Predictive, Oncogenic evidence:

Predictive: The abstract discusses how BRAF(V600E)-mutant melanoma patients generally benefit from RAF inhibitors like vemurafenib, but some do not respond, indicating a correlation between the variant and treatment response. This suggests that the presence of the V600E variant can influence the effectiveness of specific therapies, making it predictive of treatment outcomes.

Oncogenic: The variant BRAF(V600E) is implicated in driving tumor proliferation in melanoma, as indicated by its association with BRAF-mediated cell proliferation. This suggests that the variant contributes to tumor development or progression, classifying it as oncogenic.

Predictive, Oncogenic evidence:

Predictive: The study indicates that the PIK3CA-p.Glu545Lys mutation did not respond to crizotinib, suggesting that this variant may abrogate the response to the therapy. This aligns with the predictive evidence type as it discusses the variant's impact on treatment response.

Oncogenic: The mention of the PIK3CA-p.Glu545Lys mutation in the context of lung adenocarcinomas and its co-occurrence with MET exon 14 skipping mutation suggests a role in tumor development or progression, which supports the oncogenic evidence type.

Predictive, Oncogenic evidence:

Predictive: The study demonstrates that FLT3 mutations correlate with increased sensitivity to the therapy SU11248, as evidenced by the statement that "FLT3 internal tandem duplication (ITD) mutants showed increased sensitivity relative to FLT3-WT." This indicates a relationship between the variant and treatment response.

Oncogenic: The abstract mentions that activating mutations in FLT3 occur in up to 30% of patients with acute myeloid leukemia (AML), suggesting that these mutations contribute to tumor development or progression, which aligns with the definition of oncogenic variants.

Predictive evidence:

Predictive: The abstract states that responses were seen across Bcr-Abl mutants, except T315I, indicating that the presence of the T315I variant correlates with resistance to the therapy bosutinib. This suggests that T315I is predictive of treatment response in patients with chronic myeloid leukemia.

Predictive, Prognostic evidence:

Predictive: The study assesses the predictive role of KIT mutations for response to treatment with the kinase inhibitor sunitinib, indicating that the presence of these mutations correlates with treatment outcomes.

Prognostic: The results indicate that KIT mutations are associated with a significantly shortened survival time in patients with stage IV melanoma, suggesting that these mutations serve as an adverse prognostic factor independent of therapy.

nan evidence:

Missing abstract

Predictive evidence:

Predictive: The study discusses the efficacy of dasatinib in patients with imatinib-resistant chronic myeloid leukemia (CML-AP), indicating that response rates were evaluated in relation to the presence of BCR-ABL mutations, which suggests a correlation with treatment response. The mention of significant hematologic and cytogenetic responses further supports the predictive nature of the variant's role in therapy outcomes.

Predictive, Prognostic evidence:

Predictive: The study discusses the efficacy of dasatinib in patients with chronic myelogenous leukemia in accelerated phase (CML-AP) who are resistant or intolerant to imatinib, indicating that the presence of the BCR-ABL variant correlates with treatment response to dasatinib. The results show significant major and complete hematologic responses, demonstrating the predictive nature of the variant in relation to therapy outcomes.

Prognostic: The study reports on the 12-month progression-free survival and overall survival rates of patients treated with dasatinib, which indicates that the variant's presence correlates with disease outcomes independent of therapy. The overall survival rate of 82% suggests a prognostic implication of the variant in this patient population.

Predictive evidence:

Predictive: The study indicates that EGFR mutations correlate with clinical features of gefitinib response, suggesting that these mutations can predict the likelihood of a positive response to the therapy. The results show a significant difference in response rates to gefitinib based on the presence of EGFR mutations compared to tumors without these alterations.

Predictive, Oncogenic evidence:

Predictive: The abstract mentions that the novel EGFR mutations, including L858R, are "activating mutations responsive to erlotinib," indicating a correlation between the variant and response to a specific therapy. This suggests that the presence of the L858R mutation may influence treatment outcomes with erlotinib.

Oncogenic: The results section discusses the introduction of various mutations, including L858R, into the EGFR coding sequence and their evaluation in vitro, which implies that these mutations contribute to tumor development or progression. The context of assessing the responsiveness of mutant receptors to EGFR inhibitors further supports the oncogenic nature of the L858R variant.

Predictive, Oncogenic evidence:

Predictive: The study discusses how alterations in the EGFR tyrosine kinase domain, including the T790M variant, are associated with erlotinib resistance, indicating that this variant correlates with treatment response and resistance to therapy.

Oncogenic: The presence of the T790M variant is implied to contribute to tumor development or progression, as it is mentioned in the context of 'oncogene addiction' and its role in EGFR signaling, which is critical for cancer cell survival.

Predictive, Oncogenic evidence:

Predictive: The abstract mentions that "most are sensitive to erlotinib and gefitinib," indicating that the L858R variant is associated with a response to these therapies, which classifies it as predictive evidence.

Oncogenic: The results section discusses how various EGFR mutations, including substitutions for L858, contribute to tumor development in lung adenocarcinomas, demonstrating the oncogenic nature of the L858R variant.

Predictive evidence:

Predictive: The presence of the G776insV_G/C mutation in ERBB2 correlates with sensitivity to the HKI-272 therapy, indicating that patients with this mutation may benefit from this specific treatment. The study demonstrates that cells harboring this mutation respond positively to the dual-specific kinase inhibitor, which is a clear indication of predictive evidence.

Predictive, Diagnostic evidence:

Predictive: The study provides evidence that somatic mutations in the EGFR gene's TK domain are associated with sensitivity to gefitinib and erlotinib, as indicated by the significant differences in mutation presence between gefitinib-sensitive and gefitinib-refractory tumors (P = 0.004 and P = 0.003, respectively). This suggests that the presence of these mutations correlates with a positive response to these therapies.

Diagnostic: The abstract mentions that most mutation-positive tumors were adenocarcinomas from "never smokers," indicating a specific association between EGFR mutations and this subtype of lung cancer. This classification helps define a distinct subset of lung cancers based on the presence of these mutations.

Predictive, Diagnostic evidence:

Predictive: The abstract states that mutations of the epidermal growth factor receptor (EGFR) gene in non-small-cell lung cancer (NSCLC) patients predict the patients who will respond to EGFR tyrosine kinase inhibitor (TKI) treatment, indicating a direct correlation between the variant and treatment response.

Diagnostic: The study analyzes EGFR mutations in primary and metastatic tumors, which suggests that these mutations are being used to classify or define the disease state in NSCLC patients, particularly in the context of treatment planning.

Predictive, Oncogenic evidence:

Predictive: The T854A mutation is associated with acquired resistance to EGFR tyrosine kinase inhibitors, specifically gefitinib and erlotinib, indicating that this variant correlates with treatment response. The abstract mentions that the T854A mutation abrogates the inhibition of tyrosine phosphorylation by erlotinib, highlighting its role in resistance to therapy.

Oncogenic: The T854A mutation is described as a second-site acquired resistance mutation in the context of lung adenocarcinoma, suggesting that it contributes to tumor progression and development by enabling resistance to targeted therapies. The identification of this mutation in a patient with EGFR-mutant lung adenocarcinoma supports its role in oncogenesis.

Predictive, Diagnostic, Prognostic evidence:

Predictive: The study indicates that the presence of an EGFR mutation may increase responsiveness to erlotinib, suggesting a correlation between the variant and treatment response. This aligns with the predictive evidence type as it discusses the variant's impact on therapy effectiveness.

Diagnostic: The investigation of EGFR expression and mutations in tumor samples from non-small-cell lung cancer patients suggests that these variants are used to classify and potentially confirm the disease subtype. This supports the diagnostic evidence type as it relates to the association of the variant with the disease.

Prognostic: The results show that survival was longer in the erlotinib group when EGFR was expressed, indicating a correlation with disease outcome independent of therapy. This supports the prognostic evidence type as it discusses survival in relation to the variant without direct therapy context.

Predictive, Diagnostic, Oncogenic evidence:

Predictive: The study indicates that 7 of the 9 responders to gefitinib treatment had EGFR mutations, suggesting a correlation between these mutations and response to the therapy. This highlights the importance of detecting EGFR mutations for therapeutic decision-making in non-small cell lung cancer.

Diagnostic: The abstract mentions that EGFR mutations are detected in non-small cell lung cancer, particularly in adenocarcinoma, which supports the use of these mutations as a biomarker for classifying and confirming the disease subtype. The high mutation rate in adenocarcinoma further emphasizes the diagnostic relevance of these mutations.

Oncogenic: The conclusion suggests that EGFR mutations play an important role in the tumorigenesis of lung adenocarcinoma, indicating that these somatic mutations contribute to tumor development and progression. This is supported by the identification of mutations specifically in tumor tissues from patients with adenocarcinoma.

Predictive, Diagnostic evidence:

Diagnostic: The study indicates that EGFR mutations are significantly associated with adenocarcinoma histology and smoking status, suggesting that these mutations can be used to classify a distinct subset of pulmonary adenocarcinoma. The presence of EGFR mutations in specific patient demographics (e.g., female, never-smokers) further supports their role as a diagnostic marker in lung cancer.

Predictive: The abstract mentions that mutations in the EGFR gene occur in a subset of lung cancer patients showing a dramatic response to EGFR tyrosine kinase inhibitors, indicating that these mutations correlate with treatment response. This suggests that the presence of EGFR mutations can predict sensitivity to specific therapies targeting this pathway.

Predictive, Diagnostic evidence:

Diagnostic: The study identifies EGFR mutations, including the absence of L858R, in a specific subtype of lung cancer (lymphoepithelioma-like carcinomas), indicating that these mutations can be used to classify or define this disease subtype.

Predictive: The mention of the potential benefits of EGFR tyrosine kinase inhibitors for patients with inoperable LELCs suggests a correlation between the presence of EGFR mutations and response to therapy, even though L858R specifically was not present.

Predictive, Diagnostic, Prognostic evidence:

Predictive: The study discusses the association between EGFR mutations, including L858R, and gefitinib treatment response, indicating that gefitinib responsiveness is significantly associated with EGFR mutations. This suggests that the presence of the L858R variant may correlate with the response to gefitinib therapy in NSCLC patients.

Prognostic: The abstract mentions the median survival for responders and non-responders, indicating that the presence of the L858R mutation may correlate with disease outcome, specifically survival, independent of therapy. The reported median survival times for responders and non-responders provide insight into the prognostic implications of this variant.

Diagnostic: The study identifies the L858R mutation as the most common mutation in non-responders, which implies its role in classifying or associating with a specific disease subtype (in this case, non-small cell lung cancer). This suggests that the presence of this mutation can be used to define or confirm the disease in the context of treatment response.

Predictive, Diagnostic evidence:

Diagnostic: The study investigates the presence of EGFR TKD mutations in various subtypes of non-small-cell lung cancer (NSCLC), indicating that these mutations can be used to classify and define specific disease subtypes, particularly in relation to adenocarcinoma components.

Predictive: The conclusion suggests that patients with NSCLC harboring EGFR TKD mutations are considered candidates for molecular therapies targeting EGFR, indicating a correlation between the presence of these mutations and potential treatment options.

Predictive, Oncogenic evidence:

Predictive: The study discusses how the T790M variant is associated with resistance to EGFR inhibitors, indicating that it correlates with treatment response and resistance to therapy. This is highlighted by the mention of AZD9291 overcoming T790M-mediated resistance, which directly relates to the variant's impact on therapy effectiveness.

