Evidence map›Paper›PMID 34413159›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Impact of Prior Treatment on the Efficacy of Adoptive Transfer of Tumor-Infiltrating Lymphocytes in Patients with Metastatic Melanoma.

Samantha J Seitter, Richard M Sherry, James C Yang, Paul F Robbins, Mackenzie L Shindorf, Amy R Copeland, Christine T McGowan, Monica Epstein, Thomas E Shelton, Michelle M Langhan and 5 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01319565 (A Prospective Randomized Study of Cell Transfer Therapy for Metastatic Melanoma Using Short-Term Cultured Tumor-Infiltrating Lymphocytes Plus IL-2 Following Either a Non-Myeloablative Lymphocyte Depleting Chemotherapy Regimen Alone or in Conjunction With 12Gy Total Body Irradiation), which is not on this map. Cited by 82 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 3% 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.

NCT01319565 phase2completednot on this map

A Prospective Randomized Study of Cell Transfer Therapy for Metastatic Melanoma Using Short-Term Cultured Tumor-Infiltrating Lymphocytes Plus IL-2 Following Either a Non-Myeloablative Lymphocyte Depleting Chemotherapy Regimen Alone or in Conjunction With 12Gy Total Body Irradiation (TBI)

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2011 to 2024Enrolled102ConditionsMetastatic Melanoma, Skin CancerArmsAldesleukin, Cyclophosphamide, Fludarabine, Young TIL, Total Body Irradiation (TBI)
3 · Its place in the literature

Who cites it

82 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

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  11. Cell surface ADGRG1 and CD86 expression identifies antitumor CD4Proceedings of the National Academy of Sciences of the United States of America · 2026
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22 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

Samantha J SeitterSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Richard M SherrySurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
James C YangSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Paul F RobbinsSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Mackenzie L ShindorfSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.ORCID 0000-0001-8638-9317
Amy R CopelandSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.ORCID 0000-0002-2916-4098
Christine T McGowanSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Monica EpsteinSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Thomas E SheltonSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Michelle M LanghanSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Zulmarie FrancoSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
David N DanforthSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Donald E WhiteSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Steven A RosenbergSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.
Stephanie L GoffSurgery Branch, Center for Cancer Research, National Cancer Institute, NIH, Bethesda, Maryland.ORCID 0000-0003-3317-9804
National Cancer Institute · US

Funding

Identification and use of T-cell receptors recognizing common tumor mutationsZIABC011843 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI YANG, JAMES C · 2018 to 2025
$7.9M
Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

purposeAdoptive cell transfer (ACT) of autologous tumor-infiltrating lymphocytes (TIL) can mediate durable responses in patients with metastatic melanoma. This retrospective analysis provides long-term follow-up and describes the effect of prior therapy on outcomes after ACT-TIL. PATIENTS AND

methodsPatients with metastatic melanoma underwent surgical resection of a tumor for generation of TILs and were treated with a lymphodepleting preparative regimen followed by adoptive transfer of TILs and intravenous IL2. Clinical characteristics of enrolled patients and treatment characteristics of TIL infusion products over two decades of ACT were analyzed to identify predictors of objective response.

resultsAdoptive transfer of TILs mediated an objective response rate of 56% (108/192) and median melanoma-specific survival of 28.5 months in patients naïve to anti-programmed cell death-1 (PD-1) therapy compared with 24% (8/34) and 11.6 months in patients refractory to anti-PD-1 (aPD-1). Among patients with BRAF V600E/K-mutated disease, prior treatment with targeted molecular therapy was also associated with a decreased response rate (21% vs. 60%) and decreased survival (9.3 vs. 50.7 months) when compared with those patients naïve to targeted therapy. With a median potential follow-up of 89 months, 46 of 48 complete responders in the aPD-1-naïve cohort have ongoing responses after a single treatment and 10-year melanoma-specific survival of 96%.

conclusionsPatients previously treated with PD-1 or MAPK inhibition are significantly less likely to develop durable objective responses to ACT-TIL. While ACT-TIL is currently being investigated for treatment-refractory patients, it should also be considered as an initial treatment option for eligible patients with metastatic melanoma. See related commentary by Sznol, p. 5156.

Indexed as

MelanomaNeoplasms, Second PrimaryAdoptive TransferHumansImmunotherapy, AdoptiveLymphocytes, Tumor-InfiltratingRetrospective Studies

Identifiers

PMID34413159
PMCPMC8857302
OpenAlexW3193325476

What OpenQuestion holds

Textmetadata
LicenceTDM
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.