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阿柏西普联合FOLFIRI方案用于接受含奥沙利铂方案治疗的韩国转移性结直肠癌患者的安全性和有效性。

Safety and effectiveness of aflibercept in combination with FOLFIRI in Korean patients with metastatic colorectal cancer who received oxaliplatin-containing regimen.

作者信息

Beom Seung-Hoon, Kim Jong Gwang, Baik Seung Hyuk, Shin Seong Hoon, Park Inkeun, Park Young Suk, Lee Myung-Ah, Lee Soohyeon, Jeon So-Yeon, Han Sae-Won, Kang Myoung Hee, Oh Jisu, Kim Jin Soo, Kim Jin Young, Ahn Mi Sun, Zang Dae Young, Bae Byung-Noe, Jo Hong Jae, Kim Hee Kyung, Kim Jung-Han, Yoon Ji Ae, Kim Dong Han

机构信息

Division of Medical Oncology, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

Department of Oncology/Hematology, Kyungpook National University Chilgok Hospital, School of Medicine, Kyungpook National University, 807 Hoguk-ro, Buk-gu, Daegu, 41404, Republic of Korea.

出版信息

J Cancer Res Clin Oncol. 2023 Mar;149(3):1131-1143. doi: 10.1007/s00432-022-03946-x. Epub 2022 Mar 27.

Abstract

PURPOSE

To evaluate the safety and effectiveness of aflibercept in combination with fluorouracil, leucovorin, and irinotecan (FOLFIRI) in Korean patients with metastatic colorectal cancer (mCRC) who progressed with oxaliplatin-containing regimen.

METHODS

This was a prospective observational study conducted at 22 sites across Korea between February 2018 and September 2019. Patients aged > 19 years with a diagnosis of mCRC who were prescribed aflibercept plus FOLFIRI, after progression with an oxaliplatin-containing regimen were included. Disease assessment was performed every 6 weeks.

RESULTS

A total of 185 patients were included (males, 58.9%; right-sided tumors, 23.8%; and ECOG performance factor ≥ 1, 68.6%). A total of 514 adverse events (AEs) occurred in 134 patients, of which 206 (49.2%; 95% CI 42.0%, 56.4%) events were considered as adverse drug reactions (ADRs), 172 unexpected AEs (49.7%; 95% CI 42.5%, 56.9%), and 53 serious AEs (22.2%; 95% CI16.2%, 28.2%). The most common serious ADR was pneumonia (n = 2, 1.6%). The most common all grade hematological AE and non-hematological AE were neutropenia (21.6%) and nausea (16.2%), respectively. Over a median follow-up of 5.6 months, a total of five grade 5 (1.0%) AEs were reported. Median OS was 9.4 months, and median progression-free survival (PFS) was 7.3 months. The overall response rate was 14.6%. Right-sided tumor location and prior bevacizumab treatment were independent factors of poor PFS in multivariate analysis.

CONCLUSION

Aflibercept in combination with FOLFIRI was effective and showed an acceptable safety profile in Korean patients with mCRC in daily clinical practice.

摘要

目的

评估阿柏西普联合氟尿嘧啶、亚叶酸钙和伊立替康(FOLFIRI)方案在接受含奥沙利铂方案治疗后病情进展的韩国转移性结直肠癌(mCRC)患者中的安全性和有效性。

方法

这是一项前瞻性观察性研究,于2018年2月至2019年9月在韩国22个地点进行。纳入年龄>19岁、诊断为mCRC且在接受含奥沙利铂方案治疗病情进展后接受阿柏西普联合FOLFIRI治疗的患者。每6周进行一次疾病评估。

结果

共纳入185例患者(男性占58.9%;右侧肿瘤患者占23.8%;东部肿瘤协作组体能状态评分≥1分的患者占68.6%)。134例患者共发生514起不良事件(AE),其中206起(49.2%;95%置信区间42.0%,56.4%)事件被视为药物不良反应(ADR),172起意外AE(49.7%;95%置信区间42.5%,56.9%),53起严重AE(22.2%;95%置信区间16.2%,28.2%)。最常见的严重ADR是肺炎(n = 2,1.6%)。最常见的所有级别血液学AE和非血液学AE分别是中性粒细胞减少(21.6%)和恶心(16.2%)。中位随访5.6个月,共报告5起5级(1.0%)AE。中位总生存期(OS)为9.4个月,中位无进展生存期(PFS)为7.3个月。总缓解率为14.6%。多因素分析中,右侧肿瘤位置和既往贝伐单抗治疗是PFS较差率的独立因素。

结论

在日常临床实践中,阿柏西普联合FOLFIRI方案在韩国mCRC患者中有效且安全性可接受。

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