Combination of irinotecan (CPT-11) plus oxaliplatin (L-OHP) as first-line treatment in locally advanced or metastatic gastric cancer: a multicentre phase II trial

被引:36
作者
Souglakos, J
Syrigos, K
Potamianou, A
Polyzos, A
Boukovinas, I
Androulakis, N
Kouroussis, C
Vardakis, N
Christophilakis, C
Kotsakis, A
Georgoulias, V
机构
[1] Univ Gen Hosp Heraklion, Dept Med Oncol, Iraklion 71110, Crete, Greece
[2] Univ Athens, Dept Internal Med 3, Med Oncol Unit, Athens, Greece
[3] Univ Athens, Propedeut Dept, Med Oncol Unit, Athens, Greece
[4] Metaxa Hosp Athens, Dept Med Oncol 1, Athens, Greece
[5] Theagen Anticanc Hosp Thessaloniki, Dept Med Oncol 2, Thessaloniki, Greece
[6] Mil Hosp Athens 401, Dept Med Oncol, Med Oncol Unit, Athens, Greece
关键词
gastric cancer; irinotecan; oxaliplatin;
D O I
10.1093/annonc/mdh312
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The purpose of this study was to evaluate the efficacy and tolerance of irinotecan (CPT-11) in combination with oxaliplatin (L-OHP) as first-line treatment in patients with locally advanced or metastatic gastric cancer (AGC). Patients and methods: Thirty-two patients with AGC who had not received previous therapy for metastatic disease were enrolled. The median age was 62.5 years and the World Health Organization performance status was 0-1 in 29 patients; 13 (40.6%) patients had previous surgery and three (9.4%) had adjuvant chemotherapy. L-OHP (85 mg/m(2) as a 2-h i.v. infusion) followed by CPT-11 (200 m/m(2) as a 30-min i.v. infusion) was given on day 1, in cycles of 21 days. Results: All patients were evaluable for toxicity and 31 were evaluable for response. Complete response was achieved in one (3.1%) patient and a partial response was achieved in 15 (46.9%) [overall response rate = 50% (95% confidence interval 38.7-72.4%)]. Eight (25%) patients had stable disease, and eight (25%) had progressive disease. The median duration of response was 5 months and the median time to disease progression was 5.5 months. After a median follow-up period of 16 months, the median survival time was 8.5 months. Grade 3-4 neutropenia occurred in six (18.6%) patients, febrile neutropenia in two (6.2%) and grade 3 anaemia in one (3.1%). Grade 3 diarrhoea was observed in two (6.2%) patients, grade 1 neurotoxicity in five (15.6%) and grade 3 asthenia in two (6.2%). There was no treatment-related death. Conclusions: The combination of CPT-11/L-OHP is an active regimen as front-line treatment in AGC with a favourable toxicity profile and deserves further evaluation in randomised studies.
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页码:1204 / 1209
页数:6
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