Oncogenic: The T790M variant is described as a resistance mutation that contributes to disease progression in patients with advanced EGFR-mutant non-small cell lung cancer (NSCLC). This suggests that the variant plays a role in tumor development and progression, aligning with the oncogenic evidence type.

Predictive, Oncogenic evidence:

Predictive: The abstract discusses how mutations in the EGFR kinase domain, including S768I, are associated with clinical responsiveness to gefitinib in patients with non-small-cell lung cancers (NSCLC), indicating a correlation with treatment response.

Oncogenic: The abstract mentions that the S768I mutation, along with other EGFR mutations, contributes to various changes in EGFR's regulatory mechanisms, which may lead to constitutive activation and oncogenesis in NSCLC, suggesting its role in tumor development.

nan evidence:

Missing abstract

Diagnostic evidence:

Diagnostic: The abstract discusses the significant risk for intra-anal HPV-related cancers among gay and other men who have sex with men, indicating that the variant (in this case, the HPV-related cancers) is associated with a specific disease context. This suggests a role in defining or confirming a disease subtype related to anal cancer screening.

Predictive, Diagnostic evidence:

Predictive: The study discusses how EGFR mutation status, including the L858R variant, is associated with sensitivity to treatment with EGFR-tyrosine kinase inhibitors (TKIs) like erlotinib and gefitinib, indicating a correlation with treatment response.

Diagnostic: The mention of EGFR mutation status, including L858R, as a criterion for selecting patients for first-line therapy suggests that this variant is used to classify patients for treatment, thereby serving a diagnostic purpose in the context of non-small cell lung cancer.

Predictive, Functional evidence:

Predictive: The study discusses the pharmacokinetics of dactinomycin and its relationship with toxicity, indicating that patients who experienced any level of toxicity had a higher AUC0-6, suggesting a correlation between the variant (in this case, the dosing or response to dactinomycin) and treatment response or sensitivity to the therapy.

Functional: The pharmacokinetic analysis indicates that the plasma concentrations and exposure levels of dactinomycin are influenced by the administered dose, which suggests that the variant may alter the drug's molecular or biochemical function in the body, particularly in relation to its pharmacokinetics.

Predictive, Diagnostic evidence:

Diagnostic: The study identifies the presence of the L858R mutation in pleomorphic carcinomas, indicating its association with this specific subtype of lung cancer. This suggests that the mutation can be used to classify or confirm the diagnosis of pleomorphic carcinoma.

Predictive: The conclusion mentions that patients with inoperable pleomorphic carcinomas are likely to benefit from treatment with EGFR tyrosine kinase inhibitors, indicating that the presence of the L858R mutation may correlate with response to this specific therapy.

Predictive, Oncogenic evidence:

Predictive: The abstract discusses how the T790M mutation is frequently linked to resistance against first-generation EGFR inhibitors, indicating that this variant correlates with treatment resistance. This suggests that the presence of T790M can predict the response to specific therapies, particularly in the context of lung cancer treatment.

Oncogenic: The T790M mutation is described as an acquired point mutation in the EGFR kinase domain that contributes to resistance mechanisms in lung adenocarcinoma, implying its role in tumor progression. This aligns with the definition of an oncogenic variant, as it is associated with cancer-driving behavior.

Oncogenic evidence:

Oncogenic: The variant 295-298delTCAT is described as a rare sequence alteration in the context of the dihydropyrimidine dehydrogenase (DPD) gene, which is implicated in DPD malfunction. This suggests a potential role in tumor development or progression, particularly in relation to the intolerance to fluoropyrimidine drugs, indicating its relevance in cancer biology.

Predictive, Diagnostic, Oncogenic evidence:

Predictive: The abstract states that "activating mutations of EGFR are found frequently in a subgroup of patients with non-small cell lung cancer (NSCLC) and are highly correlated with the response to gefitinib and erlotinib." This indicates that the variant is associated with treatment response, classifying it as predictive evidence.

Diagnostic: The abstract mentions that "EGFR mutations were found in 102 of the total 349 tumors," suggesting that these mutations are used to classify or define a specific subgroup of NSCLC patients. This supports the classification as diagnostic evidence.

Oncogenic: The abstract discusses the implications of EGFR mutations in the context of tumor development, stating that "a dual genetic change of EGFR can occur in the same allele... which may imply a more selective growth advantage in a cancer cell." This indicates that the variant contributes to tumor progression, classifying it as oncogenic evidence.

Predictive, Diagnostic evidence:

Predictive: The study indicates that patients with EGFR mutations, including the L858R variant, had a significantly better response rate (82%) and longer time to progression (median, 12.6 months) when treated with gefitinib compared to those with wild-type EGFR, demonstrating the predictive value of this variant for treatment outcomes.

Diagnostic: The presence of the L858R mutation is mentioned as part of the broader category of EGFR mutations in patients with non-small-cell lung cancer (NSCLC), which helps classify these patients as having a specific subtype of the disease that is associated with better clinical outcomes when treated with gefitinib.

Predictive, Oncogenic evidence:

Predictive: The study discusses the resistance of the D816V mutation to the kinase inhibitor imatinib mesylate and its sensitivity to the tyrosine kinase inhibitor PKC412, indicating that the variant correlates with response to specific therapies. This suggests that D816V can influence treatment options for c-KIT-positive malignancies.

Oncogenic: The D816V mutation is associated with the transformation of cells in the murine hematopoietic cell line Ba/F3, demonstrating its role in tumor development or progression. This indicates that D816V contributes to oncogenic processes in hematologic malignancies.

Predictive evidence:

Predictive: The abstract mentions that the relapsed thymic carcinoma patient showed a positive response to sorafenib, which indicates that the C-KIT exon 11 mutation correlates with sensitivity to this specific therapy. This suggests that the variant may play a role in predicting treatment response.

