Long Yan-Yan, Chen Jing, Xie Yue, Wang Ying, Wu Yong-Zhong, Xv Ying, Weng Ke-Gui, Zhou Wei
Department of Radiation Oncology Center, Chongqing University Cancer Hospital and Chongqing Cancer Institute and Chongqing Cancer Hospital, Chongqing, China.
First School of Clinical Medicine, Southern Medical University, Guangzhou, China.
Front Oncol. 2023 Oct 6;13:1209758. doi: 10.3389/fonc.2023.1209758. eCollection 2023.
Brain metastases (BMs) are common in Small Cell Lung Cancer (SCLC), but the prognosis is very poor. Currently, there is no standard of care on what constitutes optimal treatment, and there is no consensus regarding maintenance therapy in SCLC.
We report the case of a 55-year-old man with advanced SCLC. After the initial diagnosis, he received routine chemotherapy and chest radiotherapy but developed brain metastases with 2 lesions seven months later. We used an effective combination therapy consisting of the antiangiogenic inhibitor, Anlotinib and whole-brain radiotherapy. We then administered anti-PD-L1 immunotherapy Atezolizumab in combination with Anlotinib as long-term maintenance therapy. Twelve months later, there was a progression in one of the brain metastases. The patient underwent further stereotactic radiotherapy (SRT) for the lesion. However, after four months of treatment with SRT, the lesion began to gradually grow in size. The patient underwent surgical resection of the lesion, which confirmed radioactive brain necrosis. After a full 3-year course of anti-PD-L1 therapy, the patient discontinued immunotherapy and was administered only Anlotinib as maintenance. At the time of writing up this report, the patient was alive and the overall survival reached 41 months after the onset of BM.
This indicated a potential synergistic effect of combined immunotherapy and antiangiogenic targeted therapy with local radiotherapy in patients with BM-SCLC and can provide directions for future clinical decisions.
脑转移瘤(BMs)在小细胞肺癌(SCLC)中很常见,但预后很差。目前,对于什么构成最佳治疗尚无标准治疗方案,并且在SCLC的维持治疗方面也没有共识。
我们报告了一例55岁晚期SCLC男性患者的病例。初始诊断后,他接受了常规化疗和胸部放疗,但7个月后出现了2个脑转移瘤病灶。我们采用了由抗血管生成抑制剂安罗替尼和全脑放疗组成的有效联合治疗方案。然后,我们给予抗程序性死亡受体配体1(PD-L1)免疫疗法阿替利珠单抗联合安罗替尼作为长期维持治疗。12个月后,其中一个脑转移瘤出现进展。患者对该病灶进行了进一步的立体定向放射治疗(SRT)。然而,在接受SRT治疗4个月后,病灶开始逐渐增大。患者接受了病灶的手术切除,病理证实为放射性脑坏死。在完成了为期3年的抗PD-L1治疗疗程后,患者停止免疫治疗,仅给予安罗替尼作为维持治疗。在撰写本报告时,患者仍然存活,自脑转移瘤出现后总生存期达到了41个月。
这表明免疫治疗与抗血管生成靶向治疗联合局部放疗在BM-SCLC患者中可能具有协同效应,并可为未来的临床决策提供指导。