Evidence map›Paper›PMID 37558833›Full record

ArticleCommunications medicine2023

Ablative radiotherapy improves survival but does not cure autochthonous mouse models of prostate and colorectal cancer.

Daniel R Schmidt, Iva Monique T Gramatikov, Allison Sheen, Christopher L Williams, Martina Hurwitz, Laura E Dodge, Edward Holupka, W S Kiger, Milton R Cornwall-Brady, Wei Huang and 10 more

Open access · goldAbstract read
In one paragraph

Article in Communications medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Modulation of CD8International journal of molecular sciences · 2023
    Review
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

20 authors at 6 institutions in 1 country.

Daniel R SchmidtKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA. dschmidt@bidmc.harvard.edu.ORCID http://orcid.org/0000-0001-6192-0378
Iva Monique T GramatikovKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-5789-7961
Allison SheenKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Christopher L WilliamsHarvard Medical School, Boston, MA, USA.
Martina HurwitzDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Laura E DodgeHarvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-4024-2034
Edward HolupkaDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
W S KigerDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Milton R Cornwall-BradyKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Wei HuangKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Howard H MakKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Kathleen S CormierKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Charlene CondonKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
K Dane WittrupKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0003-2398-5896
Ömer H YilmazKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.ORCID http://orcid.org/0000-0002-7577-4612
Mary Ann StevensonDepartment of Radiation Oncology, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Julian D DownKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Scott R FloydDepartment of Radiation Oncology, Duke University School of Medicine, Durham, NC, USA.ORCID http://orcid.org/0000-0002-8067-2426
Jatin RoperKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Matthew G Vander HeidenKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA. mvh@mit.edu.ORCID http://orcid.org/0000-0002-6702-4192
Massachusetts Institute of Technology · USBeth Israel Deaconess Medical Center · USDuke University · USBrigham and Women's Hospital · USDana-Farber Cancer Institute · USHarvard University · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Kristin A Knouse · 1985 to 2026
$93.9M
The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
Tumor and Circulating Markers as Links Between Obesity and Lethal Prostate CanceP50CA090381 · NCI · DANA-FARBER CANCER INSTITUTE · PI KANTOFF, PHILIP W · 2002 to 2017
$36.2M
Institutional Career Development CoreKL2TR002542 · NCATS · HARVARD MEDICAL SCHOOL · PI BREDELLA, MIRIAM ANTOINETTE, RUTKOVE, SEWARD B. · 2018 to 2022
$8.7M
Understanding the role of metabolism in cancerR35CA242379 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI VANDER HEIDEN, MATTHEW G. · 2019 to 2025
$5.8M
Adipose tissue-colorectal tumor cross-talk: new targets for breaking the obesity-cancer linkR01CA254108 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI HURSTING, STEPHEN D, ULRICH, CORNELIA M · 2021 to 2025
$3.2M
Targeting plasma membrane spatial dynamics to suppress aberrant Wnt signalingR01CA244359 · NCI · TEXAS A&M AGRILIFE RESEARCH · PI CHAPKIN, ROBERT STEPHEN, KARPAC, JASON S · 2020 to 2024
$2.7M
Role of immune regulation in colorectal cancer chemotherapeutic responseR01CA256530 · NCI · YALE UNIVERSITY · PI LU, JUN · 2021 to 2025
$2.4M
Wnt signaling in obesity-associated colorectal cancerR37CA259363 · NCI · DUKE UNIVERSITY · PI Jatin Roper · 2022 to 2026
$1.8M
Ultra-bright fluorescent nanoparticles for colorectal adenoma detectionR21DK125911 · NIDDK · DUKE UNIVERSITY · PI ROPER, JATIN, SOKOLOV, IGOR · 2021 to 2022
$461k
Inhibition of CaMKK2 sensitizes rectal cancers to radiation therapyR21CA256414 · NCI · DUKE UNIVERSITY · PI LEE, CHANG-LUNG, ROPER, JATIN · 2021 to 2022
$409k
Low Cost Spectroscopic OCT for GI ApplicationsR41EB032693 · NIBIB · LUMEDICA, INC. · PI BROWN, WILLIAM · 2021 to 2021
$256k
NCATS NIH HHS KL2 TR002542NCATS NIH HHS UL1 TR002541NCI NIH HHS P30 CA014051NCI NIH HHS P50 CA090381NCI NIH HHS R01 CA244359NCI NIH HHS R01 CA254108NCI NIH HHS R01 CA256530NCI NIH HHS R21 CA256414NCI NIH HHS R35 CA242379NCI NIH HHS R37 CA259363NIBIB NIH HHS R41 EB032693NIDDK NIH HHS R21 DK125911
6 · The paper itself

Abstract

backgroundGenetically engineered mouse models (GEMMs) of cancer are powerful tools to study mechanisms of disease progression and therapy response, yet little is known about how these models respond to multimodality therapy used in patients. Radiation therapy (RT) is frequently used to treat localized cancers with curative intent, delay progression of oligometastases, and palliate symptoms of metastatic disease.

methodsHere we report the development, testing, and validation of a platform to immobilize and target tumors in mice with stereotactic ablative RT (SART). Xenograft and autochthonous tumor models were treated with hypofractionated ablative doses of radiotherapy.

resultsWe demonstrate that hypofractionated regimens used in clinical practice can be effectively delivered in mouse models. SART alters tumor stroma and the immune environment, improves survival in GEMMs of primary prostate and colorectal cancer, and synergizes with androgen deprivation in prostate cancer. Complete pathologic responses were achieved in xenograft models, but not in GEMMs.

conclusionsWhile SART is capable of fully ablating xenografts, it is unable to completely eradicate disease in GEMMs, arguing that resistance to potentially curative therapy can be modeled in GEMMs.

Identifiers

PMID37558833
PMCPMC10412558
OpenAlexW4385700004

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.