Differences in lymphoma patients between chimeric antigen receptor T-cell therapy trials and the general population

Author:

Apaydin Eric A.ORCID,Richardson Andrea S.,Baxi Sangita,Vockley Jerry,Akinniranye Olamigoke,Larkin Jody,Motala Aneesa,Hempel Susanne

Funder

Patient-Centered Outcomes Research Institute

Office of Academic Affiliations, Department of Veterans Affairs

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference11 articles.

1. June CH. Chapter 30—adoptive cellular therapy with synthetic T cells as an “Instant Vaccine” for cancer and immunity. In: Bloom BR, Lambert P-H, ediorss. The vaccine book. 2nd ed. Academic Press; 2016. p. 581–596.

2. Lundh S, Jung IY, Dimitri A, et al. Clinical practice: chimeric antigen receptor (CAR) T cells: a major breakthrough in the battle against cancer. Clin Exp Med. 2020;20(4):469–80.

3. National Cancer Institute, Surveillance, Epidemiology and End Results Program. Cancer Stat Facts: Non-Hodgkin Lymphoma. https://seer.cancer.gov/statfacts/html/nhl.html. Accessed 31 Mar 2021.

4. Richardson A, Apaydin E, Baxi S, et al. Landscape review and evidence map of gene therapy, part II: Chimeric Antigen Receptor-T cell (CAR-T), autologous cell, antisense, RNA interference (RNAi), Zinc Finger Nuclease (ZFN), genetically modified oncolytic herpes virus. Washington, DC: Patient-Centered Outcomes Research Institute (PCORI); 2019.

5. Richardson A, Apaydin E, Baxi S, et al. Landscape review and evidence map of gene therapy, part I: adenovirus, adeno-associated virus, and clustered regularly interspaced short palindromic repeats. Washington, DC: Patient-Centered Outcomes Research Institute (PCORI); 2019.

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