<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Palani HK</submitter><funding>Indian Council of Medical Research</funding><pagination>200977</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12005290</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(2)</volume><pubmed_abstract>Decentralized or point-of-care (POC) manufacture of CAR-T cells is a potential strategy to improve accessibility and reduce cost and logistic challenges. A total of 10 relapsed/refractory patients (B cell acute lymphoblastic leukemia [B-ALL] &lt;i>N&lt;/i> = 6, diffuse large B cell lymphoma [DLBCL] &lt;i>N&lt;/i> = 4) were enrolled in this POC phase 1 study. Chimeric antigen receptor (CAR)-T cells were manufactured using the fully automated CliniMACS Prodigy system. The CAR-T cell products had a median 15-fold expansion with a median transduction rate of 38%. The immunophenotypic characterization indicates a significant increase in central memory and effector T cells. All the patients were infused with fresh CAR-T cells. Complete remission rates were 100% for B-ALL and 50% for DLBCL. At a median follow-up of 15 months, 8 of 10 patients remain without disease progression. Adverse events reported were cytokine release syndrome grade 2 or higher in 2 of 10 patients. None of the patients developed immune effector cell-associated neurotoxicity syndrome. Late hematological toxicity of grade 2 or higher was noted only in one patient. Evaluation of health care resource utilization demonstrates that the median cost was US$12,724, while the manufacturing cost was US$35,107. Our data highlight the safety, efficacy, low cost, and potential to enhance the accessibility of CAR-T cell therapy in low- and middle-income countries through a fully automated and closed manufacturing platform.</pubmed_abstract><journal>Molecular therapy. Oncology</journal><pubmed_title>Safety, efficacy and total cost of point-of-care manufactured anti-CD19 CAR-T cell therapy in India: VELCART trial.</pubmed_title><pmcid>PMC12005290</pmcid><funding_grant_id>91/06/2020-TFGTR/ BMS</funding_grant_id><pubmed_authors>Abraham A</pubmed_authors><pubmed_authors>Arunachalam AK</pubmed_authors><pubmed_authors>Palanikumar S</pubmed_authors><pubmed_authors>Rajasekaran A</pubmed_authors><pubmed_authors>George B</pubmed_authors><pubmed_authors>Korula A</pubmed_authors><pubmed_authors>Solomon M</pubmed_authors><pubmed_authors>Selvarajan S</pubmed_authors><pubmed_authors>Kulkarni U</pubmed_authors><pubmed_authors>Venkatraman A</pubmed_authors><pubmed_authors>Wirthlin L</pubmed_authors><pubmed_authors>Dash P</pubmed_authors><pubmed_authors>Schneider D</pubmed_authors><pubmed_authors>Mathews V</pubmed_authors><pubmed_authors>Palani HK</pubmed_authors><pubmed_authors>Radhakrishnan RN</pubmed_authors><pubmed_authors>Datari PVR</pubmed_authors><pubmed_authors>Yasar M</pubmed_authors><pubmed_authors>Bankar A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety, efficacy and total cost of point-of-care manufactured anti-CD19 CAR-T cell therapy in India: VELCART trial.</name><description>Decentralized or point-of-care (POC) manufacture of CAR-T cells is a potential strategy to improve accessibility and reduce cost and logistic challenges. A total of 10 relapsed/refractory patients (B cell acute lymphoblastic leukemia [B-ALL] &lt;i>N&lt;/i> = 6, diffuse large B cell lymphoma [DLBCL] &lt;i>N&lt;/i> = 4) were enrolled in this POC phase 1 study. Chimeric antigen receptor (CAR)-T cells were manufactured using the fully automated CliniMACS Prodigy system. The CAR-T cell products had a median 15-fold expansion with a median transduction rate of 38%. The immunophenotypic characterization indicates a significant increase in central memory and effector T cells. All the patients were infused with fresh CAR-T cells. Complete remission rates were 100% for B-ALL and 50% for DLBCL. At a median follow-up of 15 months, 8 of 10 patients remain without disease progression. Adverse events reported were cytokine release syndrome grade 2 or higher in 2 of 10 patients. None of the patients developed immune effector cell-associated neurotoxicity syndrome. Late hematological toxicity of grade 2 or higher was noted only in one patient. Evaluation of health care resource utilization demonstrates that the median cost was US$12,724, while the manufacturing cost was US$35,107. Our data highlight the safety, efficacy, low cost, and potential to enhance the accessibility of CAR-T cell therapy in low- and middle-income countries through a fully automated and closed manufacturing platform.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jun</publication><modification>2025-07-12T03:04:18.464Z</modification><creation>2025-07-12T03:04:18.464Z</creation></dates><accession>S-EPMC12005290</accession><cross_references><pubmed>40248244</pubmed><doi>10.1016/j.omton.2025.200977</doi></cross_references></HashMap>