Evidence map›Paper›PMID 23032743›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2012

Specific lymphocyte subsets predict response to adoptive cell therapy using expanded autologous tumor-infiltrating lymphocytes in metastatic melanoma patients.

Laszlo G Radvanyi, Chantale Bernatchez, Minying Zhang, Patricia S Fox, Priscilla Miller, Jessica Chacon, Richard Wu, Gregory Lizee, Sandy Mahoney, Gladys Alvarado and 25 more

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04165967 (A Phase I Study of Adoptive Tumor-infiltrating Lymphocyte Transfer in Combination With Nivolumab in Patients With Advanced Melanoma), which is not on this map. Cited by 261 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
261citing papers in PubMed, 5 pooled it
14.7field-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.

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

261 citing papers in PubMed, 5 syntheses or guidelines pooled it, 430 citations in OpenAlex.

  1. Pooled it
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  3. The Roles of MiRNAs (MicroRNAs) in Melanoma Immunotherapy.International journal of molecular sciences · 2022
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  11. Pilot Clinical Trial of Perioperative Durvalumab and Tremelimumab in the Treatment of Resectable Colorectal Cancer Liver Metastases.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
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  18. PD-1Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
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201 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

35 authors at 1 institution in 1 country.

Laszlo G RadvanyiDepartments of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA. lradvanyi@mdanderson.org
Chantale Bernatchez
Minying Zhang
Patricia S Fox
Priscilla Miller
Jessica Chacon
Richard Wu
Gregory Lizee
Sandy Mahoney
Gladys Alvarado
Michelle Glass
Valen E Johnson
John D McMannis
Elizabeth Shpall
Victor Prieto
Nicholas Papadopoulos
Kevin Kim
Jade Homsi
Agop Bedikian
Wen-Jen Hwu
Sapna Patel
Merrick I Ross
Jeffrey E Lee
Jeffrey E Gershenwald
Anthony Lucci
Richard Royal
Janice N Cormier
Michael A Davies
Rahmatu Mansaray
Orenthial J Fulbright
Christopher Toth
Renjith Ramachandran
Seth Wardell
Audrey Gonzalez
Patrick Hwu
The University of Texas MD Anderson Cancer Center · US

Funding

U OF TEXAS HLTH SCI CTR HOUSTON CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCESUL1RR024148 · NCRR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2006 to 2010
$27.9M
UT M.D. Anderson Cancer Center SPORE in MelanomaP50CA093459 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GRIMM, ELIZABETH A · 2004 to 2014
$23.7M
Center for Clinical and Translational SciencesTL1RR024147 · NCRR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2006 to 2011
$2.3M
DC Vaccination to Enhance Adoptive T Cell TransferR01CA111999 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HWU, PATRICK · 2006 to 2010
$1.8M
NCI NIH HHS CA093459-DRP21NCI NIH HHS CA111999NCI NIH HHS P50 CA093459NCI NIH HHS R01 CA111999NCRR NIH HHS TL1 RR024147NCRR NIH HHS UL1 RR024148
6 · The paper itself

Abstract

purposeAdoptive cell therapy (ACT) using autologous tumor-infiltrating lymphocytes (TIL) is a promising treatment for metastatic melanoma unresponsive to conventional therapies. We report here on the results of an ongoing phase II clinical trial testing the efficacy of ACT using TIL in patients with metastatic melanoma and the association of specific patient clinical characteristics and the phenotypic attributes of the infused TIL with clinical response. EXPERIMENTAL

designAltogether, 31 transiently lymphodepleted patients were treated with their expanded TIL, followed by two cycles of high-dose interleukin (IL)-2 therapy. The effects of patient clinical features and the phenotypes of the T cells infused on the clinical response were determined.

resultsOverall, 15 of 31 (48.4%) patients had an objective clinical response using immune-related response criteria (irRC) with 2 patients (6.5%) having a complete response. Progression-free survival of more than 12 months was observed for 9 of 15 (60%) of the responding patients. Factors significantly associated with the objective tumor regression included a higher number of TIL infused, a higher proportion of CD8(+) T cells in the infusion product, a more differentiated effector phenotype of the CD8(+) population, and a higher frequency of CD8(+) T cells coexpressing the negative costimulation molecule "B- and T-lymphocyte attenuator" (BTLA). No significant difference in the telomere lengths of TIL between responders and nonresponders was identified.

conclusionThese results indicate that the immunotherapy with expanded autologous TIL is capable of achieving durable clinical responses in patients with metastatic melanoma and that CD8(+) T cells in the infused TIL, particularly differentiated effectors cells and cells expressing BTLA, are associated with tumor regression.

Indexed as

Immunotherapy, AdoptiveCells, CulturedCombined Modality TherapyDisease-Free SurvivalFemaleHumansInterleukin-2Lymphocyte SubsetsMaleMelanomaMiddle AgedRemission InductionSkin NeoplasmsSurvival AnalysisTelomereT-Lymphocytes, CytotoxicInterleukin-2

Identifiers

PMID23032743
PMCPMC3525747
OpenAlexW2170403104

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.