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Splenomegaly in patients with primary or secondary myelofibrosis who are candidates for allogeneic hematopoietic cell transplantation: a Position Paper on behalf of the Chronic Malignancies Working Party of the EBMT.
Polverelli, Nicola; Hernández-Boluda, Juan Carlos; Czerw, Tomasz; Barbui, Tiziano; D'Adda, Mariella; Deeg, Hans Joachim; Ditschkowski, Markus; Harrison, Claire; Kröger, Nicolaus Martin; Mesa, Ruben; Passamonti, Francesco; Palandri, Francesca; Pemmaraju, Naveen; Popat, Uday; Rondelli, Damiano; Vannucchi, Alessandro Maria; Verstovsek, Srdan; Robin, Marie; Colecchia, Antonio; Grazioli, Luigi; Damiani, Enrico; Russo, Domenico; Brady, Jessica; Patch, David; Blamek, Slawomir; Damaj, Gandhi Laurent; Hayden, Patrick; McLornan, Donal P; Yakoub-Agha, Ibrahim.
Afiliação
  • Polverelli N; Unit of Blood Diseases and Bone Marrow Transplantation, Cell Therapies and Hematology Research Program, Department of Clinical and Experimental Sciences, University of Brescia, ASST Spedali Civili di Brescia, Brescia, Italy. Electronic address: nicola.polverelli@unibs.it.
  • Hernández-Boluda JC; Department of Hematology, Hospital Clínico Universitario, Valencia, Spain.
  • Czerw T; Department of Hematology, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice, Poland.
  • Barbui T; FROM Research Foundation, Papa Giovanni XXIII Hospital, Bergamo, Italy.
  • D'Adda M; Hematology Division, Department of Oncology, ASST Spedali Civili di Brescia, Brescia, Italy.
  • Deeg HJ; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Ditschkowski M; Department of Hematology and Stem Cell Transplantation, West German Cancer Center, University Hospital of Essen, Essen, Germany.
  • Harrison C; Department of Clinical Haematology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Kröger NM; University Medical Center Hamburg, Hamburg, Germany.
  • Mesa R; Mays Cancer Center at UT Health San Antonio, San Antonio, TX, USA.
  • Passamonti F; Department of Medicine and Surgery, University of Insubria, ASST Sette Laghi, Varese, Italy.
  • Palandri F; Institute of Hematology L and A Seràgnoli, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Pemmaraju N; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Popat U; Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Rondelli D; Blood and Marrow Transplant Program, and Center for Global Health, University of Illinois at Chicago, Chicago, IL, USA.
  • Vannucchi AM; Center for Innovation and Research in Myeloproliferative Neoplasms, Hematology Unit, Azienda Ospedaliera Universitaria Careggi, University of Florence, Florence, Italy.
  • Verstovsek S; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • Robin M; Hôpital Saint-Louis, APHP, Université de Paris Cité, Paris, France.
  • Colecchia A; Gastroenterology Unit, University Hospital of Modena, Modena, Italy.
  • Grazioli L; Department of Radiology, ASST Spedali Civili di Brescia, Brescia, Italy.
  • Damiani E; 2nd Division of General Surgery, Department of Medical and Surgical Sciences, ASST Spedali Civili di Brescia, Brescia, Italy.
  • Russo D; Unit of Blood Diseases and Bone Marrow Transplantation, Cell Therapies and Hematology Research Program, Department of Clinical and Experimental Sciences, University of Brescia, ASST Spedali Civili di Brescia, Brescia, Italy.
  • Brady J; Department of Clinical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Patch D; Hepatology and Liver Transplantation, Royal Free London NHS Foundation Trust, London, UK.
  • Blamek S; Department of Radiotherapy, Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice, Poland.
  • Damaj GL; Unit of Hematology, Centre Hospitalier Universitaire de Caen, University of Caen-Normandie, Caen, France.
  • Hayden P; Department of Haematology, Trinity College Dublin, St James's Hospital, Dublin, Ireland.
  • McLornan DP; Department of Stem Cell Transplantation and Haematology, University College London Hospitals, London, UK.
  • Yakoub-Agha I; CHU de Lille, Univ Lille, INSERM U1286, Infinite, Lille, France. Electronic address: ibrahim.yakoubagha@chru-lille.fr.
Lancet Haematol ; 10(1): e59-e70, 2023 Jan.
Article em En | MEDLINE | ID: mdl-36493799
ABSTRACT
Splenomegaly is a hallmark of myelofibrosis, a debilitating haematological malignancy for which the only curative option is allogeneic haematopoietic cell transplantation (HCT). Considerable splenic enlargement might be associated with a higher risk of delayed engraftment and graft failure, increased non-relapse mortality, and worse overall survival after HCT as compared with patients without significantly enlarged splenomegaly. Currently, there are no standardised guidelines to assist transplantation physicians in deciding optimal management of splenomegaly before HCT. Therefore, the aim of this Position Paper is to offer a shared position statement on this issue. An international group of haematologists, transplantation physicians, gastroenterologists, surgeons, radiotherapists, and radiologists with experience in the treatment of myelofibrosis contributed to this Position Paper. The key issues addressed by this group included the assessment, prevalence, and clinical significance of splenomegaly, and the need for a therapeutic intervention before HCT for the control of splenomegaly. Specific scenarios, including splanchnic vein thrombosis and COVID-19, are also discussed. All patients with myelofibrosis must have their spleen size assessed before allogeneic HCT. Myelofibrosis patients with splenomegaly measuring 5 cm and larger, particularly when exceeding 15 cm below the left costal margin, or with splenomegaly-related symptoms, could benefit from treatment with the aim of reducing the spleen size before HCT. In the absence of, or loss of, response, patients with increasing spleen size should be evaluated for second-line options, depending on availability, patient fitness, and centre experience. Splanchnic vein thrombosis is not an absolute contraindication for HCT, but a multidisciplinary approach is warranted. Finally, prevention and treatment of COVID-19 should adhere to standard recommendations for immunocompromised patients.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trombose / Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas / Mielofibrose Primária / COVID-19 Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trombose / Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas / Mielofibrose Primária / COVID-19 Idioma: En Ano de publicação: 2023 Tipo de documento: Article