Evidence map›Paper›PMID 21632855›Full record

Trial reportClinical cancer research : an official journal of the American Association for Cancer Research2011

Impact of clinical and pathologic features on tumor-infiltrating lymphocyte expansion from surgically excised melanoma metastases for adoptive T-cell therapy.

Richard W Joseph, Vijay R Peddareddigari, Ping Liu, Priscilla W Miller, Willem W Overwijk, Nebiyou B Bekele, Merrick I Ross, Jeffrey E Lee, Jeffrey E Gershenwald, Anthony Lucci and 9 more

Abstract readClinical Trial
In one paragraph

Trial report in Clinical cancer research : an official journal of the American Association for Cancer Research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 53 citations in OpenAlex.

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  11. Strategies to sensitize cancer cells to immunotherapy.Human vaccines & immunotherapeutics · 2021
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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

19 authors at 1 institution in 1 country.

Richard W JosephDepartment of Melanoma Medical Oncology, The University of Texas, M.D. Anderson Cancer Center, Houston, Texas 77030, USA.
Vijay R Peddareddigari
Ping Liu
Priscilla W Miller
Willem W Overwijk
Nebiyou B Bekele
Merrick I Ross
Jeffrey E Lee
Jeffrey E Gershenwald
Anthony Lucci
Victor G Prieto
John D McMannis
Nicholas Papadopoulos
Kevin Kim
Jade Homsi
Agop Bedikian
Wen-Jen Hwu
Patrick Hwu
Laszlo G Radvanyi
The University of Texas MD Anderson Cancer Center · US

Funding

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 1R01 CA111999-01A2NCI NIH HHS R01 CA111999
6 · The paper itself

Abstract

purposeClinical trials on adoptive T-cell therapy (ACT) using expanded tumor-infiltrating lymphocytes (TIL) have shown response rates of over 50% in refractory melanoma. However, little is known how clinical and pathologic features impact TIL outgrowth isolated from metastatic melanoma tumors. EXPERIMENTAL

designWe analyzed the impact of clinical and pathologic features on initial TIL outgrowth in 226 consecutive patients undergoing tumor resection. Successful initial TIL outgrowth was defined as ≥40 million viable lymphocytes harvested from all tumor fragments in a 5-week culture. To normalize for the different size of resected tumors and thus available tumor fragments, we divided the number of expanded TIL by the starting number of tumor fragments (TIL/fragment).

resultsOverall, initial TIL outgrowth was successful in 62% of patients, with patients ≤30 years of age (94%; P = 0.01) and female patients (71% vs. 57% for males; P = 0.04) having the highest rate of success. Systemic therapy 30 days before tumor harvest negatively impacted initial TIL outgrowth compared to patients who never received systemic therapy (47% vs. 71%, P = 0.02). Biochemotherapy within 0 to 60 days of tumor harvest negatively impacted the initial TIL outgrowth with a success rate of only 16% (P < 0.0001).

conclusionParameters such as age, sex, and the type and timing of prior systemic therapy significantly affect the success rate of the initial TIL outgrowth from tumor fragments for ACT; these parameters may be helpful in selecting patients for melanoma ACT.

Indexed as

Immunotherapy, AdoptiveAdolescentAdultAgedAntineoplastic AgentsFemaleHumansLymphocytes, Tumor-InfiltratingMaleMelanomaMiddle AgedNeoplasm MetastasisNeoplasm StagingRisk FactorsTime FactorsTreatment OutcomeAntineoplastic Agents

Identifiers

PMID21632855
PMCPMC3139726
OpenAlexW2103555907

What OpenQuestion holds

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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.