Evidence map›Paper›PMID 16946036›Full record

Trial reportScience (New York, N.Y.)2006

Cancer regression in patients after transfer of genetically engineered lymphocytes.

Richard A Morgan, Mark E Dudley, John R Wunderlich, Marybeth S Hughes, James C Yang, Richard M Sherry, Richard E Royal, Suzanne L Topalian, Udai S Kammula, Nicholas P Restifo and 6 more

4 registry-linked trialsOpen access · greenAbstract readClinical Trial
In one paragraph

Trial report in Science (New York, N.Y.), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 1,319 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,319citing papers in PubMed, 1 pooled it
79.1field-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.

NCT02632019 phase1 / phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Clinical Study of Adoptive Cellular Immunotherapy Using Precision T Cells Specific to Personalized Neo-antigen in Treating Patients With Advanced Malignant Tumor of Biliary Tract

TypeinterventionalSponsorSecond Military Medical UniversityRan2015 to 2017Enrolled40ConditionsAdvanced Biliary Tract Malignant TumorArmsGemcitabine, Dendritic cell-precision T cell for neo-antigen combined with gemcitabine treatment
NCT03159585 phase1completednot on this mapstarted 2017, after this paper: background citation

Application of NY-ESO-1-specific TCR Affinity Enhancing Specific T Cell Therapy (TAEST16001) in Solid Tumors Except Non Small Cell Lung Cancer,Including Liver Cancer,Gastric Cancer,Esophageal Cancer and so on.

TypeinterventionalSponsorZhujiang HospitalRan2017 to 2019Enrolled6ConditionsLiver Cancer Stage IV, Gastric Cancer Stage IV, Esophageal Cancer, Stage IV, Bone and Soft Tissue TumorsArmsTAEST16001
NCT03925896 phase1unknown statusnot on this mapstarted 2019, after this paper: background citation

LMP2 Antigen-specific High-affinity T Cell Receptor (TCR)-Transduced Autologous T-cell Therapy for Recurrent and Metastatic Nasopharyngeal Carcinoma, an Open-label, Single-center, Phase I Clinical Trial

TypeinterventionalSponsorSun Yat-sen UniversityRan2019 to 2022Enrolled27ConditionsNasopharyngeal CarcinomaArmsLMP2 Antigen-specific TCR T cells
NCT05438667 early_phase1recruitingnot on this mapstarted 2023, after this paper: background citation

A Prospective, One Arm Clinical Study on the Safety, Efficacy and Pharmacokinetics of KRAS Mutant Antigen Specific TCR-T Cells in the Treatment of Advanced Solid Tumors.

TypeinterventionalSponsorSun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityRan2023 to 2028Enrolled18ConditionsPancreatic CancerArmsTCR-T therapy
3 · Its place in the literature

Who cites it

1,319 citing papers in PubMed, 1 synthesis or guideline pooled it, 2,560 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Current status and challenges of TCR-T cell therapy for AML/MDS.International journal of hematology · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Cell surface ADGRG1 and CD86 expression identifies antitumor CD4Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Review
  19. Strategies to eliminate native T cell receptors for adoptive T cell therapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Review
  20. Review

1,259 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 1 institution in 1 country.

Richard A MorganSurgery Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892, USA.
Mark E Dudley
John R Wunderlich
Marybeth S Hughes
James C Yang
Richard M Sherry
Richard E Royal
Suzanne L Topalian
Udai S Kammula
Nicholas P Restifo
Zhili Zheng
Azam Nahvi
Christiaan R de Vries
Linda J Rogers-Freezer
Sharon A Mavroukakis
Steven A Rosenberg
National Cancer Institute · US

Funding

SURGICAL CONSULTATIONS AND COLLABORATIVE RESEARCH IN SURGICAL SERVICES AT NIHZ01SC003800 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI ROSENBERG, STEVEN A · 1996 to 2008
$7.5M
Building on the success of the adoptive immunotherapy of cancerZ01BC010763 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RESTIFO, NICHOLAS P · 2006 to 2008
$6.4M
THE IMMUNOTHERAPY OF ANIMAL AND HUMAN CANCERZ01SC003811 · SC · CLINICAL SCIENCES · PI ROSENBERG, STEVEN A · 1996 to 2007
$3.2M
Immunotherapy Strategies for Gastrointestinal and Hepatocellular CancerZ01BC010649 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KAMMULA, UDAI S · 2005 to 2008
$1.1M
RECOMBINANT AND SYNTHETIC ANTI-CANCER VACCINESZ01SC006670 · SC · CLINICAL SCIENCES · PI RESTIFO, NICHOLAS P · 1996 to 2005
–
Intramural NIH HHS Z01 BC010763Intramural NIH HHS Z01 SC003811Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

Through the adoptive transfer of lymphocytes after host immunodepletion, it is possible to mediate objective cancer regression in human patients with metastatic melanoma. However, the generation of tumor-specific T cells in this mode of immunotherapy is often limiting. Here we report the ability to specifically confer tumor recognition by autologous lymphocytes from peripheral blood by using a retrovirus that encodes a T cell receptor. Adoptive transfer of these transduced cells in 15 patients resulted in durable engraftment at levels exceeding 10% of peripheral blood lymphocytes for at least 2 months after the infusion. We observed high sustained levels of circulating, engineered cells at 1 year after infusion in two patients who both demonstrated objective regression of metastatic melanoma lesions. This study suggests the therapeutic potential of genetically engineered cells for the biologic therapy of cancer.

Indexed as

Adoptive TransferGenetic TherapyAdultAntigens, NeoplasmCancer VaccinesCD8-Positive T-LymphocytesCells, CulturedElectroporationFemaleGenetic EngineeringHLA-A2 AntigenHLA-A AntigensHumansInterleukin-2MaleMART-1 AntigenAntigens, NeoplasmCancer VaccinesHLA-A*02:01 antigenHLA-A2 AntigenHLA-A AntigensInterleukin-2MART-1 AntigenMLANA protein, humanNeoplasm ProteinsReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID16946036
PMCPMC2267026
OpenAlexW2094652659

What OpenQuestion holds

Textmetadata
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.