The Cell and Gene Therapy Consortium's Perspective on Harmonizing Data Collection for Patient Enrollment, Therapy Ordering and Scheduling, and Cell Collection.


Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 28 04 2023
revised: 26 06 2023
accepted: 08 08 2023
medline: 3 11 2023
pubmed: 22 8 2023
entrez: 21 8 2023
Statut: ppublish

Résumé

Established in October 2021, the Cell and Gene Therapy (CGT) Consortium convened with the goal to bring together key CGT stakeholders - manufacturers, treatment centers, regulators, services providers, and ecosystem partners - to gain alignment on process definitions, terminology, challenges, and opportunities for process and data standardization from CGT program start-up and patient enrollment to therapy administration. With the recognition that the number of investigational and commercial cell and gene therapies will scale over the next several years, so will the number of manufacturer-specific processes and solutions (e.g., portals). As a result, this will increase the burden on academic medical centers, community hospitals, standalone clinics, collection facilities, and labs. Healthcare professionals (HCPs) and other industry stakeholders agree that a multiplicity of manufacturer portals with varying data requirements and nomenclature is unsustainable and adds unnecessary complexity - risk, cost, and time - in coordinating patient treatment. Following extensive discussions and multiple stakeholder meetings and interviews, we have developed a manuscript reporting on our activities and conclusions. Through the course of the manuscript, we delineate a framework for defining common principles, terminology, and user experiences for enrolling patients, ordering therapies, and collecting starting material in a standardized way. We also provide substantial background information on opportunities to streamline communications between manufacturing and healthcare organizations from the HCP end-user's perspective.

Identifiants

pubmed: 37604251
pii: S2666-6367(23)01468-9
doi: 10.1016/j.jtct.2023.08.011
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

653-665

Informations de copyright

Copyright © 2023 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Alexandra Mora (A)

Accenture, San Francisco, California. Electronic address: alexandra.r.mora@accenture.com.

Linda Barnes (L)

Association for the Advancement of Blood & Biotherapies, Bethesda, MD.

Clint Divine (C)

The University of Kansas Cancer Center, Westwood, Kansas.

Noelle Frey (N)

University of Pennsylvania and the Abramson Cancer Center, Philadelphia, Pennsylvania.

Christian Fuchs (C)

Genentech, South San Francisco, California.

Beth Hayes (B)

Accenture, San Francisco, California.

Dawn Henke (D)

Standards Coordinating Body, Gaithersburg, Maryland.

Peter Holman (P)

ArsenalBio, South San Francisco, California.

Hien Liu (H)

H. Lee Moffitt Cancer Center, University of South Florida Morsani College of Medicine, Tampa, Florida.

David Porter (D)

University of Pennsylvania and the Abramson Cancer Center, Philadelphia, Pennsylvania.

Kirstin Powel (K)

Talaris Therapeutics, Union Bridge, Maryland.

Sanjay Srivastava (S)

Accenture, New York, New York.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH