Torka Pallawi, Feldman Tatyana, Savage Kerry J, Ganesan Nivetha, Drill Esther, Hancock Helen, Davey Theresa, Perez Leslie, Capadona Charisse, Subzwari Sarima, Galasso Natasha, Yang Jinshu, Post Michelle, Boardman Alexander, Caron Philip, David Kevin, Epstein-Peterson Zachary, Falchi Lorenzo, Ghione Paola, Hamlin Paul, Horwitz Steven M, Intlekofer Andrew M, Johnson William, Kumar Anita, Lue Jennifer, Noy Ariela, Owens Colette, Palomba M Lia, Salles Gilles A, Steiner Raphael, Stuver Robert, Vardhana Santosha, Yahalom Joachim, Dogan Ahmet, Zelenetz Andrew D, Schöder Heiko, Moskowitz Alison J
Memorial Sloan Kettering Cancer Center, New York, NY.
John Theurer Cancer Center, Hackensack, NJ.
J Clin Oncol. 2025 Mar 10;43(8):985-993. doi: 10.1200/JCO-24-01278. Epub 2024 Dec 11.
We conducted a phase I/II study evaluating nivolumab plus doxorubicin, vinblastine, dacarbazine (N-AVD) as frontline therapy for treatment-naïve older adults (OA) with classical Hodgkin lymphoma (cHL; ClinicalTrials.gov identifier: NCT03033914).
Patients age ≥60 years with newly diagnosed, any stage, cHL were treated with six cycles of AVD at standard doses plus nivolumab 240 mg intravenously once every 2 weeks (on days 1 and 15) of each cycle. A geriatric assessment was performed before therapy initiation. The primary end point was progression-free survival (PFS).
Patient characteristics (N = 40) included median age of 66 years (range, 60-78 years) with 38% ≥70 years, 78% with stage III/IV disease, 68% with International Prognostic Score of ≥3, 82% dependent in ≥1 activities of daily living, 23% dependent in ≥1 instrumental activities of daily living, 50% with impaired timed up and go test, and 40% with polypharmacy. Among 37 response-evaluable patients, the median follow-up was 49 months and 3-year PFS and overall survival (OS) were 79% and 97%, respectively. Overall, 50% patients experienced grade 3/4 treatment-related adverse events (TRAEs), including febrile neutropenia in 8%. Four (10%) patients stopped therapy due to TRAEs. There was no correlation between baseline geriatric impairments and survival outcomes or toxicities. Positron emission tomography-2 was not predictive of PFS or OS.
N-AVD is a highly effective and well-tolerated frontline regimen in OA with cHL across a wide range of geriatric impairments.
我们开展了一项I/II期研究,评估纳武利尤单抗联合多柔比星、长春花碱、达卡巴嗪(N-AVD)作为初治老年(OA)经典型霍奇金淋巴瘤(cHL)患者一线治疗方案的疗效(ClinicalTrials.gov标识符:NCT03033914)。
年龄≥60岁、新诊断的各期cHL患者接受六个周期标准剂量的AVD治疗,外加每2周(每个周期的第1天和第15天)静脉注射240mg纳武利尤单抗。在治疗开始前进行了老年评估。主要终点是无进展生存期(PFS)。
患者特征(N = 40)包括:中位年龄66岁(范围60 - 78岁),38%≥70岁;78%为III/IV期疾病;68%国际预后评分≥3;82%在至少一项日常生活活动中存在依赖;23%在至少一项工具性日常生活活动中存在依赖;50%计时起立行走测试结果不佳;40%服用多种药物。在37例可评估缓解情况的患者中,中位随访时间为49个月,3年PFS和总生存期(OS)分别为79%和97%。总体而言,50%的患者发生3/4级治疗相关不良事件(TRAEs),其中8%发生发热性中性粒细胞减少。4例(10%)患者因TRAEs停止治疗。基线老年功能障碍与生存结果或毒性之间无相关性。正电子发射断层扫描-2不能预测PFS或OS。
N-AVD是一种对存在广泛老年功能障碍的cHL老年患者高度有效且耐受性良好的一线治疗方案。