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  1. Book: Photopheresis and hematopoietic stem cell transplantation

    Couriel, Daniel R.

    mechanisms and clinical applications

    (Biology of blood and marrow transplantation ; 12,1, Suppl. 2)

    2006  

    Author's details guest ed.: Daniel R. Couriel
    Series title Biology of blood and marrow transplantation ; 12,1, Suppl. 2
    Collection
    Language English
    Size 40 S. : graph. Darst.
    Publisher Elsevier
    Publishing place New York, NY
    Publishing country United States
    Document type Book
    HBZ-ID HT014659301
    Database Catalogue ZB MED Medicine, Health

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  2. Article ; Online: Infectious complications following CAR-t cell therapy for B cell non-Hodgkin lymphoma: a single-center experience and review of the literature.

    Mercadal, Santiago / Gomez, Carlos A / Lee, Catherine J / Couriel, Daniel R

    Annals of hematology

    2023  Volume 102, Issue 7, Page(s) 1837–1843

    Abstract: Chimeric antigen receptor T-cell (CAR-T) therapy targeting CD19 has significantly improved outcomes in the treatment of refractory or relapsed (R/R) B-cell non-Hodgkin lymphoma (NHL). Several risk factors including CAR-T cell-related toxicities and their ...

    Abstract Chimeric antigen receptor T-cell (CAR-T) therapy targeting CD19 has significantly improved outcomes in the treatment of refractory or relapsed (R/R) B-cell non-Hodgkin lymphoma (NHL). Several risk factors including CAR-T cell-related toxicities and their treatments often lead to infectious complications (ICs); however, the pattern and timeline is not well established. We evaluated ICs in 48 patients with R/R B-cell NHL following CAR-T cell therapy at our institution. Overall, 15 patients experienced 22 infection events. Eight infections (4 bacterial, 3 viral and 1 fungal) occurred within the first 30 days and 14 infections (7 bacterial, 6 viral, 1 fungal) between days 31 to 180 following CAR-T infusion. Most infections were mild-to-moderate and fifteen infections involved the respiratory tract. Two patients developed mild-to-moderate COVID-19 infection and one patient a cytomegalovirus reactivation after CAR-T infusion. Two patients developed IFIs: one case each of fatal disseminated candidiasis and invasive pulmonary aspergillosis at day 16 and 77, respectively. Patients with more than 4 prior antitumor regimens and patient's ≥ 65 years had a higher infection rate. Infections in patients with relapsed/refractory B-cell NHL are common after CAR-T despite the use of infection prophylaxis. Age ≥ 65 years and having > 4 prior antitumor treatments were identified as risk factors for infection. Fungal infections carried significant impact in morbidity and mortality, suggesting a role for increase fungal surveillance and/or anti-mold prophylaxis following high-dose steroids and tocilizumab. Four of ten patients developed an antibody response following two doses of SARS-CoV-2 mRNA vaccine.
    MeSH term(s) Humans ; Aged ; Receptors, Chimeric Antigen ; COVID-19 Vaccines ; COVID-19 ; SARS-CoV-2 ; Lymphoma, B-Cell/therapy ; Cell- and Tissue-Based Therapy ; Antigens, CD19
    Chemical Substances Receptors, Chimeric Antigen ; COVID-19 Vaccines ; Antigens, CD19
    Language English
    Publishing date 2023-05-29
    Publishing country Germany
    Document type Review ; Journal Article
    ZDB-ID 1064950-5
    ISSN 1432-0584 ; 0939-5555 ; 0945-8077
    ISSN (online) 1432-0584
    ISSN 0939-5555 ; 0945-8077
    DOI 10.1007/s00277-023-05131-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Chimeric antigen receptor T-cell immunotherapies adverse events reported to FAERS database: focus on cytopenias.

    Gomez-Lumbreras, Ainhoa / Mercadal Vilchez, Santiago / Villa-Zapata, Lorenzo / Malone, Daniel C / Couriel, Daniel R

    Leukemia & lymphoma

    2023  Volume 64, Issue 13, Page(s) 2071–2080

    Abstract: Chimeric antigen receptor (CAR) T-cell therapy presents a promising treatment for hematologic malignancies, displaying high efficacy but not being exempt from toxicity. In this observational study, we assessed adverse events (AEs) reported to the Food ... ...

