Evidence map›Paper›PMID 38299667›Full record

ArticleHaematologica2024

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.

Andrew J Menssen, Chad A Hudson, Todd Alonzo, Robert Gerbing, Laura Pardo, Amanda Leonti, Jacqueline A Cook, Fan-Chi Hsu, Loren L Lott, Fangyan Dai and 13 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Haematologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01371981 (A Phase III Randomized Trial for Patients With De Novo AML Using Bortezomib and Sorafenib), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01371981 phase3completednot on this map

A Phase III Randomized Trial for Patients With De Novo AML Using Bortezomib and Sorafenib (NSC# 681239, NSC# 724772) for Patients With High Allelic Ratio FLT3/ITD

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2011 to 2026Enrolled1,645ConditionsAcute Myeloid Leukemia, Leukemia Cutis, Myeloid Neoplasm, Myeloid SarcomaArmsAsparaginase, Bortezomib, Cytarabine, Daunorubicin Hydrochloride, Etoposide
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Pediatric AML CAR T cell therapy.Molecular therapy. Oncology · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 7 institutions in 2 countries.

Andrew J MenssenHematologics Inc., Seattle, WA. amenssen@hematologics.com.
Chad A HudsonHematologics Inc., Seattle, WA.
Todd AlonzoChildren's Oncology Group, Monrovia, CA, USA; Department of Preventive Medicine, University of Southern California, Los Angeles, CA.
Robert GerbingChildren's Oncology Group, Monrovia, CA.
Laura PardoHematologics Inc., Seattle, WA.
Amanda LeontiFred Hutchinson Cancer Research Center, Seattle WA.
Jacqueline A CookHematologics Inc., Seattle, WA.
Fan-Chi HsuHematologics Inc., Seattle, WA.
Loren L LottHematologics Inc., Seattle, WA.
Fangyan DaiHematologics Inc., Seattle, WA.
Collette FearingHematologics Inc., Seattle, WA.
Keely GhirardelliHematologics Inc., Seattle, WA.
Tiffany HylkemaFred Hutchinson Cancer Research Center, Seattle WA.
Katherine TarlockFred Hutchinson Cancer Research Center, Seattle WA, USA; Seattle Children's Hospital, Cancer and Blood Disorders Center, Department of Hematology/Oncology, Seattle, WA.
Keith R LoebFred Hutchinson Cancer Research Center, Seattle WA, USA; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA.
Edward A KolbChildren's Oncology Group, Monrovia, CA, USA; Nemours Center for Cancer and Blood Disorders Nemours/A.I. DuPont Hospital for Children, Wilmington DE.
Todd CooperSeattle Children's Hospital, Cancer and Blood Disorders Center, Department of Hematology/Oncology, Seattle, WA.
Jessica PollardPediatric Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Harvard Medical School, Boston, MA.
Denise A WellsHematologics Inc., Seattle, WA.
Michael R LokenHematologics Inc., Seattle, WA.
Richard AplencChildren's Hospital of Philadelphia, Philadelphia, PA.
Soheil MeshinchiChildren's Oncology Group, Monrovia, CA, USA; Fred Hutchinson Cancer Research Center, Seattle WA.
Lisa Eidenschink BrodersenHematologics Inc., Seattle, WA.
Center for Cancer and Blood Disorders · USFred Hutch Cancer Center · USChildren's Hospital of Philadelphia · USChildren's Oncology Group · USDana-Farber Cancer Institute · USUniversity of Southern California · USUniversity of Washington · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899
6 · The paper itself

Abstract

As curative therapies for pediatric acute myleoid leukemia (AML) remain elusive, identifying potential new treatment targets is vital. We assessed the cell surface expression of CD74, also known as the major histocompatibility complex-II invariant chain, by multidimensional flow cytometry in 973 patients enrolled in the Children's Oncology Group AAML1031 clinical trial (clinicaltrials gov. Identifier: NCT01371981). Thirty-eight percent 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 white blood cells 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 preclinical 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 AML 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.

Indexed as

Antigens, Differentiation, B-LymphocyteHistocompatibility Antigens Class IILeukemia, Myeloid, AcuteAdolescentChildChild, PreschoolFemaleHumansImmunophenotypingInfantMaleMolecular Targeted TherapyPrognosisAntigens, Differentiation, B-LymphocyteHistocompatibility Antigens Class IIinvariant chain

Identifiers

PMID38299667
PMCPMC11443400
OpenAlexW4391438635

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.