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CD74 is expressed in a subset of pediatric acute myeloid leukemia patients and is a promising target for therapy: a report from the Children's Oncology Group.
Menssen, Andrew J; Hudson, Chad A; Alonzo, Todd; Gerbing, Robert; Pardo, Laura; Leonti, Amanda; Cook, Jacqueline A; Hsu, Fan-Chi; Lott, Loren L; Dai, Fangyan; Fearing, Collette; Ghirardelli, Keely; Hylkema, Tiffany; Tarlock, Katherine; Loeb, Keith R; Kolb, Edward A; Cooper, Todd; Pollard, Jessica; Wells, Denise A; Loken, Michael R; Aplenc, Richard; Meshinchi, Soheil; Brodersen, Lisa Eidenschink.
Afiliación
  • Menssen AJ; Hematologics Inc., Seattle, WA. amenssen@hematologics.com.
  • Hudson CA; Hematologics Inc., Seattle, WA.
  • Alonzo T; Children's Oncology Group, Monrovia, CA, USA; Department of Preventive Medicine, University of Southern California, Los Angeles, CA.
  • Gerbing R; Children's Oncology Group, Monrovia, CA.
  • Pardo L; Hematologics Inc., Seattle, WA.
  • Leonti A; Fred Hutchinson Cancer Research Center, Seattle WA.
  • Cook JA; Hematologics Inc., Seattle, WA.
  • Hsu FC; Hematologics Inc., Seattle, WA.
  • Lott LL; Hematologics Inc., Seattle, WA.
  • Dai F; Hematologics Inc., Seattle, WA.
  • Fearing C; Hematologics Inc., Seattle, WA.
  • Ghirardelli K; Hematologics Inc., Seattle, WA.
  • Hylkema T; Fred Hutchinson Cancer Research Center, Seattle WA.
  • Tarlock K; Fred Hutchinson Cancer Research Center, Seattle WA, USA; Seattle Children's Hospital, Cancer and Blood Disorders Center, Department of Hematology/Oncology, Seattle, WA.
  • Loeb KR; Fred Hutchinson Cancer Research Center, Seattle WA, USA; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA.
  • Kolb EA; Children's Oncology Group, Monrovia, CA, USA; Nemours Center for Cancer and Blood Disorders Nemours/A.I. DuPont Hospital for Children, Wilmington DE.
  • Cooper T; Seattle Children's Hospital, Cancer and Blood Disorders Center, Department of Hematology/Oncology, Seattle, WA.
  • Pollard J; Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Harvard Medical School, Boston, MA.
  • Wells DA; Hematologics Inc., Seattle, WA.
  • Loken MR; Hematologics Inc., Seattle, WA.
  • Aplenc R; Children's Hospital of Philadelphia, Philadelphia, PA.
  • Meshinchi S; Children's Oncology Group, Monrovia, CA, USA; Fred Hutchinson Cancer Research Center, Seattle WA.
  • Brodersen LE; Hematologics Inc., Seattle, WA.
Haematologica ; 2024 Feb 01.
Article en En | MEDLINE | ID: mdl-38299667
ABSTRACT
As curative therapies for pediatric AML remain elusive, identifying potential new treatment targets is vital. We assessed the cell surface expression of CD74, also known as the MHC-II invariant chain, by multidimensional flow cytometry in 973 patients enrolled in the Children's Oncology Group AAML1031 clinical trial. 38% of pediatric AML patients expressed CD74 at any level and a comparison to normal hematopoietic cells revealed a subset with increased expression relative to normal myeloid progenitor cells. Pediatric AML patients expressing high intensity CD74 typically had an immature immunophenotype and an increased frequency of lymphoid antigen expression. Increased CD74 expression was associated with older patients with lower WBC and peripheral blood blast counts, and was enriched for t(8;21), trisomy 8, and CEBPA mutations. Overall, high CD74 expression was associated with low-risk status, however 26% of patients were allocated to high-risk protocol status and 5-year event free survival was 53%, indicating that a significant number of high expressing patients had poor outcomes. In vitro pre-clinical studies indicate that anti-CD74 therapy demonstrates efficacy against AML cells but has little impact on normal CD34+ cells. Together, we demonstrate that CD74 is expressed on a subset of pediatric AMLs at increased levels compared to normal hematopoietic cells and is a promising target for therapy in expressing patients. Given that nearly half of patients expressing CD74 at high levels experience an adverse event within 5 years, and the availability of CD74 targeting drugs, this represents a promising line of therapy worthy of additional investigation.

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Haematologica Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Guideline Idioma: En Revista: Haematologica Año: 2024 Tipo del documento: Article