Panitumumab Provides Better Survival Outcomes Compared to Cetuximab for Metastatic Colorectal Cancer Patients Treated with Prior Bevacizumab within 6 Months

被引:3
作者
Hayashi, Kaori [1 ,4 ]
Mitani, Seiichiro [2 ]
Taniguchi, Hiroya [2 ]
Yasui, Hirofumi [1 ]
Muro, Kei [2 ]
Mori, Keita [3 ]
Gotoda, Takuji [4 ]
Yamazaki, Kentaro [1 ]
机构
[1] Shizuoka Canc Ctr, Div Gastrointestinal Oncol, 1007 Shimonagakubo, Nagaizumi, Shizuoka 4118777, Japan
[2] Aichi Canc Ctr, Dept Clin Oncol, Nagoya, Aichi, Japan
[3] Shizuoka Canc Ctr, Clin Res Ctr, Clin Res Promot Unit, Nagaizumi, Shizuoka, Japan
[4] Nihon Univ, Div Gastroenterol & Hepatol, Dept Med, Sch Med, Tokyo, Japan
关键词
Metastatic colorectal cancer; Panitumumab; Cetuximab; Epithelial growth factor receptor; Bevacizumab; Vascular endothelial growth factor; Irinotecan; Interval; WILD-TYPE KRAS; GROWTH-FACTOR RECEPTOR; PHASE-III TRIAL; OPEN-LABEL; 1ST-LINE TREATMENT; PLUS IRINOTECAN; NON-INFERIORITY; CHEMOTHERAPY; PHARMACOKINETICS; NORMALIZATION;
D O I
10.1159/000493321
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Anti-epithelial growth factor receptor (EGFR) antibodies cetuximab (Cmab) and panitumumab (Pmab) have shown survival benefit for metastatic colorectal cancer (mCRC) patients. This study aimed to compare Pmab and Cmab according to the interval between bevacizumab discontinuation and anti-EGFR antibody initiation (bevacizumab-free interval; BFI). Methods: We retrospectively evaluated mCRC patients who received Cmab or Pmab in combination with irinotecan at two institutions. Inclusion criteria were histologically confirmed mCRC, with KRAS exon 2 wild-type tumor, refractory or intolerant to fluoropyrimidines, oxali-platin, and irinotecan. Results: One-hundred-seventy-eight patients fulfilled the eligibility criteria. Among them, there was no significant difference in overall survival (OS) and progression-free survival (PFS) between the Pmab (n = 44) and Cmab groups (n = 134). Of 132 patients with BFI < 6 months, the median OS was 13.3 and 11.5 months in the Pmab (n = 39) and Cmab (n = 93) groups, respectively (p = 0.043). The median PFS was 5.8 and 4.9 months in the Pmab and Cmab groups, respectively (p = 0.055). Multivariate analysis for OS confirmed the superiority of Pmab. Conclusion: Pmab showed more favorable outcomes in patients treated with bevacizumab within the last 6 months. The interval between prior bevacizumab and subsequent anti-EGFR therapy may be useful for determining the optimal anti-EGFR therapy. (c) 2018 S. Karger AG, Basel
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收藏
页码:132 / 139
页数:8
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