Department of Oncology, Changde Hospital, Xiangya School of Medicine, Central South University (The First People's Hospital of Changde City), Changde, China.
Department of Electrocardiogram and Physiology, Changde Hospital, Xiangya School of Medicine, Central South University (The First People's Hospital of Changde City), Changde, China.
Front Immunol. 2024 Nov 1;15:1493740. doi: 10.3389/fimmu.2024.1493740. eCollection 2024.
Extensive-stage small-cell lung cancer (ES-SCLC) has a dismal prognosis owing to its high aggressiveness, rapid drug resistance, and early metastasis. ES-SCLC responds well to first-line chemotherapy, and chemotherapy coupled with immunotherapy can further improve overall survival. However, the long-term survival of patients remains unsatisfactory because of its high recurrence rate and the poor efficacy of second-line treatment. Although local radiotherapy is an important component of the overall treatment for ES-SCLC, its value in the age of immunotherapy remains controversial.
A 54-year-old male with ES-SCLC achieved a complete response (CR), as determined using enhanced computed tomography (CT) after four cycles of immunochemotherapy (serplulimab, carboplatin, and etoposide). Whole-body positron emission tomography-CT was performed during maintenance treatment with serplulimab, which showed primary lung, liver, and bone metastatic lesions with CR. However, several mediastinal lymph nodes exhibited glucose metabolism uptake, and new lesions appeared on the head. The patient underwent palliative radiotherapy of the head and consolidative thoracic radiotherapy of the chest and continued maintenance treatment with serplulimab. Subsequent magnetic resonance imaging of the head suggested good control of metastatic lesions (CR). The patient received first-line immunotherapy for approximately 20 months.
This report presents a patient with ES-SCLC who underwent local radiotherapy in addition to serplulimab as maintenance therapy. Although the programmed death-ligand 1 (PD-L1) expression level was negative and a PD-1 inhibitor instead of a PD-L1 inhibitor was used, the patient did not experience significant pneumonia during treatment, and the efficacy of the current treatment was evident. This treatment model warrants further clinical investigation.
广泛期小细胞肺癌(ES-SCLC)由于其侵袭性强、耐药迅速和早期转移等特点,预后较差。ES-SCLC 对一线化疗反应良好,化疗联合免疫治疗可进一步提高总生存期。然而,由于其高复发率和二线治疗效果不佳,患者的长期生存仍然不尽如人意。虽然局部放疗是 ES-SCLC 整体治疗的重要组成部分,但在免疫治疗时代,其价值仍存在争议。
一名 54 岁男性患有 ES-SCLC,在免疫化疗(赛普利单抗、卡铂和依托泊苷)四个周期后,增强 CT 检查显示完全缓解(CR)。在赛普利单抗维持治疗期间进行全身正电子发射断层扫描-CT 检查,显示原发性肺、肝和骨转移病灶均达到 CR。然而,几个纵隔淋巴结显示葡萄糖代谢摄取,头部出现新病灶。患者接受了头部姑息性放疗和胸部巩固性放疗,继续接受赛普利单抗维持治疗。随后的头部磁共振成像显示转移性病变得到良好控制(CR)。患者接受了约 20 个月的一线免疫治疗。
本报告介绍了一名 ES-SCLC 患者,在接受赛普利单抗维持治疗的同时还接受了局部放疗。尽管程序性死亡配体 1(PD-L1)表达水平为阴性,且使用的是 PD-1 抑制剂而不是 PD-L1 抑制剂,但患者在治疗过程中并未出现明显肺炎,且当前治疗的疗效明显。这种治疗模式值得进一步的临床研究。