Zhongshan City People's Hostipial, Zhongshan, China.
Medicine (Baltimore). 2022 Dec 30;101(52):e32459. doi: 10.1097/MD.0000000000032459.
Malignant pleural mesothelioma (MPM) is a malevolent tumor originated from pleura and often leads to poor prognosis. Chemotherapy of pemetrexed and cisplatin combined with antiangiogenic therapy of bevacizumab is recommended as the first-line regimen by guidelines. However, there are few sustainable second-line anti-tumor theraies that bring distinct survival benefit after the occurrence of drug resistance as the reported mPFS (median progression-free survival) scarcely exceeds 6 months. Immune checkpoint inhibitors are extensively investigated in pan-cancer, and dual immunotherapy has been listed in the first-line recommendation of MPM in several guidelines, while MPM patients benefit modestly from immune checkpoint inhibitors combination or monotherapy in second-line practice.
We report a 59-year-old male patient who was diagnosed with unresectable MPM in April 2021.
He received firstly pemetrexed combined with platinum and bevacizumab, which barely curbed disease progression; When the first line treatment failed, he was switched to tislelizumab combined with anlotinib.
Tislelizumab combined with anlotinib significantly relieved his clinical symptoms, and imaging examination further validated the improvement. Until present, the second-line treatment PFS is more than 10 months.
The case firstly demonstrated the efficacy of tislelizumab combined with anlotinib in the second-line management of MPM. Thus, immunotherapy combined with small-molecule multi-target anti-angiogenic medication may be alternative for the second-line schemes of MPM.
恶性胸膜间皮瘤(MPM)是一种起源于胸膜的恶性肿瘤,通常预后不良。指南推荐培美曲塞和顺铂联合贝伐珠单抗的化疗联合抗血管生成治疗作为一线方案。然而,耐药后能带来明显生存获益的二线抗肿瘤治疗方法很少,因为报道的 mPFS(无进展生存期中位数)很少超过 6 个月。免疫检查点抑制剂在泛癌中得到了广泛研究,双免疫疗法已被列入几项指南中 MPM 的一线推荐,而 MPM 患者在二线治疗中从免疫检查点抑制剂联合或单药治疗中获益有限。
我们报告了一位 59 岁男性患者,他于 2021 年 4 月被诊断为不可切除的 MPM。
他首先接受了培美曲塞联合铂类和贝伐珠单抗治疗,但几乎没有抑制疾病进展;一线治疗失败后,他改用替雷利珠单抗联合安罗替尼。
替雷利珠单抗联合安罗替尼显著缓解了他的临床症状,影像学检查进一步验证了疗效的改善。截至目前,二线治疗 PFS 已超过 10 个月。
该病例首次证明了替雷利珠单抗联合安罗替尼在 MPM 二线治疗中的疗效。因此,免疫治疗联合小分子多靶点抗血管生成药物可能是 MPM 二线治疗方案的替代选择。