Eugene Chao, Joseph P Marshalek, David Yashar, Sarah Tomassetti
{"title":"Doxorubicin, bleomycin, vinblastine, and dacarbazine for Hodgkin lymphoma: Real-world experience from a Los Angeles County hospital.","authors":"Eugene Chao, Joseph P Marshalek, David Yashar, Sarah Tomassetti","doi":"10.1177/20503121251365462","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>While there are significant ongoing advancements in the management of Hodgkin lymphoma, doxorubicin + bleomycin + vinblastine + dacarbazine remains a preferred option for early stage Hodgkin lymphoma and is a frequently used first-line treatment globally. The aim of this retrospective study is to analyze real-world doxorubicin + bleomycin + vinblastine + dacarbazine outcomes from a safety net hospital setting.</p><p><strong>Methods: </strong>This retrospective cohort consisted of 69 adult patients with classical Hodgkin lymphoma who received first-line doxorubicin + bleomycin + vinblastine + dacarbazine at Harbor-UCLA Medical Center from 2009 to 2024. Early (I-II) and advanced (III-IV) stage patients were included.</p><p><strong>Results: </strong>The median patient age was 41 years old (range 18-71). There was balanced distribution of early stage (7.2% stage I, 40.6% stage II) and advanced stage (20.3% stage III, 31.9% stage IV) Hodgkin lymphoma. With a median of six cycles (range 2-7) of doxorubicin + bleomycin + vinblastine + dacarbazine, the complete response rate was 78.3% and overall response rate was 82.6%. Five-year progression-free survival was 70.7% (70.2% for stage I-II, 71.3% for stage III-IV). Overall survival at 5 years was 95.4% (100% for stages I-II, 91.5% for stages III-IV). Bleomycin-associated lung toxicity was observed in 10 (14.5%) patients, including one treatment-related death.</p><p><strong>Conclusions: </strong>Response rates and overall survival from this real-world cohort are comparable to previously published contemporary studies. The high complete response rate, 5-year progression-free survival, and 5-year overall survival in this study further support the robust curative potential of doxorubicin + bleomycin + vinblastine + dacarbazine and validate its continued use in resource-limited settings.</p>","PeriodicalId":21398,"journal":{"name":"SAGE Open Medicine","volume":"13 ","pages":"20503121251365462"},"PeriodicalIF":2.1000,"publicationDate":"2025-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12434294/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"SAGE Open Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/20503121251365462","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: While there are significant ongoing advancements in the management of Hodgkin lymphoma, doxorubicin + bleomycin + vinblastine + dacarbazine remains a preferred option for early stage Hodgkin lymphoma and is a frequently used first-line treatment globally. The aim of this retrospective study is to analyze real-world doxorubicin + bleomycin + vinblastine + dacarbazine outcomes from a safety net hospital setting.
Methods: This retrospective cohort consisted of 69 adult patients with classical Hodgkin lymphoma who received first-line doxorubicin + bleomycin + vinblastine + dacarbazine at Harbor-UCLA Medical Center from 2009 to 2024. Early (I-II) and advanced (III-IV) stage patients were included.
Results: The median patient age was 41 years old (range 18-71). There was balanced distribution of early stage (7.2% stage I, 40.6% stage II) and advanced stage (20.3% stage III, 31.9% stage IV) Hodgkin lymphoma. With a median of six cycles (range 2-7) of doxorubicin + bleomycin + vinblastine + dacarbazine, the complete response rate was 78.3% and overall response rate was 82.6%. Five-year progression-free survival was 70.7% (70.2% for stage I-II, 71.3% for stage III-IV). Overall survival at 5 years was 95.4% (100% for stages I-II, 91.5% for stages III-IV). Bleomycin-associated lung toxicity was observed in 10 (14.5%) patients, including one treatment-related death.
Conclusions: Response rates and overall survival from this real-world cohort are comparable to previously published contemporary studies. The high complete response rate, 5-year progression-free survival, and 5-year overall survival in this study further support the robust curative potential of doxorubicin + bleomycin + vinblastine + dacarbazine and validate its continued use in resource-limited settings.