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  1. Article ; Online: Les CAR-NK allogéniques : une alternative prometteuse aux CAR-T autologues – État de la question, sources de cellules NK, limites et perspectives.

    Nguyen, Stéphanie / Lacan, Claire / Roos-Weil, Damien

    Bulletin du cancer

    2021  Volume 108, Issue 10S, Page(s) S81–S91

    Abstract: Immunotherapy with chimeric antigen receptor engineered-T cells (CAR-T) has revolutionized the landscape of treatment of relapsed or refractory B-cell. However, the use of autologous T cells has limitations: variable quality of collected effector T cells, ...

    Title translation Allogeneic CAR-NK cells: A promising alternative to autologous CAR-T cells - State of the art, sources of NK cells, limits and perspectives.
    Abstract Immunotherapy with chimeric antigen receptor engineered-T cells (CAR-T) has revolutionized the landscape of treatment of relapsed or refractory B-cell. However, the use of autologous T cells has limitations: variable quality of collected effector T cells, duration of the process sometimes incompatible with uncontrolled hemopathy, limited number of available CAR cells, sometimes fatal toxicities, extremely high cost. Natural Killer (NK) cells are an interesting alternative to T cells. NK cells are very powerful cytotoxic effectors that have demonstrated an anti-tumor effect after haploidentical hematopoietic stem cells transplantation or in adoptive cell therapy against a number of solid or hematological tumors. Mainly, they can be used in allogeneic situations without causing major toxic side effects. The sources of NK cells are multiple: cell line, cord blood, peripheral blood, induced pluripotent stem cells. Recent advances in manufacturing engineered CAR-NK cells make it possible to promote antibody-dependent cell-mediated cytotoxicity (ADCC), as well as the activation and persistence of these cells, notably via the cytokine Il-15. The majority of the reports on CAR-NK cells concern pre-clinical or early clinical trials. However, the many advantages of "off-the-shelf" allogeneic CAR-NK cells provide great potential in cancer treatments.
    MeSH term(s) Allogeneic Cells/cytology ; Allogeneic Cells/immunology ; Antibody-Dependent Cell Cytotoxicity ; Blood Cells ; Cell Engineering ; Cell Line ; Fetal Blood/cytology ; Hematologic Neoplasms/immunology ; Hematologic Neoplasms/therapy ; Hematopoietic Stem Cell Transplantation ; Humans ; Immunotherapy, Adoptive/methods ; Induced Pluripotent Stem Cells/cytology ; Killer Cells, Natural/cytology ; Killer Cells, Natural/immunology ; Killer Cells, Natural/transplantation ; Lymphocyte Activation ; Neoplasms/immunology ; Neoplasms/therapy ; Receptors, Chimeric Antigen/immunology ; T-Lymphocytes/cytology ; T-Lymphocytes/immunology ; T-Lymphocytes/transplantation
    Chemical Substances Receptors, Chimeric Antigen
    Language French
    Publishing date 2021-12-17
    Publishing country France
    Document type Journal Article ; Review
    ZDB-ID 213270-9
    ISSN 1769-6917 ; 0007-4551
    ISSN (online) 1769-6917
    ISSN 0007-4551
    DOI 10.1016/j.bulcan.2021.06.007
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Neurolymphomatosis: involvement of peripheral nervous system revealing hematologic malignancy, a report of nine cases.

    Ducatel, Pauline / Michaud, Maud / Viala, Karine / Leblond, Véronique / Charlotte, Frédéric / Roos-Weil, Damien / Benoit, Charline / Debs, Rabab / Maisonobe, Thierry

    Journal of the peripheral nervous system : JPNS

    2023  Volume 28, Issue 2, Page(s) 252–261

    Abstract: Background and aim: Neurolymphomatosis is defined as an infiltration of the peripheral nervous system (PNS) by malignant lymphoma cells. It is a rare entity and diagnosis is complicated especially when PNS involvement is the initial and leading symptom. ...

