Efficiency and Safety of Brentuximab Vedotine as a Salvage Treatment Before Autologous Stem Cell Transplantation in Patients With Relapsed or Refractory Classic Hodgkin Lymphoma: Retrospective Study.
Kateryna Filonenko, Yana Stepanishyna, Nazar Shokun, Arina Martynchyk, Yevhen Kushchevyi, Iryna Kriachok, Jan Maciej Zaucha
{"title":"Efficiency and Safety of Brentuximab Vedotine as a Salvage Treatment Before Autologous Stem Cell Transplantation in Patients With Relapsed or Refractory Classic Hodgkin Lymphoma: Retrospective Study.","authors":"Kateryna Filonenko, Yana Stepanishyna, Nazar Shokun, Arina Martynchyk, Yevhen Kushchevyi, Iryna Kriachok, Jan Maciej Zaucha","doi":"10.1155/ah/3573471","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>There is no strong evidence supporting brentuximab vedotine (BV) efficacy as a salvage regimen for relapsed/refractory Hodgkin's lymphoma (R/R HL) patients before autologous hematopoietic cell transplantation (auto-HCT).</p><p><strong>Methods: </strong>We performed multicenter retrospective analysis of efficiency of treatment with the BV monotherapy as salvage regimen versus standard salvage chemotherapy (sCT) in 44 patients with R/R HL from a high-risk group.</p><p><strong>Results: </strong>Twenty-six patients (59.1%) had primary refractory disease. Nineteen patients (43.2%) received BV salvage treatment before auto-HCT, and 12 (63.6%) achieved complete response (CR) that counts 27.3% of the whole study cohort. There was no difference in the CR rate, 2-year progression-free survival, and 2-year overall survival after BV salvage and sCT (63.2% vs. 60%, respectively, <i>p</i> = 0.35; 88.2% vs. 80.7%, <i>p</i> = 0.655; 94.1% vs. 100%, <i>p</i> = 0.735, respectively). There was no difference in neuropathy of all grades, including Grades 2-3 between groups.</p><p><strong>Conclusions: </strong>The BV as a salvage treatment showed quite high efficiency. Despite a worse clinical characteristic of the BV group, there were no significant differences in the outcomes of the auto-HCT with respect to the salvage regimen (BV versus sCT) used before auto-HCT. Our results suggest that BV before auto-HCT in patients refractory to standard 2nd line treatment equalizes their prognosis to the patient sensitive to standard CT with the same tolerance and toxicity.</p>","PeriodicalId":7325,"journal":{"name":"Advances in Hematology","volume":"2025 ","pages":"3573471"},"PeriodicalIF":0.0000,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12539663/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Hematology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/ah/3573471","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Background: There is no strong evidence supporting brentuximab vedotine (BV) efficacy as a salvage regimen for relapsed/refractory Hodgkin's lymphoma (R/R HL) patients before autologous hematopoietic cell transplantation (auto-HCT).
Methods: We performed multicenter retrospective analysis of efficiency of treatment with the BV monotherapy as salvage regimen versus standard salvage chemotherapy (sCT) in 44 patients with R/R HL from a high-risk group.
Results: Twenty-six patients (59.1%) had primary refractory disease. Nineteen patients (43.2%) received BV salvage treatment before auto-HCT, and 12 (63.6%) achieved complete response (CR) that counts 27.3% of the whole study cohort. There was no difference in the CR rate, 2-year progression-free survival, and 2-year overall survival after BV salvage and sCT (63.2% vs. 60%, respectively, p = 0.35; 88.2% vs. 80.7%, p = 0.655; 94.1% vs. 100%, p = 0.735, respectively). There was no difference in neuropathy of all grades, including Grades 2-3 between groups.
Conclusions: The BV as a salvage treatment showed quite high efficiency. Despite a worse clinical characteristic of the BV group, there were no significant differences in the outcomes of the auto-HCT with respect to the salvage regimen (BV versus sCT) used before auto-HCT. Our results suggest that BV before auto-HCT in patients refractory to standard 2nd line treatment equalizes their prognosis to the patient sensitive to standard CT with the same tolerance and toxicity.
背景:没有强有力的证据支持布伦妥昔单抗维多定(BV)作为复发/难治性霍奇金淋巴瘤(R/R HL)患者自体造血细胞移植(auto-HCT)前的补救方案的疗效。方法:我们对44名来自高危人群的R/R HL患者进行了多中心回顾性分析,以BV单药治疗作为挽救方案与标准挽救化疗(sCT)的治疗效率。结果:原发难治性疾病26例(59.1%)。19例患者(43.2%)在auto-HCT前接受了BV挽救治疗,12例(63.6%)达到完全缓解(CR),占整个研究队列的27.3%。BV抢救和sCT后的CR率、2年无进展生存率和2年总生存率均无差异(分别为63.2% vs 60%, p = 0.35; 88.2% vs 80.7%, p = 0.655; 94.1% vs 100%, p = 0.735)。两组间包括2-3级在内的所有级别的神经病变均无差异。结论:BV作为一种救助性治疗具有较高的疗效。尽管BV组的临床特征较差,但与auto-HCT之前使用的挽救方案(BV vs sCT)相比,auto-HCT的结果没有显著差异。我们的研究结果表明,对标准二线治疗难治的患者在自体hct前的BV与对标准CT敏感的患者的预后相同,并且具有相同的耐受性和毒性。