Diagnostic, Oncogenic evidence:

Diagnostic: The study evaluates the prevalence of EGFR mutations, including L858R, in thymomas and thymic carcinomas, indicating its potential role in classifying these tumors and exploring targeted therapies. The mention of specific mutations in the context of tumor types supports the diagnostic classification.

Oncogenic: The presence of the L858R mutation in EGFR, a known driver mutation in various cancers, suggests its role in tumor development or progression, particularly in the context of thymomas and thymic carcinomas. This aligns with the oncogenic classification as it indicates a somatic variant contributing to cancer.

Predictive, Diagnostic evidence:

Diagnostic: The abstract mentions that the study evaluated patients with metastatic melanoma "harboring KIT alterations, either mutations or amplifications," which includes the Leu576Pro variant. This indicates that the variant is used to classify or define a specific disease subtype.

Predictive: The study discusses the anti-tumor activity of nilotinib in patients with KIT mutations, including Leu576Pro, and reports treatment responses, indicating a correlation between the variant and response to therapy. This suggests that the variant may influence the effectiveness of the treatment.

nan evidence:

Missing abstract

nan evidence:

Missing abstract

Diagnostic, Oncogenic evidence:

Diagnostic: The study identifies a missense point mutation (Trp557Gly) in KIT exon 11 associated with neurofibromatosis type 1-related GISTs, indicating its role in classifying this specific subtype of tumors.

Oncogenic: The presence of the Trp557Gly mutation in the extramural portion of the largest tumor suggests that this somatic variant contributes to tumor development in the context of GISTs.

Oncogenic evidence:

Oncogenic: The abstract indicates that BRAF mutations (V600E) were found in gastrointestinal stromal tumors (GISTs) that were wild type for KIT and PDGFRA, suggesting that these mutations contribute to the tumor development in this context. The statement about the pathogenetic significance of BRAF mutations in wild type GISTs supports the classification of V600E as an oncogenic variant.

Oncogenic evidence:

Oncogenic: The abstract indicates that BRAF mutations (V600E) were found in gastrointestinal stromal tumors (GISTs) and suggests that these mutations have pathogenetic significance in wild type GISTs, implying that the variant contributes to tumor development or progression.

Predictive, Oncogenic evidence:

Predictive: The study discusses the detection of ALK mutations, including p.C1156Y, in post-treatment tumor samples and highlights their role in crizotinib resistance, indicating a correlation between the presence of this variant and resistance to the therapy.

Oncogenic: The mention of ALK mutations, such as C1156Y, in the context of resistance mechanisms to ALK-TKI suggests that these somatic variants contribute to tumor progression and development, particularly in the setting of non-small cell lung cancer.

Diagnostic, Oncogenic evidence:

Diagnostic: The study discusses ALK gene rearrangements as defining a distinct molecular subset of non-small cell lung cancer (NSCLC), indicating that these rearrangements are used to classify or confirm the disease subtype.

Oncogenic: The presence of ALK rearrangements is implicated in the development of ALK-positive NSCLC, and the study highlights that these rearrangements are associated with resistance to crizotinib, suggesting their role in tumor progression.

Predictive, Oncogenic evidence:

Predictive: The study discusses the efficacy of FLT3 inhibitors (sunitinib and sorafenib) against the D835Y variant, indicating that the sensitivity to these therapies varies based on the specific FLT3 mutations, including D835Y. This suggests a correlation between the presence of the D835Y variant and the response to these treatments, which aligns with the predictive evidence type.

Oncogenic: The abstract mentions that activating mutations in FLT3, including D835Y, are frequent transforming events in acute myeloid leukemia, indicating that this variant contributes to tumor development or progression. This supports the classification of D835Y as an oncogenic variant.

nan evidence:

There are no mentions of variants in the abstract or results section of the study provided. Therefore, no CIViC evidence types can be classified based on the information given.

Diagnostic, Prognostic evidence:

Prognostic: The K-ras codon-12 point mutation was identified as a strong unfavorable prognostic factor, with a significant difference in overall survival and disease-free survival between patients with and without the mutation. This indicates that the presence of the mutation correlates with poorer outcomes independent of therapy.

Diagnostic: The presence of K-ras point mutations is used to define a subgroup of patients with lung adenocarcinoma, indicating its role in classifying the disease and its associated prognosis. This classification is supported by the study's findings that highlight the mutation's prevalence in a specific cancer type.

Prognostic evidence:

Prognostic: The study investigates the prognostic importance of codon 12 K-ras mutations in early-stage non-small-cell lung cancer (NSCLC), noting that for stage II patients, the presence of K-ras mutations was associated with a statistically significant adverse effect on survival, indicating a correlation with disease outcome.

Predictive, Diagnostic, Prognostic evidence:

Diagnostic: The study aims to define patient characteristics associated with K-ras mutation, indicating its potential use as a biomarker for classifying patients with non-small-cell lung cancer (NSCLC).

Prognostic: The results show a strong association between K-ras mutation and decreased patient survival, particularly in stage I tumors, suggesting that this mutation correlates with disease outcome independent of therapy.

Predictive: The study indicates that K-ras codon 12 mutation is a statistically significant predictor of patient survival after adjusting for various factors, highlighting its potential role in predicting treatment outcomes.

Predictive, Prognostic evidence:

Predictive: The study discusses the relationship between mutations in KRAS and PIK3CA and the effectiveness of gefitinib treatment, indicating that tumors with KRAS mutations did not respond to gefitinib, while some with PIK3CA mutations showed a partial response. This suggests that the presence of these mutations can predict the response to gefitinib therapy.

Prognostic: The results indicate that survival was significantly longer in patients with EGFR mutations or in those without KRAS mutations, suggesting that these factors correlate with disease outcome independent of therapy. This highlights the prognostic value of these mutations in lung cancer patients.

Predictive, Prognostic evidence:

Predictive: The study indicates that KRAS mutations are significantly associated with the absence of response to cetuximab therapy, demonstrating that these mutations predict resistance to this treatment.

