Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates...

Autores
Apostolova, Petya; Kreutmair, Stefanie; Toffalori, Cristina; Punta, Marco; Unger, Susanne; Burk, Ann Cathrin; Wehr, Claudia; Maas Bauer, Kristina; Melchinger, Wolfgang; Haring, Eileen; Höfflin, Rouven; Shoumariyeh, Khalid; Hupfer, Valerie; Lauer, Eliza Maria; Duquesne, Sandra; Lowinus, Theresa; Núñez, Nicolás; Alberti, Chiara; da Costa Pereira, Sara; Merten, Carla Helena; Power, Laura; Weiss, Matthias; Böke, Caroline; Pfeifer, Dietmar; Marks, Reinhard; Bertz, Hartmut; Wäsch, Ralph; Ihorst, Gabriele; Gentner, Bernhard; Duyster, Justus; Boerries, Melanie; Andrieux, Geoffroy; Finke, Juergen; Becher, Burkhard; Vago, Luca; Zeiser, Robert
Año de publicación
2023
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Acute myeloid leukaemia (AML) relapse after allogeneic haematopoietic cell transplantation (allo-HCT) is often driven by immune-related mechanisms and associated with poor prognosis. Immune checkpoint inhibitors combined with hypomethylating agents (HMA) may restore or enhance the graft-versus-leukaemia effect. Still, data about using this combination regimen after allo-HCT are limited. We conducted a prospective, phase II, open-label, single-arm study in which we treated patients with haematological AML relapse after allo-HCT with HMA plus the anti-PD-1 antibody nivolumab. The response was correlated with DNA-, RNA- and protein-based single-cell technology assessments to identify biomarkers associated with therapeutic efficacy. Sixteen patients received a median number of 2 (range 1–7) nivolumab applications. The overall response rate (CR/PR) at day 42 was 25%, and another 25% of the patients achieved stable disease. The median overall survival was 15.6 months. High-parametric cytometry documented a higher frequency of activated (ICOS+, HLA-DR+), low senescence (KLRG1−, CD57−) CD8+ effector T cells in responders. We confirmed these findings in a preclinical model. Single-cell transcriptomics revealed a pro-inflammatory rewiring of the expression profile of T and myeloid cells in responders. In summary, the study indicates that the post-allo-HCT HMA/nivolumab combination induces anti-AML immune responses in selected patients and could be considered as a bridging approach to a second allo-HCT.
Fil: Apostolova, Petya. Albert Ludwigs University of Freiburg; Alemania. German Cancer Research Center; Alemania
Fil: Kreutmair, Stefanie. Universitat Zurich; Suiza. German Cancer Research Center; Alemania
Fil: Toffalori, Cristina. Istituto di Ricovero e Cura a Carattere Scientifico; Italia
Fil: Punta, Marco. Istituto di Ricovero e Cura a Carattere Scientifico; Italia
Fil: Unger, Susanne. Universitat Zurich; Suiza
Fil: Burk, Ann Cathrin. Universite de Fribourg (unifr); . German Cancer Research Center; Alemania
Fil: Wehr, Claudia. Universite de Fribourg (unifr);
Fil: Maas Bauer, Kristina. Universite de Fribourg (unifr);
Fil: Melchinger, Wolfgang. Universite de Fribourg (unifr);
Fil: Haring, Eileen. Universite de Fribourg (unifr); . German Cancer Research Center; Alemania
Fil: Höfflin, Rouven. Universite de Fribourg (unifr);
Fil: Shoumariyeh, Khalid. Universite de Fribourg (unifr);
Fil: Hupfer, Valerie. Universite de Fribourg (unifr);
Fil: Lauer, Eliza Maria. Universite de Fribourg (unifr);
Fil: Duquesne, Sandra. Universite de Fribourg (unifr);
Fil: Lowinus, Theresa. Universite de Fribourg (unifr);
Fil: Núñez, Nicolás. Universitat Zurich; Suiza. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina
Fil: Alberti, Chiara. Universitat Zurich; Suiza