    Abstract Chimeric antigen receptor (CAR) T-cell therapy presents a promising treatment for hematologic malignancies, displaying high efficacy but not being exempt from toxicity. In this observational study, we assessed adverse events (AEs) reported to the Food and Drug Adverse Event Reporting System (FAERS) including any of the six approved CAR T-cell therapies. A total of 5249 reports mentioning a CAR T-cell as a suspect product were retrieved from the FAERS database, containing a total of 24333 AEs, of which 3236 (13.3%) were cytopenias. The highest number of AEs mentioned by the report was observed for tisagenlecleucel (mean = 6.7), with the lowest for ciltacabtagene (mean = 1.3). Among all reports,
    MeSH term(s) Humans ; United States ; Receptors, Chimeric Antigen ; Cytopenia ; Drug-Related Side Effects and Adverse Reactions/epidemiology ; Drug-Related Side Effects and Adverse Reactions/etiology ; Immunotherapy, Adoptive/adverse effects ; Leukopenia/etiology ; Thrombocytopenia ; United States Food and Drug Administration ; T-Lymphocytes
    Chemical Substances Receptors, Chimeric Antigen
    Language English
    Publishing date 2023-09-14
    Publishing country United States
    Document type Observational Study ; Journal Article
    ZDB-ID 1042374-6
    ISSN 1029-2403 ; 1042-8194
    ISSN (online) 1029-2403
    ISSN 1042-8194
    DOI 10.1080/10428194.2023.2254430
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Access to CAR T-cell therapy: Focus on diversity, equity and inclusion.

    Odstrcil, Maria S / Lee, Catherine J / Sobieski, Catherine / Weisdorf, Daniel / Couriel, Daniel

    Blood reviews

    2023  Volume 63, Page(s) 101136

    Abstract: Chimeric antigen receptor T-cell (CAR T-cell) therapy has revolutionized the treatment of hematologic malignancies in patients with relapsed or refractory disease without other treatment options. However, only a very small proportion of patients with an ... ...

    Abstract Chimeric antigen receptor T-cell (CAR T-cell) therapy has revolutionized the treatment of hematologic malignancies in patients with relapsed or refractory disease without other treatment options. However, only a very small proportion of patients with an indication for CAR T-cell can access the treatment. The imbalance between supply and demand is magnified in minority and vulnerable populations. Limited access is multifactorial and in part a result of factors directly related to the cellular product such as cost, complex logistics and manufacturing limitations. On the other hand, the impact of diversity, equity, and inclusion (DEI) and their social and structural context are also key to understanding access barriers in cellular therapy and health care in general. CAR T-cell therapy provides us with a new opportunity to better understand and prioritize this gap, a key step towards proactively and strategically addressing access. The aim of this review is to provide an analysis of the current state of access to CAR T therapy with a focus on the influence of DEI. We will cover aspects related to the cellular product and the inseparable context of social and structural determinants. Identifying and addressing barriers is necessary to ensure equitable access to this and all future novel therapies.
    MeSH term(s) Humans ; Immunotherapy, Adoptive/adverse effects ; Diversity, Equity, Inclusion ; Cell- and Tissue-Based Therapy ; Hematologic Neoplasms
    Language English
    Publishing date 2023-10-05
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 639015-8
    ISSN 1532-1681 ; 0268-960X
    ISSN (online) 1532-1681
    ISSN 0268-960X
    DOI 10.1016/j.blre.2023.101136
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Allogeneic stem cell transplantation and CAR-T in B-cell Non-Hodgkin Lymphoma: a two-center experience and review of the literature.

    Mercadal, Santiago / Mussetti, Alberto / Lee, Catherine J / Arevalo, Carolina / Odstrcil, Silvina M / Peña, Esteban / Sureda, Anna / Couriel, Daniel R

    Annals of hematology

    2024  Volume 103, Issue 5, Page(s) 1717–1727

    Abstract: Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is still a potentially curative option for B-cell Non-Hodgkin Lymphoma (B-NHL) in the modern immunotherapy era. The objective of this study was to analyze long-term outcomes of patients with ... ...

