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卡瑞利珠单抗联合阿帕替尼成功治疗晚期肺泡软组织肉瘤:一例报告

Successful treatment of advanced alveolar soft part sarcoma with camrelizumab combined with apatinib: a case report.

作者信息

Xu Zhen, Zhang Yong, Yu Yong-Hua

机构信息

Cancer Hospital of Shandong First Medical University, Shandong Cancer Hospital and Institute,Jinan, China.

Department of Abdominal Radiation Oncology Ward 2, Cancer Hospital of Shandong First Medical University, Shandong Cancer Hospital and Institute, Jinan, China.

出版信息

Ann Palliat Med. 2021 Jan;10(1):785-792. doi: 10.21037/apm-20-2275.

Abstract

Alveolar soft part sarcoma (ASPS) is a rare and highly malignant mesenchymal tumor that primarily affects adolescents and young adults. ASPS is characterized by a slow growth rate, high metastatic potential, and resistance to conventional therapies. The emergence of immune checkpoint inhibitors (ICIs) has revolutionized the treatment of advanced malignancies, improving the objective response rate (ORR) and prolonging patient survival. The combination of immunotherapy with targeted therapies can overcome resistance to treatment with ICIs alone. Although substantial progress has been made in various solid tumors, the clinical relevance of ICIs, used alone or in combination with other therapies, in patients with ASPS remains unclear. This is a case report of a 32-year-old man who was diagnosed with advanced ASPS. After 8 months of anlotinib treatment, the patient's disease progressed and new cerebellar metastases were detected. Radiotherapy was administered in addition to camrelizumab combined with apatinib to treat the brain metastases. The patient achieved partial remission (46%) after 3 months of treatment and did not present any severe side effects. This is the first reported case of the successful treatment of advanced ASPS with camrelizumab combined with apatinib. This case supports the use of a novel treatment regimen for patients with inoperable ASPS or ASPS that is resistant to conventional therapies.

摘要

肺泡软组织肉瘤(ASPS)是一种罕见的高恶性间充质肿瘤,主要影响青少年和年轻成年人。ASPS的特点是生长速度缓慢、转移潜能高且对传统疗法耐药。免疫检查点抑制剂(ICI)的出现彻底改变了晚期恶性肿瘤的治疗方式,提高了客观缓解率(ORR)并延长了患者生存期。免疫疗法与靶向疗法联合使用可以克服单独使用ICI治疗的耐药性。尽管在各种实体瘤治疗方面取得了重大进展,但ICI单独使用或与其他疗法联合使用在ASPS患者中的临床相关性仍不明确。本文报告了一例32岁男性被诊断为晚期ASPS的病例。在接受8个月的安罗替尼治疗后,患者病情进展,检测到新的小脑转移灶。除了卡瑞利珠单抗联合阿帕替尼治疗脑转移外,还进行了放疗。治疗3个月后,患者达到部分缓解(46%),且未出现任何严重副作用。这是首例报道的卡瑞利珠单抗联合阿帕替尼成功治疗晚期ASPS的病例。该病例支持为无法手术的ASPS患者或对传统疗法耐药的ASPS患者采用新的治疗方案。

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