Evidence map›Paper›PMID 32162718›Full record

ArticleAmerican journal of hematology2020

Microtransplantation in older patients with AML: A pilot study of safety, efficacy and immunologic effects.

Anthony D Sung, Shekeab Jauhari, Sharareh Siamakpour-Reihani, Arati V Rao, Janet Staats, Cliburn Chan, Everett Meyer, Vijayakrishna K Gadi, Andrew B Nixon, Jing Lyu and 16 more

Open access · greenAbstract readClinical Trial, Phase I
In one paragraph

Article in American journal of hematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 24% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 13 citations in OpenAlex.

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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

26 authors at 5 institutions in 1 country.

Anthony D SungDuke University School of Medicine, Durham, North Carolina, USA.ORCID 0000-0003-3765-641X
Shekeab JauhariDuke University School of Medicine, Durham, North Carolina, USA.
Sharareh Siamakpour-ReihaniDuke University School of Medicine, Durham, North Carolina, USA.ORCID 0000-0002-2837-443X
Arati V RaoKite Pharma, San Francisco, California, USA.
Janet StaatsDuke University School of Medicine, Durham, North Carolina, USA.
Cliburn ChanDuke University School of Medicine, Durham, North Carolina, USA.
Everett MeyerStanford University Medical School, Palo Alto, California, USA.
Vijayakrishna K GadiFred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Andrew B NixonDuke University School of Medicine, Durham, North Carolina, USA.
Jing LyuDuke University School of Medicine, Durham, North Carolina, USA.
Jichun XieDuke University School of Medicine, Durham, North Carolina, USA.
Lauren BohannonDuke University School of Medicine, Durham, North Carolina, USA.
Zhiguo LiDuke University School of Medicine, Durham, North Carolina, USA.
Christopher S HouriganLaboratory of Myeloid Malignancies, Hematology Branch, National Heart, Lung and Blood Institute, Bethesda, Maryland, USA.
Laura W DillonLaboratory of Myeloid Malignancies, Hematology Branch, National Heart, Lung and Blood Institute, Bethesda, Maryland, USA.
Hong Yuen WongLaboratory of Myeloid Malignancies, Hematology Branch, National Heart, Lung and Blood Institute, Bethesda, Maryland, USA.
Rebecca ShelbyDuke University School of Medicine, Durham, North Carolina, USA.
Louis DiehlDuke University School of Medicine, Durham, North Carolina, USA.
Carlos de CastroDuke University School of Medicine, Durham, North Carolina, USA.
Thomas LeBlancDuke University School of Medicine, Durham, North Carolina, USA.
Danielle BranderDuke University School of Medicine, Durham, North Carolina, USA.
Harry ErbaDuke University School of Medicine, Durham, North Carolina, USA.
Ahmed GalalDuke University School of Medicine, Durham, North Carolina, USA.
Alexandra StefanovicDuke University School of Medicine, Durham, North Carolina, USA.
Nelson ChaoDuke University School of Medicine, Durham, North Carolina, USA.
David A RizzieriDuke University School of Medicine, Durham, North Carolina, USA.
Duke University · USNational Heart Lung and Blood Institute · USFred Hutch Cancer Center · USKite (United States) · USPalo Alto University · US

Funding

Women's Cancer Research ProgramP30CA014236 · NCI · DUKE UNIVERSITY · PI DONNA NIEDZWIECKI · 1985 to 2026
$174.8M
Resource Core 3 - Metabolomics CoreP30AG028716 · NIA · DUKE UNIVERSITY · PI Virginia B Kraus · 2006 to 2026
$24.6M
Detection, prevention and treatment of acute myeloid leukemia (AML) relapse.ZIAHL006163 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HOURIGAN, CHRISTOPHER · 2013 to 2023
$21.0M
NCI NIH HHS P30 CA014236NIA NIH HHS P30 AG028716
6 · The paper itself

Abstract

Older AML patients have low remission rates and poor survival outcomes with standard chemotherapy. Microtransplantation (MST) refers to infusion of allogeneic hematopoietic stem cells without substantial engraftment. MST has been shown to improve clinical outcomes compared with chemotherapy alone. This is the first trial reporting on broad correlative studies to define immunologic mechanisms of action of MST in older AML patients. Older patients with newly diagnosed AML were eligible for enrollment, receiving induction chemotherapy with cytarabine (100 mg/m2) on days 1-7 and idarubicin (12 mg/m2) on days 1-3 (7 + 3). MST was administered 24 hours later. Patients with complete response (CR) were eligible for consolidation with high dose cytarabine (HiDAC) and a second cycle of MST. Responses were evaluated according to standard criteria per NCCN. Immune correlative studies were performed. Sixteen patients were enrolled and received 7 + 3 and MST (median age 73 years). Nine (56%) had high-risk and seven (44%) had standard-risk cytogenetics. Ten episodes of CRS were observed. No cases of GVHD or treatment-related mortality were reported. Event-free survival (EFS) was 50% at 6 months and 19% at 1 year. Overall survival (OS) was 63% at 6 months and 44% at 1 year. Donor microchimerism was not detected. Longitudinal changes were noted in NGS, TCR sequencing, and cytokine assays. Addition of MST to induction and consolidation chemotherapy was well tolerated in older AML patients. Inferior survival outcomes in our study may be attributed to a higher proportion of very elderly patients with high-risk features. Potential immunologic mechanisms of activity of MST include attenuation of inflammatory cytokines and emergence of tumor-specific T cell clones.

Indexed as

Hematopoietic Stem Cell TransplantationInduction ChemotherapyLeukemia, Myeloid, AcuteAgedAllograftsCytarabineFemaleFollow-Up StudiesHumansIdarubicinMaleMiddle AgedPilot ProjectsRisk FactorsCytarabineIdarubicin

Identifiers

PMID32162718
PMCPMC7433709
OpenAlexW3011065608

What OpenQuestion holds

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Registered trials

None linked

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.