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Ibrutinib Treatment of Pediatric Chronic Graft-versus-Host Disease: Primary Results from the Phase 1/2 iMAGINE Study

  • Paul A. Carpenter
  • , Hyoung Jin Kang
  • , Keon Hee Yoo
  • , Marco Zecca
  • , Bin Cho
  • , Giovanna Lucchini
  • , Eneida R. Nemecek
  • , Kirk R. Schultz
  • , Polina Stepensky
  • , Sonali Chaudhury
  • , Benjamin Oshrine
  • , Seong Lin Khaw
  • , Andrew C. Harris
  • , Marta Verna
  • , Liudmila Zubarovskaya
  • , Yihua Lee
  • , Justin Wahlstrom
  • , Lori Styles
  • , Peter J. Shaw
  • , Jean Hugues Dalle
  • Fred Hutchinson Cancer Research Center
  • Seoul National University
  • Sungkyunkwan University
  • IRCCS Fondazione Policlinico San Matteo - Pavia
  • Great Ormond Street Hospital for Children NHS Foundation Trust
  • Oregon Health and Science University
  • University of British Columbia
  • Hebrew University of Jerusalem
  • Children's Memorial Hospital
  • Johns Hopkins All Children's Cancer & Blood Disorders Institute
  • Royal Children's Hospital Melbourne
  • Memorial Sloan-Kettering Cancer Center
  • MBBM Foundation
  • Pavlov First State Medical University of St. Petersburg
  • Pharmacyclics, Inc.
  • The Children's Hospital at Westmead
  • Université de Paris

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

Chronic graft-versus-host disease (cGVHD) is a potentially life-threatening complication of allogeneic hematopoietic stem cell transplantation. Clinical data surrounding cGVHD therapies in younger children are limited and critically needed. Primary endpoints were to determine the recommended pediatric equivalent dose (RPED) and assess pharmacokinetics (PK) and safety. Secondary endpoints included overall response rate (ORR; comprising complete response and partial response) according to the 2014 National Institutes of Health criteria at 24 weeks, overall survival, and duration of response (DOR). Here we present the primary results from the open-label, multicenter, international phase 1/2 iMAGINE study (PCYC-1146-IM), which evaluated the PK, safety, and efficacy of ibrutinib in patients age ≥1 to <22 years with treatment-naive (TN) or relapsed/refractory (R/R) moderate/severe cGVHD. Patients age <12 years received once-daily ibrutinib starting at 120 mg/m2 and escalating to 240 mg/m2 (full adult dose equivalent) after 14 days if free from ibrutinib-related grade ≥3 toxicity; patients age ≥12 years received once-daily ibrutinib 420 mg. Fifty-nine patients (12 TN and 47 with R/R cGVHD; median age, 13 years; range, 1 to 19 years) were enrolled. Plasma concentration-time profiles for ibrutinib 240 mg/m2 (the RPED) were comparable to those observed in adults with cGVHD at a dose of 420 mg/day. Safety was consistent with the known profile of ibrutinib in cGVHD. ORR by 24 weeks was 64% (38 of 59), including 83% (10 of 12) for the TN subgroup and 60% (28 of 47) for R/R. Among 46 responders (median follow-up, 20 months; range, 2 to 32 months), 12-month DOR for each subgroup was 60% (95% confidence interval [CI], 25% to 83%) in TN patients and 58% (95% CI, 35% to 75%) in R/R patients. Responses were durable, with numerically higher rates than those previously observed with ibrutinib in adults, demonstrating that ibrutinib provides clinically meaningful activity with acceptable safety in children with moderate/severe cGVHD.

Original languageEnglish
Pages (from-to)771.e1-771.e10
JournalTransplantation and Cellular Therapy
Volume28
Issue number11
DOIs
StatePublished - Nov 2022

Bibliographical note

Publisher Copyright:
© 2022 The American Society for Transplantation and Cellular Therapy

Keywords

  • Bruton's tyrosine kinase inhibitor
  • Chronic graft-versus-host disease
  • Ibrutinib
  • Pediatric

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