A phase III randomised study comparing concomitant radiochemotherapy as induction versus consolidation treatment in patients with locally advanced unresectable non-small cell lung cancer

• Published in: Lung cancer (Amsterdam, Netherlands) Netherlands), 2009-05, Vol.64 (2), p.187-193
• Main Authors: Berghmans, T, Van Houtte, P, Paesmans, M, Giner, V, Lecomte, J, Koumakis, G, Richez, M, Holbrechts, S, Roelandts, M, Meert, A.P, Alard, S, Leclercq, N, Sculier, J.P
• Format: Article
• Language: English
• Subjects: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols - therapeutic use; Biological and medical sciences; Carcinoma, Non-Small-Cell Lung - drug therapy; Carcinoma, Non-Small-Cell Lung - mortality; Carcinoma, Non-Small-Cell Lung - radiotherapy; Chemotherapy; Cisplatin; Cisplatin - administration & dosage; Cisplatin - adverse effects; Combined Modality Therapy; Deoxycytidine - administration & dosage; Deoxycytidine - adverse effects; Deoxycytidine - analogs & derivatives; Female; Gemcitabine; Hematology, Oncology and Palliative Medicine; Humans; Lung Neoplasms - drug therapy; Lung Neoplasms - mortality; Lung Neoplasms - radiotherapy; Male; Medical sciences; Middle Aged; Non-small cell lung carcinoma; Pneumology; Pulmonary/Respiratory; Radiotherapy; Radiotherapy - adverse effects; Radiotherapy - methods; Tumors; Tumors of the respiratory system and mediastinum; Vinblastine - administration & dosage; Vinblastine - adverse effects; Vinblastine - analogs & derivatives; Vinorelbine
• ISSN: 0169-5002; 1872-8332
• DOI: 10.1016/j.lungcan.2008.08.004

Abstract As concomitant chemoradiotherapy for stage III NSCLC is associated with survival advantage in comparison to a sequential approach, we conducted a phase III randomised study aiming to determine the best sequence and safety of chemotherapy (CT) and chemoradiotherapy (CT-RT), using a regimen with cisplatin (CDDP), gemcitabine (GEM) and vinorelbine (VNR). Unresectable stage III NSCLC patients received CDDP (60 mg/m2 ), GEM (1 g/m2 , days 1 and 8) and VNR (25 mg/m2 , days 1 and 8) with reduced dosage of GEM and VNR during radiotherapy (66 Gy). Two cycles of CT with radiotherapy followed by two further cycles of CT alone were administered in arm A or the reverse sequence in arm B. The study was prematurely closed for poor accrual due to administrative problems. Forty-nine eligible patients were randomised. Response rates and median survival times were, respectively 57% (95% CI: 36–78%) and 17 months (95% CI: 9.3–24.6 months) in arm A and 79% (95% CI: 64–94%) and 23.9 months (95% CI: 13.3–34.5 months) in arm B ( p > 0.05). Chemotherapy dose-intensity was significantly reduced in arm A. Grade 3–4 oesophagitis occurred in 5 patients. One case of grade 5 radiation pneumonitis was observed. In conclusion, chemoradiotherapy with CDDP, GEM and VNR appears feasible as initial treatment or after induction chemotherapy. Consolidation chemoradiotherapy seems less toxic with a better observed response rates and survival although no valid conclusion can be drawn from the comparison of both arms.