TY - JOUR T1 - An ELCWP Phase III Trial Comparing Ifosfamide and Cisplatin Regimens in Advanced NSCLC JF - Anticancer Research JO - Anticancer Res SP - 5477 LP - 5482 VL - 33 IS - 12 AU - THIERRY BERGHMANS AU - JEAN-JACQUES LAFITTE AU - ARNAUD SCHERPEREEL AU - MARIANNE PAESMANS AU - JACQUES LECOMTE AU - VICENTE GINER MARCO AU - ANNE-PASCALE MEERT AU - NATHALIE LECLERCQ AU - JEAN-PAUL SCULIER AU - for the European Lung Cancer Working Party Y1 - 2013/12/01 UR - http://ar.iiarjournals.org/content/33/12/5477.abstract N2 - Aim: While meta-analyses and clinical trials show improved survival in advanced NSCLC treated with platinum-containing chemotherapy, there are few data concerning front-line platinum-free ifosfamide-based regimens. We aimed to compare cisplatin-based chemotherapy to ifosfamide-gemcitabine (IG) with pre-defined second-line docetaxel. Patients and Methods: 693 Untreated advanced inoperable NSCLC cases were randomised to either GIP (gemcitabine, ifosfamide, cisplatin), DP (docetaxel, cisplatin) or IG. Primary outcome was overall survival. Results: Median age of the patients was 58 years with a predominance of males (75%), adenocarcinoma (56%), Karnofsky PS 80-100 (77%) and stage-IV disease (81%). Median survival times were 8.7, 8.8 and 8.3 months for IG, GIP and DP (p=0.79). GIP presented with (p<0.05) greater neutropenia, thrombopenia, vomiting, while greater cardiotoxicity, diarrhea, peripheral neuropathy were observed for DP and encephalopathy for IG. Conclusion: In advanced NSCLC, cisplatin-based CT is not superior to a platinum-free regimen (ifosfamide-gemcitabine) with a favourable toxicity profile. ER -