Prognostic: The overall survival of patients without KRAS mutations was significantly higher compared to those with mutations, indicating that KRAS mutations correlate with worse prognosis independent of therapy.

Predictive, Prognostic evidence:

Predictive: The study indicates that KRAS mutation status is a candidate marker for predicting survival in patients with metastatic colorectal cancer treated with cetuximab, highlighting the correlation between KRAS wild-type status and better overall survival and response to treatment.

Prognostic: The results show that median overall survival was significantly better in KRAS wild-type patients compared to KRAS mutants, indicating that KRAS status correlates with disease outcome independent of therapy.

Prognostic evidence:

Prognostic: The study reports that KRAS mutations in codon 12 and codon 13 are significantly associated with shorter disease-free survival (DFS) in patients with stage III colon adenocarcinoma, indicating that these mutations correlate with disease outcome independent of therapy. The multivariate hazard ratios provided further support the prognostic impact of these mutations on survival.

Predictive, Diagnostic evidence:

Predictive: The study discusses how patients with the KRAS p.G13D mutation are currently excluded from treatment with cetuximab, indicating that the presence of this variant correlates with a lack of response to this therapy. The analysis of progression-free survival and overall survival in relation to the mutation status further supports this predictive evidence.

Diagnostic: The abstract mentions that patients with activating mutations at codon 13 of the KRAS gene are excluded from treatment with certain therapies, which implies that the presence of the p.G13D mutation is used to classify patients regarding their eligibility for cetuximab treatment. This establishes the variant's role in defining a specific patient subgroup in metastatic colorectal cancer.

Predictive evidence:

Predictive: The study discusses the utility of KRAS gene mutation testing in predicting response to anti-EGFR monoclonal antibody therapy, indicating that patients with KRAS mutations in codon 12 or 13 do not benefit from this treatment. This clearly correlates the presence of specific KRAS mutations with resistance to therapy, fulfilling the criteria for predictive evidence.

Predictive, Diagnostic evidence:

Diagnostic: The abstract mentions "greater understanding of the genetic basis of inherited colorectal cancer and identification of patients at risk," indicating that the variant is used to classify or define a disease or subtype.

Predictive: The abstract discusses the importance of "biomarker development... to aid selection of patients likely to respond to therapy," which suggests that the variant correlates with treatment response or sensitivity to specific therapies.

Diagnostic, Oncogenic evidence:

Diagnostic: The study discusses the correlation between the intermediate-methylation epigenotype and KRAS-mutation((+)), indicating that the presence of this variant can be used to classify or define a specific subtype of colorectal cancer. This association suggests that KRAS mutations are relevant in the context of epigenotype classification in adenomas.

Oncogenic: The mention of KRAS-mutation((+)) in the context of adenoma development implies that this somatic variant contributes to tumor progression, as it is associated with the intermediate-methylation epigenotype in colorectal cancer. This suggests a role for KRAS mutations in the oncogenic process of colorectal carcinogenesis.

Prognostic, Oncogenic evidence:

Oncogenic: The study mentions a single mutation of the BRAF gene (D594G) detected in the context of locally advanced rectal cancer, indicating that this somatic variant may contribute to tumor development or progression.

Prognostic: The results indicate that CIMP positivity correlates with worse disease-free survival outcomes, suggesting that the presence of certain molecular markers, potentially including variants like D594G, may indicate a higher likelihood of poor clinical outcomes.

Predictive, Oncogenic evidence:

Predictive: The abstract mentions that assessing BRAF V600E mutations might help optimize the selection of patients for anti-EGFR monoclonal antibodies, indicating a correlation between the variant and response to therapy.

Oncogenic: The results section describes how the BRAF V600E mutation induces structural changes in the RAF protein that increase its kinase activity, suggesting that this somatic variant contributes to tumor development and progression through the dysregulation of the RAS/RAF/MAPKs signaling pathway.

Predisposing, Oncogenic evidence:

Oncogenic: The abstract discusses how oncogenic mutations in the H-ras, N-ras, or K-ras genes lead to tumor development by disrupting normal signaling pathways, indicating that these somatic mutations contribute to tumorigenesis.

Predisposing: The abstract mentions germline mutations in Ras and other components of Ras signaling pathways that are associated with familial syndromes, suggesting an inherited risk for developing certain diseases.

Oncogenic evidence:

Oncogenic: The study demonstrates that the K-ras codon 12 mutation contributes to tumor development and progression, as evidenced by the more aggressive, invasive, and metastatic characteristics of tumors derived from this mutation compared to those from codon 13. The use of in vitro and in vivo experimental systems to evaluate the tumorogenic capacity further supports the oncogenic nature of the K-ras codon 12 mutation.

Predictive, Diagnostic evidence:

Predictive: The study demonstrates that KRAS mutations correlate with poor response to panitumumab in metastatic colorectal cancer (mCRC), indicating that KRAS status can predict treatment efficacy. The results show a significant difference in progression-free survival (PFS) between wild-type and mutant KRAS groups, supporting the predictive value of KRAS status for therapy response.

Diagnostic: The abstract mentions that KRAS mutations were detected and their status was ascertained in a significant portion of patients, indicating that KRAS status is used to classify patients in terms of their eligibility for panitumumab treatment. This establishes KRAS as a potential diagnostic marker for selecting patients with mCRC for anti-EGFR therapy.

Predictive evidence:

Predictive: The study provides evidence that k-RAS mutations are significantly associated with an absence of response to EGFR tyrosine-kinase inhibitors in NSCLC and anti-EGFR monoclonal antibodies in mCRC, indicating that these mutations serve as predictive biomarkers for resistance to these therapies. The analysis highlights the specificity of k-RAS mutations as negative predictors of treatment response, reinforcing their role in therapeutic decision-making.

