Impact of type of reduced-intensity conditioning regimen on the outcomes of allogeneic haematopoietic cell transplantation in classical Hodgkin lymphoma.
Sairah AhmedNilanjan GhoshKwang W AhnManoj KhanalCarlos LitovichAlberto MussettiSaurabh ChhabraMitchell S CairoMatthew MeiBasem M WilliamSunita NathanNelli BejanyanRichard F OlssonParastoo B DahiMarjolein van der PoelAmir SteinbergJennifer KanakryJan CernyUmar FarooqSachiko SeoMohamed A Kharfan-DabajaAnna SuredaTimothy S FenskeMehdi HamadaniPublished in: British journal of haematology (2020)
Reduced-intensity conditioning (RIC) allogeneic haematopoietic cell transplantation (allo-HCT) is a curative option for select relapsed/refractory Hodgkin lymphoma (HL) patients; however, there are sparse data to support superiority of any particular conditioning regimen. We analyzed 492 adult patients undergoing human leucocyte antigen (HLA)-matched sibling or unrelated donor allo-HCT for HL between 2008 and 2016, utilizing RIC with either fludarabine/busulfan (Flu/Bu), fludarabine/melphalan (Flu/Mel140) or fludarabine/cyclophosphamide (Flu/Cy). Multivariable regression analysis was performed using a significance level of <0·01. There were no significant differences between regimens in risk for non-relapse mortality (NRM) (P = 0·54), relapse/progression (P = 0·02) or progression-free survival (PFS) (P = 0·14). Flu/Cy conditioning was associated with decreased risk of mortality in the first 11 months after allo-HCT (HR = 0·28; 95% CI = 0·10-0·73; P = 0·009), but beyond 11 months post allo-HCT it was associated with a significantly higher risk of mortality, (HR = 2·46; 95% CI = 0·1.32-4·61; P = 0·005). Four-year adjusted overall survival (OS) was similar across regimens at 62% for Flu/Bu, 59% for Flu/Mel140 and 55% for Flu/Cy (P = 0·64), respectively. These data confirm the choice of RIC for allo-HCT in HL does not influence risk of relapse, NRM or PFS. Although no OS benefit was seen between Flu/Bu and Flu/Mel 140; Flu/Cy was associated with a significantly higher risk of mortality beyond 11 months from allo-HCT (possibly due to late NRM events).
Keyphrases
- hodgkin lymphoma
- free survival
- cardiovascular events
- patients undergoing
- high dose
- stem cell transplantation
- cell cycle arrest
- risk factors
- cell therapy
- single cell
- end stage renal disease
- bone marrow
- low dose
- ejection fraction
- newly diagnosed
- stem cells
- high intensity
- cell death
- acute lymphoblastic leukemia
- rectal cancer
- adipose tissue
- multiple myeloma
- deep learning
- insulin resistance
- hematopoietic stem cell
- diffuse large b cell lymphoma