    Abstract Background and aim: Neurolymphomatosis is defined as an infiltration of the peripheral nervous system (PNS) by malignant lymphoma cells. It is a rare entity and diagnosis is complicated especially when PNS involvement is the initial and leading symptom. To improve knowledge of the disorder and shorten the time to diagnosis, we report a series of nine patients without a history of hematologic malignancy, who were diagnosed with neurolymphomatosis after evaluation and workup of peripheral neuropathy.
    Methods: The patients were included from the Department of Clinical Neurophysiology at Pitié Salpêtrière and Nancy Hospitals over a period of 15 years. Diagnosis of neurolymphomatosis was confirmed by histopathologic examination for each patient. We characterized their clinical, electrophysiological, biological, imaging, and histopathologic features.
    Results: The neuropathy was characterized by pain (78%), proximal involvement (44%) or of all four limbs (67%), asymmetrical or with multifocal distribution (78%), abundant fibrillation (78%), a tendency to worsen rapidly, and significant associated weight loss (67%). Neurolymphomatosis was diagnosed principally on nerve biopsy (89%) identifying infiltration of lymphoid cells, atypical cells (78%), a monoclonal population (78%), and supported by fluorodeoxyglucose-positron emission tomography, spine or plexus MRI, cerebrospinal fluid analysis, and blood lymphocyte immunophenotyping. Six patients had systemic disease and three impairment limited to the PNS. In the latter case, progression could be unpredictable and may be diffuse and explosive, sometimes occurring years after a seemingly indolent course.
    Interpretation: This study provides better knowledge and understanding of neurolymphomatosis when neuropathy is the initial presentation.
    MeSH term(s) Humans ; Neurolymphomatosis/diagnosis ; Neurolymphomatosis/pathology ; Peripheral Nervous System/pathology ; Peripheral Nervous System Diseases ; Hematologic Neoplasms/complications ; Hematologic Neoplasms/diagnosis ; Positron-Emission Tomography
    Language English
    Publishing date 2023-03-19
    Publishing country United States
    Document type Case Reports
    ZDB-ID 1364009-4
    ISSN 1529-8027 ; 1085-9489
    ISSN (online) 1529-8027
    ISSN 1085-9489
    DOI 10.1111/jns.12541
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Long-term results of Waldenström macroglobulinaemia treatment by bendamustine and rituximab: A study on behalf of the French Innovative Leukemia Organization (FILO).

    Laribi, Kamel / Poulain, Stéphanie / Willems, Lise / Merabet, Fatiha / Herbaux, Charles / Roos-Weil, Damien / Laribi de Materre, Inès / Roussel, Xavier / Nudel, Morgane / Tricot, Sabine / Dupuis, Jehan / Le Calloch, Ronan / Bareau, Benoit / Leblond, Véronique

    British journal of haematology

    2024  

    Abstract: The bendamustine-rituximab (BR) schedule is an efficient first-line therapy in Waldenström macroglobulinaemia (WM). A previous analysis of 69 patients who received this treatment confirmed a high response rate and good progression-free (PFS) and overall ... ...

    Abstract The bendamustine-rituximab (BR) schedule is an efficient first-line therapy in Waldenström macroglobulinaemia (WM). A previous analysis of 69 patients who received this treatment confirmed a high response rate and good progression-free (PFS) and overall survival (OS). With a median follow-up of 76.1 months (95% confidence interval [CI] 69.9-80.6), 5-year outcome is still excellent at 66.63% (95% CI 56.09-79.17) for PFS and 80.01% (95% CI 70.82-90.41) for OS. The rate of secondary cancers is 17.66% (IQR 7.99-27.64) at 66 months. Relapsed patients who received ibrutinib as second-line clearly benefited from this schedule. This confirms current recommendations suggesting BR long-term efficacy as first-line option in WM.
    Language English
    Publishing date 2024-03-19
    Publishing country England
    Document type Journal Article
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.19409
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Acute myeloid leukaemia following direct acting antiviral drugs in HCV-infected patients: A 10 years' retrospective single-center study.

