# Phase 2 multicenter maintenance study of golidocitinib, A JAK1 selective inhibitor, in patients with peripheral T cell lymphomas after first-line systemic therapy (JACKPOT26)

**Authors:** Juying Wei, Qingqing Cai, Liling Zhang, Liqun Zou, Zengjun Li, Keshu Zhou, Huijing Wu, Lihua Qiu, Liping Su, Kaiyang Ding, Hui Zhou, Li Yu, Fei Li, Wenyu Li, Li’e Lin, Qing Xiao, Erhua Wang, Hongmei Jing, Meifang Zheng, Hongyu Zhang, Yuhuan Gao, Da Gao, Lijia Chen, Jie Jin

PMC · DOI: 10.1038/s41408-026-01452-8 · Blood Cancer Journal · 2026-03-17

## TL;DR

A study tested golidocitinib as maintenance therapy for T cell lymphoma patients after initial treatment, showing promising survival rates and manageable side effects.

## Contribution

This study evaluates golidocitinib as a maintenance therapy for PTCL patients post-first-line treatment, reporting survival outcomes and safety profile.

## Key findings

- 24-month disease-free survival rate was 74.2% in patients achieving complete response.
- 50% of patients with partial response achieved complete response during golidocitinib treatment.
- Common adverse events were hematological but mostly reversible and manageable.

## Abstract

Patients with peripheral T cell lymphoma (PTCL) who achieved tumor response with first-line standard therapy were at high risk of disease relapse. We explored golidocitinib (150 mg once daily) as maintenance therapy for this group of patients (JACKPOT26, NCT06511869). This study included two cohorts: patients achieving a complete response (Cohort 1 (CR), N = 30) and a partial response (Cohort 2 (PR), N = 18) during induction stage. All enrolled patients were transplant ineligible or did not have a transplant plan. All dosed patients were included in the efficacy and safety analysis. In Cohort 1, the 24-month disease free survival (DFS) rate was 74.2% with golidocitinib treatment. In nodal subtypes (AITL, NOS, ALK- ALCL), the 24-month DFS rate was 62.7%. In Cohort 2, median progression free survival (PFS) was 17.4 months, and 24-month PFS rate was 48.6%. Nine out of 18 patients with initial PR achieved complete response, leading to a complete response rate of 50.0%, and median duration of response of 23.9 months. The most common ≥grade 3 treatment-related treatment-emergent adverse events (TRAEs) were hematological adverse events in nature, including neutrophil count decreased (47.9%), white blood cell count decreased (31.3%), lymphocyte count decreased (14.6%) and leukopenia (12.5%). The majority of these TRAEs were reversible and clinically manageable. TRAEs leading to treatment interruption and discontinuation occurred in 60.4% and 10% of patients, respectively. No TRAEs leading to fatal outcomes were reported. This study suggests the potential of golidocitinib as maintenance therapy for patients with PTCL.

## Linked entities

- **Chemicals:** golidocitinib (PubChem CID 126715380)
- **Diseases:** peripheral T cell lymphoma (MONDO:0000430), AITL (MONDO:0004977), ALK- ALCL (MONDO:0017602)

## Full-text entities

- **Genes:** TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, STAT5B (signal transducer and activator of transcription 5B) [NCBI Gene 6777] {aka GHISID2, STAT5}, PIK3R1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 5295] {aka AGM7, GRB1, IMD36, p85, p85-ALPHA, p85alpha}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, RHOA (ras homolog family member A) [NCBI Gene 387] {aka ARH12, ARHA, EDFAOB, RHO12, RHOH12}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, HDAC9 (histone deacetylase 9) [NCBI Gene 9734] {aka HD7, HD7b, HD9, HDAC, HDAC7B, HDAC9B}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, JAK3 (Janus kinase 3) [NCBI Gene 3718] {aka JAK-3, JAK3_HUMAN, JAKL, L-JAK, LJAK}, JAK1 (Janus kinase 1) [NCBI Gene 3716] {aka AIIDE, JAK1A, JAK1B, JTK3}, TNFRSF8 (TNF receptor superfamily member 8) [NCBI Gene 943] {aka CD30, D1S166E, Ki-1}
- **Diseases:** HSTCL (MESH:D016399), nodal (MESH:D013611), EATL (MESH:D058527), Tumor (MESH:D009369), ALCL (MESH:D017728), NHL (MESH:D008228), lymphoid neoplasms (MESH:D008223), NK (MESH:D054066), infection disease (MESH:D007239), subcutaneous (MESH:D013352), PTCL (MESH:D016411), Pneumonia (MESH:D011014), death (MESH:D003643), panniculitis (MESH:D015434), herpes zoster (MESH:D006562), SPTCL (MESH:C537503), TRAEs (MESH:D064420), leukopenia (MESH:D007970), anemia (MESH:D000740), NK/TCL (MESH:D000077428), Cytopenia (MESH:D006402), ECOG (MESH:D000072716)
- **Chemicals:** pegaspargase (MESH:C042705), creatinine (MESH:D003404), decitabine (MESH:D000077209), bilirubin (MESH:D001663), GemOx (MESH:C508870), Etoposide (MESH:D005047), cytarabine (MESH:D003561), AZD4205 (-), brentuximab vedotin (MESH:D000079963), chidamide (MESH:C547816), CHP (MESH:C048279), dexamethasone (MESH:D003907), cisplatin (MESH:D002945)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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Source: https://tomesphere.com/paper/PMC13005011