Alina Markova, MD, on the Rationale for Assessing Topical Ruxolitinib in Cutaneous Chronic GVHD

Article

Alina Markova, MD, discusses the rationale for assessing topical ruxolitinib INCB018424 phosphate 1.5% cream in patients with non-sclerotic and superficially sclerotic chronic cutaneous graft-versus-host disease.

In an interview with CancerNetwork® during the 2022 Tandem Meeting, Alina Markova, MD, dermatologist and director of inpatient consultative dermatology at Memorial Sloan Kettering Cancer Center, discussed the rationale for assessing topical ruxolitinib INCB018424 phosphate 1.5% cream (Opselura) in patients with non-sclerotic and superficially sclerotic chronic cutaneous graft-versus-host disease (GVHD). She highlights that other topical treatments for the disease, such as steroids, can negatively impact survivors’ quality of life due to adverse effects (AEs) such as bruising and skin thinning. This leaves an unmet need in this patient population.

Transcript:

There are currently no FDA-approved topical therapies for chronic cutaneous [GVHD]. The main topical treatment that is currently used for chronic cutaneous [GVHD] is topical steroids. Topical steroids with long-term use have significant toxicity, [such as] skin thinning and bruising—things that are irreversible and can affect the quality of life of our survivors. Other treatments that are used off label are topical calcineurin inhibitors such as tacrolimus [Protopic], and they have AEs such as burning. Ultimately, both are ineffective and we need other treatments in order to increase [the number of] tools that we have to treat cutaneous involvement of GVHD.

Reference

Markova A, Prockop SE, Dusza S, et al. Interim results of a pilot, prospective, randomized, double-blinded, vehicle-controlled trial on safety and efficacy of a topical inhibitor of Janus kinase 1/2 (ruxolitinib INCB018424 phosphate 1.5% cream) for non-sclerotic and superficially sclerotic chronic cutaneous graft-versus-host disease. Presented at: 2022 Transplantation & Cellular Therapy Meetings; Salt Lake City, UT; April 23-26, 2022. Abstract 390.

Recent Videos
“If you have a [patient in the] fourth or fifth line, [JNJ-5322] could be a valid drug of choice,” said Rakesh Popat, BSc, MBBS, MRCP, FRCPath, PhD.
Earlier treatment with daratumumab may be better tolerated for patients with pretreated MRD-negative multiple myeloma.
The trispecific antibody JNJ-5322 demonstrated superior efficacy vs approved agents in multiple myeloma in results shared at the 2025 EHA Congress.
Despite CD19 CAR T-cell therapy exhibiting efficacy in patients with relapsed/refractory large B-cell lymphoma, less than half achieve long-term remission.
Current findings from the phase 1/2 CaDAnCe-101 trial show no predictive factors of improved responses with BGB-16673 in patients with CLL or SLL.
More follow-up data will better elucidate the impact of frontline use of hypomethylating agents in patients with myelodysplastic syndromes.
Related Content