PURPOSE: Irinotecan, in combination with leucovorin/5-fluorouracil (FU) or with cisplatin, is known to be active for treating advanced gastric cancer (AGC). This pilot study evaluated a novel three-drug combination of irinotecan, leucovorin/FU and cisplatin as a first-line treatment of AGC. The primary endpoint was to assess the feasibility in anticipation of conducting a larger phase II study. MATERIALS AND METHODS: Chemotherapy-naive AGC patients received irinotecan 150 mg/m(2) on day 1, and leucovorin 200 mg/m(2) and a 22-h infusion of FU 1000 mg/m(2) on days 1 and 2. Cisplatin 30 mg/m(2) was administered on day 2. Treatment was repeated every 2 weeks until disease progression or unacceptable toxicity. RESULTS: Of the 17 eligible patients, two patients had an ECOG performance status of 2 and their median age was 48 years (range: 31 to 69). A total of 117 chemotherapy cycles were delivered (median: 6, range: 1 to 12). The causes of treatment discontinuation were disease progression in 9 patients (53%), refusal (35%) and toxicity (12%). Although grade 3 or 4 neutropenia (41% of patients) was the major toxicity that required dose adjustments, only one episode of febrile neutropenia occurred. Grade 3 or 4 nausea and vomiting, diarrhea and fatigue were observed in 35%, 35% and 29% of patients, respectively. None of the patients died of toxicity during treatment. Of the 16 patients who were evaluable for response, 7 (44%) experienced a partial response. CONCLUSION: This novel multi-drug combination was tolerated well in patients with AGC. Based on the encouraging efficacy and tolerability, a randomized phase II study is ongoing in this disease setting.
PURPOSE:Irinotecan, in combination with leucovorin/5-fluorouracil (FU) or with cisplatin, is known to be active for treating advanced gastric cancer (AGC). This pilot study evaluated a novel three-drug combination of irinotecan, leucovorin/FU and cisplatin as a first-line treatment of AGC. The primary endpoint was to assess the feasibility in anticipation of conducting a larger phase II study. MATERIALS AND METHODS: Chemotherapy-naive AGC patients received irinotecan 150 mg/m(2) on day 1, and leucovorin 200 mg/m(2) and a 22-h infusion of FU 1000 mg/m(2) on days 1 and 2. Cisplatin 30 mg/m(2) was administered on day 2. Treatment was repeated every 2 weeks until disease progression or unacceptable toxicity. RESULTS: Of the 17 eligible patients, two patients had an ECOG performance status of 2 and their median age was 48 years (range: 31 to 69). A total of 117 chemotherapy cycles were delivered (median: 6, range: 1 to 12). The causes of treatment discontinuation were disease progression in 9 patients (53%), refusal (35%) and toxicity (12%). Although grade 3 or 4 neutropenia (41% of patients) was the major toxicity that required dose adjustments, only one episode of febrile neutropenia occurred. Grade 3 or 4 nausea and vomiting, diarrhea and fatigue were observed in 35%, 35% and 29% of patients, respectively. None of the patients died of toxicity during treatment. Of the 16 patients who were evaluable for response, 7 (44%) experienced a partial response. CONCLUSION: This novel multi-drug combination was tolerated well in patients with AGC. Based on the encouraging efficacy and tolerability, a randomized phase II study is ongoing in this disease setting.
Authors: Jaffer A Ajani; Jackie Baker; Peter W T Pisters; Linus Ho; Paul F Mansfield; Barry W Feig; Chusilp Charnsangavej Journal: Cancer Date: 2002-02-01 Impact factor: 6.860
Authors: C Pozzo; C Barone; J Szanto; E Padi; C Peschel; J Bükki; V Gorbunova; V Valvere; J Zaluski; M Biakhov; E Zuber; C Jacques; R Bugat Journal: Ann Oncol Date: 2004-12 Impact factor: 32.976
Authors: Olivier Bouché; Jean Luc Raoul; Franck Bonnetain; Marc Giovannini; Pierre Luc Etienne; Gérard Lledo; Dominique Arsène; Jean Francois Paitel; Véronique Guérin-Meyer; Emmanuel Mitry; Bruno Buecher; Marie Christine Kaminsky; Jean François Seitz; Philippe Rougier; Laurent Bedenne; Chantal Milan Journal: J Clin Oncol Date: 2004-11-01 Impact factor: 44.544
Authors: C-H Köhne; J Wils; M Lorenz; P Schöffski; R Voigtmann; C Bokemeyer; M Lutz; C Kleeberg; K Ridwelski; R Souchon; M El-Serafi; U Weiss; O Burkhard; H Rückle; M Lichnitser; T Langenbuch; W Scheithauer; B Baron; M L Couvreur; H J Schmoll Journal: J Clin Oncol Date: 2003-09-08 Impact factor: 44.544
Authors: S T Kim; W K Kang; J H Kang; K W Park; J Lee; S-H Lee; J O Park; K Kim; W S Kim; C W Jung; Y S Park; Y-H Im; K Park Journal: Br J Cancer Date: 2005-05-23 Impact factor: 7.640
Authors: C-H Köhne; R Catane; B Klein; M Ducreux; P Thuss-Patience; N Niederle; M Gips; P Preusser; A Knuth; M Clemens; R Bugat; I Figer; A Shani; B Fages; D Di Betta; C Jacques; H J Wilke Journal: Br J Cancer Date: 2003-09-15 Impact factor: 7.640