Department of Surgery, Gastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
Cancer Chemotherapy Center, Osaka Medical and Pharmaceutical University, Osaka, Japan.
Int J Clin Oncol. 2023 Jan;28(1):130-138. doi: 10.1007/s10147-022-02259-w. Epub 2022 Oct 28.
Safety and effectiveness of aflibercept with 5-fluorouracil/levofolinate/irinotecan have not been reported in Japanese patients with metastatic colorectal cancer (mCRC) in a real-world clinical setting.
This post-marketing surveillance enrolled patients with un-resectable advanced or recurrent mCRC who were prescribed aflibercept from December 2017 to June 2019 in Japan. Data, collected up to 1 year from starting treatment, included patient background, safety, and effectiveness assessed by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 or physician's evaluation.
Of 261 patients registered from 64 centers, 235 [53.2% male with a median age of 67 years (range 28-84)] received treatment and were included in the safety analysis. Aflibercept was received at 1st, 2nd, and ≥ 3rd line in 1.3%, 48.1%, and 50.2% of patients, respectively. Median number of treatment cycles was 6 (range 1-22) and relative dose intensity was 75.4% (range 14.3-101.8%). Adverse events (all grades) were reported in 88.5% of patients, including neutropenia (34.5%), proteinuria (24.7%), hypertension (17.0%), diarrhea (17.0%), and decreased appetite (15.3%). Three treatment-related deaths occurred by perforation of the digestive tract, pneumonia and gastrointestinal bleeding, and sudden death. The effectiveness analysis included 198 patients. Overall response rate was 6.1% (1st line, 0%; 2nd line, 10.1%; ≥ 3rd line, 2.1%) and disease control rate was 47.5% (1st line, 100%; 2nd line, 58.6%; ≥ 3rd line, 34.4%).
No new risks of aflibercept were identified in real clinical practice. Effectiveness in patients at the 2nd line was consistent with previous reports.
在真实临床环境中,尚未有研究报告 aflibercept 联合氟尿嘧啶/左亚叶酸钙/伊立替康在日本转移性结直肠癌(mCRC)患者中的安全性和有效性。
本上市后监测研究纳入了 2017 年 12 月至 2019 年 6 月期间在日本因不可切除的晚期或复发性 mCRC 而接受 aflibercept 治疗的患者。数据收集截至治疗开始后 1 年,包括患者背景、安全性以及采用实体瘤疗效评价标准(RECIST)1.1 或医生评估的有效性。
在 64 个中心登记的 261 例患者中,235 例(53.2%为男性,中位年龄 67 岁(范围 28-84))接受了治疗并纳入安全性分析。1.3%、48.1%和 50.2%的患者分别在一线、二线和三线接受 aflibercept 治疗。中位治疗周期数为 6(范围 1-22),相对剂量强度为 75.4%(范围 14.3-101.8%)。88.5%的患者发生了不良反应(所有级别),包括中性粒细胞减少症(34.5%)、蛋白尿(24.7%)、高血压(17.0%)、腹泻(17.0%)和食欲下降(15.3%)。3 例治疗相关死亡由消化道穿孔、肺炎和胃肠道出血以及猝死引起。有效性分析包括 198 例患者。总体缓解率为 6.1%(一线,0%;二线,10.1%;三线,2.1%),疾病控制率为 47.5%(一线,100%;二线,58.6%;三线,34.4%)。
在真实临床实践中未发现 aflibercept 的新风险。二线治疗患者的疗效与既往报告一致。