Pere Barba
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Pere Barba has a total of 1000 co-authors. Here are the top co-authors by number of shared publications:
- David Valcárcel
University Hospital Vall d'Hebron, Barcelona, Spain
40 shared publications - José Luis Piñana
Department of Hematology. Hospital Clínico Universitario de Valencia, Spain. INCLIVA Biomedical Research Institute, Valencia, Spain
27 shared publications - Josep-Maria Ribera
ICO-Hospital Germans Trias i Pujol, Josep Carreras Leukemia Research Institute (IJC), Universitat Autònoma de Barcelona, Badalona, Spain
24 shared publications Rodrigo Martino
Department of Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
24 shared publications- Manuel Guerreiro
Hematology Research Group, Instituto de Investigacion Sanitaria La Fe (IIS La Fe), 46026 Valencia, Spain
21 shared publications - Javier Briones
Hematology Service, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
18 shared publications
Latest Publications
- 12 October 2026
- Published by Springer Nature in Bone Marrow Transplantation
- p. 1-10
Bridging therapy in pediatric and AYA patients under 25 years with relapsed/refractory B-ALL undergoing anti-CD19 CAR-T therapy: a multicenter retrospective study by the Spanish group GETH-TC
CAR-T therapy is a powerful treatment for pediatric B-cell acute lymphoblastic leukemia (B-ALL). However, the impact of bridging therapy prior to CAR-T infusion on patient outcomes remains insufficiently explored. In this retrospective study of patients with relapse/refractory B-ALL (N = 103), we compared outcomes across different bridging therapy groups: Low-Intensity Chemotherapy (LIC, N = 50), Immunotherapy (N = 20), or High-Intensity Chemotherapy (HIC, N = 33). At day +28 post-infusion, LIC and Immunotherapy showed significantly higher rates of Complete Remission with negative Minimal Residual Disease compared with HIC (96% vs 85% vs 75%), along with lower rates of disease progression (4% vs 10% vs 15.2%) and treatment-related mortality (0% vs 5% vs 9.1%). Additionally, patients who received three or more prior lines of therapy before CAR-T infusion exhibited significantly lower response rates. Despite potential biases, such as intrinsic disease aggressiveness or unidentified genomic alterations, present findings suggest that using LIC or immunotherapy as bridging strategies, in patients with fewer prior treatment lines, may be associated with a lower overall disease and treatment burden and could potentially contribute to improved CAR-T cell efficacy and clinical outcomes. Nevertheless, additional investigations are required to elucidate biological and clinical mechanisms by which bridging approaches and treatment history modulate CAR-T responses.
- 12 October 2026
- Published by Springer Nature in Bone Marrow Transplantation
- p. 1-10
Bridging therapy in pediatric and AYA patients under 25 years with relapsed/refractory B-ALL undergoing anti-CD19 CAR-T therapy: a multicenter retrospective study by the Spanish group GETH-TC
CAR-T therapy is a powerful treatment for pediatric B-cell acute lymphoblastic leukemia (B-ALL). However, the impact of bridging therapy prior to CAR-T infusion on patient outcomes remains insufficiently explored. In this retrospective study of patients with relapse/refractory B-ALL (N = 103), we compared outcomes across different bridging therapy groups: Low-Intensity Chemotherapy (LIC, N = 50), Immunotherapy (N = 20), or High-Intensity Chemotherapy (HIC, N = 33). At day +28 post-infusion, LIC and Immunotherapy showed significantly higher rates of Complete Remission with negative Minimal Residual Disease compared with HIC (96% vs 85% vs 75%), along with lower rates of disease progression (4% vs 10% vs 15.2%) and treatment-related mortality (0% vs 5% vs 9.1%). Additionally, patients who received three or more prior lines of therapy before CAR-T infusion exhibited significantly lower response rates. Despite potential biases, such as intrinsic disease aggressiveness or unidentified genomic alterations, present findings suggest that using LIC or immunotherapy as bridging strategies, in patients with fewer prior treatment lines, may be associated with a lower overall disease and treatment burden and could potentially contribute to improved CAR-T cell efficacy and clinical outcomes. Nevertheless, additional investigations are required to elucidate biological and clinical mechanisms by which bridging approaches and treatment history modulate CAR-T responses.
- 18 August 2026
- Published by Springer Nature in Bone Marrow Transplantation
- Vol. 61 (11) , 1566-1569
Real-world CAR-T practice patterns in patients with mantle cell lymphoma: an international survey on behalf of the EBMT lymphoma working party
- 18 August 2026
- Published by Springer Nature in Bone Marrow Transplantation
- Vol. 61 (11) , 1566-1569
Real-world CAR-T practice patterns in patients with mantle cell lymphoma: an international survey on behalf of the EBMT lymphoma working party
- Open Access
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure S1 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Kaplan-Meier landmark analysis of EFS among patients with ongoing remission without new anti-cancer therapies, by CAR T-cell persistence by intracellular flow cytometry at A) Month 3 and B) Month 6.
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure S1 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Kaplan-Meier landmark analysis of EFS among patients with ongoing remission without new anti-cancer therapies, by CAR T-cell persistence by intracellular flow cytometry at A) Month 3 and B) Month 6.
- Open Access
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Table 1 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Analysis of concordance between surface FC or intracellular FC data and ddPCR data in matched samples.
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable 1 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Analysis of concordance between surface FC or intracellular FC data and ddPCR data in matched samples.
- Open Access
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table S5 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Summary of L-Psi duplex ddPCR assay
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table S5 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Summary of L-Psi duplex ddPCR assay
- Open Access
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Figure 2 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Correlation between (A) surface and intracellular FC, (B) surface FC and VCN by ddPCR, and (C) intracellular FC and VCN by ddPCR. Spearman correlation coefficients reported for all data above the LLoQ.
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure 2 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Correlation between (A) surface and intracellular FC, (B) surface FC and VCN by ddPCR, and (C) intracellular FC and VCN by ddPCR. Spearman correlation coefficients reported for all data above the LLoQ.
- Open Access
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table S4 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Fluorescence minus multiple controls for setting gating limits
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table S4 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Fluorescence minus multiple controls for setting gating limits
- Open Access
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table S2 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Intracellular flow cytometry surface antibody master mix
- 15 July 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table S2 from CAR T-cell Kinetics, Persistence, and Clinical Outcomes in Adult Patients with Relapsed/Refractory B-cell ALL Treated with Obecabtagene Autoleucel in the FELIX Study
Intracellular flow cytometry surface antibody master mix