Allogeneic haematopoietic cell transplantation in peripheral T-cell lymphoma: recommendations from the EBMT Practice Harmonisation and Guidelines Committee
- PMID: 40610175
- DOI: 10.1016/S2352-3026(25)00073-0
Allogeneic haematopoietic cell transplantation in peripheral T-cell lymphoma: recommendations from the EBMT Practice Harmonisation and Guidelines Committee
Abstract
Allogeneic haematopoietic cell transplantation (HCT) is a potentially curative therapy for peripheral T-cell lymphoma; however, to date, there are no standardised and detailed guidelines for its application. To address gaps in clinical practice, the European Society for Blood and Marrow Transplantation (EBMT) Practice Harmonisation and Guidelines Committee convened an international expert meeting in Lille (France) on Sept 30 and Oct 1, 2024. EBMT performed funding acquisition. The chairs invited experts in T-cell lymphoma and HCT, who were organised in two work packages devoted to peripheral T-cell lymphoma and transplantation. A literature search was performed beforehand, and results were presented by subgroups of two or three experts, then discussed collectively in structured discussions, and consensus-building exercises. The recommendations presented in this Review were developed and approved based on current evidence, expert opinion, and clinical experience. These recommendations should help to further establish allogeneic HCT as the standard of care for eligible patients with refractory or relapsed peripheral T-cell lymphoma, leveraging its curative potential through the graft-versus-lymphoma effect.
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Conflict of interest statement
Declaration of interests GD: honoraria from Takeda and Amgen; travel support from Takeda; research support from Takeda and Ideogen. AB: honoraria from Takeda, Amgen, Janssen, Roche, and Maat Pharma; research support from Takeda, Roche, Novartis and Janssen. A-SC: travel support from Roche. CPF: consultancy for AbbVie, Arvinas, Atarabio, Bristol Myers Squibb (BMS), GenMab, Kite Pharma (Gilead Sciences), Incyte, Eli Lilly, MorphoSys, Ono, Roche, SERB, SOBI, and Takeda; research funding from BeiGene, AbbVie and GenMab, and Incyte. CK: research support from BMS; travel support from Takeda. KC: consulting or advisory role at Roche, Gilead, KITE, Incyte, AbbVie, BMS, Secura Bio, Autolus, and Sobi; speakers’ bureau for Acrotech, Roche, KITE, Gilead, and Incyte; conference and travel support from Roche, Kite Pharma, and BMS. P-LZ: consultancy for MSD, Takeda, Novartis, and Recordati; speakers bureau for Sobi, Kite Pharma (Gilead Sciences), Janssen, BMS, Servier, MSD, AstraZeneca, Takeda, Roche, Recordati, Kyowa Kirin, Novartis, Incyte and BeiGene; advisory board for Sobi, Kite (Gilead Sciences), Janssen, BMS, Servier, MSD, AstraZeneca, Takeda, Roche, Recordati, Kyowa Kirin, Novartis, Incyte, BeiGene Secura Bio, Sandoz, and ADC Therapeutics. OT: honoraria from Takeda and BeiGene; travel support from Takeda, AbbVie, AstraZeneca, and BeiGene; research support from Takeda. WJ: honoraria from Takeda and AbbVie. IEK: supported by Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)—493624047 (Clinician Scientist CareerS Muenster); honoraria from Kite (Gilead Sciences); travel grants from BeiGene. SN-Q: honoraria from Jazz Pharma, Novartis, AbbVie, and Gilead Sciences; travel support from AbbVie, Gilead Sciences, Sanofi, and Neovii. DB: honoraria from Kite (Gilead Sciences) and Novartis. GW: honoraria from Takeda, Gilead Sciences, Novartis, and Clinigen; travel support from Medac and Janssen. AS: honoraria from Takeda, Calgene (Bristol-Myers Squib), MSD, Janssen, Amgen, Novartis, Kite (Gilead Sciences), Sanofi, Roche, GenMab, AbbVie, Jazz Pharmaceuticals, Therakos, and Menarini; consultancy for Takeda, Calgene (Bristol-Myers Squib), Novartis, Janssen, Gilead Sciences, Sanofi, GenMab, and AbbVie; speaker's bureau for Takeda; research support from Takeda; non-profit organisations: president of the EBMT. PC: honoraria from Takeda, Gilead Sciences, Novartis, Calgene (Bristol-Myers Squib), Roche, Incyte, and Eli Lilly. MH: research support or funding from ADC Therapeutics, Spectrum Pharmaceuticals, and Astellas Pharma; consultancy for Genmab, CRISPR, Allovir, Caribou, Autolus, Forte Biosciences, and Byondis; speaker's bureau for AstraZeneca, ADC Therapeutics, BeiGene, Kite (Gilead Sciences), and Sobi. FO: honoraria from Takeda, Medac Pharma, and Kyowa Kirin; travel support from Takeda, Jazz Pharma, and Kyowa Kirin. IY-A: honoraria from novartis, Bristol-Meyers Squib, Kite (Gilead Sciences), Janssen, and Pfizer. All other authors declare no competing interests.
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