Allogeneic haematopoietic cell transplantation for myelofibrosis: proposed definitions and management strategies for graft failure, poor graft function and relapse: best practice recommendations of the EBMT Chronic Malignancies Working Party

Allogeneic haematopoietic cell transplantation (allo-HCT) remains the only curative approach in myelofibrosis (MF). Despite advances over recent decades, relapse and non-relapse mortality rates remain significant. Relapse rates vary between 15 and 25% across retrospective studies and management stra...

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Published inLeukemia Vol. 35; no. 9; pp. 2445 - 2459
Main Authors McLornan, Donal P., Hernandez-Boluda, Juan Carlos, Czerw, Tomasz, Cross, Nicholas, Joachim Deeg, H., Ditschkowski, Marcus, Moonim, Mufaddal T., Polverelli, Nicola, Robin, Marie, Aljurf, Mahmoud, Conneally, Eibhlin, Hayden, Patrick, Yakoub-Agha, Ibrahim
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.09.2021
Nature Publishing Group
Springer Nature
SeriesLeukemia
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Abstract Allogeneic haematopoietic cell transplantation (allo-HCT) remains the only curative approach in myelofibrosis (MF). Despite advances over recent decades, relapse and non-relapse mortality rates remain significant. Relapse rates vary between 15 and 25% across retrospective studies and management strategies vary widely, ranging from palliation to adoptive immunotherapy and, in some cases, a second allo-HCT. Moreover, in allo-HCT, there is a higher incidence of poor graft function and graft failure due to splenomegaly and a hostile “pro-inflammatory” marrow niche. The Practice Harmonisation and Guidelines subcommittee of the Chronic Malignancies Working Party (CMWP) of EBMT convened an international panel consisting of transplant haematologists, histopathologists and molecular biologists to propose practical, clinically relevant definitions of graft failure, poor graft function and relapse as well as management strategies following allo-HCT. A systematic approach to molecular monitoring, histopathological assessment and chimerism testing is proposed. These proposed recommendations aim to increase the accuracy and uniformity of reporting and to thereby facilitate the development of more consistent approaches to these challenging issues. In addition, we propose management strategies for these complications.
AbstractList Allogeneic haematopoietic cell transplantation (allo-HCT) remains the only curative approach in myelofibrosis (MF). Despite advances over recent decades, relapse and non-relapse mortality rates remain significant. Relapse rates vary between 15 and 25% across retrospective studies and management strategies vary widely, ranging from palliation to adoptive immunotherapy and, in some cases, a second allo-HCT. Moreover, in allo-HCT, there is a higher incidence of poor graft function and graft failure due to splenomegaly and a hostile "pro-inflammatory" marrow niche. The Practice Harmonisation and Guidelines subcommittee of the Chronic Malignancies Working Party (CMWP) of EBMT convened an international panel consisting of transplant haematologists, histopathologists and molecular biologists to propose practical, clinically relevant definitions of graft failure, poor graft function and relapse as well as management strategies following allo-HCT. A systematic approach to molecular monitoring, histopathological assessment and chimerism testing is proposed. These proposed recommendations aim to increase the accuracy and uniformity of reporting and to thereby facilitate the development of more consistent approaches to these challenging issues. In addition, we propose management strategies for these complications.Allogeneic haematopoietic cell transplantation (allo-HCT) remains the only curative approach in myelofibrosis (MF). Despite advances over recent decades, relapse and non-relapse mortality rates remain significant. Relapse rates vary between 15 and 25% across retrospective studies and management strategies vary widely, ranging from palliation to adoptive immunotherapy and, in some cases, a second allo-HCT. Moreover, in allo-HCT, there is a higher incidence of poor graft function and graft failure due to splenomegaly and a hostile "pro-inflammatory" marrow niche. The Practice Harmonisation and Guidelines subcommittee of the Chronic Malignancies Working Party (CMWP) of EBMT convened an international panel consisting of transplant haematologists, histopathologists and molecular biologists to propose practical, clinically relevant definitions of graft failure, poor graft function and relapse as well as management strategies following allo-HCT. A systematic approach to molecular monitoring, histopathological assessment and chimerism testing is proposed. These proposed recommendations aim to increase the accuracy and uniformity of reporting and to thereby facilitate the development of more consistent approaches to these challenging issues. In addition, we propose management strategies for these complications.