Fil: da Costa Pereira, Sara. Universitat Zurich; Suiza
Fil: Merten, Carla Helena. Universitat Zurich; Suiza
Fil: Power, Laura. Universitat Zurich; Suiza
Fil: Weiss, Matthias. Universite de Fribourg (unifr);
Fil: Böke, Caroline. Universite de Fribourg (unifr);
Fil: Pfeifer, Dietmar. Universite de Fribourg (unifr);
Fil: Marks, Reinhard. Universite de Fribourg (unifr);
Fil: Bertz, Hartmut. Universite de Fribourg (unifr);
Fil: Wäsch, Ralph. Universite de Fribourg (unifr);
Fil: Ihorst, Gabriele. Universite de Fribourg (unifr);
Fil: Gentner, Bernhard. Istituto di Ricovero e Cura a Carattere Scientifico; Italia. Universite de Lausanne; Suiza
Fil: Duyster, Justus. Universite de Fribourg (unifr);
Fil: Boerries, Melanie. German Cancer Research Center; Alemania. Universite de Fribourg (unifr);
Fil: Andrieux, Geoffroy. Universite de Fribourg (unifr);
Fil: Finke, Juergen. Universite de Fribourg (unifr);
Fil: Becher, Burkhard. Universitat Zurich; Suiza
Fil: Vago, Luca. Istituto di Ricovero e Cura a Carattere Scientifico; Italia. Vita Salute Universidad San Raffaele; Italia
Fil: Zeiser, Robert. German Cancer Research Center; Alemania. Universite de Fribourg (unifr);
Materia
AML
HCT
HMA
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/241849

id CONICETDig_c5de122a2df79dedf9095dce33cd4779
oai_identifier_str oai:ri.conicet.gov.ar:11336/241849
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with responseApostolova, PetyaKreutmair, StefanieToffalori, CristinaPunta, MarcoUnger, SusanneBurk, Ann CathrinWehr, ClaudiaMaas Bauer, KristinaMelchinger, WolfgangHaring, EileenHöfflin, RouvenShoumariyeh, KhalidHupfer, ValerieLauer, Eliza MariaDuquesne, SandraLowinus, TheresaNúñez, NicolásAlberti, Chiarada Costa Pereira, SaraMerten, Carla HelenaPower, LauraWeiss, MatthiasBöke, CarolinePfeifer, DietmarMarks, ReinhardBertz, HartmutWäsch, RalphIhorst, GabrieleGentner, BernhardDuyster, JustusBoerries, MelanieAndrieux, GeoffroyFinke, JuergenBecher, BurkhardVago, LucaZeiser, RobertAMLHCTHMAhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3Acute myeloid leukaemia (AML) relapse after allogeneic haematopoietic cell transplantation (allo-HCT) is often driven by immune-related mechanisms and associated with poor prognosis. Immune checkpoint inhibitors combined with hypomethylating agents (HMA) may restore or enhance the graft-versus-leukaemia effect. Still, data about using this combination regimen after allo-HCT are limited. We conducted a prospective, phase II, open-label, single-arm study in which we treated patients with haematological AML relapse after allo-HCT with HMA plus the anti-PD-1 antibody nivolumab. The response was correlated with DNA-, RNA- and protein-based single-cell technology assessments to identify biomarkers associated with therapeutic efficacy. Sixteen patients received a median number of 2 (range 1–7) nivolumab applications. The overall response rate (CR/PR) at day 42 was 25%, and another 25% of the patients achieved stable disease. The median overall survival was 15.6 months. High-parametric cytometry documented a higher frequency of activated (ICOS+, HLA-DR+), low senescence (KLRG1−, CD57−) CD8+ effector T cells in responders. We confirmed these findings in a preclinical model. Single-cell transcriptomics revealed a pro-inflammatory rewiring of the expression profile of T and myeloid cells in responders. In summary, the study indicates that the post-allo-HCT HMA/nivolumab combination induces anti-AML immune responses in selected patients and could be considered as a bridging approach to a second allo-HCT.Fil: Apostolova, Petya. Albert Ludwigs