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Outcome of patients with mantle cell lymphoma after autologous stem cell transplantation in the pre-CAR T-cell era Letter.

cris.virtual.author-orcid0000-0003-4474-3132
cris.virtualsource.author-orcid3ffc609d-4653-413a-a80f-2bf6c2b71f47
cris.virtualsource.author-orcidc441561b-2f62-41ef-8e09-fb335467e1b9
cris.virtualsource.author-orcida0f00c7b-780d-4398-9754-fe2161b10f0e
cris.virtualsource.author-orcid5f5278c3-d908-45fe-8a4a-885030ed281d
cris.virtualsource.author-orcid4cb402ea-7dca-4848-9a8a-3f49f6d6e920
cris.virtualsource.author-orcid1b65be99-ede2-4b0e-8e6d-1c720e453513
datacite.rightsopen.access
dc.contributor.authorMathys, Anina
dc.contributor.authorBacher, Vera Ulrike
dc.contributor.authorBanz Wälti, Yara Sarah
dc.contributor.authorLegros, Myriam
dc.contributor.authorMansouri Taleghani, Behrouz
dc.contributor.authorNovak, Urban
dc.contributor.authorPabst, Thomas Niklaus
dc.date.accessioned2024-10-06T18:50:56Z
dc.date.available2024-10-06T18:50:56Z
dc.date.issued2022-04
dc.description.abstractINTRODUCTION Mantle cell lymphoma (MCL) patients can be treated with intensive induction therapy, followed by high dose chemotherapy (HDCT) with autologous stem cell transplantation (ASCT) for consolidation and subsequent anti-CD20 maintenance. For patients relapsing after bruton tyrosine kinase (BTK) inhibitors, CAR T-cell therapy became available in late 2020 fueling the interest in outcomes of relapsing MCL patients. METHODS We retrospectively analyzed the outcome of MCL patients receiving HDCT/ASCT at our center between 2000 and 2021, thus, before availability of CAR-T cells. RESULTS We identified 97 MCL patients undergoing HDCT/ASCT in this period with a median follow-up of 52 months. 43 (44%) patients ultimately relapsed, and 29 (30%) have died. The median progression-free survival (PFS) for the entire cohort was 48 months and overall survival (OS) was 202 months. Relapsing patients had a median PFS of only 28 months and median OS of 105 months. The OS of relapsing patients receiving BTK inhibitors was 148 versus 78 months in patients who never received BTK inhibitors (p=0.1175). CONCLUSION Even after HDCT/ASCT, a substantial proportion of MCL patients will relapse and ultimately die of the disease, emphasizing the need for new therapeutic options including CAR T-cell treatment for this lymphoma subtype. This article is protected by copyright. All rights reserved.
dc.description.numberOfPages5
dc.description.sponsorshipUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
dc.description.sponsorshipInstitut für Pathologie
dc.description.sponsorshipUniversitätsklinik für Medizinische Onkologie
dc.identifier.doi10.48350/161613
dc.identifier.pmid34817087
dc.identifier.publisherDOI10.1002/hon.2952
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/57810
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofHematological oncology
dc.relation.issn1099-1069
dc.relation.organizationDCD5A442BF89E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C055E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C448E17DE0405C82790C4DE2
dc.subjectCAR T-cell Mantle cell lymphoma (MCL) autologous stem cell transplantation (ASCT) lymphoma outcome
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleOutcome of patients with mantle cell lymphoma after autologous stem cell transplantation in the pre-CAR T-cell era Letter.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage296
oaire.citation.issue2
oaire.citation.startPage292
oaire.citation.volume40
oairecerif.author.affiliationUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
oairecerif.author.affiliationInstitut für Pathologie
oairecerif.author.affiliationUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
oairecerif.author.affiliationUniversitätsklinik für Hämatologie und Hämatologisches Zentrallabor
oairecerif.author.affiliationUniversitätsklinik für Medizinische Onkologie
oairecerif.author.affiliationUniversitätsklinik für Medizinische Onkologie
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unibe.date.embargoChanged2022-11-25 23:25:04
unibe.date.licenseChanged2021-11-26 16:24:01
unibe.description.ispublishedpub
unibe.eprints.legacyId161613
unibe.refereedtrue
unibe.subtype.articlejournal

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