Allogeneic haematopoietic cell transplantation (allo-HCT) remains the only curative approach in myelofibrosis (MF). Despite advances over recent decades, relapse and non-relapse mortality rates remain significant. Relapse rates vary between 15 and 25% across retrospective studies and management strategies vary widely, ranging from palliation to adoptive immunotherapy and, in some cases, a second allo-HCT. Moreover, in allo-HCT, there is a higher incidence of poor graft function and graft failure due to splenomegaly and a hostile "pro-inflammatory" marrow niche. The Practice Harmonisation and Guidelines subcommittee of the Chronic Malignancies Working Party (CMWP) of EBMT convened an international panel consisting of transplant haematologists, histopathologists and molecular biologists to propose practical, clinically relevant definitions of graft failure, poor graft function and relapse as well as management strategies following allo-HCT. A systematic approach to molecular monitoring, histopathological assessment and chimerism testing is proposed. These proposed recommendations aim to increase the accuracy and uniformity of reporting and to thereby facilitate the development of more consistent approaches to these challenging issues. In addition, we propose management strategies for these complications.
Audience Academic
Author Polverelli, Nicola
Robin, Marie
Ditschkowski, Marcus
Aljurf, Mahmoud
Czerw, Tomasz
Conneally, Eibhlin
Yakoub-Agha, Ibrahim
McLornan, Donal P.
Joachim Deeg, H.
Hayden, Patrick
Moonim, Mufaddal T.
Cross, Nicholas
Hernandez-Boluda, Juan Carlos
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  organization: Department of Histopathology, Imperial College Healthcare NHS Trust
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  orcidid: 0000-0001-6297-9697
  surname: Polverelli
  fullname: Polverelli, Nicola
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  organization: Oncology Center, King Faisal Specialist Hospital and Research Center
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  surname: Yakoub-Agha
  fullname: Yakoub-Agha, Ibrahim
  email: ibrahim.yakoubagha@chru-lille.fr
  organization: CHU de Lille, Univ Lille, INSERM U1286, Infinite
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34040148$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright The Author(s), under exclusive licence to Springer Nature Limited 2021
2021. The Author(s), under exclusive licence to Springer Nature Limited.
COPYRIGHT 2021 Nature Publishing Group
The Author(s), under exclusive licence to Springer Nature Limited 2021.
Distributed under a Creative Commons Attribution 4.0 International License
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crossref_primary_10_1038_s41375_021_01294_2
springer_journals_10_1038_s41375_021_01294_2
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PublicationCentury 2000
PublicationDate 2021-09-01
PublicationDateYYYYMMDD 2021-09-01
PublicationDate_xml – month: 09
  year: 2021
  text: 2021-09-01
  day: 01
PublicationDecade 2020
PublicationPlace London
PublicationPlace_xml – name: London
– name: England
PublicationSeriesTitle Leukemia
PublicationTitle Leukemia
PublicationTitleAbbrev Leukemia
PublicationTitleAlternate Leukemia
PublicationYear 2021
Publisher Nature Publishing Group UK
Nature Publishing Group
Springer Nature
Publisher_xml – name: Nature Publishing Group UK
– name: Nature Publishing Group
– name: Springer Nature
References McLornan DP, Sirait T, Hernández-Boluda JC, Czerw T, Hayden P, Yakoub-Agha I. European wide survey on allogeneic haematopoietic cell transplantation practice for myelofibrosis on behalf of the EBMT chronic malignancies working party. Curr Res Transl Med. 2020;69:103267.
