PMID- 11268491 OWN - NLM STAT- MEDLINE DCOM- 20010412 LR - 20221207 IS - 0250-7005 (Print) IS - 0250-7005 (Linking) VI - 20 IP - 5C DP - 2000 Sep-Oct TI - New triplet chemotherapy combination with carboplatin, paclitaxel and gemcitabine plus amifostine support in advanced non small cell lung cancer: a phase II study. PG - 3999-4003 AB - New triplet chemotherapy combinations are under investigation in advanced non small cell lung cancer (NSCLC). Carboplatin, plus paclitaxel, plus gemcitabine is among the most active and promising regimens. The use of more aggressive chemotherapy in order to improve results can increase toxicity. Amifostine (WR-2721) reduces toxicity of radiotherapy and chemotherapy and protects selectively a number of normal, but not neoplastic, tissue. Based on this background, we performed a phase II study on carboplatin, plus paclitaxel, plus gemcitabine with amifostine support in advanced NSCLC. Patients received chemotherapy at the following dosage: carboplatin AUC 5, i.v., at day 1; paclitaxel 175 mg/m2, i.v. by 3-hour infusion, at day 1; gemcitabine 1000 mg/m2, i.v. by 3-hour infusion, at days 1 and 8; every 3 weeks for a maximum of 6 cycles. Amifostine was administered at the dose of 740 mg/m2, i.v., at day 1 of each cycle. Seventeen patients entered the study. They were prevalently male, median age was 62 years, PS (ECOG) was 0 in 10 cases (58.8%), 1 in 6 (35.3%) and 2 in 1 (5.9%). Histology was epidermoid in 8 cases (47%) and adenocarcinoma in 9 (53%). We observed 8 (47.5%) objective responses with 2 (11.7%) complete responses. Median time to progression and median survival were 24 and 36 weeks, respectively. Treatment was well tolerated. The main toxicity was as follows: grade 3 neutropenia, grade 2 thrombocytopenia and grade 3 anemia in one (5.8%) case; grade 2 peripheral neurologic toxicity in 3 (17.6%) patients; grade 2 cardiac toxicity (atrial fibrillation) in one case; and grade 3 respiratory toxicity (dispnoea) in one patient. These data indicate that this combination has promising activity and tolerability. A randomized trial comparing carboplatin plus paclitaxel, plus gemcitabine versus carboplatin, plus paclitaxel, plus gemcitabine, plus amifostine in advanced NSCLC is warranted. FAU - Illiano, A AU - Illiano A AD - VI Divisione di Pneumologia, Ospedale Monaldi, Napoli, Italy. FAU - Barletta, E AU - Barletta E FAU - De Marino, V AU - De Marino V FAU - Battiloro, C AU - Battiloro C FAU - Barzelloni, M AU - Barzelloni M FAU - Scognamiglio, F AU - Scognamiglio F FAU - Rossi, N AU - Rossi N FAU - Zampa, G AU - Zampa G FAU - De Bellis, M AU - De Bellis M FAU - Gridelli, C AU - Gridelli C LA - eng PT - Clinical Trial PT - Clinical Trial, Phase II PT - Journal Article PT - Multicenter Study PL - Greece TA - Anticancer Res JT - Anticancer research JID - 8102988 RN - 0 (Radiation-Protective Agents) RN - 0W860991D6 (Deoxycytidine) RN - BG3F62OND5 (Carboplatin) RN - M487QF2F4V (Amifostine) RN - P88XT4IS4D (Paclitaxel) RN - 0 (Gemcitabine) SB - IM MH - Adenocarcinoma/drug therapy/pathology MH - Aged MH - Amifostine/administration & dosage/adverse effects/*therapeutic use MH - Antineoplastic Combined Chemotherapy Protocols/adverse effects/*therapeutic use MH - Carboplatin/administration & dosage MH - Carcinoma, Non-Small-Cell Lung/*drug therapy/pathology MH - Carcinoma, Squamous Cell/drug therapy/pathology MH - Deoxycytidine/administration & dosage/analogs & derivatives MH - Female MH - Humans MH - Lung Neoplasms/*drug therapy/pathology MH - Lymphatic Metastasis MH - Male MH - Middle Aged MH - Neoplasm Metastasis MH - Paclitaxel/administration & dosage MH - Radiation-Protective Agents/administration & dosage/adverse effects/therapeutic use MH - Gemcitabine EDAT- 2001/03/28 10:00 MHDA- 2001/04/17 10:01 CRDT- 2001/03/28 10:00 PHST- 2001/03/28 10:00 [pubmed] PHST- 2001/04/17 10:01 [medline] PHST- 2001/03/28 10:00 [entrez] PST - ppublish SO - Anticancer Res. 2000 Sep-Oct;20(5C):3999-4003.