    Scheifer, Carole / Luckina, Elena / Lebrun-Vignes, Bénédicte / Diop, Abdoul-Aziz / Damais-Thabut, Dominique / Roos-Weil, Damien / Dechartres, Agnès / Lebray, Pascal

    Clinics and research in hepatology and gastroenterology

    2022  Volume 46, Issue 8, Page(s) 102000

    Abstract: Background: After several cases of peculiar hematological malignancies following introduction of new oral anti-hepatitis C virus (HCV) treatments in our recent practice, we aimed to systematically identify all cases of hematological malignancies (HM) in ...

    Abstract Background: After several cases of peculiar hematological malignancies following introduction of new oral anti-hepatitis C virus (HCV) treatments in our recent practice, we aimed to systematically identify all cases of hematological malignancies (HM) in patients with chronic HCV infection and to compare them according to the prescription of oral anti-HCV Direct Acting Antivirals (DAA) treatment or not.
    Material/methods: In this single-center retrospective observational study, we included all patients with confirmed HM and chronic HCV infection managed between 2010 and 2019 in the Pitié-Salpêtrière hospital, Paris. Non-inclusion criteria were a benign hematological disorder, an HM preceding chronic HCV infection and HCV acute infection. We compared characteristics of patients who received DAA before HM diagnosis to those with no DAA before HM.
    Results: Over the 10 years, 61 cases of HM among HCV infected patients were identified (female 29%, median age of 58.0 years [IQR 17]). Twenty-one received DAA before the onset of HM (Group DAA+) and 40 did not (Group DAA-) including 22 having received DAA after HM. In the DAA+ group, oral NS5B, NS5A and NS3A inhibitors were used in 90, 76 and 29% respectively. HM developed in the two years following DAA initiation in 76%. Eight (38%) had Non-Hodgkin Lymphoma, 5 (24%) had an Acute Myeloid Leukaemia (AML) including two with a mixed phenotype, 2 each had Hodgkin Lymphoma, Multiple Myeloma or a myeloproliferative disorder and one each had a chronic Lymphocytic Leukaemia or AL Amyloidosis. In the Group DAA-, HM were NHL in 20(50%) patients, Myeloproliferative neoplasms in 7 (17%), Multiple Myeloma in 5, Hodgkin Lymphoma in 3, Myelodysplastic syndrome and AML in 2 (5%) each and Acute Lymphoblastic Leukaemia in one. No significant difference between the groups DAA + and - was found according to age, sex, HCV genotype, viral load, co-infection or type and exposition of previous HCV treatments. AML, liver transplantation and cirrhosis were significantly more frequent in the DAA+ group (p = 0.020, 0.045 and 0.032, respectively).
    Conclusion: AML seemed more frequent after using DAA treatments, notably in severe HCV patients including cirrhotic and/or liver transplanted patients. A multicentric observational study is ongoing to confirm and explore the results.
    MeSH term(s) Antiviral Agents/therapeutic use ; Female ; Hematologic Neoplasms/chemically induced ; Hematologic Neoplasms/drug therapy ; Hepacivirus/genetics ; Hepatitis C/complications ; Hepatitis C/drug therapy ; Hepatitis C, Chronic/complications ; Hepatitis C, Chronic/drug therapy ; Humans ; Leukemia, Myeloid, Acute/chemically induced ; Leukemia, Myeloid, Acute/drug therapy ; Lymphoma/chemically induced ; Lymphoma/drug therapy ; Multiple Myeloma ; Retrospective Studies
    Chemical Substances Antiviral Agents
    Language English
    Publishing date 2022-08-03
    Publishing country France
    Document type Journal Article ; Observational Study
    ZDB-ID 2594333-9
    ISSN 2210-741X ; 2210-7401
    ISSN (online) 2210-741X
    ISSN 2210-7401
    DOI 10.1016/j.clinre.2022.102000
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: CAR-NK Cells: A Chimeric Hope or a Promising Therapy?

