Evidence map›Paper›PMID 20386463›Full record

Trial reportJournal of immunotherapy (Hagerstown, Md. : 1997)2010

Regulatory (FoxP3+) T-cell tumor infiltration is a favorable prognostic factor in advanced colon cancer patients undergoing chemo or chemoimmunotherapy.

Pierpaolo Correale, Maria Saveria Rotundo, Maria Teresa Del Vecchio, Cinzia Remondo, Cristina Migali, Chiara Ginanneschi, Kwong Y Tsang, Antonella Licchetta, Susanna Mannucci, Lucia Loiacono and 3 more

Open access · greenAbstract readClinical Trial, Phase IIIComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of immunotherapy (Hagerstown, Md. : 1997), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 4 pooled it
10.4field-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.

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

125 citing papers in PubMed, 4 syntheses or guidelines pooled it, 208 citations in OpenAlex.

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65 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

13 authors at 3 institutions in 2 countries.

Pierpaolo CorrealeDepartment Giorgio Segre of Pharmacology, Siena University School of Medicine, Italy.
Maria Saveria Rotundo
Maria Teresa Del Vecchio
Cinzia Remondo
Cristina Migali
Chiara Ginanneschi
Kwong Y Tsang
Antonella Licchetta
Susanna Mannucci
Lucia Loiacono
Pierfrancesco Tassone
Guido Francini
Pierosandro Tagliaferri
Magna Graecia University · ITUniversity of Siena · ITNational Cancer Institute · US

Funding

Identification of human tumor-associated antigensZIABC010972 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TSANG, KWONG YOK · 2009 to 2016
$6.0M
Analyses of human T regulatory cellsZIABC010973 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TSANG, KWONG YOK · 2009 to 2016
$3.7M
Analyses of human T regulatory cellsZ01BC010973 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TSANG, KWONG YOK · 2008 to 2008
$525k
Intramural NIH HHS Z01 BC010973Intramural NIH HHS ZIA BC010972
6 · The paper itself

Abstract

Antitumor immune response and chemotherapy-induced immunomodulation in colon cancer patients represented the rationale to design new strategies, like GOLFIG chemoimmunotherapy (gemcitabine, oxaliplatin, 5-fluorouracil/folinic acid, granulocyte macrophage colony-stimulating factor, and aldesleukine), that resulted a safe and very active regimen. Antitumor activity and immunity feedback to GOLFIG were strictly correlated with the best outcome observed in patients with autoimmunity signs, increase of central memory T cells, and decrease of regulatory T cells (Treg) in the peripheral blood. We thus investigated a potential correlation between the Treg tumor infiltration at diagnosis and the clinical outcome in a current randomized phase 3 trial aimed to compare the GOLFIG regimen with the standard FOLFOX chemotherapy (GOLFIG-2). An immunohistochemistry study was carried out to quantify the infiltration of Treg/FoxP3+ T lymphocytes in tumor samples of 57 patients enrolled in the GOLFIG-2 trial. Treg tumor infiltration scores were correlated with overall survival, treatment-relative survival, and progression-free survival (PFS). Higher Treg tumor infiltration scores were associated with a better prognosis in the whole series (Treg high score vs. low score: overall survival=mean 43.2 mo vs. 28.6 mo, P=0.0005) and a better outcome after treatment (Treg high score vs. low score: PFS=mean 15.8 mo vs. 8.8 mo, P=0.0009; treatment-relative survival=mean 23.1 mo vs. 18.2 mo, P=0.004). PFS was significantly longer in GOLFIG high versus all other subgroups (mean 18.1 mo vs. 9.9 mo, P=0.01). Our results suggest that a higher FoxP3+ T-lymphocyte tumor infiltration score is a favorable prognostic factor in colon cancer patients undergoing chemo or chemoimmunotherapy.

Indexed as

ImmunotherapyAntineoplastic Combined Chemotherapy ProtocolsCarcinomaColonic NeoplasmsCombined Modality TherapyDeoxycytidineDisease ProgressionFemaleFluorouracilForkhead Transcription FactorsGemcitabineGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunohistochemistryLeucovorinLymphocytes, Tumor-InfiltratingDeoxycytidineFluorouracilForkhead Transcription FactorsFOXP3 protein, humanGemcitabineGranulocyte-Macrophage Colony-Stimulating FactorLeucovorinOrganoplatinum CompoundsOxaliplatinRecombinant Proteins

Identifiers

PMID20386463
PMCPMC7322625
OpenAlexW1993546867

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.