For the Nordic MPD Study Group, Abelsson J, Merup M, Birgegård G, WeisBjerrum O, Brinch L, et al.The outcome of allo-HSCT for 92 patients with myelofibrosis in the Nordic countriesBone Marrow Transplant201247Mar3806
ShahMVPatelKPLuthraRShamannaRKMehrotraMChamplinREReal time PCR detects relapse of JAK2 V617F myelofibrosis earlier than pyrosequencing after allogeneic transplantationBiol Blood Marrow Transplant201723S298910.1016/j.bbmt.2016.12.217
NabergojMWangJRobinMKrögerNAngelucciEPoireXOutcomes following second allogenic haematopoietic Cell transplantation in patients with myelofibrosis: a retrospective study on behalf of the Chronic Malignancies Working Party of EBMTBlood.201913469810.1182/blood-2019-125802
CuadradoMRichardMSzydloMWattsMPatelNRenshawHPredictors of recovery following allogeneic CD34+-selected cell infusion without conditioning to correct poor graft functionHaematologica.2019105263946760461810.3324/haematol.2019.2263401:CAS:528:DC%2BB3cXisFKmtrbP
KeyznerAHanSShapiroSMoshierESchorrEPetersenBOutcome of allogeneic hematopoietic stem cell transplantation for patients with chronic and advanced phase myelofibrosisBiol Blood Marrow Transplant201622218062759613010.1016/j.bbmt.2016.08.029
WolschkeCBadbaranAZabelinaTChristopeitMAyukFTriviaiIImpact of molecular residual disease post allografting in myelofibrosis patientsBone Marrow Transplant201752152691:CAS:528:DC%2BC2sXhtFOrurzE2871494510.1038/bmt.2017.157
TamariRMughalTIRondelliDHasserjianRGuptaVOdenikeOAllo-SCT for myelofibrosis: reversing the chronic phase in the JAK inhibitor era?Bone Marrow Transplant201550628361:CAS:528:DC%2BC2MXotVCjsb8%3D25665047639421510.1038/bmt.2014.323
Luque PazDRiouJVergerECassinatBChauveauAIanottoJ-CGenomic analysis of primary and secondary myelofibrosis redefines the prognostic impact of ASXL1 mutations: a FIM studyBlood Adv202151442511:CAS:528:DC%2BB3MXnt1Smt74%3D33666653794826010.1182/bloodadvances.2020003444
PetrovicAHaleGClinical options after failure of allogeneic hematopoietic stem cell transplantation in patients with hematologic malignanciesExpert Rev Clin Immunol20117515271:CAS:528:DC%2BC3MXpsVajtr4%3D2178719510.1586/eci.11.24
OlssonRRembergerMSchafferMBerggrenDMSvahnB-MMattssonJGraft failure in the modern era of allogeneic hematopoietic SCTBone Marrow Transplant201348537431:CAS:528:DC%2BC3sXlsVeqsL0%3D2322238410.1038/bmt.2012.239
RobinMEspérouHDe LatourRPPetropoulouADXhaardARibaudPcorrespondence: splenectomy after allogeneic haematopoietic stem cell transplantation in patients with primary myelofibrosis: correspondenceBr J Haematol201015072142061833310.1111/j.1365-2141.2010.08276.x
De VosJBaudouxEBayJ-OCalmelsBCrasAEl CheikhJInjections de lymphocytes du donneur (DLI): recommandations de la Société francophone de greffe de moelle et de thérapie cellulaire (SFGM-TC)Bull du Cancer.2019106S35910.1016/j.bulcan.2018.10.002
JansonDAyukFAWolschkeCChristopeitMBadbaranAvon PeinU-MRuxolitinib for myelofibrosis patients relapsing after allogeneic hematopoietic transplantationBlood.2016128194810.1182/blood.V128.22.1948.1948
KrögerNZabelinaTAlchalbyHStübigTWolschkeCAyukFDynamic of bone marrow fibrosis regression predicts survival after allogeneic stem cell transplantation for myelofibrosisBiol Blood Marrow Transplant20142081252458954910.1016/j.bbmt.2014.02.019
PolverelliNMauffKKrögerNRobinMBeelenDBeauvaisDImpact of spleen size and splenectomy on outcomes of allogeneic hematopoietic cell transplantation for myelofibrosis: a retrospective analysis by the chronic malignancies working party on behalf of European society for blood and marrow transplantation (EBMT)Am J Hematol20219669791:CAS:528:DC%2BB3MXlvFWqtw%3D%3D3306430110.1002/ajh.26020