    Sabbah, Mohamad / Jondreville, Ludovic / Lacan, Claire / Norol, Francoise / Vieillard, Vincent / Roos-Weil, Damien / Nguyen, Stéphanie

    Cancers

    2022  Volume 14, Issue 15

    Abstract: Immunotherapy with chimeric antigen receptor-engineered T cells (CAR-T) has revolutionized the treatment landscape of relapsed/refractory B-cell malignancies. Nonetheless, the use of autologous T cells has certain limitations, including the variable ... ...

    Abstract Immunotherapy with chimeric antigen receptor-engineered T cells (CAR-T) has revolutionized the treatment landscape of relapsed/refractory B-cell malignancies. Nonetheless, the use of autologous T cells has certain limitations, including the variable quality and quantity of collected effector T cells, extended time of cell processing, limited number of available CAR cells, toxicities, and a high cost. Thanks to their powerful cytotoxic capabilities, with proven antitumor effects in both haploidentical hematopoietic stem cell transplantation and adoptive cell therapy against solid tumors and hematological malignancies, Natural Killer cells could be a promising alternative. Different sources of NK cells can be used, including cellular lines, cord blood, peripheral blood, and induced pluripotent stem cells. Their biggest advantage is the possibility of using them in an allogeneic context without major toxic side effects. However, the majority of the reports on CAR-NK cells concern preclinical or early clinical trials. Indeed, NK cells might be more difficult to engineer, and the optimization and standardization of expansion and transfection protocols need to be defined. Furthermore, their short persistence after infusion is also a major setback. However, with recent advances in manufacturing engineered CAR-NK cells exploiting their cytolytic capacities, antibody-dependent cellular cytotoxicity (ADCC), and cytokine production, "off-the-shelf" allogeneic CAR-NK cells can provide a great potential in cancer treatments.
    Language English
    Publishing date 2022-08-08
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers14153839
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Circulating tumor cells in Waldenström macroglobulinemia.

    Boccon-Gibod, Clémentine / Sourdeau, Elise / Morel, Pierre / Chapiro, Elise / Nguyen-Khac, Florence / Bravetti, Clotilde / Davi, Frédéric / Morel, Véronique / Gauthier, Nicolas / Grenier, Adrien / Boussen, Inès / Choquet, Sylvain / Leblond, Véronique / Le Garff-Tavernier, Magali / Baron, Marine / Roos-Weil, Damien

    Leukemia

    2024  Volume 38, Issue 4, Page(s) 903–907

    MeSH term(s) Humans ; Waldenstrom Macroglobulinemia/pathology ; Neoplastic Cells, Circulating ; Mutation ; Cell Proliferation
    Language English
    Publishing date 2024-02-09
    Publishing country England
    Document type Journal Article
    ZDB-ID 807030-1
    ISSN 1476-5551 ; 0887-6924
    ISSN (online) 1476-5551
    ISSN 0887-6924
    DOI 10.1038/s41375-024-02156-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Invasive Aspergillosis with impaired neutrophil responses against Aspergillus fumigatus in patients treated with Acalabrutinib-findings from three cases.

    Blaize, Marion / Thizy, Guillaume / Boissonnas, Alexandre / Portalier, Anaïs / Lanternier, Fanny / de La Porte des Vaux, Clémentine / Suarez, Felipe / Bougnoux, Marie-Elisabeth / Guitard, Juliette / Jabet, Arnaud / Stocker, Nicolas / Aoudjhane, Abdelmalek / Roos-Weil, Damien / Fekkar, Arnaud

    International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases

    2024  Volume 142, Page(s) 107000

    Abstract: Objectives: Ibrutinib, a first-generation covalent Bruton's tyrosine kinase inhibitor (BTKi) was found to be a risk factor for the occurrence of invasive fungal complications. Acalabrutinib is a second-generation covalent BTKi used to treat B-cell ... ...