University of Freiburg; Alemania. German Cancer Research Center; AlemaniaFil: Kreutmair, Stefanie. Universitat Zurich; Suiza. German Cancer Research Center; AlemaniaFil: Toffalori, Cristina. Istituto di Ricovero e Cura a Carattere Scientifico; ItaliaFil: Punta, Marco. Istituto di Ricovero e Cura a Carattere Scientifico; ItaliaFil: Unger, Susanne. Universitat Zurich; SuizaFil: Burk, Ann Cathrin. Universite de Fribourg (unifr); . German Cancer Research Center; AlemaniaFil: Wehr, Claudia. Universite de Fribourg (unifr);Fil: Maas Bauer, Kristina. Universite de Fribourg (unifr);Fil: Melchinger, Wolfgang. Universite de Fribourg (unifr);Fil: Haring, Eileen. Universite de Fribourg (unifr); . German Cancer Research Center; AlemaniaFil: Höfflin, Rouven. Universite de Fribourg (unifr);Fil: Shoumariyeh, Khalid. Universite de Fribourg (unifr);Fil: Hupfer, Valerie. Universite de Fribourg (unifr);Fil: Lauer, Eliza Maria. Universite de Fribourg (unifr);Fil: Duquesne, Sandra. Universite de Fribourg (unifr);Fil: Lowinus, Theresa. Universite de Fribourg (unifr);Fil: Núñez, Nicolás. Universitat Zurich; Suiza. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; ArgentinaFil: Alberti, Chiara. Universitat Zurich; SuizaFil: da Costa Pereira, Sara. Universitat Zurich; SuizaFil: Merten, Carla Helena. Universitat Zurich; SuizaFil: Power, Laura. Universitat Zurich; SuizaFil: Weiss, Matthias. Universite de Fribourg (unifr);Fil: Böke, Caroline. Universite de Fribourg (unifr);Fil: Pfeifer, Dietmar. Universite de Fribourg (unifr);Fil: Marks, Reinhard. Universite de Fribourg (unifr);Fil: Bertz, Hartmut. Universite de Fribourg (unifr);Fil: Wäsch, Ralph. Universite de Fribourg (unifr);Fil: Ihorst, Gabriele. Universite de Fribourg (unifr);Fil: Gentner, Bernhard. Istituto di Ricovero e Cura a Carattere Scientifico; Italia. Universite de Lausanne; SuizaFil: Duyster, Justus. Universite de Fribourg (unifr);Fil: Boerries, Melanie. German Cancer Research Center; Alemania. Universite de Fribourg (unifr);Fil: Andrieux, Geoffroy. Universite de Fribourg (unifr);Fil: Finke, Juergen. Universite de Fribourg (unifr);Fil: Becher, Burkhard. Universitat Zurich; SuizaFil: Vago, Luca. Istituto di Ricovero e Cura a Carattere Scientifico; Italia. Vita Salute Universidad San Raffaele; ItaliaFil: Zeiser, Robert. German Cancer Research Center; Alemania. Universite de Fribourg (unifr);Wiley Blackwell Publishing, Inc2023-10info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/241849Apostolova, Petya; Kreutmair, Stefanie; Toffalori, Cristina; Punta, Marco; Unger, Susanne; et al.; Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response; Wiley Blackwell Publishing, Inc; British Journal of Haematology; 203; 2; 10-2023; 264-2811365-2141CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1111/bjh.19007info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1111/bjh.19007info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:00:39Zoai:ri.conicet.gov.ar:11336/241849instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:00:39.717CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response
title Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response
spellingShingle Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response
Apostolova, Petya
AML
HCT
HMA
title_short Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response
title_full Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response
title_fullStr Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response
title_full_unstemmed Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response
