Journal
THORACIC CANCER
Volume 12, Issue 13, Pages 1943-1951Publisher
WILEY
DOI: 10.1111/1759-7714.13977
Keywords
extensive‐ stage; prognosis; small cell lung cancer; survival
Categories
Funding
- CAMS Innovation Fund for Medical Sciences (CIFMS) [2016-I2M-1-001]
- China National Major Project for New Drug Innovation [2017ZX09304015]
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This study retrospectively collected detailed medical records of 358 patients with ES-SCLC from January 1, 2011 to December 31, 2018 in a top-level cancer hospital in China. It identified age ≥70, smoking index ≥400, bone multimetastasis, two tumor biomarkers (cyfra211, CA125), and two laboratory indexes (decreased Na, PLR <76) as independent prognostic factors for OS in this patient population, providing real-world evidence for survival and prognosis.
Background Extensive-stage small cell lung cancer (ES-SCLC) is deemed as a fatal malignancy with a poor prognosis. Although immunotherapy has gradually played an important role in the treatment of ES-SCLC since 2018, ES-SCLC treatment data and patient outcome before 2018, when chemotherapy served as a fundamental therapeutic strategy, is still meaningful as a summary of the situation regarding previous medical treatment and is a baseline for comparative data. In addition, the prognostic factors of ES-SCLC have failed to reach a consensus until now. Therefore, this study aimed to evaluate survival and identify the prognostic factors in an ES-SCLC population. Methods We retrospectively collected the detailed medical records of 358 patients with ES-SCLC from January 1, 2011 to December 31, 2018 in a Chinese top-level cancer hospital. The prognostic factors were evaluated by Cox univariate and multivariate analysis. Results The median overall survival (OS) of ES-SCLC patients (N = 358) was 14.0 months, the one- and two-year OS rates were 56.2% and 21.7%, respectively. Moreover, we identified two demographic characters (age >= 70, smoking index >= 400), one tumor burden factor (bone multimetastasis), two tumor biomarkers (cyfra211, CA125) and two laboratory indexes (decreased Na, PLR < 76) as independent prognostic factors for OS in this patient population. Progression-free survival (PFS) data of 238 patients was obtained for further analysis, and the median PFS was 6.2 months, and six-month and one-year PFS rates were 51.7% and 14.3%, respectively. Elevated cyfra211, decreased Hb and Na were identified as independent prognostic factors for PFS. Conclusions This study provides real-world evidence of the survival and prognosis of ES-SCLC patients which will enable better evaluation and clinical decision-making in the future.
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