Predictive evidence:

Predictive: The study evaluates whether mutation status of k-ras, b-raf, or p53 could predict which patients were more likely to respond to bevacizumab, indicating a focus on the relationship between these variants and treatment response. The mention of hazard ratios for death among patients with different mutation statuses further supports this classification as it relates to therapy outcomes.

nan evidence:

Missing abstract

Predictive, Prognostic evidence:

Prognostic: The study indicates that the BRAF V600E mutation is associated with a significantly higher likelihood of disease progression and death, marking it as a poor prognostic factor independent of treatment regimen. This is supported by the reported hazard ratios for early relapse and death, demonstrating its impact on patient outcomes.

Predictive: The BRAF V600E mutation is mentioned as a predictor for early relapse on first-line therapy, suggesting that it correlates with treatment response. The study discusses the implications of this mutation for patient selection and stratification in clinical trials, indicating its relevance in predicting therapy outcomes.

Predictive, Prognostic evidence:

Predictive: The study indicates that the mutation status of the K-ras gene significantly affects the response to cetuximab treatment, with wild-type K-ras tumors showing improved overall and progression-free survival compared to those with mutated K-ras tumors. This correlation between K-ras mutation status and treatment response classifies the evidence as predictive.

Prognostic: The abstract mentions that the mutation status of the K-ras gene has treatment-independent prognostic value, suggesting that it correlates with survival outcomes regardless of therapy. This aligns with the definition of prognostic evidence, as it indicates the potential impact of K-ras mutation status on overall survival and progression-free survival.

Predictive evidence:

Predictive: The study discusses how BCR-ABL kinase domain point mutations lead to resistance against the ABL kinase inhibitor imatinib, indicating that these mutations correlate with treatment response and resistance to specific therapies. The mention of BMS-354825's effectiveness against imatinib-resistant mutants further supports the predictive nature of these variants in relation to therapy outcomes.

Oncogenic evidence:

Oncogenic: The study identifies a novel double L858R + E884K somatic mutation of the EGFR, indicating that this variant contributes to tumor development or progression in the context of the patient's lung adenocarcinoma. The presence of this mutation is associated with the patient's disease state and treatment resistance, highlighting its role in oncogenesis.

Predictive, Diagnostic evidence:

Predictive: The study discusses the T790M mutation as a secondary mutation that contributes to acquired resistance to gefitinib, indicating a correlation with treatment response. This aligns with the definition of predictive evidence, as it relates to how the presence of the T790M variant affects the efficacy of a specific therapy.

Diagnostic: The T790M mutation is mentioned in the context of identifying tumors with acquired resistance to gefitinib, suggesting its role in classifying or confirming a subtype of non-small cell lung cancer. This supports the diagnostic evidence type, as it is used to define a specific condition related to treatment resistance.

Predictive, Oncogenic, Functional evidence:

Predictive: The abstract discusses a patient with an EGFR mutation who was initially responsive to gefitinib but later relapsed due to a second mutation (threonine-to-methionine) that resulted in gefitinib resistance, indicating a correlation between the variant and treatment response.

Oncogenic: The presence of the threonine-to-methionine mutation is described as contributing to gefitinib resistance, which suggests that this somatic variant plays a role in tumor progression and development in the context of non-small-cell lung cancer.

Functional: The abstract mentions that structural modeling and biochemical studies demonstrated that the threonine-to-methionine mutation alters the response to gefitinib, indicating a change in molecular function related to drug interaction.

Predictive, Diagnostic evidence:

Predictive: The study discusses the use of erlotinib as maintenance therapy for patients with non-small-cell lung cancer (NSCLC) and reports that median progression-free survival (PFS) was significantly longer with erlotinib compared to placebo, indicating a correlation between the EGFR status and response to the therapy. This suggests that the variant related to EGFR may predict sensitivity to erlotinib treatment.

Diagnostic: The study stratified patients by EGFR immunohistochemistry status, indicating that the presence of EGFR protein overexpression is used to classify patients and assess their eligibility for erlotinib treatment. This demonstrates the role of the EGFR variant in defining a specific disease subtype within NSCLC.

Predictive, Oncogenic evidence:

Predictive: The study discusses the response of a patient with a BRAF V600E mutation to vemurafenib, indicating that the presence of this variant correlates with a dramatic therapeutic response, thus providing evidence for its predictive value in treatment outcomes.

Oncogenic: The BRAF V600E mutation is mentioned in the context of contributing to the activity of the mitogen-activated protein kinase pathway in malignant peripheral nerve sheath tumors, suggesting its role in tumor development or progression.

Predictive, Oncogenic evidence:

Predictive: The study discusses how the presence of the BRAF(V600E) variant correlates with the clinical activity of RAF inhibitors in melanoma patients, indicating that this variant is associated with treatment response and resistance mechanisms.

Oncogenic: The evidence presented shows that the BRAF(V600E) variant contributes to tumor development and progression, particularly through its role in dimerization and resistance to RAF inhibitors, which is characteristic of oncogenic behavior.

nan evidence:

Missing abstract

Predictive, Prognostic evidence:

Predictive: The study discusses the response rates to high-dose IL-2 therapy in patients with metastatic melanoma, indicating that baseline performance status and prior systemic therapy are predictive factors for response to treatment. This aligns with the predictive evidence type as it correlates the variant's presence with treatment response.

Prognostic: The results mention that 28% of responding patients remain progression-free, and disease did not progress in any patient responding for more than 30 months, indicating a correlation between the variant and disease outcome independent of therapy. This supports the classification as prognostic evidence.

Predictive, Oncogenic evidence:

Predictive: The study discusses the response rate to the RAF-selective inhibitor PLX4032 in patients with B-RAF(V600E)-positive melanomas, indicating that the presence of this variant correlates with treatment response. The mention of an "80% anti-tumour response rate" highlights the predictive nature of the variant in relation to therapy effectiveness.

