Your browser doesn't support javascript.
loading
Influence of invasive aspergillosis during acute leukaemia treatment on survival after allogeneic stem cell transplantation: a prospective study of the EBMT Infectious Diseases Working Party.
Penack, Olaf; Tridello, Gloria; Salmenniemi, Urpu; Martino, Rodrigo; Khanna, Nina; Perruccio, Katia; Fagioli, Franca; Richert-Przygonska, Monika; Labussière-Wallet, Hélène; Maertens, Johan; Jubert, Charlotte; Aljurf, Mahmoud; Pichler, Herbert; Kriván, Gergely; Kunadt, Desiree; Popova, Marina; Gabriel, Melissa; Calore, Elisabetta; Blau, Igor Wolfgang; Benedetti, Fabio; Itäla-Remes, Maija; de Kort, Elizabeth; Russo, Domenico; Faraci, Maura; Ménard, Anne-Lise; Borne, Peter von dem; Poiré, Xavier; Yesilipek, Akif; Gozdzik, Jolanta; Yegin, Zeynep Arzu; Yañez, Lucrecia; Facchini, Luca; Van Gorkom, Gwendolyn; Thurner, Lorenz; Kocak, Ulker; Sampol, Antònia; Zuckerman, Tsila; Bierings, Marc; Mielke, Stephan; Ciceri, Fabio; Wendel, Lotus; Knelange, Nina; Mikulska, Malgorzata; Averbuch, Dina; Styczynski, Jan; Camara, Rafael de la; Cesaro, Simone.
Afiliação
  • Penack O; Medizinische Klinik m. S. Hämatologie, Onkologie und Tumorimmunologie, Berlin, Germany.
  • Tridello G; EBMT Leiden Study Unit, Leiden, the Netherlands.
  • Salmenniemi U; HUCH Comprehensive Cancer Center, Helsinki, Finland.
  • Martino R; Hospital Santa Creu i Sant Pau, Barcelona, Spain.
  • Khanna N; Division of Infectious Diseases, University Hospital, Basel, Switzerland.
  • Perruccio K; Pediatric Oncology Hematology and Stem Cell Transplantation Program, Santa Maria Della Misericordia Hospital, Perugia.
  • Fagioli F; Ospedale Infantile Regina Margherita, Torino, Italy.
  • Richert-Przygonska M; Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
  • Labussière-Wallet H; Hopital Lyon Sud, Hospices Civils de Lyon, Pierre Bénite, France.
  • Maertens J; University Hospital Gasthuisberg, Leuven, Belgium.
  • Jubert C; CHU Bordeaux Groupe Hospitalier Pellegrin-Enfants, Bordeaux, France.
  • Aljurf M; King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
  • Pichler H; Department of Pediatrics and Adolescent Medicine, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.
  • Kriván G; Central Hospital of Southern Pest, Budapest, Hungary.
  • Kunadt D; University Hospital, TU Dresden, Germany.
  • Popova M; RM Gorbacheva Research Institute, Pavlov University, St. Petersburg, Russian Federation.
  • Gabriel M; Cancer Centre for Children, The Children's Hospital at Westmead, Sydney, Australia.
  • Calore E; Pediatric Hematology Oncology and Stem Cell Transplant Division, Department of Women's and Children's Health, Azienda Ospedale-UniversitàPadova, Italy.
  • Blau IW; Medizinische Klinik m. S. Hämatologie, Onkologie und Tumorimmunologie, Berlin, Germany.
  • Benedetti F; Policlinico G.B. Rossi, Verona, Italy.
  • Itäla-Remes M; Turku University Hospital, Turku, Finland.
  • de Kort E; Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands.
  • Russo D; Unit of Blood Diseases and Bone Marrow Transplantation, Brescia University, Italy.
  • Faraci M; HSCT Unit, Department of Hematology-Oncology, IRCCS Istituto G. Gaslini, Genova, Italy.
  • Ménard AL; Centre Henri Becquerel, Rouen, France.
  • Borne PVD; Leiden University Hospital, Leiden, the Netherlands.
  • Poiré X; Cliniques Universitaires St. Luc, Brussels, Belgium.
  • Yesilipek A; Medical Park Antalya Hospital, Antalya, Turkey.
  • Gozdzik J; Department of Clinical Immunology and Transplantation, Jagiellonian University Medical Collage, University Children's Hospital in Krakow, Poland.
  • Yegin ZA; Gazi University Faculty of Medicine, Ankara, Turkey.
  • Yañez L; Hospital U. Marqués de Valdecilla-IDIVAL, Santander, Spain.
  • Facchini L; Hematology, AUSL-IRCCS Reggio Emilia, Italy.
  • Van Gorkom G; University Hospital Maastricht, Maastricht, the Netherlands.
  • Thurner L; Lorenz Thurner, University of Saarland, Homburg, Germany.
  • Kocak U; Gazi University School of Medicine, Ankara, Turkey.
  • Sampol A; Hospital Son Espases, Palma de Mallorca, Balearic Islands, Spain.
  • Zuckerman T; Rambam Medical Center, Technion -Faculty of Medicine. Haifa, Israel.
  • Bierings M; Princess Maxima Center/ University Hospital for Children (WKZ), Utrecht, the Netherlands.
  • Mielke S; Karolinska University Hospital, Stockholm, Sweden.
  • Ciceri F; Università Vita Salute San Raffaele, Milan, Italy.
  • Wendel L; EBMT Leiden Study Unit, Leiden, the Netherlands.
  • Knelange N; EBMT Leiden Study Unit, Leiden, the Netherlands.
  • Mikulska M; Division of Infectious Diseases, University of Genoa and Ospedale Policlinico San Martino, Genoa, Italy.
  • Averbuch D; Pediatric Infectious Diseases, Faculty of Medicine, Hebrew University of Jerusalem, Hadassah Medical Center, Israel.
  • Styczynski J; Department of Pediatric Hematology and Oncology, Collegium Medicum, Nicolaus Copernicus University Torun, Bydgoszcz, Poland.
  • Camara R; Rafael de la Camara, Hospital de la Princesa, Madrid, Spain.
  • Cesaro S; Pediatric Hematology Oncology, Department of Mother and Child, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
EClinicalMedicine ; 67: 102393, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38152413
ABSTRACT

