Clinical Research and Public HealthIn-Press PreviewHematologyImmunology Free access | 10.1172/jci.insight.130195
Find articles by Li, C. in: PubMed | Google Scholar
Find articles by Zhang, Y. in: PubMed | Google Scholar
Find articles by Zhang, C. in: PubMed | Google Scholar
Find articles by Chen, J. in: PubMed | Google Scholar
Find articles by Lou, X. in: PubMed | Google Scholar
Find articles by Chen, X. in: PubMed | Google Scholar
Find articles by Kang, L. in: PubMed | Google Scholar
Find articles by Xu, N. in: PubMed | Google Scholar
Find articles by Li, M. in: PubMed | Google Scholar
Find articles by Tan, J. in: PubMed | Google Scholar
Find articles by Sun, X. in: PubMed | Google Scholar
Find articles by Zhou, J. in: PubMed | Google Scholar
Find articles by Yang, Z. in: PubMed | Google Scholar
Find articles by Zong, X. in: PubMed | Google Scholar
Find articles by Wang, P. in: PubMed | Google Scholar
Find articles by Xu, T. in: PubMed | Google Scholar
Find articles by Qu, C. in: PubMed | Google Scholar
Find articles by Huang, H. in: PubMed | Google Scholar
Find articles by Jin, Z. in: PubMed | Google Scholar
Find articles by Yu, L. in: PubMed | Google Scholar
Find articles by Wu, D. in: PubMed | Google Scholar
Published July 23, 2019 - More info
BACKGROUND. Autologous stem-cell transplantation (ASCT) is the standard treatment for R/R B-NHL, while chimeric antigen receptor T (CAR-T) therapy targeting CD19 emerges as an alternative strategy. Here we report a comparative analysis of the two strategies in a single center.
METHODS. We performed a prospective single-arm study of CAR-T therapy in 29 patients with R/R B-NHL and compared the outcomes with contemporaneous 27 patients who received ASCT. NHL was diagnosed by histopathological assessments, and the safety and efficacy were compared.
RESULTS. The CAR-T group exhibited better rates of CR (48.0% vs. 20.8%, P=0.046) and one-year OS (74.4% vs. 44.5%, P=0.044) compared with the ASCT group. Subpopulation analysis showed that patients with IPI scores ≥ 3 achieved significantly higher ORR and CR rates in the CAR-T group than in the ASCT group (ORR: 72.0% vs. 10.0%, P=0.002; CR: 38.9% vs 0% P=0.030, respectively). The most common severe adverse events in the CAR-T group were cytokine release syndrome, neurotoxicity and infection compared with cytopenia, gastrointestinal toxicity and infection in the ASCT group. Additionally, the incidence of non-hematologic severe adverse events (SAEs) was markedly lower in the CAR-T group than in the ASCT group (20.7% vs. 48.1% P=0.030).
CONCLUSION. CAR-T therapy exhibited superior clinical outcomes in safety and efficacy over ASCT in patients with R/R B-NHL, suggesting CAR-T may be a recommended alternative to ASCT.