Neutropenia is an indicator of outcomes in metastatic colorectal cancer patients treated with FTD/TPI plus bevacizumab: a retrospective study

被引:17
作者
Nose, Yohei [1 ,2 ]
Kagawa, Yoshinori [1 ]
Hata, Taishi [1 ]
Mori, Ryota [1 ,2 ]
Kawai, Kenji [1 ]
Naito, Atsushi [1 ,3 ]
Sakamoto, Takuya [1 ]
Murakami, Kohei [1 ]
Katsura, Yoshiteru [1 ]
Ohmura, Yoshiaki [1 ]
Masuzawa, Toru [1 ]
Takeno, Atsushi [1 ]
Takeda, Yutaka [1 ]
Kato, Takeshi [1 ,4 ]
Murata, Kohei [1 ]
机构
[1] Kansai Rosai Hosp, Dept Surg, Japan Org Occupat Hlth & Safety, Amagasaki, Hyogo, Japan
[2] Osaka Univ, Grad Sch Med, Dept Gastroenterol Surg, Suita, Osaka, Japan
[3] Osaka Police Hosp, Dept Surg, Osaka, Japan
[4] Osaka Natl Hosp, Natl Hosp Org, Dept Surg, Osaka, Japan
关键词
FTD; TPI plus bevacizumab; Metastatic colorectal cancer; Neutropenia; Chemotherapy; OPEN-LABEL; TAS-102; COMBINATION;
D O I
10.1007/s00280-020-04129-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Trifluridine/tipiracil (FTD/TPI) improves the overall survival (OS) of metastatic colorectal cancer (mCRC) patients. Additionally, FTD/TPI plus bevacizumab (BEV) has demonstrated promising efficacy for mCRC patients who are refractory to standard chemotherapy. Chemotherapy-induced neutropenia (CIN) has been reported to be an indicator of efficacy for FTD/TPI. This study investigated whether CIN was an indicator of efficacy for FTD/TPI plus BEV. Methods We reviewed chemo-refractory mCRC patients who were treated with FTD/TPI alone (monotherapy) or FTD/TPI plus BEV (combination) at our institution and compared the safety and efficacy of the two. Progression-free survival (PFS) and OS were analyzed using Kaplan-Meier curves. We also investigated correlations between CIN and outcomes. Results In total, 56 patients received FTD/TPI, among whom 24 and 32 were treated with monotherapy and combination therapy, respectively. The median PFS was 1.8 and 4.7 months for the monotherapy and combination arms, respectively (hazard ratio [HR]: 0.28; 95% confidence interval [CI]: 0.15-0.51;P < 0.001). The median OS was 6.3 and 11.7 months for the monotherapy and combination arms, respectively (HR 0.25; 95% CI 0.13-0.48;P < 0.001). CIN (Grade 3 or worse) developed in five (20.8%) and 17 (53.1%) patients from the monotherapy and combination arms, respectively (P = 0.030). Patients with CIN in the combination arm had improved PFS and OS compared with non-CIN patients (P = 0.033 andP = 0.045, respectively). Conclusions FTD/TPI plus BEV prolonged PFS and OS and had tolerable toxicity compared with FTD/TPI alone. CIN is an indicator of patients who will benefit from FTD/TPI plus BEV.
引用
收藏
页码:427 / 433
页数:7
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