Efficacy of Second-Line Bevacizumab-Containing Chemotherapy for Patients with Metastatic Colorectal Cancer following First-Line Treatment with an Anti-Epidermal Growth Factor Receptor Antibody

被引:9
|
作者
Hasegawa, Hiroko [1 ,3 ]
Taniguchi, Hiroya [1 ]
Mitani, Seiichiro [1 ]
Masuishi, Toshiki [1 ]
Komori, Azusa [1 ]
Narita, Yukiya [1 ]
Kadowaki, Shigenori [1 ]
Ura, Takashi [1 ]
Ando, Masashi [1 ]
Yatabe, Yasushi [2 ]
Muro, Kei [1 ]
机构
[1] Aichi Canc Ctr Hosp, Dept Clin Oncol, Nagoya, Aichi, Japan
[2] Aichi Canc Ctr Hosp, Dept Pathol & Mol Diag, Nagoya, Aichi, Japan
[3] Osaka Natl Hosp, Dept Gastroenterol & Hepatol, Osaka, Japan
关键词
Metastatic colorectal cancer; Effect of prior use of anti-epidermal growth factor receptor antibody; Efficacy of second-line bevacizumab therapy; WILD-TYPE KRAS; K-RAS MUTATIONS; ACQUIRED-RESISTANCE; PHASE-II; FLUOROURACIL; MULTICENTER; OXALIPLATIN; LEUCOVORIN; CETUXIMAB; FOLFIRI;
D O I
10.1159/000453336
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Anti-epidermal growth factor receptor (EGFR) antibodies and bevacizumab are commonly used, sequentially, as palliative chemotherapies for patients with metastatic colorectal cancer. However, little is known about the efficacy of second-line treatments containing bevacizumab after first-line treatment with an anti-EGFR antibody. Methods: We retrospectively reviewed 128 patients who received second -line bevacizumab-containing chemotherapy and evaluated the effect of prior use of anti-EGFR antibody on the efficacy of the second-line treatment. Results: As first-line treatments, 35 of these patients received only cytotoxic chemotherapy (cohort A), 58 received bevacizumab-containing chemotherapy (cohort B), and 35 received anti-EGFR-containing chemotherapy (cohort C). The median progression free survival (PFS) with the second-line bevacizumab-containing therapy was 8.3 months in cohort C, 6.9 months in cohort A (hazard ratio [1-1R], 1.43; 95% confidence interval [CI], 0.83-2.51), and 5.6 months in cohort B (HR, 1.95; 95% CI, 1.18-3.22). Multivariate analysis showed that PFS in cohort C was the same as that in cohort A, but better than that in cohort B. The overall response rate in cohort C (25.7%) was also similar to that in cohort A (20.0%), but better than that in cohort B (10.3%). Conclusions: Prior use of anti-EGFR antibody did not adversely affect the efficacy of subsequent bevacizumab-containing chemotherapy. (C) 2017 S. Ka rger AG, Basel
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页码:205 / 212
页数:8
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