Omar Castaneda Puglianini

ORCID: 0000-0003-0423-5870
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Multiple Myeloma Research and Treatments
  • CAR-T cell therapy research
  • Immunotherapy and Immune Responses
  • RNA Interference and Gene Delivery
  • Protein Degradation and Inhibitors
  • Chronic Lymphocytic Leukemia Research
  • Chronic Myeloid Leukemia Treatments
  • vaccines and immunoinformatics approaches
  • Viral Infectious Diseases and Gene Expression in Insects
  • Lymphoma Diagnosis and Treatment
  • Cancer Treatment and Pharmacology
  • Hematopoietic Stem Cell Transplantation
  • Acute Lymphoblastic Leukemia research
  • Cancer Mechanisms and Therapy
  • Acute Myeloid Leukemia Research
  • Biosimilars and Bioanalytical Methods
  • T-cell and B-cell Immunology
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Synthesis and Biological Evaluation
  • Monoclonal and Polyclonal Antibodies Research
  • Nanowire Synthesis and Applications
  • Semiconductor materials and devices
  • Mesenchymal stem cell research
  • Pharmacological Effects and Toxicity Studies
  • Advanced Breast Cancer Therapies

Moffitt Cancer Center
2019-2025

VCU Massey Comprehensive Cancer Center
2022

University of South Florida
2022

Virginia Commonwealth University
2020-2021

Abstract Most patients with multiple myeloma experience disease relapse after treatment a B-cell maturation antigen-targeted therapy (BCMA-TT), and data describing outcomes for treated sequential BCMA-TT are limited. We analyzed clinical infused standard-of-care idecabtagene vicleucel, an anti-BCMA chimeric antigen receptor (CAR) T-cell therapy, at 11 US medical centers. A total of 50 prior exposure (38 antibody-drug conjugate, 7 bispecific, 5 CAR T) 153 no were ide-cel, median follow-up...

10.1038/s41408-023-00886-8 article EN cc-by Blood Cancer Journal 2023-08-09

Idecabtagene vicleucel (ide-cel) was FDA-approved in March 2021 for the treatment of relapsed/refractory multiple myeloma after 4 lines therapy. On KarMMa trial, grade ≥ 3 cytopenias and infections were common. We sought to characterize within 100 days ide-cel standard-of-care (SOC) setting. This multi-center retrospective study included 52 patients who received SOC ide-cel; 47 reached day-90 follow-up. Data censored at day 100. Grade cytopenia present among 65% 30 40% 90. Granulocyte colony...

10.1182/bloodadvances.2022008320 article EN cc-by-nc-nd Blood Advances 2022-08-08

While response rates and survival outcomes have been very promising for idecabtagene vicleucel (ide-cel), a proportion of patients do not respond or relapse early after this B-cell maturation antigen (BCMA) targeted CAR T-cell therapy. Understanding the characteristics these is important patient selection development novel strategies to improve outcomes. We evaluated factors associated with progression (progression death due myeloma ≤ 3 months T infusion) in treated standard care ide-cel at...

10.3324/haematol.2023.283888 article EN cc-by-nc Haematologica 2023-10-19

PURPOSE Idecabtagene vicleucel (ide-cel) and ciltacabtagene autoleucel (cilta-cel), two B-cell maturation antigen–directed chimeric antigen receptor (CAR) T-cell therapies have demonstrated remarkable efficacy in relapsed/refractory multiple myeloma (RRMM). We compare safety, efficacy, survival among patients with RRMM treated standard-of-care (SOC) ide-cel or cilta-cel. METHODS Data were from a retrospective chart review of leukapheresed by December 31, 2022, the intent to receive SOC...

10.1200/jco-24-01730 article EN Journal of Clinical Oncology 2025-02-18

PURPOSE This phase I-Ib trial evaluated a novel CD40L blocking antibody, BMS-986004, for the prevention of graft-versus-host disease (GVHD) after unrelated donor allogeneic hematopoietic cell transplantation (HCT). PATIENTS AND METHODS A total 34 patients were treated at three centers. The safety and biologic activity single-dose BMS-986004 (675 mg [n = 6] 1,500 6]; one-time dose) evaluated. Safety prolonged dosing was then examined in separate cohorts (drug administration every 2 weeks × 3...

10.1200/oa-24-00040 article EN JCO oncology advances. 2025-02-01

Abstract Idecabtagene vicleucel (ide-cel) is a type of B-cell maturation antigen (BCMA)–targeting chimeric receptor T-cell (CAR-T) approved for the treatment relapsed and refractory multiple myeloma (RRMM). Currently, incidence cardiac events associated with ide-cel remains unclear. This was retrospective single-center observational study patients treated RRMM. We included all consecutive who received standard-of-care at least 1-month follow-up. Baseline clinical risk factors, safety...

10.1182/bloodadvances.2023009766 article EN cc-by-nc-nd Blood Advances 2023-06-12

Idecabtagene vicleucel (ide-cel) was the first chimeric antigen receptor T-cell therapy to gain US Food and Drug Administration approval for patients with relapsed/refractory multiple myeloma (RRMM). The clinical outcomes of standard care (SOC) ide-cel in racially ethnically diverse populations have been understudied. This study pooled data from 207 RRMM (28% racial ethnic minority groups) treated SOC across 11 institutions examine differences incidence toxicities adverse events, response...

10.1182/bloodadvances.2023010894 article EN cc-by-nc-nd Blood Advances 2023-10-19

Abstract Purpose: We investigated whether a dendritic cell (DC) vaccine transduced with an adenoviral vector encoded full-length survivin (Ad-S), mutations neutralizing its antiapoptotic function, could safely generate immune response and deepen clinical responses when administered before after autologous stem transplant (ASCT) for multiple myeloma. Patients Methods: This phase I first-in-human trial (NCT02851056) evaluated the safety of DC:Ad-S in newly diagnosed myeloma not having achieved...

10.1158/1078-0432.ccr-22-3987 article EN Clinical Cancer Research 2023-09-22

8013 Background: Ide-cel is an FDA-approved treatment for RRMM patients (pts). However, there limited data on how BT disease control during its manufacturing process affects clinical outcomes. Methods: Eleven US academic centers contributed to this analysis without involvement from the manufacturer. By 5/1/2022, 235 pts had undergone leukapheresis, with 214 infused a median follow up of 9 months (mos). was given between leukapheresis and CAR-T infusion. Results: In analysis, 79% (n = 170)...

10.1200/jco.2023.41.16_suppl.8013 article EN Journal of Clinical Oncology 2023-06-01

12052 Background: Multiple myeloma is a disease of older adults with median age at diagnosis 68 years (y). Patients (pts) receiving chimeric antigen receptor T-cell (CAR-T) therapy for relapsed/refractory MM (RRMM) often experience detrimental effects due to frailty, comorbidity, and cumulative toxicities. In this study, we evaluated the prevalence impact defined by simplified frailty score, (SFS; Facon et al, Leukemia 2020), immuno-nutritional status, using Glasgow-prognostic score (GPS;...

10.1200/jco.2023.41.16_suppl.12052 article EN Journal of Clinical Oncology 2023-06-01
Coming Soon ...