Posoleucel, an Allogeneic, Off-the-Shelf Multivirus-Specific T-Cell Therapy, for the Treatment of Refractory Viral Infections in the Post-HCT Setting.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
17 01 2023
Historique:
received: 03 08 2022
revised: 22 09 2022
accepted: 09 11 2022
pubmed: 12 1 2023
medline: 19 1 2023
entrez: 11 1 2023
Statut: ppublish

Résumé

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 off-the-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. 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. 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. In this open-label trial, treatment of refractory viral infections/disease in allo-HCT recipients with posoleucel was feasible, safe, and effective.

Identifiants

pubmed: 36628536
pii: 712758
doi: 10.1158/1078-0432.CCR-22-2415
pmc: PMC9843433
doi:

Substances chimiques

Antiviral Agents 0

Banques de données

ClinicalTrials.gov
['NCT02108522']

Types de publication

Clinical Trial, Phase II Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

324-330

Subventions

Organisme : NCI NIH HHS
ID : K12 CA090433
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA125123
Pays : United States

Informations de copyright

©2023 The Authors; Published by the American Association for Cancer Research.

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Auteurs

Thomas Pfeiffer (T)

Division of Hematology/Oncology, Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri.
Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Ifigeneia Tzannou (I)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Mengfen Wu (M)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.
Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.

Carlos Ramos (C)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Ghadir Sasa (G)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Caridad Martinez (C)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Premal Lulla (P)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Robert A Krance (RA)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Lauren Scherer (L)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Daniel Ruderfer (D)

Section of Pediatric Infectious Disease, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.

Swati Naik (S)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Claire Bocchini (C)

Section of Pediatric Infectious Disease, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.

Iain P Fraser (IP)

AlloVir, Waltham, Massachusetts.

Badrish Patel (B)

AlloVir, Waltham, Massachusetts.

Dany Ward (D)

AlloVir, Waltham, Massachusetts.

Tao Wang (T)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.
Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, Texas.

Helen E Heslop (HE)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

Ann M Leen (AM)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.
AlloVir, Waltham, Massachusetts.

Bilal Omer (B)

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, Houston Methodist Hospital, Houston, Texas.

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Classifications MeSH