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Is neoadjuvant chemoradiotherapy a feasible strategy for stage IIIA-N2 non-small cell lung cancer? Mature results of the randomized IFCT-0101 phase II trial

Nicolas Girardab, Françoise Mornexab, Jean-Yves Douillardbc, Nadine Bossardd, Elisabeth Quoixbe, Véronique Beckendorfbf, Dominique Grunenwaldbg, Elodie Amourb, Bernard MilleronbhCorresponding Author Informationemail address

Received 28 July 2009; received in revised form 24 September 2009; accepted 1 October 2009. published online 30 October 2009.
Corrected Proof

Abstract 

Locally advanced non-small cell lung cancers share a risk of both local and systemic recurrence and justifies a therapeutic strategy combining focal and systemic treatment. In resectable stage IIIA-N2 tumors, peri-operative chemotherapy significantly increases survival rates. Chemoradiotherapy, which is the standard treatment of non-resectable locally advanced tumors, may have a role as an induction treatment to reduce locoregional recurrence rates.

In the present phase II trial, we aimed at comparing standard induction chemotherapy (arm A: cisplatin and gemcitabine) with 2 different regimens of induction chemoradiotherapy (total dose: 46Gy) including third-generation cytotoxic agents (arm B: cisplatin and vinorelbine; arm C: carboplatin and paclitaxel) in patients with resectable stage IIIA-N2 NSCLC, using feasibility of the whole strategy, including surgery, as a primary endpoint.

A total of 46 patients were included. Response rate was significantly higher after induction chemoradiotherapy vs. chemotherapy (87% vs. 57%, p=0.049). A total of 44 patients underwent operation. The feasibility rate of the proposed therapeutic strategy was 89% for the whole cohort, 93% in arm A (induction chemotherapy with cisplatin and gemcitabine), 88% in arm B (induction chemoradiotherapy with cisplatin and vinorelbine), and 87% in arm C (induction chemoradiotherapy with carboplatin and paclitaxel) (p=0.857). Overall median, 1-year, and 3-year survival were 30 months, 87%, and 43%, respectively.

Induction chemoradiotherapy with modern treatment regimens is highly feasible and may show promises in the current and future developments of multimodal therapeutic strategies in locally advanced NSCLC.

a Department of Radiotherapy-Oncology, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, Université Claude Bernard-Lyon 1, Lyon, France

b French-speaking Intergroup of Thoracic Oncology (IFCT), Paris, France

c Department of Medical Oncology, Centre René Gauducheau, Saint-Herblain, France

d Department of Epidemiology and Biostatistics, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, Université Claude Bernard-Lyon 1, Lyon, France

e Department of Respiratory Medicine, Centre Hospitalier Universitaire de Strasbourg, France

f Centre Alexis Vautrin, Vandoeuvre-les-Nancy, Paris, France

g Department of Thoracic Surgery, Hôpital Tenon, Paris, France

h Department of Respiratory Medicine and Thoracic Oncology, Hôpital Tenon, Paris, France

Corresponding Author InformationCorresponding author at: Service de Pneumologie, Assistance Publique - Hôpitaux de Paris, Hôpital Tenon, 4, rue de la Chine, 75020 Paris, France. Tel.: +33 1 56 01 62 04; fax: +33 1 56 01 70 02.

PII: S0169-5002(09)00502-9

doi:10.1016/j.lungcan.2009.10.003