    Abstract Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is still a potentially curative option for B-cell Non-Hodgkin Lymphoma (B-NHL) in the modern immunotherapy era. The objective of this study was to analyze long-term outcomes of patients with B-NHL who received allo-HSCT. We analyzed overall survival (OS), progression-free survival (PFS) and graft versus host disease (GVHD) relapse-free survival (GRFS) in 53 patients undergoing allo-HSCT from two institutions. The median follow-up of the study was 72 months (range 29-115 months). The median number of lines of therapy before allo-HSCT was 3 (range 1-6) and twenty-eight patients (53%) had received a previous autologous transplant. The 3-year PFS, OS and GRFS were 55%, 63%, and 55%, respectively. One-year non-relapse mortality was 26%. Karnofsky Performance Scale < 90 was associated with worse OS in multivariable analysis. A non-comparative analysis of a cohort of 44 patients with similar characteristics who received chimeric antigen receptor T-cell therapy was done, showing a 1-year PFS and OS were 60% and 66%, respectively. Our data shows that allo-HSCT is still a useful option for treating selected patients with R/R B-NHL. Our retrospective analysis and review of the literature demonstrate that allo-HSCT can provide durable remissions in a subset of patients with R/R B-NHL.
    MeSH term(s) Humans ; Receptors, Chimeric Antigen ; Retrospective Studies ; Hematopoietic Stem Cell Transplantation ; Transplantation, Homologous ; Graft vs Host Disease ; Recurrence ; Lymphoma, Non-Hodgkin/therapy
    Chemical Substances Receptors, Chimeric Antigen
    Language English
    Publishing date 2024-03-02
    Publishing country Germany
    Document type Review ; Journal Article
    ZDB-ID 1064950-5
    ISSN 1432-0584 ; 0939-5555 ; 0945-8077
    ISSN (online) 1432-0584
    ISSN 0939-5555 ; 0945-8077
    DOI 10.1007/s00277-024-05677-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Extracorporeal photopheresis: Focus on therapeutic immunomodulation.

    Couriel, Daniel R

    Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

    2015  Volume 52, Issue 2, Page(s) 149–150

    MeSH term(s) Apoptosis ; Graft vs Host Disease/etiology ; Hematopoietic Stem Cell Transplantation/adverse effects ; Humans ; Immune System ; Immunomodulation/physiology ; Leukocytes/cytology ; Lymphoma, T-Cell, Cutaneous/therapy ; Off-Label Use ; Organ Transplantation/methods ; Photopheresis/methods ; Photopheresis/trends
    Language English
    Publishing date 2015-04
    Publishing country England
    Document type Editorial
    ZDB-ID 2046795-3
    ISSN 1878-1683 ; 1473-0502
    ISSN (online) 1878-1683
    ISSN 1473-0502
    DOI 10.1016/j.transci.2015.02.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Chronic graft-versus-host disease exacerbation after SARS-CoV-2 vaccination.

    Trunk, Andrew D / Shewan, Samuel K / Lee, Catherine J / Parker, Charles J / Couriel, Daniel R

    Bone marrow transplantation

    2022  Volume 57, Issue 3, Page(s) 502–503

    MeSH term(s) COVID-19/prevention & control ; COVID-19 Vaccines/adverse effects ; Graft vs Host Disease/etiology ; Humans ; SARS-CoV-2 ; Vaccination
    Chemical Substances COVID-19 Vaccines
    Language English
    Publishing date 2022-01-11
    Publishing country England
    Document type Letter
    ZDB-ID 632854-4
    ISSN 1476-5365 ; 0268-3369 ; 0951-3078
    ISSN (online) 1476-5365
    ISSN 0268-3369 ; 0951-3078
    DOI 10.1038/s41409-021-01543-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Hedgehog blockade in steroid-refractory sclerotic chronic graft-versus-host disease.

    Radojcic, Vedran / Pletneva, Maria / Lee, Catherine J / Ivcevic, Sanja / Sarantopoulos, Stefanie / Couriel, Daniel

    British journal of haematology

    2021  Volume 195, Issue 2, Page(s) e120–e122

    MeSH term(s) Administration, Oral ; Anilides/administration & dosage ; Anilides/adverse effects ; Anilides/pharmacology ; Anilides/therapeutic use ; Biopsy ; Chronic Disease ; Graft vs Host Disease/drug therapy ; Graft vs Host Disease/pathology ; Hedgehog Proteins/antagonists & inhibitors ; Hedgehog Proteins/pharmacology ; Hematopoietic Stem Cell Transplantation/adverse effects ; Humans ; Pyridines/administration & dosage ; Pyridines/adverse effects ; Pyridines/pharmacology ; Pyridines/therapeutic use ; Sclerosis/diagnosis ; Skin/pathology ; Steroids/therapeutic use
    Chemical Substances Anilides ; Hedgehog Proteins ; HhAntag691 ; Pyridines ; Steroids
    Language English
    Publishing date 2021-06-17
    Publishing country England
    Document type Clinical Trial ; Letter ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.17657
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Multifaceted Burden of Chronic Graft-versus-Host Disease.