title_sort Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response
dc.creator.none.fl_str_mv Apostolova, Petya
Kreutmair, Stefanie
Toffalori, Cristina
Punta, Marco
Unger, Susanne
Burk, Ann Cathrin
Wehr, Claudia
Maas Bauer, Kristina
Melchinger, Wolfgang
Haring, Eileen
Höfflin, Rouven
Shoumariyeh, Khalid
Hupfer, Valerie
Lauer, Eliza Maria
Duquesne, Sandra
Lowinus, Theresa
Núñez, Nicolás
Alberti, Chiara
da Costa Pereira, Sara
Merten, Carla Helena
Power, Laura
Weiss, Matthias
Böke, Caroline
Pfeifer, Dietmar
Marks, Reinhard
Bertz, Hartmut
Wäsch, Ralph
Ihorst, Gabriele
Gentner, Bernhard
Duyster, Justus
Boerries, Melanie
Andrieux, Geoffroy
Finke, Juergen
Becher, Burkhard
Vago, Luca
Zeiser, Robert
author Apostolova, Petya
author_facet Apostolova, Petya
Kreutmair, Stefanie
Toffalori, Cristina
Punta, Marco
Unger, Susanne
Burk, Ann Cathrin
Wehr, Claudia
Maas Bauer, Kristina
Melchinger, Wolfgang
Haring, Eileen
Höfflin, Rouven
Shoumariyeh, Khalid
Hupfer, Valerie
Lauer, Eliza Maria
Duquesne, Sandra
Lowinus, Theresa
Núñez, Nicolás
Alberti, Chiara
da Costa Pereira, Sara
Merten, Carla Helena
Power, Laura
Weiss, Matthias
Böke, Caroline
Pfeifer, Dietmar
Marks, Reinhard
Bertz, Hartmut
Wäsch, Ralph
Ihorst, Gabriele
Gentner, Bernhard
Duyster, Justus
Boerries, Melanie
Andrieux, Geoffroy
Finke, Juergen
Becher, Burkhard
Vago, Luca
Zeiser, Robert
author_role author
author2 Kreutmair, Stefanie
Toffalori, Cristina
Punta, Marco
Unger, Susanne
Burk, Ann Cathrin
Wehr, Claudia
Maas Bauer, Kristina
Melchinger, Wolfgang
Haring, Eileen
Höfflin, Rouven
Shoumariyeh, Khalid
Hupfer, Valerie
Lauer, Eliza Maria
Duquesne, Sandra
Lowinus, Theresa
Núñez, Nicolás
Alberti, Chiara
da Costa Pereira, Sara
Merten, Carla Helena
Power, Laura
Weiss, Matthias
Böke, Caroline
Pfeifer, Dietmar
Marks, Reinhard
Bertz, Hartmut
Wäsch, Ralph
Ihorst, Gabriele
Gentner, Bernhard
Duyster, Justus
Boerries, Melanie
Andrieux, Geoffroy
Finke, Juergen
Becher, Burkhard
Vago, Luca
Zeiser, Robert
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv AML
HCT
HMA
topic AML
HCT
HMA
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Acute myeloid leukaemia (AML) relapse after allogeneic haematopoietic cell transplantation (allo-HCT) is often driven by immune-related mechanisms and associated with poor prognosis. Immune checkpoint inhibitors combined with hypomethylating agents (HMA) may restore or enhance the graft-versus-leukaemia effect. Still, data about using this combination regimen after allo-HCT are limited. We conducted a prospective, phase II, open-label, single-arm study in which we treated patients with haematological AML relapse after allo-HCT with HMA plus the anti-PD-1 antibody nivolumab. The response was correlated with DNA-, RNA- and protein-based single-cell technology assessments to identify biomarkers associated with therapeutic efficacy. Sixteen patients received a median number of 2 (range 1–7) nivolumab applications. The overall response rate (CR/PR) at day 42 was 25%, and another 25% of the patients achieved stable disease. The median overall survival was 15.6 months. High-parametric cytometry documented a higher frequency of activated (ICOS+, HLA-DR+), low senescence (KLRG1−, CD57−) CD8+ effector T cells in responders. We confirmed these findings in a preclinical model. Single-cell transcriptomics revealed a pro-inflammatory rewiring of the expression profile of T and myeloid cells in responders. In summary, the study indicates that the post-allo-HCT HMA/nivolumab combination induces anti-AML immune responses in selected patients and could be considered as a bridging approach to a second allo-HCT.
