The impact of smoking status on the progression-free survival of non-small cell lung cancer patients receiving molecularly target therapy or immunotherapy versus chemotherapy: A meta-analysis

被引:23
作者
Li, Xinyi [1 ]
Huang, Cong [1 ]
Xie, Xiaohui [1 ,2 ]
Wu, Ziyang [1 ]
Tian, Xia [2 ]
Wu, Yibo [1 ]
Du, Xin [1 ]
Shi, Luwen [1 ,2 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, Dept Pharm Adm & Clin Pharm, Beijing 100191, Peoples R China
[2] Peking Univ, Int Res Ctr Med Adm, Beijing 100191, Peoples R China
关键词
immunotherapy; molecularly target therapy; non‐ small cell lung cancer; smoking status; TYROSINE KINASE INHIBITORS; OPEN-LABEL; PHASE-III; 1ST-LINE TREATMENT; EGFR MUTATIONS; WILD-TYPE; ERLOTINIB; DOCETAXEL; NIVOLUMAB; ADENOCARCINOMA;
D O I
10.1111/jcpt.13309
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
What is known and Objective Smoking has a notable influence on the efficacy of medications for lung cancer. Previous studies illustrated the correlation between smoking and the efficacy of first-line Epidermal Growth Factor Receptors-Tyrosine Kinase Inhibitors (EGFR-TKIs). The benefit of smokers in immunotherapy was still controversial. Here, we investigated the impact of smoking on clinical outcomes of molecularly targeted therapies or immunotherapy in Non-Small Cell Lung Cancer (NSCLC). Methods We performed meta-analysis including trials comparing EGFR-TKIs, Anaplastic Lymphoma Kinase (ALK) inhibitors or Immune Checkpoint Inhibitors (ICIs) against chemotherapy in NSCLC. The Progression-Free Survival (PFS)-Hazard Ratios (HRs) of two groups served as the index and we used random effects to pool outcomes. Results and discussion Twenty randomized trials were selected. Compared with chemotherapy, treatment with EGFR-TKIs had similar benefit in never-smokers (PFS: HR = 0.46, 95% CI 0.30 to 0.69) and smokers (PFS: HR = 0.68, 95% CI 0.50 to 0.91; p = 0.135) while non-smokers (PFS: HR = 0.32, 95% CI 0.23 to 0.44) had better benefit from first-line EGFR-TKIs than smokers (PFS: HR = 0.54, 95% CI 0.41 to 0.71; p = 0.02). Treatment with ALK inhibitors had similar benefits in never-smokers (PFS: HR = 0.43, 95% CI 0.35 to 0.53) and smokers (PFS: HR = 0.56, 95% CI 0.44 to 0.71; p = 0.406). The benefit of ICIs in smokers (PFS: HR = 0.79, 95% CI 0.64 to 0.98) was significantly greater than never-smokers (PFS: HR = 1.81, 95% CI 1.27 to 2.57; p = 0.004). What is new and Conclusion Smoking status is an important clinical predictor of therapy in NSCLC. Never-smokers and smokers have similar benefit with EGFR-TKIs therapy compared with chemotherapy, while never-smokers have greater benefit after first-line EGFR-TKIs therapy. There was similar benefit in never-smokers and smokers when using ALK inhibitors over chemotherapy. Additionally, ICIs treatment over chemotherapy leads to more favourable PFS in smokers both in first-line and second-line settings.
引用
收藏
页码:256 / 266
页数:11
相关论文
共 39 条
[2]   Avelumab versus docetaxel in patients with platinum-treated advanced non-small-cell lung cancer (JAVELIN Lung 200): an open-label, randomised, phase 3 study [J].
Barlesi, Fabrice ;
Vansteenkiste, Johan ;
Spigel, David ;
Ishii, Hidenobu ;
Garassino, Marina ;
de Marinis, Filippo ;
Ozguroglu, Mustafa ;
Szczesna, Aleksandra ;
Polychronis, Andreas ;
Uslu, Ruchan ;
Krzakowski, Maciej ;
Lee, Jong-Seok ;
Calabro, Luana ;
Frontera, Osvaldo Aren ;
Ellers-Lenz, Barbara ;
Bajars, Marcis ;
Ruisi, Mary ;
Park, Keunchil .
LANCET ONCOLOGY, 2018, 19 (11) :1468-1479
[3]   Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer [J].
