Evidence map›Paper›PMID 25869387›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2015

Ablative Tumor Radiation Can Change the Tumor Immune Cell Microenvironment to Induce Durable Complete Remissions.

Alexander Filatenkov, Jeanette Baker, Antonia M S Mueller, Justin Kenkel, G-One Ahn, Suparna Dutt, Nigel Zhang, Holbrook Kohrt, Kent Jensen, Sussan Dejbakhsh-Jones and 4 more

2 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 270 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
270citing papers in PubMed, 3 pooled it
15.8field-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.

NCT04289792 phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

Chemotherapy-based Split Stereotactic Body Radiation Therapy for Borderline Resectable and Locally Advanced Pancreatic Cancer: Study Protocol of a Prospective, Single-arm Phase II Trial

TypeinterventionalSponsorFujian Medical University Union HospitalRan2020 to 2025Enrolled27ConditionsPancreatic NeoplasmsArmsnab-Paclitaxel+Gemcitabine, split-course SBRT
NCT07052669 phase3recruitingnot on this mapstarted 2025, after this paper: background citation

Hypofractionated Chemoradiotherapy Followed by Consolidative Immunotherapy Versus Conventional Fractionated Chemoradiotherapy Followed by Consolidative Immunotherapy in Locally Advanced Non-small Cell Lung Cancer: A Randomized, Phase III Controlled Study

TypeinterventionalSponsorSun Yat-sen UniversityRan2025 to 2029Enrolled311ConditionsLocally Advanced Non-Small Cell Lung CancerArmsHypofractionated Radiation Therapy, Conventionally Fractionated Radiation Therapy, Concurrent Chemotherapy, concurrent chemotherapy, Consolidative immunotherapy
3 · Its place in the literature

Who cites it

270 citing papers in PubMed, 3 syntheses or guidelines pooled it, 470 citations in OpenAlex.

  1. Journal of gastrointestinal cancer · 2025
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210 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

14 authors at 3 institutions in 1 country.

Alexander FilatenkovDivision of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, California. sstrober@stanford.edu afilaten@standord.edu.
Jeanette BakerDivision of Blood and Bone Marrow Transplantation, Department of Medicine, Stanford University, School of Medicine, Stanford, California.
Antonia M S MuellerDivision of Blood and Bone Marrow Transplantation, Department of Medicine, Stanford University, School of Medicine, Stanford, California.
Justin KenkelDepartment of Pathology, Stanford University School of Medicine, Stanford, California.
G-One AhnDivision of Radiation and Cancer Biology, Department of Radiation Oncology, Stanford University School of Medicine, Stanford, California.
Suparna DuttDivision of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Nigel ZhangDivision of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Holbrook KohrtDivision of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Kent JensenDivision of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Sussan Dejbakhsh-JonesDivision of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Judith A ShizuruDivision of Blood and Bone Marrow Transplantation, Department of Medicine, Stanford University, School of Medicine, Stanford, California.
Robert N NegrinDivision of Blood and Bone Marrow Transplantation, Department of Medicine, Stanford University, School of Medicine, Stanford, California.
Edgar G EnglemanDepartment of Pathology, Stanford University School of Medicine, Stanford, California.
Samuel StroberDivision of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, California. sstrober@stanford.edu afilaten@standord.edu.
Stanford University · USStanford Blood Center · USStanford Medicine · US

Funding

Radiotherapy as Immunotherapy of TumorsR01CA163441 · NCI · STANFORD UNIVERSITY · PI STROBER, SAMUEL · 2012 to 2016
$2.2M
NCI NIH HHS R01 CA-163441NCI NIH HHS R01 CA163441
6 · The paper itself

Abstract

purposeThe goals of the study were to elucidate the immune mechanisms that contribute to desirable complete remissions of murine colon tumors treated with single radiation dose of 30 Gy. This dose is at the upper end of the ablative range used clinically to treat advanced or metastatic colorectal, liver, and non-small cell lung tumors. EXPERIMENTAL

designChanges in the tumor immune microenvironment of single tumor nodules exposed to radiation were studied using 21-day (>1 cm in diameter) CT26 and MC38 colon tumors. These are well-characterized weakly immunogenic tumors.

resultsWe found that the high-dose radiation transformed the immunosuppressive tumor microenvironment resulting in an intense CD8(+) T-cell tumor infiltrate, and a loss of myeloid-derived suppressor cells (MDSC). The change was dependent on antigen cross-presenting CD8(+) dendritic cells, secretion of IFNγ, and CD4(+)T cells expressing CD40L. Antitumor CD8(+) T cells entered tumors shortly after radiotherapy, reversed MDSC infiltration, and mediated durable remissions in an IFNγ-dependent manner. Interestingly, extended fractionated radiation regimen did not result in robust CD8(+) T-cell infiltration.

conclusionsFor immunologically sensitive tumors, these results indicate that remissions induced by a short course of high-dose radiotherapy depend on the development of antitumor immunity that is reflected by the nature and kinetics of changes induced in the tumor cell microenvironment. These results suggest that systematic examination of the tumor immune microenvironment may help in optimizing the radiation regimen used to treat tumors by adding a robust immune response.

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorColonic NeoplasmsDendritic CellsHumansMiceMyeloid CellsRemission InductionTumor Microenvironment

Identifiers

PMID25869387
PMCPMC4537844
OpenAlexW2150293352

What OpenQuestion holds

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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.