Service d'Hépato-Gastroentérologie et d'Oncologie Digestive, CHU de Reims, Hôpital Robert-Debré, Reims F-51092 Cedex, France.
Dig Liver Dis. 2011 Nov;43(11):912-6. doi: 10.1016/j.dld.2011.07.001. Epub 2011 Aug 9.
Pancreatic endocrine carcinomas are rare and heterogeneous. Published results concerning treatment of advanced tumours are inconsistent and responses to standard chemotherapy remain unsatisfactory.
To investigate the ability of the FOLFIRI regimen to manage progressive unresectable metastatic well-differentiated endocrine carcinomas of the pancreas as first-line chemotherapy.
20 patients with metastatic or advanced well-differentiated endocrine carcinomas of the pancreas and progressive disease were enrolled in a prospective multicentre phase II trial to receive chemotherapy with FOLFIRI schedule (irinotecan 180mg/m(2) infusion combined with simplified LV5FU2) every 14 days. The primary end point was the non-progression rate at 6 months.
The 6-month non-progression rate was 80% (95% confidence interval [56-94%]), with stabilisation in 15 patients and 1 objective response. Overall survival at 24 months was 65% [40-82%]. Median progression-free survival was 9.1 months [6.5-17.3 months]. The median number of administered cycles was 12 [range 1-28]. Grade 3/4 haematologic toxicity occurred in 5 patients (25%) and grade 3 digestive toxicity in 11.
The FOLFIRI regimen, as first-line chemotherapy, achieved stabilisation in most patients whose tumours had been progressing and was well-tolerated. It could be an alternative therapy for advanced well-differentiated endocrine carcinomas of the pancreas.
胰腺内分泌癌罕见且异质性高。关于晚期肿瘤治疗的已有研究结果并不一致,且标准化疗的反应仍不令人满意。
研究 FOLFIRI 方案作为一线化疗治疗不可切除的进展性转移性高分化胰腺内分泌癌的疗效。
20 例转移性或晚期高分化胰腺内分泌癌患者,疾病进展,入组一项前瞻性多中心 II 期试验,接受 FOLFIRI 方案(伊立替康 180mg/m² 输注联合简化 LV5FU2)化疗,每 14 天一次。主要终点为 6 个月时的无进展率。
6 个月无进展率为 80%(95%置信区间 [56-94%]),15 例患者稳定,1 例客观缓解。24 个月总生存率为 65%[40-82%]。中位无进展生存期为 9.1 个月[6.5-17.3 个月]。中位给药周期数为 12 个[范围 1-28]。5 例(25%)患者发生 3/4 级血液学毒性,11 例患者发生 3 级消化系统毒性。
FOLFIRI 方案作为一线化疗,使多数进展性肿瘤患者病情稳定且耐受性良好。它可能是晚期高分化胰腺内分泌癌的一种替代治疗方法。