Infectious complications of chimeric antigen receptor (CAR) T-cell therapies
Seminars in Hematology, ISSN: 0037-1963, Vol: 60, Issue: 1, Page: 52-58
2023
- 8Citations
- 31Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations8
- Citation Indexes8
- Captures31
- Readers31
- 31
Article Description
CAR T-cells have revolutionized the treatment of many hematological malignancies. Thousands of patients with lymphoma, acute lymphoblastic leukemia, and multiple myeloma have received this “living medicine” and achieved durable remissions. Their place in therapy continues to evolve, and there is ongoing development of new generation CAR constructs, CAR T-cells against solid tumors and CAR T-cells against chronic infections like human immunodeficiency virus and hepatitis B. A significant fraction of CAR T-cell recipients, unfortunately, develop infections. This is in part due to factors intrinsic to the patient, but also to the treatment, which requires lymphodepletion (LD), causes neutropenia and hypogammaglobulinemia and necessarily increases the state of immunosuppression of the patient. The goal of this review is to present the infectious complications of CAR T-cell therapy, explain their temporal course and risk factors, and provide recommendations for their prevention, diagnosis, and management.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0037196323000197; http://dx.doi.org/10.1053/j.seminhematol.2023.02.003; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85150849195&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/37080711; https://linkinghub.elsevier.com/retrieve/pii/S0037196323000197; https://dx.doi.org/10.1053/j.seminhematol.2023.02.003
Elsevier BV
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