Real World Analysis of Small Cell Lung Cancer Patients: Prognostic Factors and Treatment Outcomes

被引:16
作者
Moser, Sarah Sharman [1 ]
Bar, Jair [2 ,3 ]
Kan, Inna [4 ]
Ofek, Keren [4 ]
Cohen, Raanan [4 ]
Khandelwal, Nikhil [5 ]
Shalev, Varda [1 ,3 ]
Chodick, Gabriel [1 ,3 ]
Siegelmann-Danieli, Nava [1 ]
机构
[1] Maccabi Healthcare Serv, Maccabi Inst Res & Innovat, Maccabitech, IL-6812509 Tel Aviv, Israel
[2] Sheba Med Ctr, Inst Oncol, IL-5262000 Ramat Gan, Israel
[3] Tel Aviv Univ, Sackler Fac Med, IL-6997801 Tel Aviv, Israel
[4] Abbvie Biopharmaceut Ltd, IL-4524075 Hod Hasharon, Israel
[5] Abbvie Inc, Chicago, IL 60064 USA
关键词
SCLC; survival; observational study; platinum sensitive; limited stage; PROPHYLACTIC CRANIAL IRRADIATION; RANDOMIZED PHASE-II; LONG-TERM SURVIVORS; 3RD-LINE CHEMOTHERAPY; 2ND-LINE CHEMOTHERAPY; 1ST-LINE CHEMOTHERAPY; CHECKMATE; 032; OPEN-LABEL; PROGRESS; REGIMEN;
D O I
10.3390/curroncol28010036
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this observational study, we assessed treatment patterns and prognostic factors in patients with small cell lung cancer (SCLC) in a large state-mandated healthcare organization in Israel. Methods: All incident cases with histologically confirmed SCLC who initiated systemic anti-cancer treatment between 2011 and 2017 were identified. Treatment patterns and overall survival (OS) were evaluated for each line of therapy. Results: A total of 235 patients were identified (61% male, median age 64 years, 95% ever smokers, 64% had extensive stage). The first-line treatment was platinum-etoposide regimen for 98.7% of the cohort. The second and third-line regimen were given to 43% and 12% of patients, respectively. Mean OS for extensive and limited stage patients was 9.1 and 23.5 months respectively. In a multivariable model, increased risk for mortality was observed among patients with an ECOG performance status (PS) of 2 compared to a PS of 0-1 for the extensive stage patients (Hazard ratio (HR) = 1.63, 95% confidence ratios (CI): 1.00-2.65); and for males compared to females for the limited stage patients (HR = 2.17; 95% CI: 1.12-4.20). Regarding all 2nd line patients in a multivariable model incorporating relevant confounding factors, demonstrated a significantly better outcome with platinum-based regimens compared to topotecan. Median survival after initiation of 2nd line in platinum-sensitive patients was longer (p = 0.056) for those re-challenged with platinum-based regimen (n = 7): 6.8mo (6.1-not reported (NR)), compared with those switched to a different treatment (n = 27): 4.5 mo (2.6-6.6) for extensive stage patients, and a non-significant difference was also observed for limited stage patients. Conclusion: To our knowledge, this is one of the largest real-world studies of SCLC patients. OS for SCLC patients was similar to that reported in clinical trials. PS for extensive stage patients and sex for limited stage patients were significant correlates of prognosis. Re-challenge of the platinum-based doublet was associated with longer OS compared to switching treatment in extensive stage patients.
引用
收藏
页码:317 / 331
页数:15
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