Evidence map›Paper›PMID 15585832›Full record

Trial reportJournal of immunology (Baltimore, Md. : 1950)2004

Cutting edge: persistence of transferred lymphocyte clonotypes correlates with cancer regression in patients receiving cell transfer therapy.

Paul F Robbins, Mark E Dudley, John Wunderlich, Mona El-Gamil, Yong F Li, Juhua Zhou, Jianping Huang, Daniel J Powell, Steven A Rosenberg

Open access · bronzeAbstract readClinical TrialComparative Study
In one paragraph

Trial report in Journal of immunology (Baltimore, Md. : 1950), 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 256 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
256citing papers in PubMed, 1 pooled it
11.1field-weighted citation impact, top 1% 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

256 citing papers in PubMed, 1 synthesis or guideline pooled it, 459 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  5. Trial
  6. A pilot trial using lymphocytes genetically engineered with an NY-ESO-1-reactive T-cell receptor: long-term follow-up and correlates with response.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Trial
  7. Persistence of CTL clones targeting melanocyte differentiation antigens was insufficient to mediate significant melanoma regression in humans.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Trial
  8. Trial
  9. Trial
  10. Durable complete responses in heavily pretreated patients with metastatic melanoma using T-cell transfer immunotherapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    Trial
  11. Trial
  12. Trial
  13. Article
  14. Review
  15. Article
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  20. Novel Arf1 Inhibitors Drive Cancer Stem Cell Aging and Potentiate Anti-Tumor Immunity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article

196 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Paul F RobbinsSurgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA. Paul_Robbins@nih.gov
Mark E Dudley
John Wunderlich
Mona El-Gamil
Yong F Li
Juhua Zhou
Jianping Huang
Daniel J Powell
Steven A Rosenberg
National Institutes of Health · US

Funding

THE IMMUNOTHERAPY OF ANIMAL AND HUMAN CANCERZ01SC003811 · SC · CLINICAL SCIENCES · PI ROSENBERG, STEVEN A · 1996 to 2007
$3.2M
Intramural NIH HHS Z01 SC003811
6 · The paper itself

Abstract

The lack of persistence of transferred autologous mature lymphocytes in humans has been a major limitation to the application of effective cell transfer therapies. The results of a pilot clinical trial in 13 patients with metastatic melanoma suggested that conditioning with nonmyeloablative chemotherapy before adoptive transfer of activated tumor-reactive T cells enhances tumor regression and increases the overall rates of objective clinical responses. The present report examines the relationship between T cell persistence and tumor regression through analysis of the TCR beta-chain V region gene products expressed in samples obtained from 25 patients treated with this protocol. Sequence analysis demonstrated that there was a significant correlation between tumor regression and the degree of persistence in peripheral blood of adoptively transferred T cell clones, suggesting that inadequate T cell persistence may represent a major factor limiting responses to adoptive immunotherapy.

Indexed as

Immunotherapy, AdoptiveLymphocyte TransfusionCell ProliferationCell SurvivalClone CellsGene Rearrangement, beta-Chain T-Cell Antigen ReceptorHumansImmunoglobulin Variable RegionLymphocyte CountLymphocytes, Tumor-InfiltratingMelanomaPilot ProjectsReceptors, Antigen, T-Cell, alpha-betaImmunoglobulin Variable RegionReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID15585832
PMCPMC2175171
OpenAlexW2115278843

What OpenQuestion holds

Textmetadata
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.