Thiruvengadam Swetha Kambhampati, Mei Matthew G, Godfrey James, Siddiqi Tanya, Salhotra Amandeep, Chen Robert, Smith Eileen, Popplewell Leslie L, Herrera Alex F
Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
Clin Lymphoma Myeloma Leuk. 2022 Oct;22(10):e893-e897. doi: 10.1016/j.clml.2022.06.004. Epub 2022 Jun 6.
Anti-PD-1 directed therapy is safe and effective in patients with relapsed/refractory (r/r) cHL and is currently being studied in the frontline setting. There are currently little data regarding the safety and efficacy of PD-1 blockade after prior PD-L1 blockade with agents such as avelumab.
This is a retrospective case series evaluating r/r cHL patients treated with avelumab who subsequently received at least 1 dose of PD-1 blockade. Primary objective is efficacy as measured by overall response rate. Secondary objectives include duration of response and time to progression on PD-1 blockade as well as safety as evaluated by incidence and severity of immune-related adverse events (irAE) with PD-1 blockade.
There were 7 patients treated with PD-1 blockade after avelumab, of whom 4 were re-treated. The median follow-up was 46.8 months. At the time of PD-1 blockade initiation median age was 36.6 years, all patients had advanced stage, 1 patient had B symptoms, and 4 patients had extranodal disease. Patients received median 7 prior lines of therapy including avelumab. Median duration on anti-PD-1 treatment was 15.9 months. A response was observed in 86% of patients with median duration of response of 26.4 months and median time to progression of 22.2 months. Only 1 patient experienced an irAE (grade 2 pneumonitis).
Our study suggests that PD-1 blockade after PD-L1 blockade in r/r cHL appears safe and may be effective with durable responses observed in a subset of patients.
抗程序性死亡蛋白1(PD-1)定向治疗对复发/难治性(r/r)经典型霍奇金淋巴瘤(cHL)患者安全有效,目前正在一线治疗中进行研究。目前,关于使用阿维鲁单抗等药物进行先前程序性死亡配体1(PD-L1)阻断后PD-1阻断的安全性和有效性的数据很少。
这是一项回顾性病例系列研究,评估接受阿维鲁单抗治疗后随后接受至少1剂PD-1阻断的r/r cHL患者。主要目标是通过总缓解率衡量的疗效。次要目标包括PD-1阻断的缓解持续时间和疾病进展时间,以及通过PD-1阻断的免疫相关不良事件(irAE)的发生率和严重程度评估的安全性。
有7例患者在接受阿维鲁单抗治疗后接受了PD-1阻断,其中4例接受了再治疗。中位随访时间为46.8个月。在开始PD-1阻断时,中位年龄为36.6岁,所有患者均为晚期,1例患者有B症状,4例患者有结外病变。患者接受的中位治疗线数为7线,包括阿维鲁单抗。抗PD-1治疗的中位持续时间为15.9个月。86%的患者观察到缓解,中位缓解持续时间为26.4个月,中位疾病进展时间为22.2个月。只有1例患者发生了irAE(2级肺炎)。
我们的研究表明,r/r cHL患者在PD-L1阻断后进行PD-1阻断似乎是安全的,并且在一部分患者中观察到持久缓解,可能是有效的。