Evidence map›Paper›PMID 29597002›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2018

A Phase 1 Trial of CNDO-109-Activated Natural Killer Cells in Patients with High-Risk Acute Myeloid Leukemia.

Todd A Fehniger, Jeffrey S Miller, Robert K Stuart, Sarah Cooley, Amandeep Salhotra, Julie Curtsinger, Peter Westervelt, John F DiPersio, Timothy M Hillman, Nova Silver and 4 more

2 registry-linked trialsAbstract readClinical Trial, Phase I
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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.

NCT05933070 phase1terminatednot on this mapstarted 2020, after this paper: background citation

A Phase I Open-Label Dose Escalation Study Of Intravenous INKmune In Patients With Myelodysplastic Syndrome With Excess Blasts (MDS-EB-1/2 - MDS-CMML 1/2) Or Acute Myeloid Leukaemia (AML)

TypeinterventionalSponsorInmune Bio, Inc.Ran2020 to 2024Enrolled2ConditionsCancer, MDS-EB, Myelodysplastic Syndromes, Acute Myeloid LeukemiaArmsINKmune
NCT06056791 phase1 / phase2completednot on this mapstarted 2023, after this paper: background citation

An Open-label, Phase I/IIa Dose Escalation and Expansion Study to Determine the Safety and Clinical Activity of an Immune Priming Cell Therapy (INKmune) in Patients With Metastatic Castration Resistant Prostate Cancer (mCRPC)

TypeinterventionalSponsorInmune Bio, Inc.Ran2023 to 2025Enrolled12ConditionsCancer, Metastatic Castration-resistant Prostate Cancer, mCRPCArmsINKmune
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  7. Article
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  9. Natural killer cell-based immunotherapy for cancer.Journal of immunology (Baltimore, Md. : 1950) · 2025
    Review
  10. Review
  11. Review
  12. Adoptive NK cell therapy in AML: progress and challenges.Clinical and experimental medicine · 2025
    Review
  13. Article
  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Todd A FehnigerDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri. Electronic address: tfehnige@wustl.edu.
Jeffrey S MillerDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota.
Robert K StuartDepartment of Hematology and Oncology, Medical University of South Carolina, Charleston, South Carolina.
Sarah CooleyDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota.
Amandeep SalhotraDepartment of Hematology and Hematopoietic Cell Transplantation, Beckman Research Institute of City of Hope, City of Hope Comprehensive Cancer Center, Duarte, California.
Julie CurtsingerDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota.
Peter WesterveltDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
John F DiPersioDivision of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
Timothy M HillmanFortress Biotech, Inc., New York, New York.
Nova SilverFortress Biotech, Inc., New York, New York.
Michael SzarekDepartment of Epidemiology and Biostatistics, SUNY Downstate School of Public Health, Brooklyn New York.
Leonid GorelikFortress Biotech, Inc., New York, New York.
Mark W LowdellDepartment of Hematology, Royal Free Hospital, UCL Medical School, London, United Kingdom.
Eric RowinskyFortress Biotech, Inc., New York, New York.

Funding

TRANSLATING NK CELL BIOLOGY INTO CLINICAL CANCER IMMUNOTHERAPYR01CA205239 · NCI · WASHINGTON UNIVERSITY · PI FEHNIGER, TODD A · 2017 to 2020
$2.4M
NCI NIH HHS R01 CA205239
6 · The paper itself

Abstract

Natural killer (NK) cells are an emerging immunotherapy approach to acute myeloid leukemia (AML); however, the optimal approach to activate NK cells before adoptive transfer remains unclear. Human NK cells that are primed with the CTV-1 leukemia cell line lysate CNDO-109 exhibit enhanced cytotoxicity against NK cell-resistant cell lines. To translate this finding to the clinic, CNDO-109-activated NK cells (CNDO-109-NK cells) isolated from related HLA-haploidentical donors were evaluated in a phase 1 dose-escalation trial at doses of 3 × 10

Indexed as

AdultAgedCell CountCell Line, TumorDisease-Free SurvivalFemaleHumansImmunotherapy, AdoptiveKiller Cells, NaturalLeukemia, Myeloid, AcuteMaleMiddle AgedSecondary PreventionTissue DonorsTransplantation, HaploidenticalTreatment OutcomeAcute myeloid leukemiaCNDO-109–activated natural killer cells

Identifiers

PMID29597002
PMCPMC6232080

What OpenQuestion holds

Textmetadata
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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.