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Treatment Patterns and Prognosis of Palliative Chemotherapy Combined With Targeting Agents in Patients With Unresectable Metastatic Colorectal Cancer: CHOICE, A Multicenter Longitudinal Observational Study

贝伐单抗 福尔菲里 西妥昔单抗 医学 福克斯 内科学 肿瘤科 结直肠癌 化疗 伊立替康 养生 奥沙利铂 胃肠病学 癌症
作者
Jae‐Hoon Kim,Yongjun Cha,Sang Joon Shin,YOUNG SUK PARK,Jung Hun Kang,Chan Kim,Sung Hee Lim,Myoung Joo Kang,Jong Gwang Kim,In Gyu Hwang,J.H. Choi,Seong Hoon Shin,Seok Yun Kang,SANG-CHEOL LEE,Seung Taek Lim,JUNG SUN KIM,Hei‐Cheul Jeung,Myoung Hee Kang,In Sil Choi,Hye Won Ryu
出处
期刊:Anticancer Research [Anticancer Research USA Inc.]
卷期号:44 (1): 347-359 被引量:2
标识
DOI:10.21873/anticanres.16818
摘要

Background/Aim: This study investigated the treatment patterns and prognosis of patients with metastatic or unresectable colorectal cancer (mCRC) treated with chemotherapy with targeting agents. Patients and Methods: This longitudinal multicenter study included 963 patients with mCRC who were treated in Korea between 2016 and 2020. Treatment patterns and efficacy were compared according to the mutation status and clinical factors. Results: As first-line therapy, most of the patients (83.5%) received FOLFOX plus bevacizumab (35.4%), followed by FOLFIRI plus bevacizumab (18.8%), FOLFIRI plus cetuximab (17.0%), and FOLFOX plus cetuximab (12.3%). Bevacizumab was the most frequent agent (78.8%) combined with chemotherapy in RAS-mutated CRC, while cetuximab (57.2%) in RAS wild-type CRC. Cetuximab was frequently combined with a doublet regimen in patients with left-sided CRC than in those with right-sided CRC (34.4% vs. 16%). As second-line therapy, most patients (63.4%) also received doublet regimens with bevacizumab, and FOLFIRI plus aflibercept was administered in 15.1%. The objective response rate with FOLFIRI plus cetuximab was significantly higher in patients with left-sided CRC than in those with right-sided CRC (59.2% vs. 30.8%, p=0.008) and marginally higher in patients with RAS wild-type CRC than in those with RAS-mutated CRC (55.6% vs. 0.0%, p=0.092). Progression-free survival (PFS) with FOLFOX plus bevacizumab was significantly shorter than that with FOLFIRI plus bevacizumab (p=0.030) in RAS-mutated CRC, whereas there were no significant differences between regimens in RAS wild-type CRC. Conclusion: In patients with unresectable metastatic colorectal cancer, doublet chemotherapy with targeting agents is the most common therapy and efficacy depends on the mutation status as well as clinical factors.

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