Clinical and molecular features in patients with advanced non-small-cell lung carcinoma refractory to first-line platinum-based chemotherapy

被引:34
作者
Leprieur, E. Giroux [1 ,2 ]
Antoine, M. [1 ,3 ]
Vieira, T. [1 ]
Duruisseaux, M. [1 ]
Poulot, V. [1 ]
Rabbe, N. [1 ]
Belmont, L. [4 ]
Gounant, V. [4 ]
Lavole, A. [4 ]
Milleron, B. [4 ]
Lacave, R. [1 ,5 ]
Cadranel, J. [1 ]
Wislez, M. [1 ,4 ]
机构
[1] GRC Univ Paris 6, Hop Tenon, APHP, Equipe Rech 2, F-75970 Paris, France
[2] Univ Versailles St Quentin Yvelines, Hop Ambroise Pare, APHP, Serv Pneumol, F-92100 Boulogne, France
[3] Univ Paris 06, Hop Tenon, APHP, Serv Anat Pathol, F-75970 Paris, France
[4] Univ Paris 06, Hop Tenon, APHP, Serv Pneumol, F-75970 Paris, France
[5] Univ Paris 06, Hop Tenon, APHP, Serv Histol Biol Tumorale, F-75970 Paris, France
关键词
Non-small-cell lung cancer; Early progressive disease; Refractory patients; Platinum-based chemotherapy; Sarcomatoid carcinoma; EGFR mutations; KRAS mutations; ALK translocation; GROWTH-FACTOR RECEPTOR; PHASE-III TRIAL; VINORELBINE PLUS CISPLATIN; PULMONARY PLEOMORPHIC CARCINOMA; HA-RAS ONCOGENE; RANDOMIZED TRIAL; SARCOMATOID CARCINOMAS; ADJUVANT CHEMOTHERAPY; OPEN-LABEL; CANCER;
D O I
10.1016/j.lungcan.2012.10.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Most of the cases of non-small-cell lung cancer (NSCLC) are diagnosed at an advanced stage and are treated with platinum-doublet chemotherapy. However, some patients are refractory to this treatment. The aim of this study was to identify the clinical and molecular characteristics of patients with refractory disease. All consecutive patients between 2003 and 2006, who received a platinum-doublet chemotherapy as first-line treatment for stage IIIb-IV NSCLC, were included. Refractory patients were defined as early progressive disease (PD) at the first evaluation of chemotherapy according to WHO criteria. The clinical, histo-pathological, and molecular characteristics (EGFR: exon 19, 20, 21 and KRAS: exon 2 by PCR sequencing; ALK by immunohistochemistry) and survival of refractory patients with initial PD (r-patients) and controlled disease (c-patients) were compared by univariate analyses. Factors that differed between the two groups (p-value <0.25 in univariate analyses) were entered into multivariate analysis. In this study, 178 patients were included. The first tumor assessment was carried out after a median of three cycles (range 1-4). Forty-six (25.8%) patients were refractory. Clinical presentation was similar between r- and c-patients. The sarcomatoid histological subtype was more common in r-patients than c-patients (10.9% vs. 1.5%, respectively; p = 0.057). The proportion of EGFR (5.2% vs. 9.6%, p = 0.224) and KRAS mutations (11.1% vs. 5.7%, p = 0.357), and the expression of ALK (6.3% vs. 2.5%, p = 0.327) did not differ significantly between the two groups. In multivariate analysis, sarcomatoid histological subtype was the only factor associated with early PD (OR = 7.50; 95%CI: 1.02-55.45; p = 0.048). r-Patients had significantly shorter survival than c-patients (medians months (IQR 3.2-9.9) vs. 15.4 months (IQR 9.9-22.5), respectively; p < 0.0001). In conclusion, patients with early PD under platinum-doublet chemotherapy had shorter survival than c-patients. Sarcomatoid histological subtype was the only independent factor associated with early PD. (c) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:167 / 172
页数:6
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