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Vaughn, John L

Mayo Clinic

Long Island University

Citations 1

Evaluation of prognostic factors in patients with high-risk classical Hodgkin lymphoma undergoing autologous transplantation
Huang, Ying , Cashen, Amanda F. , Vaughn, John L, Badar, Talha , Sethi, Tarsheen , Reddy, Nishitha , Bello, Celeste, Kothari, Shalin , Hernandez‐Ilizaliturri, Francisco J. , Svoboda, Jakub , Glenn, Martha, Cohen, Jonathon B. , Sorge, Caryn, Christian, Beth , Herrera, Alex F. , Vaughn, John L. , Epperla, Narendranath , Badar, Talha , Karmali, Reem , Cohen, Jonathon B , Herrera, Alex F , Hamadani, Mehdi , Costa, Luciano J , Xavier, Ana C , Epperla, Narendranath , Hanel, Walter G. , Barta, Stefan K , Caimi, Paolo F. , Karmali, Reem , Chavez, Julio C , Lansigan, Frederick , Hamadani, Mehdi , Costa, Luciano J.

Blood Advances | August 30, 2024 | Volume: 8 | Issue: 21 | Pages: 5458-5466

10.1182/bloodadvances.2024013743 Get It

Abstract There are limited data assessing the risk scores for primary treatment failure (PTF) in patients with classical Hodgkin lymphoma (cHL; PTF-cHL) undergoing autologous hematopoietic cell transplantation (auto-HCT). ECLIPSE (Evaluation of Classical Hodgkin Lymphoma patients wIth Primary treatment failure and analySis of outcomEs) is a multicenter retrospective cohort of patients with PTF-cHL (aged ≄15 years) diagnosed on or after 1 January 2005, at 15 US medical centers. PTF was defined as 1 of the following patterns of failure: (1) progressive disease by imaging during or within 6 weeks of completion of frontline chemotherapy (primary progression [PP]); (2) partial response (PR) or stable disease (SD) by imaging after completion of frontline treatment (PR/SD); (3) progression of disease by imaging (and confirmed by biopsy) within 12 months of frontline therapy completion after prior documentation of complete response (CR; early relapse [ER]). A total of 478 patients were included in the analysis. Among these, 217 (45%) were PP, 86 (18%) were PR/SD, and 175 (37%) were ER. The 6-month and 1-year cumulative incidence of nonrelapse mortality after auto-HCT were 0.9% and 1.1%, respectively. The median progression-free survival (PFS) and overall survival (OS) after auto-HCT were 4.33 and 10.09 years, respectively. Although those not in CR at the time of auto-HCT were associated with inferior PFS and OS, advanced age and diagnosis before 2011 were associated with inferior OS. This study showcases the safety and long-term efficacy of auto-HCT, even in patients with high-risk disease who are traditionally considered chemotherapy refractory, and will serve as a benchmark for the ongoing transplant vs no transplant trials.