Background:

Infections are the main reason for mortality during acute leukaemia treatment and invasive aspergillosis (IA) is a major concern. Allogeneic stem cell transplantation (alloSCT) is a standard therapy and often is the only live-saving procedure in leukaemia patients. The profound immunodeficiency occurring after alloSCT led to high IA-associated mortality in the past. Therefore, patients with IA were historically considered transplant-ineligible. Recently, there has been improvement of anti-fungal management including novel anti-fungal agents. As a result, more leukaemia patients with IA are undergoing alloSCT. Outcome has not been prospectively assessed.

Methods:

We performed a prospective study in acute leukaemia patients undergoing alloSCT to analyse the impact of a prior history of probable or proven IA (pre-SCT IA). The primary endpoint was 1-year non-relapse mortality (NRM). Relapse free survival and overall survival were analysed as secondary endpoints.

Findings:

1439 patients were included between 2016 and 2021. The incidence of probable or proven pre-SCT IA was 6.0% (n = 87). The cumulative incidence of 1-year NRM was 17.3% (95% CI 10.2-26.0) and 11.2% (9.6-13.0) for patients with and without pre-SCT IA. In multivariate analyses the hazard ratio (HR) for 1-year NRM was 2.1 (1.2-3.6; p = 0.009) for patients with pre-SCT IA. One-year relapse-free survival was inferior in patients with pre-SCT IA (59.4% [48.3-68.9] vs. 70.4 [67.9-72.8]; multivariate HR 1.5 [1.1-2.1]; p = 0.02). Consequently, 1-year overall survival was lower in patients with pre-SCT IA (68.8% [57.8-77.4] vs. 79.0% [76.7-81.1]; multivariate HR 1.7 [1.1-2.5]; p = 0.01).

Interpretation:

Pre-SCT IA remains to be significantly associated with impaired alloSCT outcome. On the other hand, more than two thirds of patients with pre-SCT IA were alive at one year after alloSCT. IA is not anymore an absolute contraindication for alloSCT because the majority of patients with IA who undergo alloSCT benefit from this procedure.

Funding:

There was no external funding source for this study.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: EClinicalMedicine Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: EClinicalMedicine Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha