Evidence map›Paper›PMID 29757889›Full record

Trial reportJournal of immunotherapy (Hagerstown, Md. : 1997)

Utilizing T-cell Activation Signals 1, 2, and 3 for Tumor-infiltrating Lymphocytes (TIL) Expansion: The Advantage Over the Sole Use of Interleukin-2 in Cutaneous and Uveal Melanoma.

René J Tavera, Marie-Andrée Forget, Young Uk Kim, Donastas Sakellariou-Thompson, Caitlin A Creasy, Ankit Bhatta, Orenthial J Fulbright, Renjith Ramachandran, Shawne T Thorsen, Esteban Flores and 12 more

Abstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Journal of immunotherapy (Hagerstown, Md. : 1997). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

32 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. IL-2-independent expansion, persistence, and antitumor activity in TIL expressing regulatable membrane-bound IL-15.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  5. Review
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  8. Article
  9. Review
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  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Genomic Correlates of Outcome in Tumor-Infiltrating Lymphocyte Therapy for Metastatic Melanoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Article
  18. Article
  19. Article
  20. Article
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

22 authors at 2 institutions in 2 countries.

René J TaveraDepartments of Melanoma Medical Oncology.
Marie-Andrée ForgetDepartments of Melanoma Medical Oncology.
Young Uk KimDepartments of Melanoma Medical Oncology.
Donastas Sakellariou-ThompsonDepartments of Melanoma Medical Oncology.
Caitlin A CreasyDepartments of Melanoma Medical Oncology.
Ankit BhattaDepartments of Melanoma Medical Oncology.
Orenthial J FulbrightDepartments of Melanoma Medical Oncology.
Renjith RamachandranDepartments of Melanoma Medical Oncology.
Shawne T ThorsenDepartments of Melanoma Medical Oncology.
Esteban FloresDepartments of Melanoma Medical Oncology.
Arely WahlDepartments of Melanoma Medical Oncology.
Audrey M GonzalezDepartments of Melanoma Medical Oncology.
Christopher TothDepartments of Melanoma Medical Oncology.
Seth WardellDepartments of Melanoma Medical Oncology.
Rahmatu MansarayDepartments of Melanoma Medical Oncology.
Laszlo G RadvanyiDepartments of Melanoma Medical Oncology.
Dan S GombosHead and Neck Surgery, The University of Texas MD Anderson Cancer Center (MDACC), Houston, TX.
Sapna P PatelDepartments of Melanoma Medical Oncology.
Patrick HwuDepartments of Melanoma Medical Oncology.
Rodabe N AmariaDepartments of Melanoma Medical Oncology.
Chantale BernatchezDepartments of Melanoma Medical Oncology.
Cara HaymakerDepartments of Melanoma Medical Oncology.
Melanoma Institute Australia · AUThe University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

In this study, we address one of the major critiques for tumor-infiltrating lymphocyte (TIL) therapy-the time needed for proper expansion of a suitable product. We postulated that T-cell receptor activation in the first phase of expansion combined with an agonistic stimulation of CD137/4-1BB and interleukin-2 would favor preferential expansion of CD8 TIL. Indeed, this novel 3-signal approach for optimal T-cell activation resulted in faster and more consistent expansion of CD8CD3 TIL. This new method allowed for successful expansion of TIL from cutaneous and uveal melanoma tumors in 100% of the cultures in <3 weeks. Finally, providing the 3 signals attributed to optimal T-cell activation led to expansion of TIL capable of recognizing their tumor counterpart in cutaneous and uveal melanoma. This new methodology for the initial phase of TIL expansion brings a new opportunity for translation of TIL therapy in challenging malignancies such as uveal melanoma.

Indexed as

FemaleHumansImmunotherapy, AdoptiveInterleukin-2Lymphocytes, Tumor-InfiltratingMaleMelanomaSkin NeoplasmsT-LymphocytesUveal MelanomaUveal NeoplasmsInterleukin-2

Identifiers

PMID29757889
PMCPMC6177302
OpenAlexW2801302797

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.