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Autografting

Tandem autologous-allo-SCT is feasible in patients with high-risk relapsed non-Hodgkin’s lymphoma

Abstract

Allo-SCT is used to exploit GVL effect in high-risk relapsed non-Hodgkin’s lymphoma (NHL). Here, we retrospectively analyzed 34 high-risk NHL patients who underwent auto-SCT followed closely by reduced-intensity allo-SCT (‘tandem auto–allo’) from January 2002 to November 2010. The search for an allogeneic donor was started at the beginning of salvage regimen. Median patients’ age was 47 (27–68) years; histotypes were: diffuse large B-cell n=5, follicular n=14, transformed follicular n=4, mantle-cell n=5, plasmocytoid lymphoma n=1, anaplastic large T-cell n=2, peripheral T-cell n=3. Donors were HLA-identical siblings (n=29) or 10/10-matched unrelated individuals (n=5). Median interval between auto-SCT and allo-SCT was 77 days (36–197). At a median follow-up of 46 (8–108) months since allo-SCT, 5-year OS is 77% (61–93) and PFS is 68% (51–85). Disease relapse or progression occurred in six patients, 100-day TRM was 0%, 2-year TRM incidence was 6%. In conclusion, tandem transplantation is feasible in high-risk NHL patients having a HLA-identical donor. This approach could represent a suitable therapeutic option for those patients with high-risk NHL potentially benefitting from further therapy after auto-SCT. Donor searches should be started promptly whenever such an approach is chosen.

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Acknowledgements

We thank all personnel working at Hematology Department and Cellular Therapy Unit at Institut Paoli-Calmettes and at Hematology Department at Istituto Humanitas for their remarkable contribution in patients’ care and assistance to their families.

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Correspondence to R Crocchiolo.

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Crocchiolo, R., Castagna, L., Fürst, S. et al. Tandem autologous-allo-SCT is feasible in patients with high-risk relapsed non-Hodgkin’s lymphoma. Bone Marrow Transplant 48, 249–252 (2013). https://doi.org/10.1038/bmt.2012.116

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