Gao Guangbin, Wu Yajing, Liu Qing, Zhai Chang, Inoue Yusuke, Zhang Xinyuan, Lv Xiaoyan, Zhang Wei, Wang Jun
Department of Radiation Oncology, Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Transl Lung Cancer Res. 2024 Dec 31;13(12):3795-3806. doi: 10.21037/tlcr-24-981. Epub 2024 Dec 26.
Small-cell lung cancer (SCLC) is highly malignant. Despite being highly sensitive to initial chemotherapy and radiotherapy, the recurrence rate is high. Atezolizumab is the first immune checkpoint inhibitor (ICI) that has been proven to provide an overall survival (OS) benefit for extensive-stage SCLC (ES-SCLC), making ICIs in combination with chemotherapy the standard first-line treatment for ES-SCLC. However, the real-world treatment of SCLC is more complex, and multimodal therapy may be needed to achieve long-term patient survival. Few reports on later-line chemotherapy combined with immunotherapy have been published thus far. Moreover, there is limited data on the efficacy and safety of thoracic radiotherapy and radiotherapy for metastatic lesions after multiple lines of treatment have failed in ES-SCLC, and the value of small-molecule antiangiogenesis combined with immunotherapy also needs further exploration.
A patient was diagnosed with mediastinal limited-stage SCLC (LS-SCLC) and experienced local progression following standard chemoradiotherapy and prophylactic cranial irradiation. Subsequently, the patient underwent second-line irinotecan chemotherapy, which resulted in severe hematological toxicity. Upon initiation of third-line therapy with anlotinib, the disease remained stable for 9 months. Unfortunately, imaging revealed the presence of a new lesion at the right lung apex. Nevertheless, there was renewed hope for survival when atezolizumab was introduced as part of the treatment regimen. Despite the later development of brain metastases and metastasis adjacent to the aortic arch, long-term survival was achieved through combination therapy involving immunotherapy, antiangiogenic therapy, and radiotherapy targeting the metastatic lesions. By March 2024, the OS had reached 70 months, with a duration of treatment with atezolizumab of 48 months, and only grade II hypothyroidism occurred during treatment, with no other immunotherapy-related adverse events being observed.
This case report suggests the potential efficacy and safety of integrating chemotherapy, immunotherapy, radiotherapy, and antiangiogenic therapy for the treatment of SCLC. Further clinical trials are warranted to validate the value of combining chemotherapy, immunotherapy, radiotherapy, and antiangiogenic therapy.
小细胞肺癌(SCLC)具有高度恶性。尽管对初始化疗和放疗高度敏感,但复发率很高。阿替利珠单抗是首个被证实可使广泛期小细胞肺癌(ES-SCLC)患者总生存期(OS)获益的免疫检查点抑制剂(ICI),这使得ICI联合化疗成为ES-SCLC的标准一线治疗方案。然而,SCLC的实际治疗更为复杂,可能需要多模式治疗才能实现患者长期生存。迄今为止,关于后线化疗联合免疫治疗的报道很少。此外,对于ES-SCLC在多线治疗失败后进行胸部放疗和转移灶放疗的疗效和安全性数据有限,小分子抗血管生成联合免疫治疗的价值也需要进一步探索。
一名患者被诊断为纵隔局限期小细胞肺癌(LS-SCLC),在接受标准放化疗和预防性颅脑照射后出现局部进展。随后,该患者接受了二线伊立替康化疗,但出现了严重的血液学毒性。在开始使用安罗替尼进行三线治疗后,疾病稳定了9个月。不幸的是,影像学检查发现右肺尖出现了一个新病灶。然而,当将阿替利珠单抗引入治疗方案时,患者重燃了生存希望。尽管后来出现了脑转移和主动脉弓旁转移,但通过免疫治疗、抗血管生成治疗和针对转移灶的放疗联合治疗,患者实现了长期生存。截至2024年3月,OS已达70个月,阿替利珠单抗治疗时长为48个月,治疗期间仅出现II级甲状腺功能减退,未观察到其他免疫治疗相关不良事件。
本病例报告提示了化疗、免疫治疗、放疗和抗血管生成治疗联合用于SCLC治疗的潜在疗效和安全性。有必要进行进一步的临床试验来验证化疗、免疫治疗、放疗和抗血管生成治疗联合的价值。