TY - JOUR
T1 - Non-small cell lung cancer recurrence following surgery and perioperative chemotherapy
T2 - Comparison of two chemotherapy regimens (IFCT-0702: A randomized phase 3 final results study)
AU - Moro-Sibilot, Denis
AU - Audigier-Valette, Clarisse
AU - Merle, Patrick
AU - Quoix, Elisabeth
AU - Souquet, Pierre Jean
AU - Barlesi, Fabrice
AU - Chouaid, Christos
AU - Molinier, Olivier
AU - Bennouna, Jaafar
AU - Lavolé, Armelle
AU - Mazières, Julien
AU - Toffart, Anne Claire
AU - Langlais, Alexandra
AU - Morin, Franck
AU - Zalcman, Gérard
N1 - Publisher Copyright:
© 2015 Elsevier Ireland Ltd.
PY - 2015/8/1
Y1 - 2015/8/1
N2 - Introduction: This study compared the efficacy of docetaxel alone vs. docetaxel plus cisplatin/carboplatin in resected NSCLC patients relapsing after preoperative, adjuvant, or perioperative platinum-based chemotherapy. Materials and methods: Patients were randomly assigned to receive docetaxel plus cisplatin/carboplatin (Arm A) or docetaxel alone (Arm B). Primary endpoint was progression-free survival (PFS). Secondary endpoints were response rate at 6 weeks, toxicity, quality of life, and overall survival (OS). Results: From November 2007 to August 2012, 88 patients were enrolled. Due to an unexpectedly slow accrual, the trial was prematurely stopped. Adding platinum to docetaxel caused a non-significant increase in PFS. Median PFS was 8.0 months (95% CI: 5.3-10.4) for Arm A vs. 5.6 months (95% CI: 4.0-7.3) for Arm B (HR: 0.71, 95% CI: 0.45-1.1, p=. 0.15). Median OS was 16.0 months (95% CI: 10.1-23.9) for Arm A vs. 12.4 months (95% CI: 8.2-19.6) for Arm B. In pre-planned subgroup analyses, a time to recurrence ≥12 months and non-squamous histology favorably influenced OS (HR: 0.51, 95% CI: 0.29-0.91, p= 0.02 and HR: 0.54, 95% CI: 0.33-0.91, p= 0.02, respectively). There were no unexpected adverse events, and Grade 3-4 toxicity was comparable in both groups. Conclusions: Our study failed to demonstrate significant PFS improvement with the docetaxel-platinum doublet compared to single-agent docetaxel. The 3.6-month improvement in OS with the cisplatin-based doublet proves, however, appealing and merits further investigation.
AB - Introduction: This study compared the efficacy of docetaxel alone vs. docetaxel plus cisplatin/carboplatin in resected NSCLC patients relapsing after preoperative, adjuvant, or perioperative platinum-based chemotherapy. Materials and methods: Patients were randomly assigned to receive docetaxel plus cisplatin/carboplatin (Arm A) or docetaxel alone (Arm B). Primary endpoint was progression-free survival (PFS). Secondary endpoints were response rate at 6 weeks, toxicity, quality of life, and overall survival (OS). Results: From November 2007 to August 2012, 88 patients were enrolled. Due to an unexpectedly slow accrual, the trial was prematurely stopped. Adding platinum to docetaxel caused a non-significant increase in PFS. Median PFS was 8.0 months (95% CI: 5.3-10.4) for Arm A vs. 5.6 months (95% CI: 4.0-7.3) for Arm B (HR: 0.71, 95% CI: 0.45-1.1, p=. 0.15). Median OS was 16.0 months (95% CI: 10.1-23.9) for Arm A vs. 12.4 months (95% CI: 8.2-19.6) for Arm B. In pre-planned subgroup analyses, a time to recurrence ≥12 months and non-squamous histology favorably influenced OS (HR: 0.51, 95% CI: 0.29-0.91, p= 0.02 and HR: 0.54, 95% CI: 0.33-0.91, p= 0.02, respectively). There were no unexpected adverse events, and Grade 3-4 toxicity was comparable in both groups. Conclusions: Our study failed to demonstrate significant PFS improvement with the docetaxel-platinum doublet compared to single-agent docetaxel. The 3.6-month improvement in OS with the cisplatin-based doublet proves, however, appealing and merits further investigation.
KW - Chemotherapy
KW - Cisplatin
KW - Docetaxel
KW - Non-small cell lung cancer
KW - Prognosis
KW - Second line
UR - http://www.scopus.com/inward/record.url?scp=84937630369&partnerID=8YFLogxK
U2 - 10.1016/j.lungcan.2015.05.016
DO - 10.1016/j.lungcan.2015.05.016
M3 - Article
C2 - 26059274
AN - SCOPUS:84937630369
SN - 0169-5002
VL - 89
SP - 139
EP - 145
JO - Lung Cancer
JF - Lung Cancer
IS - 2
ER -