Axatilimab for Chronic Graft-Versus-Host Disease After Failure of at Least Two Prior Systemic Therapies: Results of a Phase I/II Study

Author:

Kitko Carrie L.1ORCID,Arora Mukta2ORCID,DeFilipp Zachariah3ORCID,Zaid Mohammad Abu4ORCID,Di Stasi Antonio5,Radojcic Vedran67ORCID,Betts Courtney B.8ORCID,Coussens Lisa M.8ORCID,Meyers Michael L.7,Qamoos Hope79,Ordentlich Peter7,Kumar Vinit710,Quaranto Christine711,Schmitt Aaron7,Gu Yu7,Blazar Bruce R.12ORCID,Wang Trent P.13ORCID,Salhotra Amandeep14ORCID,Pusic Iskra15,Jagasia Madan16ORCID,Lee Stephanie J.17ORCID

Affiliation:

1. Vanderbilt University Medical Center, Nashville, TN

2. University of Minnesota Masonic Cancer Center, Minneapolis, MN

3. Massachusetts General Hospital, Boston, MA

4. Indiana University Simon Cancer Center, Indianapolis, IN

5. University of Alabama, Birmingham, AL

6. University of Utah Huntsman Cancer Institute, Salt Lake City, UT

7. Syndax Pharmaceuticals, Inc, Waltham, MA

8. Department of Cell, Developmental, and Cancer Biology, Knight Cancer Institute, Oregon Health and Science University, Portland, OR

9. Kartos Therapeutics, Inc, Redwood City, CA

10. Daiichi Sankyo, Inc, Basking Ridge, NJ

11. Aerovate Therapeutics, Inc, Waltham, MA

12. Division of Blood & Marrow Transplant & Cellular Therapy, Department of Pediatrics, University of Minnesota, Minneapolis, MN

13. Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL

14. City of Hope Medical Center, Duarte, CA

15. Washington University School of Medicine, Saint Louis, MO

16. Iovance Biotherapeutics, San Carlos, CA

17. Fred Hutchinson Cancer Center, Seattle, WA

Abstract

PURPOSE Chronic graft-versus-host disease (cGVHD) remains the major cause of late morbidity after allogeneic hematopoietic cell transplantation. Colony-stimulating factor 1 receptor (CSF-1R)–dependent macrophages promote cGVHD fibrosis, and their elimination in preclinical studies ameliorated cGVHD. Axatilimab is a humanized monoclonal antibody that inhibits CSF-1R signaling and restrains macrophage development. PATIENTS AND METHODS This phase I (phI)/phase II (phII) open-label study (ClinicalTrials.gov identifier: NCT03604692 ) evaluated safety, tolerability, and efficacy of axatilimab in patients age ≥ 6 years with active cGVHD after ≥ 2 prior systemic therapy lines. Primary objectives in phI were to identify the optimal biologic and recommended phII dose and in phII to evaluate the overall (complete and partial) response rate (ORR) at the start of treatment cycle 7. RESULTS Forty enrolled patients (17 phI; 23 phII) received at least one axatilimab dose. In phI, a dose of 3 mg/kg given once every 4 weeks met the optimal biologic dose definition. Two dose-limiting toxicities occurred at the 3 mg/kg dose given once every 2 weeks. At least one treatment-related adverse event (TRAE) was observed in 30 patients with grade ≥ 3 TRAEs in eight patients, the majority known on-target effects of CSF-1R inhibition. No cytomegalovirus reactivations occurred. With the 50% ORR at cycle 7 day 1, the phII cohort met the primary efficacy end point. Furthermore, the ORR in the first six cycles, an end point supporting regulatory approvals, was 82%. Responses were seen in all affected organs regardless of prior therapy. Fifty-eight percent of patients reported significant improvement in cGVHD-related symptoms using the Lee Symptom Scale. On-target activity of axatilimab was suggested by the decrease in skin CSF-1R–expressing macrophages. CONCLUSION Targeting profibrotic macrophages with axatilimab is a therapeutically promising novel strategy with a favorable safety profile for refractory cGVHD.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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