Randomized trial of three combinations of cisplatin with vindesine and/or VP-16-213 in the treatment of advanced non-small-cell lung cancer

• Published in: Journal of clinical oncology Vol. 3; no. 2; p. 176
• Main Authors: Dhingra, H M, Valdivieso, M, Carr, D T, Chiuten, D F, Farha, P, Murphy, W K, Spitzer, G, Umsawasdi, T
• Format: Journal Article
• Language: English
• Published: United States 01-02-1985
• Subjects: Adenocarcinoma - drug therapy; Adenocarcinoma, Bronchiolo-Alveolar - drug therapy; Adult; Antineoplastic Combined Chemotherapy Protocols - adverse effects; Antineoplastic Combined Chemotherapy Protocols - therapeutic use; Carcinoma, Small Cell - drug therapy; Carcinoma, Squamous Cell - drug therapy; Cisplatin - administration & dosage; Clinical Trials as Topic; Drug Administration Schedule; Etoposide - administration & dosage; Humans; Lung Neoplasms - drug therapy; Lung Neoplasms - mortality; Male; Middle Aged; Prognosis; Random Allocation; Vinblastine - administration & dosage; Vinblastine - analogs & derivatives; Vindesine
• ISSN: 0732-183X
• DOI: 10.1200/JCO.1985.3.2.176

One hundred sixty-seven evaluable patients with non-small-cell lung cancer were randomized to receive high-dose cisplatin and vindesine (PVD), or cisplatin and VP-16-213 (etoposide epipodophyllotoxin) (PVP), or cisplatin with VP-16-213 and vindesine (PVPVD). The patient distribution and characteristics were similar in all the treatment arms. The response rate differences (35% in PVD arm, 30% in PVP arm, and 22% in PVPVD arm) were not statistically significant (P = .33). Response durations were 43 weeks in the PVD arm, 20 weeks in the PVP arm, and 27 weeks in the PVPVD arm. Median survival was 29 weeks in the PVD and PVP arms and 28 weeks in the PVPVD arm. Median survival time of responding patients was 76 weeks in the PVD arm and 65 weeks in the PVP arm; 78% of patients were alive at 22+ to 87+ weeks follow-up in the PVPVD arm. Myelosuppression was similar in all three treatment arms. Significantly more azotemia occurred in the PVD arm than in the PVP and PVPVD arms (P = .002), and significantly more neuropathy in the PVD and PVPVD arms than in the PVP arm (P = .003 and .005). All the treatment arms have similar antitumor activity in non-small-cell lung cancer, but the PVP combination is slightly less toxic than the PVD and PVPVD treatment arms.