GuardiolaPAndersonJEBandiniGCervantesFRundeVArceseWAllogeneic stem cell transplantation for agnogenic myeloid metaplasia: a European Group for Blood and Marrow Transplantation, Société Française de Greffe de Moelle, Gruppo Italiano per il Trapianto del Midollo Osseo, and Fred Hutchinson Cancer Research Center Collaborative StudyBlood.199993283181:CAS:528:DyaK1MXivVyltrc%3D10216077
ThieleJKvasnickaHMDietrichHSteinGHannMKaminskiADynamics of bone marrow changes in patients with chronic idiopathic myelofibrosis following allogeneic stem cell transplantationHistol Histopathol200520879891:STN:280:DC%2BD2M3psl2rsg%3D%3D15944939
AliHAldossIYangDMokhtariSKhaledSAribiAMIPSS70+ v2.0 predicts long-term survival in myelofibrosis after allogeneic HCT with the Flu/Mel conditioning regimenBlood Adv2019383951:CAS:528:DC%2BC1MXhslyht7nL30622146632530510.1182/bloodadvances.2018026658
KlyuchnikovEEl-CheikhJSputtekALioznovMCalmelsBFurstSCD34+-selected stem cell boost without further conditioning for poor graft function after allogeneic stem cell transplantation in patients with hematological malignanciesBiol Blood Marrow Transplant20142038261:CAS:528:DC%2BC2cXjs1Ojurs%3D2432174710.1016/j.bbmt.2013.11.034
JainTKunzeKLMountjoyLPartainDKKosiorekHKheraNEarly post-transplantation factors predict survival outcomes in patients undergoing allogeneic hematopoietic cell transplantation for myelofibrosisBlood Cancer J20201032157091706450410.1038/s41408-020-0302-9
DholariaBSavaniBNLabopinMLuznikLRuggeriAMielkeSClinical applications of donor lymphocyte infusion from an HLA-haploidentical donor: consensus recommendations from the Acute Leukemia Working Party of the EBMTHaematologica.202010547581:CAS:528:DC%2BB3cXhvVarsrnE31537691693953210.3324/haematol.2019.219790
Hernández-BoludaJCPereiraAKrögerNBeelenDRobinMBornhäuserMDeterminants of survival in myelofibrosis patients undergoing allogeneic hematopoietic cell transplantationLeukemia.202135215243228654410.1038/s41375-020-0815-z
ZhaoYGaoFShiJLuoYTanYLaiXIncidence, risk factors, and outcomes of primary poor graft function after allogeneic hematopoietic stem cell transplantationBiol Blood Marrow Transplant20192518989073117679010.1016/j.bbmt.2019.05.036
McLornanDPSzydloRRobinMvan BiezenAKosterLBlokHJPOutcome of patients with Myelofibrosis relapsing after allogeneic stem cell transplant: a retrospective study by the Chronic Malignancies Working Party of EBMTBr J Haematol.2018182418222980892610.1111/bjh.15407
CervantesFRoviraMUrbano-IspizuaARozmanMCarrerasEMontserratEComplete remission of idiopathic myelofibrosis following donor lymphocyte infusion after failure of allogeneic transplantation: demonstration of a graft-versus-myelofibrosis effectBone Marrow Transplant20002669791:STN:280:DC%2BD3cvptVejtQ%3D%3D1103537710.1038/sj.bmt.1702568
AtagunduzIKChristopeitMAyukFZeckGWolschkeCKrögerNIncidence and outcome of late relapse after allogeneic stem cell transplantation for myelofibrosisBiol Blood Marrow Transplant2020262279841:CAS:528:DC%2BB3cXhvFyit7jK3294975310.1016/j.bbmt.2020.09.006
ArberDAOraziAHasserjianRBorowitzMJBeauMMBloomfieldCDThe 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemiaBlood.201612723914061:CAS:528:DC%2BC2sXjs1agu7g%3D2706925410.1182/blood-2016-03-643544
KrögerNPanagiotaVBadbaranAZabelinaTTriviaiIAraujo CruzMMImpact of molecular genetics on outcome in myelofibrosis patients after allogeneic stem cell transplantationBiol Blood Marrow Transplant20172310951012838925610.1016/j.bbmt.2017.03.0341:CAS:528:DC%2BC2sXntVKlu7o%3D
LangeTEdelmannASieboltsUKrahlRNehringCJäkelNJAK2 p.V617F allele burden in myeloproliferative neoplasms one month after allogeneic stem cell transplantation significantly predicts outcome and risk of relapseHaematologica.20139872281:CAS:528:DC%2BC3sXhsFSmu7fK23300178364011610.3324/haematol.2012.076901
Srour SA, Olson A, Ciurea SO, Desai P, Bashir Q, Oran B, et al. Mixed myeloid chimerism and relapse of myelofibrosis after allogeneic stem cell transplantation. Haematologica. 2019. https://doi.org/10.3324/haematol.2019.223503.
