A Multicenter Phase II Trial of Ruxolitinib for Treatment of Corticosteroid Refractory Sclerotic Chronic Graft-Versus-Host Disease

Author(s): Vijaya Raj Bhatt, MS, MBBS1,2; Valerie K. Shostrom, MS3; Hannah K. Choe, MD4; Betty K. Hamilton, MD5; Krishna Gundabolu, MD, MS1,2; Lori J. Maness, MD1,2; Virender Kumar, PhD6; Ram I. Mahato, PhD6; Lynette M. Smith, PhD7; Taiga Nishihori, MD8; Stephanie J. Lee, MD, MPH9
Source: https://doi.org/10.1200/JCO.24.00205

Dr. Anjan Patel's Thoughts

Most of us don’t have many autologous stem cell transplant (Auto-HSCT) patients whom we follow, but this topic seems ripe for an American Board of Internal Medicine (ABIM) question.  Ruxolitinib seems quite effective for steroid refractory sclerotic chronic graft-versus-host disease (cGHVD).

PURPOSE

Sclerotic chronic graft-versus-host disease (cGVHD) represents a highly morbid and refractory form of cGVHD, and novel therapies for sclerotic cGVHD are critically needed. This study aimed to determine the efficacy of ruxolitinib in patients with corticosteroid refractory sclerotic cGVHD.

PATIENTS AND METHODS

In a single-arm multicenter phase II trial (N = 47), adults with sclerotic cGVHD refractory to corticosteroids and ≥one additional line of systemic therapy for cGVHD received ruxolitinib for ≥six months (ClinicalTrials.gov identifier: NCT03616184). The primary end point was complete or partial response (PR) in skin and/or joint defined according to the 2014 National Institute of Health cGVHD Consensus Criteria.

RESULTS

Following the use of ruxolitinib for a median of 11 months, PR in skin and/or joints was noted in 49% (95% CI, 34 to 64) at 6 months, with 45% having joint and fascia response and 19% having skin response. The duration of skin/joint response was 77% (95% CI, 48 to 91) at 12 months. Overall cGVHD PR was noted in 47% (95% CI, 32 to 61). Improvement in Lee Symptom Scale summary and skin subscale scores was noted in 38% of patients. With a cumulative incidence of treatment failure of 20.8% (95% CI, 10.0 to 34.1), nonrelapse mortality (NRM) of 2.2% (95% CI, 0.17 to 10.3), and no recurrent malignancy, failure-free survival (FFS) was 77.1% (95% CI, 61.3 to 87.0) at 12 months. Ruxolitinib was overall well tolerated with no new safety signals.

CONCLUSION

The use of ruxolitinib was associated with relatively high rates of skin/joint responses and overall cGVHD responses, improvement in patient-reported outcomes, low NRM, and high FFS in patients with refractory sclerotic cGVHD. Ruxolitinib offers an effective treatment option for refractory sclerotic cGVHD.

Author Affiliations

1Division of Hematology-Oncology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE; 2Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE; 3Department of Biostatistics, University of Nebraska Medical Center, Omaha, NE; 4Division of Hematology, The Ohio State University Comprehensive Cancer Center, Columbus, OH; 5Blood and Marrow Transplant Program, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH; 6Department of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, NE; 7Department of Biostatistics, University of Nebraska Medical Center, Omaha, NE; 8Department of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, FL; 9Clinical Research Division, Fred Hutchinson Cancer Center and Department of Medicine, University of Washington, Seattle, WA

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