| Thoracic Cancer | |
| Real‐life effectiveness of first‐line anticancer treatments in stage IIIB/IV NSCLC patients: Data from the Czech TULUNG Registry | |
| Helena Coupkova1  Milada Zemanova2  Michal Hrnciarik3  Leona Koubkova4  Martin Svaton5  Milos Pesek5  Jana Krejci6  Kristian Brat7  Monika Bratova7  Jana Skrickova7  Libor Havel8  Ondrej Fischer9  Magda Barinova1,10  Karolina Hurdalkova1,10  | |
| [1] Clinic of Comprehensive Cancer Care Masaryk Memorial Cancer Institute Brno Czech Republic;Department of Oncology General Teaching Hospital Prague Czech Republic;Department of Pneumology University Hospital Hradec Kralove Hradec Kralove Czech Republic;Department of Pneumology University Hospital Motol Prague Czech Republic;Department of Pneumology University Hospital Pilsen Pilsen Czech Republic;Department of Pneumology and Thoracic Surgery Bulovka Hospital Prague Czech Republic;Department of Respiratory Diseases University Hospital Brno Brno Czech Republic;Department of Respiratory Medicine Thomayer Hospital Prague Czech Republic;Department of Respiratory Medicine University Hospital Olomouc Olomouc Czech Republic;Institute of Biostatistics and Analyses, Ltd. Brno Czech Republic; | |
| 关键词: Anticancer treatment; non‐small cell lung cancer; progression‐free survival; real‐life effectiveness; tyrosinkinase inhibitors; | |
| DOI : 10.1111/1759-7714.13679 | |
| 来源: DOAJ | |
【 摘 要 】
Background Data regarding real‐life effectiveness of any treatment may improve clinical decision‐making. The aim of this study was to evaluate real‐life effectiveness of tyrosin‐kinase inhibitors, bevacizumab and pemetrexed as first‐line treatments in patients with advanced/metastatic non‐small cell lung cancer (NSCLC). Methods We analyzed data of 2157 patients of the Czech TULUNG Registry of patients with advanced/metastatic NSCLC who received modern‐era treatments between 2011 and 2018. Patients treated with gefitinib, erlotinib, afatinib, bevacizumab (+ maintenance), pemetrexed (+ maintenance) as first‐line therapy were included in the study. A systematic literature search separately identified clinical trials suitable for calculation of comparator pooled OS and PFS for each regimen. For each subgroup, basic characteristics and survival data (Kaplan‐Meier estimates) are shown. We propose the “index of real‐life effectiveness” (IRE), a ratio of real‐life OS/PFS and comparator pooled OS/PFS. Univariate and multivariate logistic regression identified factors were associated with longer OS (ie, IRE>1.1). Results Survival analysis showed median OS of 23 months for erlotinib, 29.3 months for afatinib, 19.6 months for gefitinib, 12.2 months for pemetrexed, 17.5 months for pemetrexed maintenance, 15.8 months for bevacizumab and 15.8 months for bevacizumab maintenance. Calculated IREs for OS for the regimens were: erlotinib 1.013, afatinib 1.184, gefitinib 0.736, pemetrexed 1.188, pemetrexed maintenance 1.294, bevacizumab 1.178, and bevacizumab maintenance 1.189. Multivariate regression analysis showed that these factors were associated with longer OS: lower PS for afatinib; lower PS, absence of adverse events and female sex for bevacizumab; and lower PS and female sex for pemetrexed. Conclusions This study clearly demonstrated that real‐life effectiveness of certain treatment regimens may strongly differ in various populations/health care systems, and comparison between TULUNG data and pooled survival data from trials showed higher real‐life effectiveness for most of the studied first‐line regimens. Lower ECOG PS, younger age, female sex and adverse events were associated with longer survival in most regimens. Key points Significant findings of the study Comparison between TULUNG data and pooled survival data from trials showed higher real‐life effectiveness for most of the studied first‐line regimens; for most regimens, lower ECOG PS, younger age, female sex and adverse events were associated with longer survival. What this study adds Real‐life effectiveness of certain treatment regimens may strongly differ in various populations/health care systems.
【 授权许可】
Unknown