    Radojcic, Vedran / Lee, Catherine J / Couriel, Daniel R

    Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation

    2018  Volume 24, Issue 9, Page(s) 1774–1775

    MeSH term(s) Bone Marrow Transplantation ; Cost-Benefit Analysis ; Graft vs Host Disease ; Humans ; Transplantation, Homologous
    Language English
    Publishing date 2018-08-09
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 1474865-4
    ISSN 1523-6536 ; 1083-8791
    ISSN (online) 1523-6536
    ISSN 1083-8791
    DOI 10.1016/j.bbmt.2018.07.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Regenerating islet-derived protein 3-α is a prognostic biomarker for gastrointestinal chronic graft-versus-host disease.

    DePriest, Brittany Paige / Li, Hong / Bidgoli, Alan / Onstad, Lynn / Couriel, Daniel / Lee, Stephanie J / Paczesny, Sophie

    Blood advances

    2022  Volume 6, Issue 10, Page(s) 2981–2986

    Abstract: Prognostic biomarkers used to identify likelihood of disease progression have not been identified for chronic graft-versus-host disease (cGVHD), the leading cause of late nonrelapse mortality (NRM) in survivors of allogeneic hematopoietic cell ... ...

    Abstract Prognostic biomarkers used to identify likelihood of disease progression have not been identified for chronic graft-versus-host disease (cGVHD), the leading cause of late nonrelapse mortality (NRM) in survivors of allogeneic hematopoietic cell transplantation. Gastrointestinal cGVHD (GI-cGVHD) has been particularly challenging to classify. Here, we analyzed 3 proteomics markers (Regenerating islet-derived protein 3-α [Reg3α], C-X-C motif ligand 9 [CXCL9], and Stimulation-2 [ST2]) in 2 independent cohorts of patients with cGVHD totaling 289 patients. Plasma concentrations of Reg3α were significantly increased in patients with GI-cGVHD (P = .0012) compared with those without (P = .01), but plasma concentrations of CXCL9 and ST2 were not. Patients with high Reg3α (≥72 ng/mL) vs low Reg3α had higher NRM (23% vs 11%; P = .015). Because Reg3α has been identified as a lower GI tract marker in acute GVHD, we correlated Reg3α with lower acute-like GI-cGVHD vs classical fibrotic-like esophageal manifestations and found that Reg3α did not differ between the subtypes. No difference was observed between upper GI tract and lower GI tract subtypes. Patients with extremely high Reg3α (≥180 ng/mL) had higher GI scores but not higher scores for the lower GI tract. In a multivariable Cox regression model, patients with high Reg3α were 1.9 times more likely to die without relapse. Our findings demonstrate the utility of Reg3α as a prognostic marker for GI-cGVHD. These data warrant prospective biomarker validation studies.
    MeSH term(s) Biomarkers ; Chemokine CXCL9 ; Graft vs Host Disease/diagnosis ; Graft vs Host Disease/etiology ; Humans ; Interleukin-1 Receptor-Like 1 Protein ; Pancreatitis-Associated Proteins/genetics ; Prognosis ; Prospective Studies
    Chemical Substances Biomarkers ; CXCL9 protein, human ; Chemokine CXCL9 ; IL1RL1 protein, human ; Interleukin-1 Receptor-Like 1 Protein ; Pancreatitis-Associated Proteins ; REG3A protein, human
    Language English
    Publishing date 2022-01-13
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2915908-8
    ISSN 2473-9537 ; 2473-9529
    ISSN (online) 2473-9537
    ISSN 2473-9529
    DOI 10.1182/bloodadvances.2021005420
    Database MEDical Literature Analysis and Retrieval System OnLINE

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