Borghaei, H. ;
Paz-Ares, L. ;
Horn, L. ;
Spigel, D. R. ;
Steins, M. ;
Ready, N. E. ;
Chow, L. Q. ;
Vokes, E. E. ;
Felip, E. ;
Holgado, E. ;
Barlesi, F. ;
Kohlhaeufl, M. ;
Arrieta, O. ;
Burgio, M. A. ;
Fayette, J. ;
Lena, H. ;
Poddubskaya, E. ;
Gerber, D. E. ;
Gettinger, S. N. ;
Rudin, C. M. ;
Rizvi, N. ;
Crino, L. ;
Blumenschein, G. R. ;
Antonia, S. J. ;
Dorange, C. ;
Harbison, C. T. ;
Finckenstein, F. Graf ;
Brahmer, J. R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (17) :1627-1639
[4]   Molecular analysis of the RET and NTRK1 gene rearrangements in papillary thyroid carcinoma in the Polish population [J].
Brzezianska, Ewa ;
Karbownik, Malgorzata ;
Migdalska-Sek, Monika ;
Pastuszak-Lewandoska, Dorota ;
Wloch, Jan ;
Lewinski, Andrzej .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2006, 599 (1-2) :26-35
[5]   First-Line Nivolumab in Stage IV or Recurrent Non-Small-Cell Lung Cancer [J].
Carbone, D. P. ;
Reck, M. ;
Paz-Ares, L. ;
Creelan, B. ;
Horn, L. ;
Steins, M. ;
Felip, E. ;
van den Heuvel, M. M. ;
Ciuleanu, T. -E. ;
Badin, F. ;
Ready, N. ;
Hiltermann, T. J. N. ;
Nair, S. ;
Juergens, R. ;
Peters, S. ;
Minenza, E. ;
Wrangle, J. M. ;
Rodriguez-Abreu, D. ;
Borghaei, H. ;
Blumenschein, G. R. ;
Villaruz, L. C. ;
Havel, L. ;
Krejci, J. ;
Corral Jaime, J. ;
Chang, H. ;
Geese, W. J. ;
Bhagavatheeswaran, P. ;
Chen, A. C. ;
Socinski, M. A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 376 (25) :2415-2426
[6]   Impact of smoking on lung cancer treatment effectiveness: a review [J].
Condoluci, Adalgisa ;
Mazzara, Calogero ;
Zoccoli, Alice ;
Pezzuto, Aldo ;
Tonini, Giuseppe .
FUTURE ONCOLOGY, 2016, 12 (18) :2149-2161
[7]   Clinicopathological and Demographical Characteristics of Non-Small Cell Lung Cancer Patients with ALK Rearrangements: A Systematic Review and Meta-Analysis [J].
Fan, Liang ;
Feng, Yun ;
Wan, Huanying ;
Shi, Guochao ;
Niu, Wenquan .
PLOS ONE, 2014, 9 (06)
[8]   Erlotinib versus docetaxel as second-line treatment of patients with advanced non-small-cell lung cancer and wild-type EGFR tumours (TAILOR): a randomised controlled trial [J].
Garassino, Marina Chiara ;
Martelli, Olga ;
Broggini, Massimo ;
Farina, Gabriella ;
Veronese, Silvio ;
Rulli, Eliana ;
Bianchi, Filippo ;
Bettini, Anna ;
Longo, Flavia ;
Moscetti, Luca ;
Tomirotti, Maurizio ;
Marabese, Mirko ;
Ganzinelli, Monica ;
Lauricella, Calogero ;
Labianca, Roberto ;
Floriani, Irene ;
Giaccone, Giuseppe ;
Torri, Valter ;
Scanni, Alberto ;
Marsoni, Silvia .
LANCET ONCOLOGY, 2013, 14 (10) :981-988
[9]   Effects of smoking on the pharmacokinetics of erlotinib [J].
Hamilton, M ;
Wolf, JL ;
Rusk, J ;
Beard, SE ;
Clark, GM ;
Witt, K ;
Cagnoni, PJ .
CLINICAL CANCER RESEARCH, 2006, 12 (07) :2166-2171
[10]   Overcoming CYP1A1/1A2 Mediated Induction of Metabolism by Escalating Erlotinib Dose in Current Smokers [J].
Hughes, Andrew N. ;
O'Brien, Mary E. R. ;
Petty, W. Jeffrey ;
Chick, Jonathan B. ;
Rankin, Elaine ;
Woll, Penella J. ;
Dunlop, David ;
Nicolson, Marianne ;
Boinpally, Ramesh ;
Wolf, Julie ;
Price, Allan .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (08) :1220-1226