KlyuchnikovEHollerEBornhäuserMKobbeGNaglerAShimoniADonor lymphocyte infusions and second transplantation as salvage treatment for relapsed myelofibrosis after reduced-intensity allograftingBr J Haematol2012159172812290919210.1111/bjh.12013
TefferiACervantesFMesaRPassamontiFVerstovsekSVannucchiAMRevised response criteria for myelofibrosis: International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) and European LeukemiaNet (ELN) consensus reportBlood.2013122139581:CAS:528:DC%2BC3sXhsVSqu73O23838352482807010.1182/blood-2013-03-488098
McLornanDSzydloRKosterLChalandonYRobinMWolschkeCMyeloablative and reduced-intensity conditioned allogeneic hematopoietic stem cell transplantation in myelofibrosis: a retrospective study by the Chronic Malignancies Working Party of the European Society for Blood and Marrow TransplantationBiol Blood Marrow Transplant2019252167713128406910.1016/j.bbmt.2019.06.034
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KrögerNMDeegJHOlavarriaENiederwieserDBacigalupoABarbuiTIndication and management of allogeneic stem cell transplantation in primary myelofibrosis: a consensus process by an EBMT/ELN international working groupLeukemia2015292126332629364710.1038/leu.2015.2331:CAS:528:DC%2BC2MXhsFCrur%2FI
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StevensEAJenkinsICBeppuLWZhangQSalitRLoebKRTargeted sequencing improves DIPSS-Plus prognostic scoring in myelofibrosis patients undergoing allogeneic transplantationBiol Blood Marrow Transplant202026137141:CAS:528:DC%2BB3cXnslelurc%3D3219428910.1016/j.bbmt.2020.03.007
AtagunduzIKKlyuchnikovEWolschkeCJansonDHeidenreichSChristopeitMTreosulfan-based conditioning regimen fo
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34471230 - Leukemia. 2021 Sep 1
References_xml – reference: CervantesFRoviraMUrbano-IspizuaARozmanMCarrerasEMontserratEComplete remission of idiopathic myelofibrosis following donor lymphocyte infusion after failure of allogeneic transplantation: demonstration of a graft-versus-myelofibrosis effectBone Marrow Transplant20002669791:STN:280:DC%2BD3cvptVejtQ%3D%3D1103537710.1038/sj.bmt.1702568
– reference: OlssonRRembergerMSchafferMBerggrenDMSvahnB-MMattssonJGraft failure in the modern era of allogeneic hematopoietic SCTBone Marrow Transplant201348537431:CAS:528:DC%2BC3sXlsVeqsL0%3D2322238410.1038/bmt.2012.239
– reference: TamariRRapaportFZhangNMcNamaraCKuykendallASallmanDAImpact of high-molecular-risk mutations on transplantation outcomes in patients with myelofibrosisBiol Blood Marrow Transplant2019251142511:CAS:528:DC%2BC1MXitlOjs7s%3D30625392691882310.1016/j.bbmt.2019.01.002
– reference: For the Nordic MPD Study Group, Abelsson J, Merup M, Birgegård G, WeisBjerrum O, Brinch L, et al.The outcome of allo-HSCT for 92 patients with myelofibrosis in the Nordic countriesBone Marrow Transplant201247Mar3806
– reference: WolschkeCBadbaranAZabelinaTChristopeitMAyukFTriviaiIImpact of molecular residual disease post allografting in myelofibrosis patientsBone Marrow Transplant201752152691:CAS:528:DC%2BC2sXhtFOrurzE2871494510.1038/bmt.2017.157
– reference: JainTKunzeKLMountjoyLPartainDKKosiorekHKheraNEarly post-transplantation factors predict survival outcomes in patients undergoing allogeneic hematopoietic cell transplantation for myelofibrosisBlood Cancer J20201032157091706450410.1038/s41408-020-0302-9
– reference: Valcárcel D, Sureda A. Graft failure. In: Carreras E, Dufour C, Mohty M, Kröger N, editors. The EBMT Handbook. Cham: Springer International Publishing; 2019. p. 307–13. http://link.springer.com/10.1007/978-3-030-02278-5_41.