    Abstract Objectives: Ibrutinib, a first-generation covalent Bruton's tyrosine kinase inhibitor (BTKi) was found to be a risk factor for the occurrence of invasive fungal complications. Acalabrutinib is a second-generation covalent BTKi used to treat B-cell malignancies. Healthy donor neutrophils incubated ex vivo with acalabrutinib lose ability to control Aspergillus conidia germination. In patients receiving acalabrutinib, the potential effect on neutrophil antifungal activity is unknown. Furthermore, only two cases of invasive aspergillosis have been reported during treatment with acalabrutinib, outside of a few cases in a clinical trial.
    Methods: We describe three new cases of invasive aspergillosis occurring within the first months of acalabrutinib therapy in patients with chronic lymphocytic leukemia. We used videomicroscopy and flow cytometry approaches to investigate the basic functional responses against Aspergillus of neutrophils from acalabrutinib-treated patients.
    Results: We showed an alteration in the anti-Aspergillus response after 1 month of acalabrutinb therapy: neutrophils lost their capacities of killing Aspergillus fumigatus germinating conidia and decreased their reactive oxygen species production when stimulated by Aspergillus.
    Conclusions: It is important to follow-up patients treated with acalabrutinib for the risk of aspergillosis as well as those treated with ibrutinib.
    MeSH term(s) Humans ; Agammaglobulinaemia Tyrosine Kinase ; Aspergillus fumigatus ; Neutrophils ; Aspergillosis/drug therapy ; Protein Kinase Inhibitors/therapeutic use ; Benzamides ; Pyrazines
    Chemical Substances Agammaglobulinaemia Tyrosine Kinase (EC 2.7.10.2) ; acalabrutinib (I42748ELQW) ; Protein Kinase Inhibitors ; Benzamides ; Pyrazines
    Language English
    Publishing date 2024-03-08
    Publishing country Canada
    Document type Case Reports
    ZDB-ID 1331197-9
    ISSN 1878-3511 ; 1201-9712
    ISSN (online) 1878-3511
    ISSN 1201-9712
    DOI 10.1016/j.ijid.2024.107000
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Prognostic impact of genetic abnormalities in 536 first-line chronic lymphocytic leukaemia patients without 17p deletion treated with chemoimmunotherapy in two prospective trials: Focus on IGHV-mutated subgroups (a FILO study).

    Nguyen-Khac, Florence / Baron, Marine / Guièze, Romain / Feugier, Pierre / Fayault, Alexandra / Raynaud, Sophie / Troussard, Xavier / Droin, Nathalie / Damm, Frederik / Smagghe, Luce / Susin, Santos / Leblond, Véronique / Dartigeas, Caroline / Van den Neste, Eric / Leprêtre, Stéphane / Bernard, Olivier A / Roos-Weil, Damien

    British journal of haematology

    2024  

    Abstract: The potential prognostic influence of genetic aberrations on chronic lymphocytic leukaemia (CLL) can vary based on various factors, such as the immunoglobulin heavy variable (IGHV) status. We conducted an integrative analysis on genetic abnormalities ... ...

    Abstract The potential prognostic influence of genetic aberrations on chronic lymphocytic leukaemia (CLL) can vary based on various factors, such as the immunoglobulin heavy variable (IGHV) status. We conducted an integrative analysis on genetic abnormalities identified through cytogenetics and targeted next-generation sequencing in 536 CLL patients receiving first-line chemo(immuno)therapies (CIT) as part of two prospective trials. We evaluated the prognostic implications of the main abnormalities, with specific attention to their relative impact according to IGHV status. In the entire cohort, unmutated (UM)-IGHV, complex karyotype, del(11q) and ATM mutations correlated significantly with shorter progression-free survival (PFS). Focusing on the subset of mutated IGHV (M-IGHV) patients, univariate analysis showed that complex karyotype, del(11q), SF3B1 and SAMHD1 mutations were associated with significant lower PFS. The prognostic influence varied based on the patient's IGHV status, as these abnormalities did not affect outcomes in the UM-IGHV subgroup. TP53 mutations had no significant impact on outcomes in the M-IGHV subgroup. Our findings highlight the diverse prognostic influence of genetic aberrations depending on the IGHV status in symptomatic CLL patients receiving first-line CIT. The prognosis of gene mutations and cytogenetic abnormalities needs to be investigated with a compartmentalized methodology, taking into account the IGVH status of patients receiving first-line BTK and/or BCL2 inhibitors.
    Language English
    Publishing date 2024-04-23
    Publishing country England
    Document type Journal Article
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.19459
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Norovirus and sapovirus infections after allogeneic hematopoietic stem cell transplantation: is it worth it to look for them?

