Pioneered by Our Group, 2015

Novel Haploidentical BMT — Abatacept & PTCy

Our team is one of only four groups in the world to have established an accepted method for Haploidentical Bone Marrow Transplantation. Abatacept and Post-Transplant Cyclophosphamide is our 2015 contribution to the field.

The Challenge

Why Haploidentical BMT is the hardest transplant in medicine

Haploidentical Donor (HID) BMT is immunologically the most challenging procedure in clinical medicine. This was successfully carried out by the Perugia Group led by Aversa and Martelli in 1995. Since then, several approaches to HID-BMT have been tried.


The Four Accepted Methods

The global lineage of Haploidentical BMT

Only four methods are accepted worldwide for carrying out a Haploidentical BMT. Our group is one of them.

1
Graft manipulation (TCRalfa-beta depletion)

By Aversa and Martelli (1995) — the Perugia Group. The first successful Haploidentical BMT, achieved by depleting alpha-beta T cells from the graft to prevent graft-versus-host disease.

2
Post-Transplant Cyclophosphamide

By Jones, O'Donnell and Luznick (2008) — the Johns Hopkins approach. Cyclophosphamide given after transplant selectively kills the alloreactive donor T cells.

3
ATG and multiagent GVHD prophylaxis

By Huang and Xao (2010) — the Beijing protocol. Combines anti-thymocyte globulin with multi-agent immunosuppression.

4
Abatacept and PTCy — Our Method

By Chakrabarti and Team (2015) — Bloods R Us / Action Cancer Hospital. Our pioneering contribution to the global Haploidentical BMT toolkit, combining the costimulation blockade of Abatacept with Post-Transplant Cyclophosphamide.


Our Two Protocols

Abatacept & PTCy — Adapted for Two Disease Categories

Our group has developed two protocols based on Abatacept & PTCy — one for non-malignant diseases, one for malignant diseases.

Protocol A — Non-Malignant Diseases

AbaCyS

Abatacept & PTCy with Sirolimus — for Thalassemia, Sickle Cell Anemia, Aplastic Anemia and other non-malignant diseases of the bone marrow.

Survival 85–90%

Protocol B — Malignant Diseases

AbaDCyC

Abatacept & PTCy with short-course Cyclosporine and Abatacept-primed DLI — for Leukemia, Lymphoma, Myeloma and other haematological malignancies requiring Haploidentical BMT.

Survival 70–80%

No matched donor? You still have options

A half-matched family member can be your donor. Discuss your case with one of the world's pioneering haploidentical BMT teams.