LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 6 of total 6

Search options

  1. Article ; Online: Impact of disease burden and late loss of B cell aplasia on the risk of relapse after CD19 chimeric antigen receptor T Cell (Tisagenlecleucel) infusion in pediatric and young adult patients with relapse/refractory acute lymphoblastic leukemia: role of B-cell monitoring.

    Molinos-Quintana, Águeda / Alonso-Saladrigues, Anna / Herrero, Blanca / Caballero-Velázquez, Teresa / Galán-Gómez, Víctor / Panesso, Melissa / Torrebadell, Montserrat / Delgado-Serrano, Javier / Pérez de Soto, Concepción / Faura, Anna / González-Martínez, Berta / Castillo-Robleda, Ana / Diaz-de-Heredia, Cristina / Pérez-Martínez, Antonio / Pérez-Hurtado, José María / Rives, Susana / Pérez-Simón, José Antonio

    Frontiers in immunology

    2024  Volume 14, Page(s) 1280580

    Abstract: Introduction: Loss of B-cell aplasia (BCA) is a well-known marker of functional loss of CD19 CAR-T. Most relapses and loss of BCA occur in the first months after CD19 CAR-T infusion. In addition, high tumor burden (HTB) has shown to have a strong impact ...

    Abstract Introduction: Loss of B-cell aplasia (BCA) is a well-known marker of functional loss of CD19 CAR-T. Most relapses and loss of BCA occur in the first months after CD19 CAR-T infusion. In addition, high tumor burden (HTB) has shown to have a strong impact on relapse, especially in CD19-negative. However, little is known about the impact of late loss of BCA or the relationship between BCA and pre-infusion tumor burden in patients infused with tisagenlecleucel for relapsed/refractory B-cell acute lymphoblastic leukemia. Therefore, the optimal management of patients with loss of BCA is yet to be defined.
    Methods: We conducted a Spanish, multicentre, retrospective study in patients infused with tisagenlecleucel after marketing authorization. A total of 73 consecutively treated patients were evaluated.
    Results: Prior to infusion, 39 patients had HTB (≥ 5% bone marrow blasts) whereas 34 had a low tumor burden (LTB) (<5% blasts). Complete remission was achieved in 90.4% of patients, of whom 59% relapsed. HTB was associated with inferior outcomes, with a 12-month EFS of 19.3% compared to 67.2% in patients with LTB (p<0.001) with a median follow-up of 13.5 months (95% CI 12.4 - 16.2). In the HTB subgroup relapses were mainly CD19-negative (72%) whereas in the LTB subgroup they were mainly CD19-positive (71%) (p=0.017). In the LTB group, all CD19-positive relapses were preceded by loss of BCA whereas only 57% (4/7) of HTB patients experienced CD19-positive relapse. We found a positive correlation between loss of BCA and CD19-positive relapse (R-squared: 74) which persisted beyond six months post-infusion. We also explored B-cell recovery over time using two different definitions of loss of BCA and found a few discrepancies. Interestingly, transient immature B-cell recovery followed by BCA was observed in two pediatric patients. In conclusion, HTB has an unfavorable impact on EFS and allo-SCT might be considered in all patients with HTB, regardless of BCA. In patients with LTB, loss of BCA preceded all CD19-positive relapses. CD19-positive relapse was also frequent in patients who lost BCA beyond six months post-infusion. Therefore, these patients are still at significant risk for relapse and close MRD monitoring and/or therapeutic interventions should be considered.
    MeSH term(s) Humans ; Child ; Young Adult ; Receptors, Chimeric Antigen/therapeutic use ; Retrospective Studies ; Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy ; Recurrence ; T-Lymphocytes ; Cost of Illness ; Receptors, Antigen, T-Cell ; Salicylates
    Chemical Substances tisagenlecleucel (Q6C9WHR03O) ; Receptors, Chimeric Antigen ; 4-trifluoromethylsalicylic acid (328-90-5) ; Receptors, Antigen, T-Cell ; Salicylates
    Language English
    Publishing date 2024-01-16
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2023.1280580
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Corrigendum: Impact of disease burden and late loss of B cell aplasia on the risk of relapse after CD19 chimeric antigen receptor T Cell (Tisagenlecleucel) infusion in pediatric and young adult patients with relapse/refractory acute lymphoblastic leukemia: role of B-cell monitoring.