Oncogenic: The abstract states that B-RAF(V600E) mutations occur in a significant percentage of melanomas and are implicated in tumor development, which supports the classification of this variant as oncogenic. The evidence of acquired resistance mechanisms further emphasizes its role in tumor progression.

Predictive, Prognostic, Oncogenic evidence:

Predictive: The study demonstrates that the BRAF V600E mutation correlates with improved response rates to the BRAF kinase inhibitor vemurafenib, indicating its predictive value for treatment efficacy in metastatic melanoma.

Prognostic: The results show that patients with the BRAF V600E mutation treated with vemurafenib had significantly improved overall survival rates compared to those treated with dacarbazine, suggesting that this variant is prognostic for better disease outcomes.

Oncogenic: The presence of the BRAF V600E mutation is implicated in the tumor development and progression in melanoma, as evidenced by the improved survival outcomes associated with targeted therapy.

Predictive, Diagnostic, Prognostic, Oncogenic evidence:

Predictive: The study discusses how KRAS mutations correlate with resistance to cetuximab, indicating that these mutations are predictive of treatment response. Specifically, it highlights that KRAS mutants had a significantly lower response rate compared to wild types, demonstrating the variant's role in predicting therapy efficacy.

Diagnostic: The abstract mentions that tumors are profiled for KRAS mutations before treatment, indicating that the presence of these mutations is used to classify patients for therapy. This suggests that KRAS mutations serve as a diagnostic marker in determining treatment eligibility for cetuximab.

Prognostic: The findings indicate that KRAS mutations are associated with worse overall survival and progression-free survival, independent of therapy. The reported median overall survival and progression-free survival rates for KRAS mutants versus wild types provide evidence of the prognostic implications of these variants.

Oncogenic: The study implies that KRAS mutations contribute to tumor behavior, as they are associated with a lack of benefit from cetuximab treatment. This suggests that KRAS mutations play a role in tumor development or progression, aligning with the definition of oncogenic variants.

Predictive, Prognostic evidence:

Predictive: The study identifies that patients with tumors lacking K-ras mutations have a significantly higher disease control rate with cetuximab treatment, indicating a correlation between the K-ras variant status and treatment response. Additionally, high expression levels of the EGFR ligands epiregulin and amphiregulin are associated with better clinical responses to cetuximab, further supporting the predictive nature of these markers for therapy outcomes.

Prognostic: The results indicate that patients with high expression of EREG or AREG have significantly longer progression-free survival compared to those with low expression, suggesting that these expression levels correlate with disease outcome independent of therapy.

Oncogenic evidence:

Oncogenic: The abstract discusses BRAF mutations, including V599E, as contributing to tumor development in colorectal cancer, indicating that these mutations are biologically similar to RAS mutations and occur at a specific stage of neoplastic transformation. The presence of BRAF mutations in colorectal adenocarcinomas suggests their role in tumor progression, which aligns with the definition of oncogenic variants.

Predictive, Prognostic evidence:

Prognostic: The study reports that patients with K-ras mutations had significantly poorer overall survival compared to those without K-ras mutations, indicating that the presence of K-ras mutations correlates with disease outcome independent of therapy. The multivariate analysis further supports this association with a hazard ratio of 2.9, confirming the prognostic significance of K-ras mutations in colorectal cancer.

Predictive: The abstract states that the presence of K-ras mutations predicts poor patient prognosis in colorectal cancer, suggesting a correlation with treatment response or resistance, which aligns with the predictive evidence type.

Predictive evidence:

Predictive: The study discusses the association of mutations, including the V600E BRAF mutation, with tumor resistance to panitumumab, indicating that the presence of certain mutations may correlate with treatment response. The conclusion suggests that the absence of a K-ras mutation is associated with a better response to panitumumab, which implies a predictive role for these mutations in treatment outcomes.

Predisposing, Functional evidence:

Predisposing: The abstract mentions "germline mutations that affect components of the Ras-Raf-MEK-ERK pathway," indicating that these inherited mutations confer risk for developmental disorders, which aligns with the definition of predisposing variants.

Functional: The abstract states that "many of these mutant alleles encode proteins with aberrant biochemical and functional properties," suggesting that the variants alter molecular or biochemical function, which supports the functional evidence type.

Predictive, Diagnostic evidence:

Predictive: The study indicates that CRBN depletion leads to resistance to lenalidomide and pomalidomide, suggesting that the variant correlates with treatment response, specifically highlighting the role of CRBN in the efficacy of these therapies.

Diagnostic: The mention of CRBN as a possible biomarker for the clinical assessment of antimyeloma efficacy implies that it is used to classify or define the response to treatment in patients, thus supporting its role in diagnostic contexts.

Predictive, Oncogenic evidence:

Predictive: The study discusses how secondary kinase mutations in KIT or PDGFRA are associated with decreased imatinib sensitivity, indicating a correlation between these mutations and resistance to therapy. This suggests that the presence of these mutations can predict the response to imatinib treatment in patients with advanced GISTs.

Oncogenic: The abstract mentions that gastrointestinal stromal tumors (GISTs) commonly harbor oncogenic mutations of the KIT or PDGFRA kinases, which contribute to tumor development and progression. This indicates that these mutations play a role in the oncogenic process within GISTs.

Oncogenic, Functional evidence:

Oncogenic: The study demonstrates that KMT2D functions as a tumor suppressor and that its genetic ablation in B cells promotes lymphoma development in mice, indicating that mutations in KMT2D contribute to tumor progression.

Functional: The research shows that KMT2D affects the methylation of lysine 4 on histone H3 (H3K4) and alters the expression of a set of genes involved in critical signaling pathways, suggesting that the variant alters molecular function related to gene regulation.

nan evidence:

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nan evidence:

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nan evidence:

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nan evidence:

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Predictive evidence:

Predictive: The study indicates that IDH1 and IDH2 mutations may predict a favorable response to DNA methyltransferase inhibitors (DNMTIs) in patients with AML, as evidenced by the higher remission rates in patients with these mutations compared to those without. The odds ratio of achieving a response after treatment further supports the predictive nature of these mutations in relation to therapy outcomes.

