Outcome of High-Dose Chemotherapy Followed by Autologous Stem Cell Transplantation in Relapsed/Refractory Hodgkin Lymphoma after Different Numbers of Salvage Regimens.
Jacopo MariottiFrancesca RicciLaura GiordanoDaniela TaurinoBarbara SarinaChiara De PhilippisDaniele ManninaCarmello Carlo-StellaStefania BramantiArmando SantoroPublished in: Cells (2024)
The introduction of novel drugs ( PD-1 inhibitors and/or brentuximab vedotin) into salvage regimens has improved the response rate and the outcome of patients with relapsed/refractory Hodgkin lymphoma. However, the impact of new drugs on the outcome has not been adequately investigated so far. We retrospectively analyzed 42 consecutive patients treated at our institution with high-dose chemotherapy/autologous stem cell transplantation after either one standard chemotherapy represented by BEGEV ( n = 28) or >1 salvage therapy (ST) comprising novel drugs ( n = 14). With a median follow-up of 24 months, the 2-year cumulative incidence of relapse was similar between the two cohorts: 26% for 1 ST and 18% for >1 ST ( p = 0.822). Consistently, overall survival and progression-free survival did not differ among the two groups: 3-year overall survival was 91% and 89% ( p = 0.731), respectively, and 3-year progression-free survival was 74% and 83% ( p = 0.822) for only one and more than one salvage regimens, respectively. Of note, the post-transplant side effects and engraftment rates were similar between the 1 ST and >1 ST cohorts. In conclusion, consolidation with high-dose chemotherapy/autologous stem cell transplantation is a safe and curative option, even for patients achieving disease response after more than one rescue line of therapy.
Keyphrases
- hodgkin lymphoma
- stem cell transplantation
- high dose
- free survival
- low dose
- locally advanced
- cell therapy
- bone marrow
- end stage renal disease
- rectal cancer
- prognostic factors
- ejection fraction
- newly diagnosed
- platelet rich plasma
- risk factors
- chronic kidney disease
- radiation therapy
- stem cells
- drug induced
- mass spectrometry
- atomic force microscopy
- patient reported