Fil: Apostolova, Petya. Albert Ludwigs University of Freiburg; Alemania. German Cancer Research Center; Alemania
Fil: Kreutmair, Stefanie. Universitat Zurich; Suiza. German Cancer Research Center; Alemania
Fil: Toffalori, Cristina. Istituto di Ricovero e Cura a Carattere Scientifico; Italia
Fil: Punta, Marco. Istituto di Ricovero e Cura a Carattere Scientifico; Italia
Fil: Unger, Susanne. Universitat Zurich; Suiza
Fil: Burk, Ann Cathrin. Universite de Fribourg (unifr); . German Cancer Research Center; Alemania
Fil: Wehr, Claudia. Universite de Fribourg (unifr);
Fil: Maas Bauer, Kristina. Universite de Fribourg (unifr);
Fil: Melchinger, Wolfgang. Universite de Fribourg (unifr);
Fil: Haring, Eileen. Universite de Fribourg (unifr); . German Cancer Research Center; Alemania
Fil: Höfflin, Rouven. Universite de Fribourg (unifr);
Fil: Shoumariyeh, Khalid. Universite de Fribourg (unifr);
Fil: Hupfer, Valerie. Universite de Fribourg (unifr);
Fil: Lauer, Eliza Maria. Universite de Fribourg (unifr);
Fil: Duquesne, Sandra. Universite de Fribourg (unifr);
Fil: Lowinus, Theresa. Universite de Fribourg (unifr);
Fil: Núñez, Nicolás. Universitat Zurich; Suiza. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina
Fil: Alberti, Chiara. Universitat Zurich; Suiza
Fil: da Costa Pereira, Sara. Universitat Zurich; Suiza
Fil: Merten, Carla Helena. Universitat Zurich; Suiza
Fil: Power, Laura. Universitat Zurich; Suiza
Fil: Weiss, Matthias. Universite de Fribourg (unifr);
Fil: Böke, Caroline. Universite de Fribourg (unifr);
Fil: Pfeifer, Dietmar. Universite de Fribourg (unifr);
Fil: Marks, Reinhard. Universite de Fribourg (unifr);
Fil: Bertz, Hartmut. Universite de Fribourg (unifr);
Fil: Wäsch, Ralph. Universite de Fribourg (unifr);
Fil: Ihorst, Gabriele. Universite de Fribourg (unifr);
Fil: Gentner, Bernhard. Istituto di Ricovero e Cura a Carattere Scientifico; Italia. Universite de Lausanne; Suiza
Fil: Duyster, Justus. Universite de Fribourg (unifr);
Fil: Boerries, Melanie. German Cancer Research Center; Alemania. Universite de Fribourg (unifr);
Fil: Andrieux, Geoffroy. Universite de Fribourg (unifr);
Fil: Finke, Juergen. Universite de Fribourg (unifr);
Fil: Becher, Burkhard. Universitat Zurich; Suiza
Fil: Vago, Luca. Istituto di Ricovero e Cura a Carattere Scientifico; Italia. Vita Salute Universidad San Raffaele; Italia
Fil: Zeiser, Robert. German Cancer Research Center; Alemania. Universite de Fribourg (unifr);
description Acute myeloid leukaemia (AML) relapse after allogeneic haematopoietic cell transplantation (allo-HCT) is often driven by immune-related mechanisms and associated with poor prognosis. Immune checkpoint inhibitors combined with hypomethylating agents (HMA) may restore or enhance the graft-versus-leukaemia effect. Still, data about using this combination regimen after allo-HCT are limited. We conducted a prospective, phase II, open-label, single-arm study in which we treated patients with haematological AML relapse after allo-HCT with HMA plus the anti-PD-1 antibody nivolumab. The response was correlated with DNA-, RNA- and protein-based single-cell technology assessments to identify biomarkers associated with therapeutic efficacy. Sixteen patients received a median number of 2 (range 1–7) nivolumab applications. The overall response rate (CR/PR) at day 42 was 25%, and another 25% of the patients achieved stable disease. The median overall survival was 15.6 months. High-parametric cytometry documented a higher frequency of activated (ICOS+, HLA-DR+), low senescence (KLRG1−, CD57−) CD8+ effector T cells in responders. We confirmed these findings in a preclinical model. Single-cell transcriptomics revealed a pro-inflammatory rewiring of the expression profile of T and myeloid cells in responders. In summary, the study indicates that the post-allo-HCT HMA/nivolumab combination induces anti-AML immune responses in selected patients and could be considered as a bridging approach to a second allo-HCT.
publishDate 2023
dc.date.none.fl_str_mv 2023-10
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/241849
Apostolova, Petya; Kreutmair, Stefanie; Toffalori, Cristina; Punta, Marco; Unger, Susanne; et al.; Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response; Wiley Blackwell Publishing, Inc; British Journal of Haematology; 203; 2; 10-2023; 264-281
1365-2141
CONICET Digital
CONICET
url http://hdl.handle.net/11336/241849
identifier_str_mv Apostolova, Petya; Kreutmair, Stefanie; Toffalori, Cristina; Punta, Marco; Unger, Susanne; et al.; Phase II trial of hypomethylating agent combined with nivolumab for acute myeloid leukaemia relapse after allogeneic haematopoietic cell transplantation—Immune signature correlates with response; Wiley Blackwell Publishing, Inc; British Journal of Haematology; 203; 2; 10-2023; 264-281
1365-2141
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1111/bjh.19007
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1111/bjh.19007
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Wiley Blackwell Publishing, Inc
publisher.none.fl_str_mv Wiley Blackwell Publishing, Inc
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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