Factors affecting survival and prognosis in extensive stage small cell lung cancer.

IF 2.8 3区 医学 Q2 RESPIRATORY SYSTEM BMC Pulmonary Medicine Pub Date : 2025-04-08 DOI:10.1186/s12890-025-03625-w
Mert Erciyestepe, Ömer Burak Ekinci, Hale Gülçin Yıldırım Doğan, Ahmet Emin Öztürk, Okan Aydın, Aslı Büyükkuşcu, Tugay Atasever, Beyza Soylu Uslu, Kübra Akkaya, Emir Çelik, Kayhan Ertürk, Muhammed Mustafa Atcı
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Abstract

Although chemotherapy significantly improves the quality of life and prolongs survival in patients with extensive-stage small cell lung cancer (ES-SCLC), relapse is almost inevitable, with only 5% of patients surviving two years after the initial diagnosis. Prophylactic cranial irradiation (PCI) is considered for patients who achieve a complete response, as it has been shown to improve survival rates in this population. Recent studies have also demonstrated that adding PD-L1 inhibitors, such as atezolizumab or durvalumab, to chemotherapy in first-line treatment significantly enhances survival compared to chemotherapy alone. Our study was conducted retrospectively at a single center, including 280 patients with ES-SCLC who began therapy at our institution between July 2009 and February 2023. Patients who underwent thoracic residual radiotherapy (p< 0.001) and PCI (p< 0.001) showed statistically significant improvements in OS. In the first-line treatment group, the median overall survival (OS) for patients receiving cisplatin+etoposide was 12.0 months (10.71 - 13.28), while those treated with carboplatin+etoposide had a median OS of 7.0 months (4.58 - 9.41). For patients receiving carboplatin+etoposide+atezolizumab, the median OS was 35.0 months (21.32 - 48.67), and a statistically significant difference was observed (p< 0.001). In our study, the median OS was 7 months in patients who received ≤ 4 cycles of treatment in the first line and 14 months in patients who received > 4 cycles of treatment. After first-line treatment, the proportion of patients with progression-free survival (PFS) between 0 - 3 months was 21%, and between 3 - 6 months was 24%. PFS was notably worse in those with bone, liver, or brain metastases at diagnosis in the first-line treatment. Multivariate analysis revealed that carboplatin+etoposide+atezolizumab in the first line and cisplatin+etoposide in the second line reduced the risk of both progression and death, while PCI reduced the risk of death. In conclusion, ES-SCLC remains one of the most challenging malignancies, characterized by poor survival rates and short progression-free intervals. Multiple factors influence OS and PFS, some of which are intrinsic to the patient and disease at diagnosis. In contrast, others, such as treatment modalities, the number of treatment cycles, and the application of radiotherapy, can be modified by clinicians.

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影响广泛期小细胞肺癌生存和预后的因素。
尽管化疗显著改善了广泛期小细胞肺癌(ES-SCLC)患者的生活质量并延长了生存期,但复发几乎是不可避免的,只有5%的患者在初次诊断后存活两年。预防性颅脑照射(PCI)被认为是达到完全缓解的患者,因为它已被证明可以提高这一人群的生存率。最近的研究也表明,在一线化疗中加入PD-L1抑制剂,如atezolizumab或durvalumab,与单独化疗相比,可显着提高生存率。我们的研究是在一个单中心回顾性进行的,包括280例ES-SCLC患者,他们于2009年7月至2023年2月在我们的机构开始治疗。接受胸部残余放疗(p< 0.001)和PCI (p< 0.001)的患者OS改善有统计学意义。在一线治疗组,顺铂+依托泊苷组患者的中位总生存期(OS)为12.0个月(10.71 - 13.28),而卡铂+依托泊苷组患者的中位OS为7.0个月(4.58 - 9.41)。卡铂+依托泊苷+atezolizumab组的中位OS为35.0个月(21.32 ~ 48.67),差异有统计学意义(p< 0.001)。在我们的研究中,在一线接受≤4个周期治疗的患者中位OS为7个月,而接受≤4个周期治疗的患者中位OS为14个月。一线治疗后,0 - 3个月无进展生存(PFS)患者比例为21%,3 - 6个月无进展生存(PFS)患者比例为24%。在一线治疗中,骨、肝或脑转移患者的PFS明显更差。多因素分析显示,一线卡铂+依托泊苷+atezolizumab和二线顺铂+依托泊苷均降低了进展和死亡风险,而PCI降低了死亡风险。总之,ES-SCLC仍然是最具挑战性的恶性肿瘤之一,其特点是生存率低,无进展时间短。多种因素影响OS和PFS,其中一些是患者和疾病在诊断时固有的。相比之下,其他方面,如治疗方式、治疗周期的数量和放疗的应用,可以由临床医生修改。
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来源期刊
BMC Pulmonary Medicine
BMC Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
4.40
自引率
3.20%
发文量
423
审稿时长
6-12 weeks
期刊介绍: BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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