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– reference: KlyuchnikovEEl-CheikhJSputtekALioznovMCalmelsBFurstSCD34+-selected stem cell boost without further conditioning for poor graft function after allogeneic stem cell transplantation in patients with hematological malignanciesBiol Blood Marrow Transplant20142038261:CAS:528:DC%2BC2cXjs1Ojurs%3D2432174710.1016/j.bbmt.2013.11.034
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– reference: McLornanDPSzydloRRobinMvan BiezenAKosterLBlokHJPOutcome of patients with Myelofibrosis relapsing after allogeneic stem cell transplant: a retrospective study by the Chronic Malignancies Working Party of EBMTBr J Haematol.2018182418222980892610.1111/bjh.15407
– reference: ZhaoYGaoFShiJLuoYTanYLaiXIncidence, risk factors, and outcomes of primary poor graft function after allogeneic hematopoietic stem cell transplantationBiol Blood Marrow Transplant20192518989073117679010.1016/j.bbmt.2019.05.036
– reference: KrögerNZabelinaTAlchalbyHStübigTWolschkeCAyukFDynamic of bone marrow fibrosis regression predicts survival after allogeneic stem cell transplantation for myelofibrosisBiol Blood Marrow Transplant20142081252458954910.1016/j.bbmt.2014.02.019
– reference: Luque PazDRiouJVergerECassinatBChauveauAIanottoJ-CGenomic analysis of primary and secondary myelofibrosis redefines the prognostic impact of ASXL1 mutations: a FIM studyBlood Adv202151442511:CAS:528:DC%2BB3MXnt1Smt74%3D33666653794826010.1182/bloodadvances.2020003444
– reference: GuardiolaPAndersonJEBandiniGCervantesFRundeVArceseWAllogeneic stem cell transplantation for agnogenic myeloid metaplasia: a European Group for Blood and Marrow Transplantation, Société Française de Greffe de Moelle, Gruppo Italiano per il Trapianto del Midollo Osseo, and Fred Hutchinson Cancer Research Center Collaborative StudyBlood.199993283181:CAS:528:DyaK1MXivVyltrc%3D10216077
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– reference: DeegHJSalitRBMonahanTSchochGMcFarlandCScottBLEarly mixed lymphoid donor/host chimerism is associated with improved transplant outcome in patients with primary or secondary myelofibrosisBiol Blood Marrow Transplant.20202621972033269321110.1016/j.bbmt.2020.07.0138816377
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– reference: KrögerNMDeegJHOlavarriaENiederwieserDBacigalupoABarbuiTIndication and management of allogeneic stem cell transplantation in primary myelofibrosis: a consensus process by an EBMT/ELN international working groupLeukemia2015292126332629364710.1038/leu.2015.2331:CAS:528:DC%2BC2MXhsFCrur%2FI
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Snippet Allogeneic haematopoietic cell transplantation (allo-HCT) remains the only curative approach in myelofibrosis (MF). Despite advances over recent decades,...
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SubjectTerms 692/699/1541
692/699/1541/1990/2331
Adoptive immunotherapy
Best practice
Cancer Research
Care and treatment
Chimerism
Complications
Critical Care Medicine
Development and progression
Disease Management
Failure
Graft rejection
Graft Rejection - etiology
Graft Rejection - pathology
Graft Rejection - prevention & control
Graft vs Host Disease - etiology
Graft vs Host Disease - metabolism
Graft vs Host Disease - prevention & control
Grafting
Grafts
Hematology
Hematopoietic Stem Cell Transplantation - adverse effects
Humans
Immunotherapy
Inflammation
Intensive
Internal Medicine
Life Sciences
Medicine
Medicine & Public Health
Myelofibrosis
Oncology
Palliation
Practice Guidelines as Topic - standards
Primary Myelofibrosis - pathology
Primary Myelofibrosis - therapy
Recurrence
Review Article
Splenomegaly
Stem cells
Transplantation
Transplantation, Homologous
Transplants & implants
Title Allogeneic haematopoietic cell transplantation for myelofibrosis: proposed definitions and management strategies for graft failure, poor graft function and relapse: best practice recommendations of the EBMT Chronic Malignancies Working Party
URI https://link.springer.com/article/10.1038/s41375-021-01294-2
https://www.ncbi.nlm.nih.gov/pubmed/34040148
https://www.proquest.com/docview/2568103264
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https://hal.univ-lille.fr/hal-04487980
Volume 35
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