Phase II study of FOLFIRI with low-dose irinotecan plus ramucirumab as second-line treatment in Japanese patients with metastatic colorectal cancer (study rindo).
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
62 patients were enrolled from 15 institutions between January 2018 and August 2021.
I · Intervention 중재 / 시술
8 mg/kg RAM, followed by the FOLFIRI regimen with low-dose irinotecan (150 mg/m2)
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
The observed Grade ≥ 3 adverse events included neutropenia (40%), diarrhea (8.6%), decreased appetite (10%), hypertension (6.9%), and proteinuria (3.4%). [CONCLUSION] FOLFIRI with low-dose irinotecan plus RAM is a feasible second-line treatment in Japanese patients with mCRC.
[OBJECTIVE] This multicenter, single-arm, Phase II study aimed to evaluate the efficacy and safety of fluorouracil, levofolinate, and irinotecan (150 mg/m2, standard dose in Japan) (FOLFIRI) plus ramu
- 95% CI 4.8-6.9
APA
Hattori N, Nakayama G, et al. (2026). Phase II study of FOLFIRI with low-dose irinotecan plus ramucirumab as second-line treatment in Japanese patients with metastatic colorectal cancer (study rindo).. Japanese journal of clinical oncology, 56(3), 267-273. https://doi.org/10.1093/jjco/hyaf198
MLA
Hattori N, et al.. "Phase II study of FOLFIRI with low-dose irinotecan plus ramucirumab as second-line treatment in Japanese patients with metastatic colorectal cancer (study rindo).." Japanese journal of clinical oncology, vol. 56, no. 3, 2026, pp. 267-273.
PMID
41359440
Abstract
[OBJECTIVE] This multicenter, single-arm, Phase II study aimed to evaluate the efficacy and safety of fluorouracil, levofolinate, and irinotecan (150 mg/m2, standard dose in Japan) (FOLFIRI) plus ramucirumab (RAM) as second-line treatment for metastatic colorectal cancer (mCRC) in Japanese patients.
[METHODS] On Day 1 of each 2-week cycle, patients with unresectable mCRC who were refractory to oxaliplatin and fluoropyrimidine in combination with bevacizumab or anti-epidermal growth factor receptor antibodies as first-line treatment received 8 mg/kg RAM, followed by the FOLFIRI regimen with low-dose irinotecan (150 mg/m2). The primary endpoint was progression-free survival (PFS), and secondary endpoints were overall survival (OS), treatment compliance, and safety.
[RESULTS] A total of 62 patients were enrolled from 15 institutions between January 2018 and August 2021. The intent-to-treat and safety populations included 61 and 58 patients. Median PFS and OS were 5.9 months (95% CI, 4.8-6.9 months) and 17.0 months (95% CI, 12.0-21.0 months), respectively. The objective response rate and disease control rate were 8.2% and 74%, respectively. The median time to treatment failure was 4.8 months (95% CI, 3.2-5.9 months). The median relative dose intensities of irinotecan, 5-fluorouracil, and RAM were 73.8% (range, 40.3%-102.4%), 58.5% (range, 22.8%-102.4%), and 80.8% (range, 36.1%-102.4%), respectively. Frequencies of Grade ≥ 3 hematologic, non-hematologic, and RAM-associated adverse events were 43%, 24%, and 17%, respectively. The observed Grade ≥ 3 adverse events included neutropenia (40%), diarrhea (8.6%), decreased appetite (10%), hypertension (6.9%), and proteinuria (3.4%).
[CONCLUSION] FOLFIRI with low-dose irinotecan plus RAM is a feasible second-line treatment in Japanese patients with mCRC.
[METHODS] On Day 1 of each 2-week cycle, patients with unresectable mCRC who were refractory to oxaliplatin and fluoropyrimidine in combination with bevacizumab or anti-epidermal growth factor receptor antibodies as first-line treatment received 8 mg/kg RAM, followed by the FOLFIRI regimen with low-dose irinotecan (150 mg/m2). The primary endpoint was progression-free survival (PFS), and secondary endpoints were overall survival (OS), treatment compliance, and safety.
[RESULTS] A total of 62 patients were enrolled from 15 institutions between January 2018 and August 2021. The intent-to-treat and safety populations included 61 and 58 patients. Median PFS and OS were 5.9 months (95% CI, 4.8-6.9 months) and 17.0 months (95% CI, 12.0-21.0 months), respectively. The objective response rate and disease control rate were 8.2% and 74%, respectively. The median time to treatment failure was 4.8 months (95% CI, 3.2-5.9 months). The median relative dose intensities of irinotecan, 5-fluorouracil, and RAM were 73.8% (range, 40.3%-102.4%), 58.5% (range, 22.8%-102.4%), and 80.8% (range, 36.1%-102.4%), respectively. Frequencies of Grade ≥ 3 hematologic, non-hematologic, and RAM-associated adverse events were 43%, 24%, and 17%, respectively. The observed Grade ≥ 3 adverse events included neutropenia (40%), diarrhea (8.6%), decreased appetite (10%), hypertension (6.9%), and proteinuria (3.4%).
[CONCLUSION] FOLFIRI with low-dose irinotecan plus RAM is a feasible second-line treatment in Japanese patients with mCRC.
MeSH Terms
Humans; Antineoplastic Combined Chemotherapy Protocols; Colorectal Neoplasms; Female; Male; Fluorouracil; Leucovorin; Middle Aged; Aged; Ramucirumab; Antibodies, Monoclonal, Humanized; Camptothecin; Irinotecan; Adult; Japan; Neoplasm Metastasis; Aged, 80 and over; Broadly Neutralizing Antibodies; East Asian People