Treatment of peritoneal metastases from small bowel adenocarcinoma |
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Authors: | Koen P. Rovers Eelco de Bree Yutaka Yonemura |
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Affiliation: | 1. Department of Surgical Oncology, Catharina Hospital, Eindhoven, the Netherlands;2. Department of Surgical Oncology, Medical School of Crete University Hospital, Heraklion, Greece;3. Asian and Japanese School of Peritoneal Surface Oncology, Kyoto, Japan |
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Abstract: | AbstractBackground/purpose: Peritoneal metastases (PM) affect approximately one third of patients with metastatic small bowel adenocarcinoma (SBA). Treatment options are (1) systemic therapy?±?palliative surgery and (2) cytoreductive surgery with intraperitoneal chemotherapy (CRS?+?IPC). Due to scarce evidence, PM from SBA represents a therapeutic challenge. This narrative review summarised and discussed the evidence that investigated available treatment options.Methods: Studies were discussed if they investigated first line systemic therapy for advanced SBA or CRS?+?IPC for PM from SBA. Extracted outcomes were objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), disease-free survival (DFS), overall survival (OS), and grade III–V toxicity/morbidity.Results: Eighteen studies (15 observational, 3 phase II) that investigated systemic therapy and six observational studies that investigated CRS?+?IPC were reviewed. In studies that investigated systemic therapy, ORR, DCR, median PFS, median OS, and grade III–V toxicity ranged from 6% to 50%, 50% to 90%, 3 to 11 months, 8 to 20 months, and 10% to 68%, respectively. Fluoropyrimidine–oxaliplatin revealed favourable survival outcomes compared to fluoropyrimidine–irinotecan, fluoropyrimidine–cisplatin, fluoropyrimidine monotherapy, and other regimens. In studies that investigated CRS?+?IPC, median DFS, median OS, and grade III–V morbidity ranged from 10 to 12 months, 16 to 47 months, and 12% to 35%, respectively.Conclusion: Based on available evidence, fluoropyrimidine–oxaliplatin should be regarded as optimal first line systemic treatment. In selected patients, CRS?+?IPC appears safe and may be more effective than systemic therapy as single treatment. Future studies should evaluate survival and morbidity of CRS?+?IPC in larger cohorts, as well as the value of chemotherapy with targeted agents in metastatic SBA with subgroup analysis for PM from SBA. |
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Keywords: | Small bowel adenocarcinoma peritoneal carcinomatosis peritoneal metastases surgery HIPEC chemotherapy |
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