    Molinos-Quintana, Águeda / Alonso-Saladrigues, Anna / Herrero, Blanca / Caballero-Velázquez, Teresa / Galán-Gómez, Víctor / Panesso, Melissa / Torrebadell, Montserrat / Delgado-Serrano, Javier / Pérez de Soto, Concepción / Faura, Anna / González-Martínez, Berta / Castillo-Robleda, Ana / Diaz-de-Heredia, Cristina / Pérez-Martínez, Antonio / Pérez-Hurtado, José María / Rives, Susana / Pérez-Simón, José Antonio

    Frontiers in immunology

    2024  Volume 15, Page(s) 1373852

    Abstract: This corrects the article DOI: 10.3389/fimmu.2023.1280580.]. ...

    Abstract [This corrects the article DOI: 10.3389/fimmu.2023.1280580.].
    Language English
    Publishing date 2024-02-07
    Publishing country Switzerland
    Document type Published Erratum
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2024.1373852
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Eosinophils engulfing platelets and with ring-shaped nuclei in nivolumab-associated eosinophilia.

    Delgado-Serrano, Javier / Morales-Camacho, Rosario M / Caballero-Velázquez, Teresa / García-Canale, Silvia / Vargas, M Teresa / Prats-Martín, Concepción

    British journal of haematology

    2020  Volume 188, Issue 6, Page(s) 812

    MeSH term(s) Blood Platelets/metabolism ; Cell Nucleus Shape/immunology ; Eosinophilia/chemically induced ; Eosinophils/metabolism ; Humans ; Male ; Middle Aged ; Nivolumab/adverse effects
    Chemical Substances Nivolumab (31YO63LBSN)
    Language English
    Publishing date 2020-02-10
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.16376
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Monitoring of kinetics and exhaustion markers of circulating CAR-T cells as early predictive factors in patients with B-cell malignancies.

    García-Calderón, Clara Beatriz / Sierro-Martínez, Belén / García-Guerrero, Estefanía / Sanoja-Flores, Luzalba / Muñoz-García, Raquel / Ruiz-Maldonado, Victoria / Jimenez-Leon, María Reyes / Delgado-Serrano, Javier / Molinos-Quintana, Águeda / Guijarro-Albaladejo, Beatriz / Carrasco-Brocal, Inmaculada / Lucena, José-Manuel / García-Lozano, José-Raúl / Blázquez-Goñi, Cristina / Reguera-Ortega, Juan Luis / González-Escribano, María-Francisca / Reinoso-Segura, Marta / Briones, Javier / Pérez-Simón, José Antonio /
    Caballero-Velázquez, Teresa

    Frontiers in immunology

    2023  Volume 14, Page(s) 1152498

    Abstract: Purpose: CAR-T cell therapy has proven to be a disruptive treatment in the hematology field, however, less than 50% of patients maintain long-term response and early predictors of outcome are still inconsistently defined. Here, we aimed to optimize the ... ...

