Evidence map›Paper›PMID 35172204›Full record

ArticleTransplantation and cellular therapy2022

A Phase I Study to Determine the Maximum Tolerated Dose of ex Vivo Expanded Natural Killer Cells Derived from Unrelated, HLA-Disparate Adult Donors.

Folashade Otegbeye, Brenda Cooper, Paolo Caimi, Kayla Zamborsky, Jane Reese-Koc, Antoinette Hillian, Yeritza Hernandez-Collazo, Grace Lee, Kirsten Boughan, Benjamin Tomlinson and 8 more

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

Article in Transplantation and cellular therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 11% 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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  12. Good manufacturing practice production of an off-the-shelf CD34Cellular and molecular life sciences : CMLS · 2025
    Article
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  15. Reprogramming natural killer cells for cancer therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
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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

18 authors at 3 institutions in 1 country.

Folashade OtegbeyeUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio. Electronic address: fotegbey@fredhutch.org.
Brenda CooperUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Paolo CaimiUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Kayla ZamborskyCase Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Jane Reese-KocCase Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Antoinette HillianUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio.
Yeritza Hernandez-CollazoUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio.
Grace LeeCase Western Reserve University for Lazarus, Cleveland, Ohio.
Kirsten BoughanUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Benjamin TomlinsonUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Molly GalloglyUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Leland MethenyUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
David BajorUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Jennifer SelfridgeUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Joel SaltzmanUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
Hillard LazarusCase Western Reserve University for Lazarus, Cleveland, Ohio.
Marcos de LimaUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
David WaldUniversity Hospitals Seidman Cancer Center, Cleveland, Ohio; Case Comprehensive Cancer Center for Saltzman, de Lima and Wald, Cleveland, Ohio.
University Hospitals Seidman Cancer Center · USCase Comprehensive Cancer CenterCase Western Reserve University · US

Funding

Targeting 15-PGDH in Colon Cancer Prognosis, Prediction, Treatment and PreventionP50CA150964 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI MARKOWITZ, SANFORD D. · 2011 to 2022
$24.6M
NCI NIH HHS P50 CA150964
6 · The paper itself

Abstract

The administration of allogeneic natural killer (NK) cells following a lymphodepleting chemotherapy regimen is emerging as a well-tolerated therapeutic approach in the management of various malignancies. Contrary to the expected complications of allogeneic T cell therapy, there remains no evidence of graft-versus-host disease (GVHD) mediated by NK cells in numerous clinical trials. On the contrary, preclinical and clinical studies suggest that NK cells do not induce GVHD and in fact may prevent its development following allogeneic hematopoietic cell transplantation (HCT). In this study, we sought to determine the maximum tolerated dose of non-HLA-matched donor NK cells derived from peripheral blood and ex vivo expanded using a novel feeder cell platform. In a single-center Phase I clinical trial using a 3 × 3 design, 9 subjects each received 2 infusions of NK cells 2 weeks apart following a preparative regimen of cyclophosphamide (60 mg/kg i.v.) and fludarabine (25 mg/m

Indexed as

Graft vs Host DiseaseMyelodysplastic SyndromesAdultHumansKiller Cells, NaturalMaximum Tolerated DoseTransplantation, HomologousUnrelated DonorsNK cell therapyUniversal donor NK cells

Identifiers

PMID35172204
PMCPMC9489303
OpenAlexW4213280743

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.