All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a Healthcare Professional.

  TRANSLATE

The gvhd Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the gvhd Hub cannot guarantee the accuracy of translated content. The gvhd and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.

The GvHD Hub is an independent medical education platform, sponsored by Medac and supported through grants from Sanofi and Therakos. Funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders.

Now you can support HCPs in making informed decisions for their patients

Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.

Find out more

PTCy vs standard GvHD prophylaxis in matched donor allo‑HSCT

By Nathan Fisher

Share:

Feb 18, 2026

Learning objective: After reading this article, learners will be able to cite a new clinical development in graft-versus-host disease.


Results from a single-center retrospective study, comparing post-transplant cyclophosphamide (PTCy) vs standard (non-PTCy) graft-versus-host disease (GvHD) prophylaxis in matched donor allogeneic hematopoietic stem cell transplantation (allo-HSCT), were published in Transplantation Proceedings by Kim et al. The analysis included patients undergoing matched donor allo-HSCT with tacrolimus-methotrexate-based GvHD prophylaxis treated prior to 2016 (n  =  252) and those transplanted following institutional adoption of PTCy from 2016 onward (n =  99). The primary endpoint was overall survival (OS), with additional analyses including relapse incidence, non-relapse mortality (NRM), and incidence of acute GvHD (aGvHD) and chronic GvHD (cGvHD).

Key data: PTCy demonstrated superior 1‑year OS compared with non-PTCy treatment (90% vs 62%; p < 0.0001), with this benefit maintained at 2  years (82% vs 50%) and 3  years (75% vs 44%). NRM at 1 year was lower with PTCy (7% vs 22%; p = 0.0002), while 1‑year relapse incidence was comparable between groups (19% vs 26%; p = 0.356). The cumulative incidence of Grade  2–4 aGvHD at Day  100 was lower with PTCy (16% vs 33%; p = 0.0013), while 1‑year cumulative incidence of cGvHD was similar between groups (35% vs 42%; p = 0.1235); however, extensive cGvHD occurred less frequently with PTCy (15% vs 29%; p = 0.0078). 

Key learning: PTCy-based GvHD prophylaxis demonstrates superior outcomes in matched donor allo-HSCT compared with standard non-PTCy treatment. 

References

Please indicate your level of agreement with the following statements:

The content was clear and easy to understand

The content addressed the learning objectives

The content was relevant to my practice

I will change my clinical practice as a result of this content

Your opinion matters

Which consideration most strongly guides your decision to escalate therapy in SR-aGvHD?