    Abstract Purpose: CAR-T cell therapy has proven to be a disruptive treatment in the hematology field, however, less than 50% of patients maintain long-term response and early predictors of outcome are still inconsistently defined. Here, we aimed to optimize the detection of CD19 CAR-T cells in blood and to identify phenotypic features as early biomarkers associated with toxicity and outcomes.
    Experimental design: In this study, monitoring by flow cytometry and digital PCR (dPCR), and immunophenotypic characterization of circulating CAR-T cells from 48 patients treated with Tisa-cel or Axi-cel was performed.
    Results: Validation of the flow cytometry reagent for the detection of CAR-T cells in blood revealed CD19 protein conjugated with streptavidin as the optimal detection method. Kinetics of CAR-T cell expansion in blood confirmed median day of peak expansion at seven days post-infusion by both flow cytometry and digital PCR. Circulating CAR-T cells showed an activated, proliferative, and exhausted phenotype at the time of peak expansion. Patients with increased expansion showed more severe CRS and ICANs. Immunophenotypic characterization of CAR-T cells at the peak expansion identified the increased expression of co-inhibitory molecules PD1 and LAG3 and reduced levels of the cytotoxicity marker CD107a as predictors of a better long-term disease control.
    Conclusions: These data show the importance of CAR-T cells in vivo monitoring and identify the expression of PD1LAG3 and CD107a as early biomarkers of long-term disease control after CAR-T cell therapy.
    MeSH term(s) Humans ; Receptors, Chimeric Antigen/genetics ; Kinetics ; B-Lymphocytes/pathology ; T-Lymphocytes/pathology ; Lymphoma, Large B-Cell, Diffuse/pathology
    Chemical Substances Receptors, Chimeric Antigen
    Language English
    Publishing date 2023-04-14
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2023.1152498
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Recent Bendamustine Treatment Before Apheresis Has a Negative Impact on Outcomes in Patients With Large B-Cell Lymphoma Receiving Chimeric Antigen Receptor T-Cell Therapy.

    Iacoboni, Gloria / Navarro, Víctor / Martín-López, Ana África / Rejeski, Kai / Kwon, Mi / Jalowiec, Katarzyna Aleksandra / Amat, Paula / Reguera-Ortega, Juan Luis / Gallur, Laura / Blumenberg, Viktoria / Gutiérrez-Herrero, Sara / Roddie, Claire / Benzaquén, Ana / Delgado-Serrano, Javier / Sánchez-Salinas, Mario Andrés / Bailén, Rebeca / Carpio, Cecilia / López-Corral, Lucia / Hernani, Rafael /
    Bastos, Mariana / O'Reilly, Maeve / Martín-Martín, Lourdes / Subklewe, Marion / Barba, Pere

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology

    2023  Volume 42, Issue 2, Page(s) 205–217

    Abstract: Purpose: Approximately 30%-40% of patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL) infused with CD19-targeted chimeric antigen receptor (CAR) T cells achieve durable responses. Consensus guidelines suggest avoiding bendamustine ... ...

    Abstract Purpose: Approximately 30%-40% of patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL) infused with CD19-targeted chimeric antigen receptor (CAR) T cells achieve durable responses. Consensus guidelines suggest avoiding bendamustine before apheresis, but specific data in this setting are lacking. We report distinct outcomes after CAR T-cell therapy according to previous bendamustine exposure.
    Methods: The study included CAR T-cell recipients from seven European sites. Safety, efficacy, and CAR T-cell expansion kinetics were analyzed according to preapheresis bendamustine exposure. Additional studies on the impact of the washout period and bendamustine dose were performed. Inverse probability treatment weighting (IPTW) and propensity score matching (PSM) analyses were carried out for all efficacy comparisons between bendamustine-exposed and bendamustine-naïve patients.
    Results: The study included 439 patients with R/R LBCL infused with CD19-targeted commercial CAR T cells, of whom 80 had received bendamustine before apheresis. Exposed patients had significantly lower CD3
    Conclusion: Recent bendamustine exposure before apheresis was associated with negative treatment outcomes after CD19-targeted CAR T-cell therapy and should be therefore avoided in CAR T-cell candidates.
    MeSH term(s) Humans ; Receptors, Chimeric Antigen ; Bendamustine Hydrochloride/adverse effects ; Immunotherapy, Adoptive/adverse effects ; Blood Component Removal ; Lymphoma, Large B-Cell, Diffuse ; Antigens, CD19 ; Cell- and Tissue-Based Therapy
    Chemical Substances Receptors, Chimeric Antigen ; Bendamustine Hydrochloride (981Y8SX18M) ; Antigens, CD19
    Language English
    Publishing date 2023-10-24
    Publishing country United States
    Document type Journal Article
    ZDB-ID 604914-x
    ISSN 1527-7755 ; 0732-183X
    ISSN (online) 1527-7755
    ISSN 0732-183X
    DOI 10.1200/JCO.23.01097
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Best Treatment Option for Patients With Refractory Aggressive B-Cell Lymphoma in the CAR-T Cell Era: Real-World Evidence From GELTAMO/GETH Spanish Groups.

