Evidence map›Paper›PMID 40237436›Full record

ArticleThe Journal of dermatology2025

Oral and Topical Janus Kinase Inhibitors in Patients With Cutaneous T-Cell Lymphoma: A Real-World Single-Center Experience.

Viviane Liao, Leore Lavin, Michael M Ong, Melissa P Pulitzer, Alison J Moskowitz, Patricia L Myskowski, Shamir Geller

Abstract read
In one paragraph

Article in The Journal of dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Viviane LiaoDermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0000-0001-9355-1298
Leore LavinDermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Michael M OngDermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Melissa P PulitzerDepartment of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Alison J MoskowitzLymphoma Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Patricia L MyskowskiDermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Shamir GellerDermatology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0000-0003-1206-1057

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748NIH HHS P30 CA008748
6 · The paper itself

Abstract

The JAK/STAT pathway is implicated in the pathogenesis of cutaneous T-cell lymphoma (CTCL), with early studies suggesting that JAK inhibitors (JAKi) may be used for treating CTCL. Patients with CTCL may have other indications for JAKi use, but data on JAKi agents in CTCL is limited due to warnings against their use in malignancy. We retrospectively characterized the experience of our tertiary cancer center with JAKi in patients seen for CTCL between the years 2011 and 2024. We identified 26 CTCL patients who received a JAKi: 7 received a JAKi prior to their CTCL diagnosis (topical (n = 5) or oral (n = 2) for itchy rash or eczema), 6 received a JAKi as CTCL treatment, and 13 received a JAKi for other indications following a diagnosis of CTCL (oral ruxolitinib for graft versus host disease (GvHD) following allogeneic stem cell transplant (n = 9), oral ruxolitinib for hemophagocytic lymphohistiocytosis (n = 3), or topical ruxolitinib for alopecia areata (n = 1)). Of the six patients treated for CTCL with a JAKi, four received oral ruxolitinib and two received topical ruxolitinib. One patient treated orally has had a complete response for 3 years and another patient has had a diminishing lesion size for 1 year. One patient treated topically for skin-limited CTCL demonstrated plaque thinning. Of the nine patients treated for GvHD, five experienced CTCL relapse a median of 8 weeks following ruxolitinib exposure. This study provides initial insights into the real-world use of JAKi in patients with CTCL. Further studies, however, are required to characterize any association between JAKi use and CTCL development, as well as the safety of JAKi use in the context of pre-existing CTCL.

Indexed as

Janus Kinase InhibitorsLymphoma, T-Cell, CutaneousSkin NeoplasmsAdministration, CutaneousAdministration, OralAdministration, TopicalAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedNitrilesPyrazolesPyrimidinesJanus Kinase InhibitorsNitrilesPyrazolesPyrimidinesruxolitinibJanus kinase inhibitorslymphoma T‐cell cutaneousmycosis fungoidesSezary syndrometherapeutics

Identifiers

PMID40237436
PMCPMC12151751

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.