Evidence map›Paper›PMID 29844122›Full record

ArticleCancer research2018

Radiotherapy and CD40 Activation Separately Augment Immunity to Checkpoint Blockade in Cancer.

Andrew J Rech, Hannah Dada, Jonathan J Kotzin, Jorge Henao-Mejia, Andy J Minn, Christina Twyman-Saint Victor, Robert H Vonderheide

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

80 citing papers in PubMed, 108 citations in OpenAlex.

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20 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

7 authors at 1 institution in 1 country.

Andrew J RechAbramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, Pennsylvania.
Hannah DadaDepartment of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Jonathan J KotzinDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Jorge Henao-MejiaDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Andy J MinnAbramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, Pennsylvania.
Christina Twyman-Saint Victor *Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Robert H Vonderheide *Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, Pennsylvania. rhv@upenn.edu.
University of Pennsylvania · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
Radiation and checkpoint blockade for cancer immune therapyP01CA210944 · NCI · UNIVERSITY OF PENNSYLVANIA · PI MINN, ANDY J · 2017 to 2022
$11.5M
HEMATOPOIESIS TRAINING GRANTT32DK007780 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI TONG, WEI · 1999 to 2023
$6.7M
Immunobiology and immunotherapy of pancreatic cancerR01CA169123 · NCI · UNIVERSITY OF PENNSYLVANIA · PI STANGER, BEN Z, VONDERHEIDE, ROBERT H · 2012 to 2016
$3.1M
Regulation of short-lived myeloid cells by the novel long non-coding RNA MorrbidR01HL136572 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI HENAO-MEJIA, JORGE · 2017 to 2021
$2.0M
Regulation of a DNA damage response network in glioblastomaR01CA172651 · NCI · UNIVERSITY OF PENNSYLVANIA · PI MINN, ANDY J · 2013 to 2017
$1.7M
Regulation of adipose tissue inflammation by the miR-181 familyR21DK111755 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI HENAO-MEJIA, JORGE · 2016 to 2018
$604k
Regulation of group 1 ILCs by a novel lncRNAR21AI128060 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI HENAO-MEJIA, JORGE · 2017 to 2018
$443k
Long non-coding RNA regulation of short-lived myeloid homeostasisF30HL138739 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI KOTZIN, JONATHAN J · 2017 to 2018
$39k
NCI NIH HHS P01 CA210944NCI NIH HHS P30 CA016520NCI NIH HHS R01 CA169123NCI NIH HHS R01 CA172651NHLBI NIH HHS F30 HL138739NHLBI NIH HHS R01 HL136572NIAID NIH HHS R21 AI128060NIDDK NIH HHS R21 DK111755NIDDK NIH HHS T32 DK007780
6 · The paper itself

Abstract

Immunotherapy in pancreatic ductal adenocarcinoma (PDA) remains a difficult clinical problem despite success in other disease types with immune checkpoint blockade (ICB) and chimeric antigen receptor T-cell therapy. Mechanisms driving immunosuppression and poor T-cell infiltration in PDA are incompletely understood. Here, we use genetically engineered mouse models of PDA that recapitulate hallmarks of human disease to demonstrate that CD40 pathway activation is required for clinical response to radiotherapy and ICB with αCTLA-4 and αPD-1. The combination of an agonist αCD40 antibody, radiotherapy, and dual ICB eradicated irradiated and unirradiated (i.e., abscopal) tumors, generating long-term immunity. Response required T cells and also short-lived myeloid cells and was dependent on the long noncoding RNA myeloid regulator

Indexed as

Adaptive ImmunityAnimalsAntigen-Presenting CellsCarcinoma, Pancreatic DuctalCD40 AntigensCD8-Positive T-LymphocytesCell Line, TumorFemaleImmune ToleranceImmunotherapyImmunotherapy, AdoptiveMaleMiceMice, Inbred C57BLPancreatic NeoplasmsTumor MicroenvironmentCD40 Antigens

Identifiers

PMID29844122
PMCPMC6415684
OpenAlexW2807087106

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.