TY - JOUR
T1 - Posoleucel, an Allogeneic, Off-the-Shelf Multivirus-Specific T-Cell Therapy, for the Treatment of Refractory Viral Infections in the Post-HCT Setting
AU - Pfeiffer, Thomas
AU - Tzannou, Ifigeneia
AU - Wu, Mengfen
AU - Ramos, Carlos
AU - Sasa, Ghadir
AU - Martinez, Caridad
AU - Lulla, Premal
AU - Krance, Robert A.
AU - Scherer, Lauren
AU - Ruderfer, Daniel
AU - Naik, Swati
AU - Bocchini, Claire
AU - Fraser, Iain P.
AU - Patel, Badrish
AU - Ward, Dany
AU - Wang, Tao
AU - Heslop, Helen E.
AU - Leen, Ann M.
AU - Omer, Bilal
N1 - Funding Information:
David McNeel of AlloVir provided editorial assistance in the writing of this article. Supported by a National Heart, Lung, and Blood Institute Production Assistance for Cellular Therapy grant (to B. Omer for the clinical virus-specific T-cell manufacture of this investigator-initiated study); by a Conquer Cancer Foundation/American Society for Clinical Oncology grant (to B. Omer for correlative studies); and by Dan L. Duncan Comprehensive Cancer Center Support grant no. P30CA125123 (for shared resources). B. Omer was supported by an educational National Institutes of Health K12 faculty fellowship grant at Texas Children’s Hospital (K12CA090433).
Funding Information:
I. Tzannou reports other support from AlloVir during the conduct of the study. C. Ramos reports grants and personal fees from Tessa Therapeutics; grants from Athenex Therapeutics; and personal fees from Novartis, Genentech, and CRSPR Therapeutics outside the submitted work. P. Lulla reports grants from AlloVir and other support from Karypharm outside the submitted work. C. Bocchini reports other support from Pfizer outside the submitted work. I.P. Fraser reports personal fees from AlloVir during the conduct of the study. H.E. Heslop reports grants and other support from AlloVir during the conduct of the study as well as grants and personal fees from Tessa Therapeutics; grants from Athenex; personal fees and other support from Marker Therapeutics; personal fees from GSK, Gilead, Novartis, and Kiadis; and other support from Fresh Wind Biotherapeutics outside the submitted work. In addition, H.E. Heslop has the potential for royalties as cofounder of AlloVir. A.M. Leen reports grants, personal fees, and other support from AlloVir during the conduct of the study as well as other support from Marker Therapeutics outside the submitted work. In addition, A.M. Leen is an inventor on patents for making and using VSTs; these patents are owned by Baylor College of Medicine and are pending, issued, and licensed and have royalty payments. B. Omer reports research funding from AlloVir for a 1-year period after completion of the study. No disclosures were reported by the other authors.
Publisher Copyright:
© 2023 The Authors; Published by the American Association for Cancer Research.
PY - 2023/1/15
Y1 - 2023/1/15
N2 - Purpose: Viral infections are a major cause of morbidity and mortality following allogeneic hematopoietic cell transplantation (allo-HCT). In the absence of safe and effective antiviral treatments, virus-specific T cells have emerged as a promising therapeutic option. Posoleucel is a multivirus-specific T-cell therapy for offthe- shelf use against six viral infections that commonly occur in allo-HCT recipients: adenovirus, BK virus (BKV), cytomegalovirus, Epstein-Barr virus, human herpes virus-6, and JC virus. Patients and Methods: We conducted an open-label, phase II trial to determine the feasibility and safety of posoleucel in allo-HCT recipients infected with one or more of these viruses. Infections were either unresponsive to or patients were unable to tolerate standard antiviral therapies. Fifty-eight adult and pediatric patients were enrolled and treated. Results: Posoleucel was well tolerated, with no cytokine release syndrome or other infusion-related toxicities; two patients (3.4%) developed Grade 2 and one patient (1.7%) Grade 3 GvHD during the trial. The overall response rate 6 weeks after the first posoleucel infusion was 95%, with a median plasma viral load reduction of 97%. Of the 12 patients who had two or more target viral infections identified at study entry, 10 (83%) had a clinical response for all evaluable viruses. Of the 23 patients treated for refractory BKV-associated hemorrhagic cystitis, 74% had resolution of symptoms and macroscopic hematuria by 6 weeks post-infusion. Conclusions: In this open-label trial, treatment of refractory viral infections/disease in allo-HCT recipients with posoleucel was feasible, safe, and effective.
AB - Purpose: Viral infections are a major cause of morbidity and mortality following allogeneic hematopoietic cell transplantation (allo-HCT). In the absence of safe and effective antiviral treatments, virus-specific T cells have emerged as a promising therapeutic option. Posoleucel is a multivirus-specific T-cell therapy for offthe- shelf use against six viral infections that commonly occur in allo-HCT recipients: adenovirus, BK virus (BKV), cytomegalovirus, Epstein-Barr virus, human herpes virus-6, and JC virus. Patients and Methods: We conducted an open-label, phase II trial to determine the feasibility and safety of posoleucel in allo-HCT recipients infected with one or more of these viruses. Infections were either unresponsive to or patients were unable to tolerate standard antiviral therapies. Fifty-eight adult and pediatric patients were enrolled and treated. Results: Posoleucel was well tolerated, with no cytokine release syndrome or other infusion-related toxicities; two patients (3.4%) developed Grade 2 and one patient (1.7%) Grade 3 GvHD during the trial. The overall response rate 6 weeks after the first posoleucel infusion was 95%, with a median plasma viral load reduction of 97%. Of the 12 patients who had two or more target viral infections identified at study entry, 10 (83%) had a clinical response for all evaluable viruses. Of the 23 patients treated for refractory BKV-associated hemorrhagic cystitis, 74% had resolution of symptoms and macroscopic hematuria by 6 weeks post-infusion. Conclusions: In this open-label trial, treatment of refractory viral infections/disease in allo-HCT recipients with posoleucel was feasible, safe, and effective.
KW - Adult
KW - Child
KW - Humans
KW - Antiviral Agents/adverse effects
KW - Cell- and Tissue-Based Therapy/adverse effects
KW - Epstein-Barr Virus Infections/therapy
KW - Hematopoietic Stem Cell Transplantation/adverse effects
KW - Herpesvirus 4, Human
KW - Virus Diseases/epidemiology
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U2 - 10.1158/1078-0432.CCR-22-2415
DO - 10.1158/1078-0432.CCR-22-2415
M3 - Article
C2 - 36628536
AN - SCOPUS:85146365355
SN - 1078-0432
VL - 29
SP - 3240330
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 2
ER -