10.3389/fonc.2019.00723.s001 Xia-Hong You Xia-Hong You Can Wen Can Wen Zi-Jin Xia Zi-Jin Xia Fan Sun Fan Sun Yao Li Yao Li Wei Wang Wei Wang Zhou Fang Zhou Fang Qing-Gen Chen Qing-Gen Chen Lei Zhang Lei Zhang Yu-Huang Jiang Yu-Huang Jiang Xiao-Zhong Wang Xiao-Zhong Wang Hou-Qun Ying Hou-Qun Ying Zhen Zong Zhen Zong Data_Sheet_1_Primary Tumor Sidedness Predicts Bevacizumab Benefit in Metastatic Colorectal Cancer Patients.docx Frontiers 2019 primary tumor sidedness bevacizumab mCRC prognosis survival 2019-08-14 04:15:27 Dataset https://frontiersin.figshare.com/articles/dataset/Data_Sheet_1_Primary_Tumor_Sidedness_Predicts_Bevacizumab_Benefit_in_Metastatic_Colorectal_Cancer_Patients_docx/9600437 <p>The emerging debate between primary tumor location and clinical outcome of bevacizumab treated metastatic colorectal cancer (mCRC) continues. The aim of the present study is to investigate the association between the primary tumor location and clinical outcome of 115 mCRC patients receiving bevacizumab based treatment. A meta-analysis including 21 studies was carried out to confirm the conclusion. In our prospective study, we found that right-sided mCRC commonly occurred in older cases (p = 0.03) with multiple-site metastasis (p = 0.03). Progression-free survival (PFS) of the left-sided patients undergoing bevacizumab plus a FOLFIRI regimen was superior to the right-sided cases (p = 0.03, crude HR = 0.31, 95%CI = 0.11–0.87; adjusted HR = 0.21, 95%CI = 0.06–0.66). The meta-analysis confirmed that efficacy of bevacizumab-based treatment in left-sided mCRC patients was better than the right-sided cases in the overall population (P<sub>h</sub> = 0.24, combined OR = 1.36, 95%CI = 1.07–1.72), RAS/BRAF wild-type (P<sub>h</sub> = 0.19, combined OR = 1.66, 95%CI = 1.17–2.34), clinical trial (P<sub>h</sub> = 0.23, combined OR = 1.42, 95%CI = 1.07–1.88), Caucasian population (P<sub>h</sub> = 0.18, combined OR = 1.37, 95%CI = 1.02–1.85) and first-line (P<sub>h</sub> = 0.19, combined OR = 1.48, 95%CI = 1.13–1.96) subgroups. Improved survival of bevacizumab plus chemotherapy treated left-sided mCRC patients was observed in the overall population [P<sub>h</sub> < 0.01, combined MSR = 1.09, 95%CI = 1.00–1.18 for PFS; P<sub>h</sub> < 0.01, combined MSR = 1.24, 95%CI = 1.13–1.36 for overall survival (OS)], especially in the RAS/BRAF wild-type (P<sub>h</sub> = 0.09, combined MSR = 1.10, 95%CI = 1.03–1.19 for PFS; P<sub>h</sub> = 0.02, combined MSR = 1.34, 95%CI = 1.21–1.49 for OS). These findings indicate that primary tumor sidedness can predict clinical outcome of bevacizumab-treated RAS/BRAF wild-type mCRC patients and the left-sided patients may benefit more from bevacizumab plus FOLFIRI.</p>