Combined immunochemotherapy in patients with refractory/relapsed classical Hodgkin's lymphoma as a 2nd line treatment before autologous hematopoietic stem cell transplantation (preliminary results)

Q4 Medicine
A. Mamedova, N. Mochkin, V. Sarzhevskiy, E. Demina, V. Bogatyrev, A. Spornik, A. Samoylova, A. Rukavitsin, E. Smirnova, A. Bannikova, V. Melnichenko, N. Mikhaylova, E. Borzenkova, L. Stelmakh, Y. Zalyalov, A. A. Semenova, G. Tumyan, M. Danilova, O. Konova, N. Falaleeva, A. Terekhova, M. A. Vernyuk, A. Chervontseva, L. S. Khayrullina, A. Maslov, I. Lysenko, Yuliya Alekseeva, E. S. Pavlyuchenko, A. A. Mirsaitov, A. Zverkova, I. Ishmatova, S. Volchenkov, M. Motalkina, I. Zyuzgin
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引用次数: 1

Abstract

Aim. To study the efficacy and safety of combined immunochemotherapy according to the DHAp protocol + nivolumab in patients with refractory/relapsed classical Hodgkin's lymphoma before autologous hematopoietic stem cell transplantation.Materials and methods. The study consisted of 2 phases: 1st - immunotherapy with nivolumab (2 injections as monotherapy at a dose of 240 mg/day with 14 days interval); 2nd - combined immunochemotherapy according to the DHAp protocol + nivolumab (14 days after the 2nd administration of nivolumab): nivolumab 480 mg/day on day 1 in combination with chemotherapy according to the DHAp protocol, 4 cycles in total. The effectiveness of therapy was evaluated after 2 injections of nivolumab, after 2 and 4 cycles of combination therapy. from March 2020 to November 2021, 32 patients were included in the study. The median age was 34 (18-55) years.Results. As of November 2021, the result was evaluated in 32 patients after the 1st stage of treatment (nivolumab monotherapy). A complete response was obtained in 4 (12.5 %) patients, a partial response in 20 (62.5 %) patients, disease stabilization was noted in 5 (16 %) patients, an indeterminate response in 3 (9 %) patients. At the 2nd phase, the efficacy after the 2nd cycle of DHAp + nivolumab was evaluated in 31 patients (complete response was obtained in 19 (61 %), partial response in 11 (36 %)); the final efficacy evaluation (after the 4th cycle of DHAp + nivolumab) was performed in 30 patients, and all patients achieved response to therapy (complete response in 25 (83 %), partial response in 5 (17 %)). 2 patients were excluded from the study.Conclusion. preliminary results of combined immuno- and chemotherapy according to the DHAp protocol showed high efficacy and relatively low toxicity in patients with refractory/relapsed classical Hodgkin's lymphoma before autologous hematopoietic stem cell transplantation.
自体造血干细胞移植前联合免疫化疗作为难治性/复发的经典霍奇金淋巴瘤患者的二线治疗(初步结果)
的目标。研究在自体造血干细胞移植前,按照dhp方案联合免疫化疗+纳沃单抗治疗难治性/复发的经典霍奇金淋巴瘤患者的疗效和安全性。材料和方法。该研究包括两个阶段:第一阶段-纳武单抗免疫治疗(2次注射作为单药治疗,剂量为240 mg/天,间隔14天);根据DHAp方案第二次联合免疫化疗+纳武单抗(第二次给药后14天):第1天纳武单抗480 mg/天,根据DHAp方案联合化疗,共4个周期。在2次注射纳武单抗、2和4个周期联合治疗后评估治疗的有效性。从2020年3月到2021年11月,32名患者被纳入研究。中位年龄34岁(18-55岁)。截至2021年11月,32名患者在第一阶段治疗(纳武单抗单药治疗)后进行了结果评估。4例(12.5%)患者完全缓解,20例(62.5%)患者部分缓解,5例(16%)患者疾病稳定,3例(9%)患者不确定缓解。在第二阶段,评估了31例患者在DHAp + nivolumab的第二个周期后的疗效(19例(61%)获得完全缓解,11例(36%)获得部分缓解);30例患者进行了最终疗效评估(在DHAp + nivolumab的第4个周期后),所有患者都对治疗产生了反应(完全缓解25例(83%),部分缓解5例(17%))。2例患者被排除在研究之外。初步结果显示,在自体造血干细胞移植前对难治性/复发的经典霍奇金淋巴瘤患者进行免疫联合化疗的疗效高,毒性相对较低。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
20
审稿时长
12 weeks
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