Title : Oxaliplatin-based chemotherapy is more beneficial in KRAS mutant than in KRAS wild-type metastatic colorectal cancer patients.

Pub. Date : 2014

PMID : 24505265






8 Functional Relationships(s)
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1 Oxaliplatin-based chemotherapy is more beneficial in KRAS mutant than in KRAS wild-type metastatic colorectal cancer patients. Oxaliplatin KRAS proto-oncogene, GTPase Homo sapiens
2 Oxaliplatin-based chemotherapy is more beneficial in KRAS mutant than in KRAS wild-type metastatic colorectal cancer patients. Oxaliplatin KRAS proto-oncogene, GTPase Homo sapiens
3 In KRAS mutant patients who had used oxaliplatin-based regimens (N = 131), the OS was significantly longer than that in KRAS mutant patients who had never-used oxaliplatin-based regimens (N = 38). Oxaliplatin KRAS proto-oncogene, GTPase Homo sapiens
4 The OS was 28.8 months [95% confidence interval (CI): 23.2-34.4] in KRAS mutant patients who had used oxaliplatin-based regimens versus 17.8 months [95% CI: 6.5-29.1] in KRAS mutant patients who had never-used oxaliplatin-based regimens (P = 0.026). Oxaliplatin KRAS proto-oncogene, GTPase Homo sapiens
5 The OS was 28.8 months [95% confidence interval (CI): 23.2-34.4] in KRAS mutant patients who had used oxaliplatin-based regimens versus 17.8 months [95% CI: 6.5-29.1] in KRAS mutant patients who had never-used oxaliplatin-based regimens (P = 0.026). Oxaliplatin KRAS proto-oncogene, GTPase Homo sapiens
6 In multivariate analyses, patients who had used oxaliplatin-based regimens remains an independent prognostic factor for longer OS in KRAS mutant mCRC patients. Oxaliplatin KRAS proto-oncogene, GTPase Homo sapiens
7 In conclusion, oxaliplatin-based regimens are more beneficial in KRAS mutant than in KRAS wild-type mCRC patients. Oxaliplatin KRAS proto-oncogene, GTPase Homo sapiens
8 In conclusion, oxaliplatin-based regimens are more beneficial in KRAS mutant than in KRAS wild-type mCRC patients. Oxaliplatin KRAS proto-oncogene, GTPase Homo sapiens