Predictive evidence:

Predictive: The study indicates that mutated TET2 status independently predicted a higher response rate to azacitidine (AZA) treatment, with a response rate of 82% in patients with TET2 mutations compared to 45% in wild-type patients (P=0.007). This suggests that the presence of TET2 mutations correlates with sensitivity to the therapy, fulfilling the criteria for predictive evidence.

Functional evidence:

Functional: The variant R111A is referenced in the context of immunohistochemical staining with the antibody clone EPNCIR111A, indicating that it is being studied for its impact on protein expression or function. This suggests that the variant may alter the molecular or biochemical function of the protein involved.

Oncogenic evidence:

Oncogenic: The abstract discusses the identification of inactivating mutations in the SMARCA4 gene, which is implicated in the development of small cell carcinoma of the ovary, hypercalcemic type (SCCOHT). The presence of the p.Pro1180fs variant in the SCCOHT-1 tumor cell line suggests that it contributes to tumor development or progression, aligning with the definition of an oncogenic variant.

Predisposing, Oncogenic evidence:

Predisposing: The study identifies deleterious germline mutations in SMARCA4 that segregate within families affected by small cell carcinoma of the ovary, hypercalcemic type (SCCOHT), indicating that these mutations confer inherited risk for developing this malignancy.

Oncogenic: The presence of somatic mutations or loss of the wild-type allele of SMARCA4 in familial tumors suggests that these alterations contribute to tumor development or progression in SCCOHT.

Predisposing evidence:

Predisposing: The study discusses germline mutations and deletions of SMARCB1/INI1 that predispose patients to rhabdoid tumors and schwannomatosis, indicating that these variants confer inherited risk for developing these diseases. The mention of parent-to-child transmission of mutated copies of SMARCB1 further supports the classification as predisposing.

Diagnostic, Oncogenic evidence:

Oncogenic: The study identifies a rare activating mutation of AKT1 (E17K) in melanoma, suggesting that this somatic variant contributes to tumor development or progression, as it is associated with activation of the AKT pathway in human melanoma cells.

Diagnostic: The presence of the AKT1 E17K mutation is discussed in the context of its identification in melanoma specimens, indicating its potential role in classifying or defining a subtype of melanoma with specific genetic alterations.

Predictive, Oncogenic evidence:

Oncogenic: The study demonstrates that mutations at the PH-KD interface of AKT1 lead to constitutive activation of the protein, contributing to oncogenic signaling, which indicates that these somatic mutations play a role in tumor development or progression.

Predictive: The findings suggest that the AKT1 somatic mutants are not effectively inhibited by allosteric AKT inhibitors, indicating a potential resistance to therapy, which correlates with the variant's impact on treatment response.

Predictive, Oncogenic evidence:

Oncogenic: The study demonstrates that mutations at the PH-KD interface of AKT1 lead to constitutive activation of the protein, contributing to oncogenic signaling, which indicates that these somatic variants play a role in tumor development or progression.

Predictive: The findings suggest that the AKT1 somatic mutants are not effectively inhibited by allosteric AKT inhibitors, indicating a potential resistance to therapy, which correlates with the variant's impact on treatment response.

Predictive, Oncogenic evidence:

Oncogenic: The study demonstrates that mutations at the PH-KD interface of AKT1 lead to constitutive activation of the protein, contributing to oncogenic signaling, which indicates that these somatic variants play a role in tumor development or progression.

Predictive: The findings suggest that the AKT1 somatic mutants are not effectively inhibited by allosteric AKT inhibitors, indicating a potential resistance to therapy, which correlates with the variant's impact on treatment response.

Prognostic, Oncogenic evidence:

Oncogenic: The study identifies somatic mutations in gallbladder carcinoma (GBC) and highlights the role of the ErbB signaling pathway in GBC pathogenesis, indicating that these mutations contribute to tumor development or progression.

Prognostic: The multivariate analyses show that cases with ErbB pathway mutations have a worse outcome, suggesting a correlation between these mutations and disease prognosis independent of therapy.

Oncogenic evidence:

Oncogenic: The study reports the identification of ERBB3 somatic mutations that transformed colonic and breast epithelial cells in a ligand-independent manner, indicating that these mutations contribute to tumor development. Additionally, the mutant ERBB3's oncogenic activity was shown to be dependent on kinase-active ERBB2, further supporting its role in cancer progression.

Diagnostic, Oncogenic, Functional evidence:

Diagnostic: The study presents evidence that a germline mutation involving codon 600 of BRAF is associated with the development of cardio-facio-cutaneous (CFC) syndrome, indicating its role in defining a specific disease phenotype.

Oncogenic: The abstract discusses the somatic mutation p.V600E as frequently found in various tumor types, suggesting that mutations at codon 600, including p.V600G, contribute to tumor development or progression.

Functional: The in vitro analysis demonstrates that the p.V600G mutation alters the molecular function of BRAF by leading to increased ERK and ELK phosphorylation compared to wild-type BRAF, indicating a change in biochemical activity.

Oncogenic, Functional evidence:

Oncogenic: The study demonstrates that NRAS mutation leads to increased cellular proliferation and is potently tumorigenic, indicating that this somatic variant contributes to tumor development in melanoma. The comparison of transformation efficiencies between NRAS and KRAS further supports the oncogenic role of NRAS in this context.

Functional: The findings indicate that NRAS mutation enhances MYC activity in melanocytes, suggesting that this variant alters molecular function, specifically in the context of signaling pathways. This alteration in activity is critical for understanding the mechanisms behind NRAS's role in melanoma.