Second-line Chemotherapy for Previously Treated Metastatic Small Bowel Adenocarcinoma: A Retrospective Analysis

被引:3
作者
Nakazawa, Taiko [1 ]
Narita, Yukiya [1 ]
Kumanishi, Ryosuke [1 ]
Ogata, Takatsugu [1 ]
Matsubara, Yuki [1 ]
Nozawa, Kazuki [1 ]
Kato, Kyoko [1 ]
Honda, Kazunori [1 ]
Masuishi, Toshiki [1 ]
Bando, Hideaki [1 ]
Kadowaki, Shigenori [1 ]
Ando, Masashi [1 ]
Hara, Kazuo [2 ]
Tajika, Masahiro [3 ]
Muro, Kei [1 ]
机构
[1] Aichi Canc Ctr Hosp, Dept Clin Oncol, Nagoya, Aichi, Japan
[2] Aichi Canc Ctr Hosp, Dept Gastroenterol, Nagoya, Aichi, Japan
[3] Aichi Canc Ctr Hosp, Dept Endoscopy, Nagoya, Aichi, Japan
关键词
Adenocarcinoma; chemotherapy; microsatellite instability; second-line treatment; small bowel cancer; OPEN-LABEL; PHASE-II; CANCER; CAPECITABINE; OXALIPLATIN; AMPULLA; BEVACIZUMAB; PANITUMUMAB; CETUXIMAB; COLON;
D O I
10.21873/anticanres.15332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Metastatic small bowel adenocarcinoma (SBA) is a rare disease with poor prognosis. This study aimed to explore the efficacy and safety of secondline chemotherapy for patients with SBA. Patients and Methods: We retrospectively reviewed the clinical characteristics of 27 metastatic patients with SBA after progression on first-line chemotherapy. The patients were divided into Cohort A, receiving second-line chemotherapy, and Cohort B, receiving best supportive care. Results: Patients in Cohort B had higher age, worse performance status, and higher neutrophil-to-lymphocyte ratio compared with those in Cohort A. Cohort A showed significantly better overall survival (OS) compared with Cohort B (median OS, 15.6 vs. 3.4 months; p=0.002). Objective response rate, disease control rate, and median progression-free survival (PFS) for Cohort A were 7%, 74%, and 5.0 months, respectively. Patients who underwent irinotecan-based chemotherapy showed longer PFS and OS compared with those who underwent taxane-based chemotherapy. No significant adverse events were reported. Conclusion: Second-line chemotherapy for metastatic SBA demonstrated clinical activity with acceptable toxicities.
引用
收藏
页码:5147 / 5155
页数:9
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