Your browser doesn't support javascript.
loading
Treatment approach and outcomes of patients with accelerated/blast-phase myeloproliferative neoplasms in the current era.
Patel, Anand A; Yoon, James J; Johnston, Hannah; Davidson, Marta B; Shallis, Rory M; Chen, Evan C; Burkart, Madelyn; Oh, Timothy S; Iyer, Sunil G; Madarang, Ellen; Muthiah, Chandrasekar; Gross, Iyana; Dean, Raven; Kassner, Joshua; Viswabandya, Auro; Madero-Marroquin, Rafael; Rampal, Raajit K; Guru Murthy, Guru Subramanian; Bradley, Terrence; Abaza, Yasmin; Garcia, Jacqueline S; Gupta, Vikas; Pettit, Kristen M; Cursio, John F; Odenike, Olatoyosi.
Afiliação
  • Patel AA; Department of Medicine, Section of Hematology-Oncology, University of Chicago, Chicago, IL.
  • Yoon JJ; Division of Hematologic Malignancies, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
  • Johnston H; Department of Medicine, Internal Medicine Residency, University of Chicago, Chicago, IL.
  • Davidson MB; Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Shallis RM; Department of Internal Medicine, Section of Hematology, Yale School of Medicine and Yale Cancer Center, New Haven, CT.
  • Chen EC; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Burkart M; Atrium Health Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC.
  • Oh TS; Division of Hematology and Oncology, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Iyer SG; Division of Hematology and Oncology, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY.
  • Madarang E; University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.
  • Muthiah C; Department of Internal Medicine, Medical College of Wisconsin, Milwaukee, WI.
  • Gross I; University of Chicago Comprehensive Cancer Center, Chicago, IL.
  • Dean R; University of Chicago Comprehensive Cancer Center, Chicago, IL.
  • Kassner J; Memorial Sloan Kettering Cancer Center, New York, NY.
  • Viswabandya A; Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Madero-Marroquin R; Department of Medicine, Section of Hematology-Oncology, University of Chicago, Chicago, IL.
  • Rampal RK; Department of Medicine, Leukemia Service, Memorial Sloan Kettering Cancer Center, New York, NY.
  • Guru Murthy GS; Division of Hematology & Oncology, Medical College of Wisconsin, Milwaukee, WI.
  • Bradley T; University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.
  • Abaza Y; Division of Hematology and Oncology, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Garcia JS; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Gupta V; Medical Oncology and Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada.
  • Pettit KM; Division of Hematology and Medical Oncology, Department of Internal Medicine, University of Michigan Medical School, Michigan Medicine, Ann Arbor, MI.
  • Cursio JF; Department of Public Health Sciences, University of Chicago, Chicago, IL.
  • Odenike O; Department of Medicine, Section of Hematology-Oncology, University of Chicago, Chicago, IL.
Blood Adv ; 8(13): 3468-3477, 2024 Jul 09.
Article em En | MEDLINE | ID: mdl-38739724
ABSTRACT
ABSTRACT Progression of myeloproliferative neoplasms (MPNs) to accelerated or blast phase is associated with poor survival outcomes. Since 2017 there have been several therapies approved for use in acute myeloid leukemia (AML); these therapies have been incorporated into the management of accelerated/blast-phase MPNs (MPN-AP/BP). We performed a multicenter analysis to investigate outcomes of patients diagnosed with MPN-AP/BP in 2017 or later. In total, 202 patients were identified; median overall survival (OS) was 0.86 years. We also analyzed patients based on first-line treatment; the 3 most common approaches were intensive chemotherapy (n = 65), DNA methyltransferase inhibitor (DNMTi)-based regimens (n = 65), and DNMTi + venetoclax-based regimens (n = 54). Median OS was not significantly different by treatment type. In addition, we evaluated response by 2017 European LeukemiaNet AML criteria and 2012 MPN-BP criteria in an effort to understand the association of response with survival outcomes. We also analyzed outcomes in 65 patients that received allogeneic hematopoietic stem cell transplant (allo-HSCT); median OS was 2.30 years from time of allo-HSCT. Our study demonstrates that survival among patients with MPN-AP/BP is limited in the absence of allo-HSCT even in the current era of therapeutics and underscores the urgent need for new agents and approaches.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Mieloproliferativos Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Mieloproliferativos Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article