Regorafenib combined with immune checkpoint inhibitors versus regorafenib monotherapy as a late-line treatment for metastatic colorectal cancer: a single-center, retrospective cohort study

被引:0
|
作者
Chen, Can [1 ]
Luo, Xi [1 ]
Tang, Wenhua [1 ]
Geng, Haofei [1 ]
Martinez-Perez, Julia [2 ,3 ]
Price, Timothy [4 ,5 ]
Kang, Lili [1 ]
Lu, Honglian [1 ]
Zhang, Yanling [1 ]
机构
[1] Army Med Univ, Affiliated Hosp 1, Dept Oncol, 29 Gaotanyan Zhengjie, Chongqing 400038, Peoples R China
[2] Univ Hosp Virgen Rocio, Med Oncol Dept, Seville, Spain
[3] Univ Seville, CSIC, HUVR, Inst Biomed Sevilla IBIS, Seville, Spain
[4] Queen Elizabeth Hosp, Dept Med Oncol, Woodville, Australia
[5] Univ Adelaide, Sch Med, Adelaide, Australia
关键词
Colorectal cancer (CRC); metastatic; immune checkpoint inhibitors (ICIs); regorafenib; prognosis; GENDER-DIFFERENCES; SURVIVAL; ALCOHOL;
D O I
10.21037/jgo-24-468
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Few data are available on metastatic colorectal cancer (mCRC) treated with late-line regorafenib monotherapy or combined with other therapies. This study thus aimed to examine regorafenib combined with immune checkpoint inhibitors (ICIs) compared with regorafenib monotherapy in patients with advanced CRC. Methods: This single-center retrospective cohort study included patients with advanced CRC who experienced recurrence and progression after standard first- and second-line treatments treatment from November 2018 to December 2021. The patients received regorafenib plus ICIs or regorafenib monotherapy. Treatment response was evaluated based on Response Evaluation Criteria in Solid Tumors (RECIST). Overall survival (OS) and progression-free survival (PFS) were analyzed via multivariate analysis. Results: The combined group and the monotherapy group included 30 and 43 patients, respectively. The median OS (13.7 vs. 10.1 months; P=0.10) and PFS (4 vs. 3.6 months; P=0.32) were not significantly different between the two groups. In males, the median OS was significantly longer in the combined group compared with the monotherapy group (not reached vs. 8.03 months; P=0.02), but the median PFS showed no significant difference (7.23 vs. 3.90 months; P=0.16). There was no significant difference in OS (P=0.71) or PFS (P=0.89) in females. Eastern Cooperative Oncology Group performance status (ECOG PS) 1 [vs. 0; hazard ratio (HR) =3.13, 95% confidence interval (CI): 1.61-6.10; P<0.001] was independently associated with PFS. ECOG PS 1 (vs. 0; HR =3.63, 95% CI: 1.54-8.56; P=0.003) and combined therapy (vs. monotherapy; HR =0.47, 95% CI: 0.22-0.99; P=0.048) were associated with OS. Conclusions: Regorafenib combined with ICIs led to numerically longer PFS and significantly prolonged OS in patients with mCRC compared to regorafenib monotherapy, especially in male patients.
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收藏
页码:1497 / 1507
页数:11
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