    Mageau, Arthur / Ambert-Balay, Katia / Boutolleau, David / Schuffenecker, Isabelle / Burrel, Sonia / Kaplon, Jérome / Nguyen Quoc, Stéphanie / Uzunov, Madalina / Souchet, Laetitia / de Rougemont, Alexis / Roos-Weil, Damien / Baron, Marine

    Leukemia & lymphoma

    2023  Volume 64, Issue 7, Page(s) 1295–1303

    Abstract: Norovirus (NoV) and Sapovirus (SaV) are potential causative agents of diarrhea after allogeneic HSCT but little is known in this population. We performed a retrospective analysis by RT-PCR of calicivirus (NoV and SaV), Human adenovirus (HAdV), rotavirus ( ...

    Abstract Norovirus (NoV) and Sapovirus (SaV) are potential causative agents of diarrhea after allogeneic HSCT but little is known in this population. We performed a retrospective analysis by RT-PCR of calicivirus (NoV and SaV), Human adenovirus (HAdV), rotavirus (RV), Aichi virus (AiV), enterovirus (EV), human parechovirus (HPeV) and Human bocavirus (HBoV) in the diarrheal stools of patients after allogeneic HSCT. 49/162 patients had positive viral assays: HAdV (17%), EV (7%), NoV (4.3%), RV and HBoV (3.1% each), SaV (1.9%), AiV (1.2%), HPeV (0.6%). Seven patients were positive for NoV and 3 for SaV. Among viruses-positive samples, the frequency of caliciviruses cases was 7% in the 6 months post-HSCT compared to 40% after (
    MeSH term(s) Humans ; Infant ; Sapovirus/genetics ; Norovirus/genetics ; Gastroenteritis/diagnosis ; Gastroenteritis/epidemiology ; Gastroenteritis/etiology ; Retrospective Studies ; Diarrhea/diagnosis ; Diarrhea/etiology ; Diarrhea/epidemiology ; Hematopoietic Stem Cell Transplantation/adverse effects
    Language English
    Publishing date 2023-05-10
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1042374-6
    ISSN 1029-2403 ; 1042-8194
    ISSN (online) 1029-2403
    ISSN 1042-8194
    DOI 10.1080/10428194.2023.2211186
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Successful treatment by CAR T-cells in multi-refractory mantle cell lymphoma with central nervous system involvement.

    Caillet, Adrien / Houillier, Caroline / Sourdeau, Elise / Gazzano, Marianne / Uzunov, Madalina / Friser, Valérie / Ribeiro, Monica / Nicelli, Lucia / Azar, Nabih / Baron, Marine / Phina-Ziebin, Xavier / Choquet, Sylvain / Roos-Weil, Damien

    Annals of hematology

    2023  Volume 102, Issue 11, Page(s) 3295–3297

    MeSH term(s) Adult ; Humans ; Lymphoma, Mantle-Cell/drug therapy ; Neoplasm Recurrence, Local ; Receptors, Chimeric Antigen ; T-Lymphocytes ; Central Nervous System/pathology ; Antigens, CD19 ; Central Nervous System Neoplasms/therapy ; Central Nervous System Neoplasms/pathology
    Chemical Substances Receptors, Chimeric Antigen ; Antigens, CD19
    Language English
    Publishing date 2023-08-15
    Publishing country Germany
    Document type Letter
    ZDB-ID 1064950-5
    ISSN 1432-0584 ; 0939-5555 ; 0945-8077
    ISSN (online) 1432-0584
    ISSN 0939-5555 ; 0945-8077
    DOI 10.1007/s00277-023-05408-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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