Evidence map›Paper›PMID 20668005›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2010

CD8+ enriched "young" tumor infiltrating lymphocytes can mediate regression of metastatic melanoma.

Mark E Dudley, Colin A Gross, Michelle M Langhan, Marcos R Garcia, Richard M Sherry, James C Yang, Giao Q Phan, Udai S Kammula, Marybeth S Hughes, Deborah E Citrin and 10 more

3 registry-linked trialsOpen access · bronzeAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 175 papers.

0numbers the graph read from it
0cells of the map it votes in
175citing papers in PubMed
13.0field-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.

NCT01462903 phase1unknown statusnot on this mapstarted 2011, after this paper: background citation

A Phase I Study of Adoptive Immunotherapy With Autologous Tumor Infiltrating Lymphocytes in Solid Tumors

TypeinterventionalSponsorSun Yat-sen UniversityRan2011 to 2014Enrolled20ConditionsNasopharyngeal Carcinoma, Hepatocellular Carcinoma, Breast CarcinomaArmstumor infiltrating lymphocytes, IL-2
NCT02421640 phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Study of Adoptive Immunotherapy With Autologous Tumor Infiltrating Lymphocytes and Concurrent Chemoradiotherapy in Nasopharyngeal Carcinoma

TypeinterventionalSponsorSun Yat-sen UniversityRan2015 to 2020Enrolled116ConditionsNasopharyngeal CarcinomaArmsCisplatin+TIL, Cisplatin
NCT04165967 phase1completednot on this mapstarted 2020, after this paper: background citation

A Phase I Study of Adoptive Tumor-infiltrating Lymphocyte Transfer in Combination With Nivolumab in Patients With Advanced Melanoma

TypeinterventionalSponsorUniversity Hospital, Basel, SwitzerlandRan2020 to 2023Enrolled9ConditionsAdvanced MelanomaArmsCombination of TIL Transfer with anti-PD-1 Therapy and low dose IL-2
3 · Its place in the literature

Who cites it

175 citing papers in PubMed, 311 citations in OpenAlex.

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  5. 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
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  6. Review
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  8. Cellular immunotherapy in melanoma: the next frontier in cancer treatment.Journal of experimental & clinical cancer research : CR · 2026
    Review
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115 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

20 authors at 2 institutions in 1 country.

Mark E DudleySurgery Branch and Radiation Oncology Branch, National Cancer Institute, Bethesda, Maryland 20892-1201, USA. med@nih.gov
Colin A Gross
Michelle M Langhan
Marcos R Garcia
Richard M Sherry
James C Yang
Giao Q Phan
Udai S Kammula
Marybeth S Hughes
Deborah E Citrin
Nicholas P Restifo
John R Wunderlich
Peter A Prieto
Jenny J Hong
Russell C Langan
Daniel A Zlott
Kathleen E Morton
Donald E White
Carolyn M Laurencot
Steven A Rosenberg
National Cancer Institute · USNational Institutes of Health · US

Funding

Building on the success of the adoptive immunotherapy of cancerZIABC010763 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ROSENBERG, STEVEN · 2009 to 2020
$25.0M
Surgery Branch Cell Prep CoreZICBC010905 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HALAS, HYUNMI · 2009 to 2025
$23.9M
Cell Production Facility CoreZICBC011020 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DUDLEY, MARK · 2009 to 2013
$6.5M
Cell Production Facility CoreZ01BC011020 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DUDLEY, MARK · 2008 to 2008
$1.2M
Intramural NIH HHS Z01 BC011020Intramural NIH HHS ZIC BC011020
6 · The paper itself

Abstract

purposeTumor-infiltrating lymphocytes (TIL) and interleukin (IL)-2 administered following lymphodepletion can cause the durable complete regression of bulky metastatic melanoma in patients refractory to approved treatments. However, the generation of a unique tumor-reactive TIL culture for each patient may be prohibitively difficult. We therefore investigated the clinical and immunologic impact of unscreened, CD8+ enriched "young" TIL. EXPERIMENTAL

designMethods were developed for generating TIL that minimized the time in culture and eliminated the individualized tumor-reactivity screening step. Thirty-three patients were treated with these CD8+ enriched young TIL and IL-2 following nonmyeloablative lymphodepletion (NMA). Twenty-three additional patients were treated with CD8+ enriched young TIL and IL-2 after lymphodepletion with NMA and 6 Gy of total body irradiation.

resultsYoung TIL cultures for therapy were successfully established from 83% of 122 consecutive melanoma patients. Nineteen of 33 patients (58%) treated with CD8+ enriched young TIL and NMA had an objective response (Response Evaluation Criteria in Solid Tumors) including 3 complete responders. Eleven of 23 patients (48%) treated with TIL and 6 Gy total body irradiation had an objective response including 2 complete responders. At 1 month after TIL infusion the absolute CD8+ cell numbers in the periphery were highly correlated with response.

conclusionsThis study shows that a rapid and simplified method can be used to reliably generate CD8+ enriched young TIL for administration as an individualized therapy for advanced melanoma, and may allow this potentially effective treatment to be applied at other institutions and to reach additional patients.

Indexed as

AdultAgedAged, 80 and overCD8-Positive T-LymphocytesCells, CulturedCombined Modality TherapyCytotoxicity, ImmunologicFemaleHumansImmunotherapy, AdoptiveLymphocyte CountLymphocytes, Tumor-InfiltratingMaleMelanomaMiddle AgedNeoplasm Metastasis

Identifiers

PMID20668005
PMCPMC2978753
OpenAlexW2153590293

What OpenQuestion holds

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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.