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Tandem Meetings 2026 | The current standard of care for GvHD prophylaxis in older patients undergoing transplantation

Sameem Abedin, MD, Medical College of Wisconsin, Milwaukee, WI, discusses the standard of care (SoC) for graft-versus-host disease (GvHD) prophylaxis in older patients undergoing reduced-intensity conditioning (RIC) allogeneic stem cell transplantation (SCT). The current SoC regimen combines post-transplant cyclophosphamide (PTCy) at a dose of 50 mg/kg on days +3 and +4 with a calcineurin inhibitor (CNI) and mycophenolate mofetil (MMF), and reduces the incidence of clinically significant acute and chronic GvHD compared to CNI-based prophylaxis alone. Dr Abedin also mentions alternative approaches being explored, including adding a JAK inhibitor, such as ruxolitinib, to CNI-based prophylaxis. This interview took place virtually.

These works are owned by Magdalen Medical Publishing (MMP) and are protected by copyright laws and treaties around the world. All rights are reserved.

Transcript

So, the standard of care right now is to utilize post-transplant cyclophosphamide. The standard dose, again, is at a double dose, so at 50 mg per kg on days 3 and 4, alongside calcineurin inhibitor and MMF. Really, this is because it’s been compared to CNI-based prophylaxis alone, and there were significant improvements in terms of clinically significant graft-versus-host disease...

So, the standard of care right now is to utilize post-transplant cyclophosphamide. The standard dose, again, is at a double dose, so at 50 mg per kg on days 3 and 4, alongside calcineurin inhibitor and MMF. Really, this is because it’s been compared to CNI-based prophylaxis alone, and there were significant improvements in terms of clinically significant graft-versus-host disease. In other words, much lower clinically significant acute graft-versus-host disease and chronic graft-versus-host disease with post-transplant cyclophosphamide use. 

As I mentioned, while that was an improvement, what has also been seen on studies is compared to our old standard of care, there hasn’t been a demonstrated improvement in overall survival. And that could be for a number of reasons, one of which being, you know, while there is improvement in graft versus host disease control, overall transplant remains, you know, sort of a burdensome process, and so for that reason, there are sort of baked in morbidities that still exist, you know, particularly with post-transplant cyclophosphamide as well. But despite that, you know, with an equivalent survival, with better GVH control, you know, at least what we’re offering for patients with post-transplant cyclophosphamide is a better quality of life at one year if we’re not seeing clinically significant GVH. And that’s why I think that represents really the standard of care. 

You know, sort of, if you want to comment on sort of recent developments, you know, I think what’s in this space right now that’s, you know, being investigated further is, as I mentioned, the addition of a JAK inhibitor, ruxolitinib to CNI-based prophylaxis. So we know just giving tacrolimus and methotrexate is not a relatively toxic treatment regimen for GVH prophylaxis. It lacks efficacy, you know, in terms of preventing clinically significant graft-versus-host disease, but there has been a phase two study, you know, performed or led by MGH that demonstrated sort of the addition of ruxolitinib really attenuates severe acute and chronic graft-versus-host disease. So that’s something that’s under investigation and being compared against post-transplant cyclophosphamide. There have been also sort of graft manipulation studies, primarily led by ORCA, that look at sort of separating out populations of T-cells that may impact graft-versus-host disease. And these studies are demonstrating potentially an attenuation of toxicity with that approach and potentially, compared to post-transplant cyclophosphamide attenuated toxicity as well, with comparable sort of GVH outcomes.

 

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