Chau Ian, Fakih Marwan, García-Alfonso Pilar, Linke Zdenĕk, Ruiz Casado Ana, Marques Eduardo Polo, Picard Pascaline, Celanovic Marina, Cartwright Thomas
The Royal Marsden NHS Foundation Trust, London and Surrey, Sutton SM2 5PT, UK.
City of Hope Comprehensive Cancer Center, Duarte, CA 91010, USA.
Cancers (Basel). 2020 Mar 11;12(3):657. doi: 10.3390/cancers12030657.
For patients with metastatic colorectal cancer (mCRC) that have failed a first-line oxaliplatin-based regimen, the preferred treatment option is an irinotecan-based regimen. This prospective, observational, noncomparative, post-authorization safety study (OZONE) evaluated the safety and effectiveness of aflibercept plus fluorouracil, leucovorin, and irinotecan (FOLFIRI) in patients with mCRC treated in daily practice after failure of an oxaliplatin-based regimen. Patients were grouped by age, renal impairment, hepatic impairment, race, number, and type of prior anticancer therapy. Of 766 treated patients enrolled, 59.5% were male, 94.8% had an Eastern Cooperative Oncology Group performance status of 0-1, all received previous chemotherapy (97.8% including oxaliplatin), and 58.6% had prior exposure to bevacizumab. At least one grade ≥ 3 treatment-emergent adverse event (TEAE) was reported in 68.3% of patients. Neutropenia, hypertension, diarrhea, and asthenia were the most frequently occurring grade ≥ 3 TEAEs. Antivascular endothelial growth factor class events were infrequent. Subgroup analyses did not reveal major differences in the safety profile according to age, renal and hepatic status, race, or prior anticancer therapy. For the total population, median overall survival was 12.5 months, median progression-free survival was 6.1 months, and overall response rate was 16.3%. Aflibercept in combination with FOLFIRI is a safe and efficacious regimen administered in current clinical practice to patients with mCRC previously treated with oxaliplatin. The study results, conducted in real-world clinical practice with a less selected patient population, are aligned with the VELOUR (NCT00561470) trial and no new safety issues were identified.
对于一线含奥沙利铂方案治疗失败的转移性结直肠癌(mCRC)患者,首选治疗方案是含伊立替康的方案。这项前瞻性、观察性、非对比性、上市后安全性研究(OZONE)评估了阿柏西普联合氟尿嘧啶、亚叶酸钙和伊立替康(FOLFIRI)在奥沙利铂方案治疗失败后接受日常治疗的mCRC患者中的安全性和有效性。患者按年龄、肾功能损害、肝功能损害、种族、既往抗癌治疗的次数和类型进行分组。在纳入治疗的766例患者中,59.5%为男性,94.8%的东部肿瘤协作组体能状态为0 - 1,所有患者均接受过先前的化疗(97.8%包括奥沙利铂),58.6%曾接受过贝伐单抗治疗。68.3%的患者报告了至少1次≥3级治疗中出现的不良事件(TEAE)。中性粒细胞减少、高血压、腹泻和乏力是最常出现的≥3级TEAE。抗血管内皮生长因子类事件不常见。亚组分析未显示在年龄、肾和肝状态、种族或既往抗癌治疗方面安全性存在重大差异。对于总体人群,中位总生存期为12.5个月,中位无进展生存期为6.1个月,总缓解率为16.3%。阿柏西普联合FOLFIRI是一种在当前临床实践中用于先前接受过奥沙利铂治疗的mCRC患者的安全有效的方案。在选择标准较宽松的真实世界临床实践中进行的研究结果与VELOUR(NCT00561470)试验一致,未发现新的安全问题。