Transplant-ineligible but chimeric antigen receptor T-cells eligible: a real and relevant population
European Journal of Cancer, ISSN: 0959-8049, Vol: 175, Page: 246-253
2022
- 11Citations
- 17Captures
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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.
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Metrics Details
- Citations11
- Citation Indexes11
- 11
- CrossRef1
- Captures17
- Readers17
- 17
Review Description
Autologous stem cell transplantation (ASCT) and chimeric antigen receptor (CAR) T-cells are two therapeutic options for relapsed/refractory diffuse large B-cell lymphoma. Both are intensive and potentially curative therapies but differ in their efficacy and toxicity. ASCT may be offered to ‘fit’ patients (i.e. usually young with limited comorbidities) with chemosensitive disease. On the other hand, real world studies have shown that CAR T-cells may be safely administered to less fit and older patients. Thus, there is a potentially significant population of patients who may be offered CAR T-cell therapy despite not being eligible for ASCT. As the relative role of ASCT and CAR T-cells evolves, recognising and defining this population may be increasingly relevant. Here, we review criteria which may help identify this ‘ASCT-ineligible but CAR T-cells eligible’ population of patients.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0959804922005068; http://dx.doi.org/10.1016/j.ejca.2022.08.019; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85140144959&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/36166850; https://linkinghub.elsevier.com/retrieve/pii/S0959804922005068; https://dx.doi.org/10.1016/j.ejca.2022.08.019
Elsevier BV
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