
ACCESS Study: <7/8 HLA Mismatch Outcomes Comparable to 7/8 with PTCy
The ACCESS study reveals that posttransplant cyclophosphamide improves survival rates for patients with mismatched unrelated donor transplants, expanding donor options.
The ACCESS trial (NCT04904588) addressed significant barriers to allogeneic hematopoietic cell transplantation (HCT) caused by the limited availability of matched unrelated donors, a challenge that disproportionately affects patients of non-European ancestry. While single-HLA mismatched donors (7/8) generally yield acceptable outcomes, donors with mismatches at ≥2 HLA alleles (<7/8) have historically been associated with prohibitive toxicity and poor survival.This study prospectively evaluated the use of posttransplant cyclophosphamide (PTCy) as graft-vs-host disease (GVHD) prophylaxis to determine if it could mitigate the risks associated with greater HLA disparity.
The analysis comprised 268 adult recipients of peripheral blood stem cell grafts: 85 recipients had <7/8 matches (primarily 6/8), and 183 recipients had 7/8 matches. Notably, the <7/8 cohort was racially and ethnically diverse, with 61% identifying as other than non-Hispanic white. The primary end point measured was 1-year overall survival (OS).
Outcomes at one year demonstrated that high-degree mismatching did not adversely affect patient survival when PTCy was utilized. The <7/8 cohort achieved a 1-year OS of 86%, which was comparable to, and numerically higher than, the 79% observed in the 7/8 cohort. Secondary end points showed similar parity between the 2 groups:
- Relapse: 23% in the <7/8 group vs 17% in the 7/8 group.
- Nonrelapse Mortality (NRM): 8% for <7/8 recipients compared with 14% for 7/8 recipients.
- GVHD-Free Relapse-Free Survival (GRFS): 55% for <7/8 recipients vs 51% for 7/8 recipients.
Furthermore, rates of grade 2 to 4 acute GVHD and chronic GVHD were similar across both cohorts. The authors concluded that outcomes for <7/8 recipients using PTCy are favorable and consistent with 7/8 recipients. These findings support extending donor matching criteria to include 4–6/8 matches, potentially enabling near-universal donor access.





