    Bastos-Oreiro, Mariana / Gutierrez, Antonio / Reguera, Juan Luís / Iacoboni, Gloria / López-Corral, Lucía / Terol, María José / Ortíz-Maldonado, Valentín / Sanz, Jaime / Guerra-Dominguez, Luisa / Bailen, Rebeca / Mussetti, Alberto / Abrisqueta, Pau / Hernani, Rafael / Luzardo, Hugo / Sancho, Juan-Manuel / Delgado-Serrano, Javier / Salar, Antonio / Grande, Carlos / Bento, Leyre /
    González de Villambrosía, Sonia / García-Belmonte, Daniel / Sureda, Anna / Pérez-Martínez, Antonio / Barba, Pere / Kwon, Mi / Martín García-Sancho, Alejandro

    Frontiers in immunology

    2022  Volume 13, Page(s) 855730

    Abstract: Real-world evidence comparing the efficacy of chimeric antigen receptor (CAR) T-cell therapy against that of the previous standard of care (SOC) for refractory large B-cell lymphoma (LBCL) is scarce. We retrospectively collected data from patients with ... ...

    Abstract Real-world evidence comparing the efficacy of chimeric antigen receptor (CAR) T-cell therapy against that of the previous standard of care (SOC) for refractory large B-cell lymphoma (LBCL) is scarce. We retrospectively collected data from patients with LBCL according to SCHOLAR-1 criteria treated with commercial CAR T-cell therapy in Spain (204 patients included and 192 treated, 101 with axicabtagene ciloleucel [axi-cel], and 91 with tisagenlecleucel [tisa-cel]) and compared the results with a historical refractory population of patients (n = 81) obtained from the GELTAMO-IPI study. We observed superior efficacy for CAR-T therapy (for both axi-cel and tisa-cel) over pSOC, with longer progression-free survival (PFS) (median of 5.6 vs. 4-6 months, p ≤ 0.001) and overall survival (OS) (median of 15 vs. 8 months, p < 0.001), independently of other prognostic factors (HR: 0.59 (95% CI: 0.44-0.80); p < 0.001] for PFS, and 0.45 [(95% CI: 0.31-0.64)] for OS). Within the CAR-T cohort, axi-cel showed longer PFS (median of 7.3 versus 2.8 months, respectively, p = 0.027) and OS (58% versus 42% at 12 months, respectively, p = 0.048) than tisa-cel. These differences were maintained in the multivariable analysis. On the other hand, axi-cel was independently associated with a higher risk of severe cytokine release syndrome and neurotoxicity. Our results suggest that the efficacy of CAR-T cell therapy is superior to pSOC in the real-world setting. Furthermore, axi-cel could be superior in efficacy to tisa-cel, although more toxic, in this group of refractory patients according to SCHOLAR-1 criteria.
    MeSH term(s) Antigens, CD19 ; Humans ; Lymphoma, Large B-Cell, Diffuse/pathology ; Receptors, Chimeric Antigen/genetics ; Retrospective Studies ; T-Lymphocytes
    Chemical Substances Antigens, CD19 ; Receptors, Chimeric Antigen
    Language English
    Publishing date 2022-07-12
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2606827-8
    ISSN 1664-3224 ; 1664-3224
    ISSN (online) 1664-3224
    ISSN 1664-3224
    DOI 10.3389/fimmu.2022.855730
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top