Jair Bar, Qingqing Xu, Sudeep Karve, Pooja Hingorani, Amin A. Virani, Neal E. Ready
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Patients with other/multiple primary malignancies, non-SCLC histology, or treated through a clinical trial were excluded. Clinical outcomes included RW physician-reported response rates, duration of response (DOR), duration of clinical benefit (DoCB), overall survival (OS), and progression-free survival (PFS), stratified by platinum sensitivity and Eastern Cooperative Oncology Group performance status (ECOG-PS). Time-to-event outcomes were estimated via Kaplan–Meier. Treatment patterns were assessed, including the sequence of regimens by LOT and first-line (1L) platinum sensitivity status.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Among 113 eligible patients (median age 58 years), 54% were female, and 46% had a chemotherapy-free interval after 1L of < 90 days. Tumor shrinkage, complete response, and stable disease were reported in 19%, 1%, and 13% of patients at 3L, respectively. The median DOR, DoCB, OS, and PFS were 2.8, 2.5, 5.8, and 2.4 months in 3L, respectively. Platinum-resistant versus sensitive patients in 1L had shorter time-to-event outcomes. Clinical outcomes were similar regardless of ECOG-PS status. Platinum-based chemotherapy rates decreased from 94% and 93% in 1L to 17% and 16% in 3L in platinum-sensitive and resistant patients, respectively.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>These RW findings validate 3L results from clinical trials, demonstrating the limited clinical benefits with current therapies in 3L ES SCLC, and highlighting the urgent need for novel therapies that improve outcomes in this difficult-to-treat patient population.</p>\n </section>\n </div>","PeriodicalId":9440,"journal":{"name":"Cancer reports","volume":"8 8","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cnr2.70289","citationCount":"0","resultStr":"{\"title\":\"Real-World Response and Survival Outcomes and Treatment Patterns in Patients With Extensive Stage Small-Cell Lung Cancer Receiving Third-Line Treatment\",\"authors\":\"Jair Bar, Qingqing Xu, Sudeep Karve, Pooja Hingorani, Amin A. 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引用次数: 0
摘要
背景:小细胞肺癌(SCLC)患者主要表现为广泛分期(ES)疾病,5年生存率较低。在三线(3L) ES SCLC中,很少有治疗选择和有限的结果数据来量化未满足的医疗需求。本图表回顾评估了这些患者的真实世界(RW)临床结果和治疗模式。方法采用电子病历进行回顾性研究,纳入在美国癌症治疗中心(现为City of Hope)接受≥3线治疗(LOT)的ES - SCLC成年患者(≥2例转移性肺癌)。排除了其他/多种原发性恶性肿瘤,非sclc组织学或通过临床试验治疗的患者。临床结果包括RW医生报告的缓解率、缓解持续时间(DOR)、临床获益持续时间(DoCB)、总生存期(OS)和无进展生存期(PFS),并根据铂敏感性和东部肿瘤合作组的表现状态(ECOG-PS)进行分层。通过Kaplan-Meier法估计事件发生时间。评估治疗模式,包括LOT的方案顺序和一线(1L)铂敏感性状态。结果在113例符合条件的患者中(中位年龄58岁),54%为女性,46%的患者在90天的1L后无化疗间隔。3L时,分别有19%、1%和13%的患者报告肿瘤缩小、完全缓解和疾病稳定。3L中位DOR、DoCB、OS和PFS分别为2.8、2.5、5.8和2.4个月。与铂耐药患者相比,1L患者的事件发生时间更短。无论ECOG-PS状态如何,临床结果相似。铂敏感和耐药患者的铂基化疗率分别从1L组的94%和93%下降到3L组的17%和16%。这些RW研究结果验证了临床试验的3L结果,表明目前治疗3L ES SCLC的临床益处有限,并强调迫切需要新的治疗方法来改善这一难以治疗的患者群体的预后。
Real-World Response and Survival Outcomes and Treatment Patterns in Patients With Extensive Stage Small-Cell Lung Cancer Receiving Third-Line Treatment
Background
Patients with small-cell lung cancer (SCLC) primarily present with extensive stage (ES) disease and poor 5-year survival. There are few treatment options and limited data on outcomes in third-line (3L) ES SCLC to quantify unmet medical needs. This chart review evaluated real-world (RW) clinical outcomes and treatment patterns in these patients.
Methods
This retrospective study using electronic medical records included adult patients with ES SCLC (≥ 2 claims for metastasized lung cancer) who received ≥ 3 lines of therapy (LOT) at Cancer Treatment Centers of America (now City of Hope). Patients with other/multiple primary malignancies, non-SCLC histology, or treated through a clinical trial were excluded. Clinical outcomes included RW physician-reported response rates, duration of response (DOR), duration of clinical benefit (DoCB), overall survival (OS), and progression-free survival (PFS), stratified by platinum sensitivity and Eastern Cooperative Oncology Group performance status (ECOG-PS). Time-to-event outcomes were estimated via Kaplan–Meier. Treatment patterns were assessed, including the sequence of regimens by LOT and first-line (1L) platinum sensitivity status.
Results
Among 113 eligible patients (median age 58 years), 54% were female, and 46% had a chemotherapy-free interval after 1L of < 90 days. Tumor shrinkage, complete response, and stable disease were reported in 19%, 1%, and 13% of patients at 3L, respectively. The median DOR, DoCB, OS, and PFS were 2.8, 2.5, 5.8, and 2.4 months in 3L, respectively. Platinum-resistant versus sensitive patients in 1L had shorter time-to-event outcomes. Clinical outcomes were similar regardless of ECOG-PS status. Platinum-based chemotherapy rates decreased from 94% and 93% in 1L to 17% and 16% in 3L in platinum-sensitive and resistant patients, respectively.
Conclusion
These RW findings validate 3L results from clinical trials, demonstrating the limited clinical benefits with current therapies in 3L ES SCLC, and highlighting the urgent need for novel therapies that improve outcomes in this difficult-to-treat patient population.