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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/241849
Ver los metadatos del registro completo
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network_name_str |
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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 |
_version_ |
1844613790186864640 |
score |
13.070432 |