Evidence map›Paper›PMID 34530092›Full record

ArticleInternational journal of radiation oncology, biology, physics2022

Boosting the Abscopal Effect Using Immunogenic Biomaterials With Varying Radiation Therapy Field Sizes.

Sayeda Yasmin-Karim, Bashkim Ziberi, Johanna Wirtz, Noella Bih, Michele Moreau, Romy Guthier, Victoria Ainsworth, Juergen Hesser, G Mike Makrigiorgos, Michael D Chuong and 3 more

Registry-linked trialAbstract read
In one paragraph

Article in International journal of radiation oncology, biology, physics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06363773 (Pilot, Exploratory, Prospective Study to Assess the Ability of Stereotactic Radiotherapy to Restore the Efficacy of Anti-PD1 Immunotherapy in Initially Long-responder Patients With Metastatic Progression.), which is not on this map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT06363773 narecruitingnot on this mapstarted 2026, after this paper: background citation

Pilot, Exploratory, Prospective Study to Assess the Ability of Stereotactic Radiotherapy to Restore the Efficacy of Anti-PD1 Immunotherapy in Initially Long-responder Patients With Metastatic Progression.

TypeinterventionalSponsorElsanRan2026 to 2028Enrolled35ConditionsMetastatic CancerArmsStereotactic Radiotherapy
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. Democratizing FLASH Radiotherapy.Seminars in radiation oncology · 2024
    Review
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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

13 authors.

Sayeda Yasmin-KarimDana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts. Electronic address: sayeda_yasmin-karim@dfci.harvard.edu.
Bashkim ZiberiDana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts; University of Tetova, Tetova, Republic of North Macedonia.
Johanna WirtzDana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts; Medical Faculty of University Ulm, Ulm, Germany.
Noella BihDana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Michele MoreauDana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts; University of Massachusetts, Lowell, Massachusetts; Department of Radiation Oncology and Molecular Radiation Sciences, Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Romy GuthierDana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts; Data Analysis and Modeling in Medicine, Mannheim Institute for Intelligent Systems in Medicine (MIISM), Heidelberg University, Heidelberg, Germany.
Victoria AinsworthDana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts; University of Massachusetts, Lowell, Massachusetts.
Juergen HesserData Analysis and Modeling in Medicine, Mannheim Institute for Intelligent Systems in Medicine (MIISM), Heidelberg University, Heidelberg, Germany.
G Mike MakrigiorgosDana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Michael D ChuongMiami Cancer Institute, Baptist Health South Florida, Miami, Florida.
Xiao WeiDana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Paul L NguyenDana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Wilfred NgwaDana Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts; University of Massachusetts, Lowell, Massachusetts; Department of Radiation Oncology and Molecular Radiation Sciences, Dana Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.

Funding

Biomaterial Drones for Image-Guided Drug Delivery during radiotherapyR01CA239042 · NCI · JOHNS HOPKINS UNIVERSITY · PI NGWA, WILFRED · 2019 to 2023
$3.2M
Primers: Combining Radiotherapy and Immunotherapy using next genertaion radiotherapy biomaterialsR21CA205094 · NCI · DANA-FARBER CANCER INST · PI NGWA, WILFRED · 2017 to 2018
$421k
NCI NIH HHS R01 CA239042NCI NIH HHS R21 CA205094
6 · The paper itself

Abstract

purposePersistent immunosuppression in the tumor microenvironment is a major limitation to boosting the abscopal effect, whereby radiation therapy at 1 site can lead to regression of tumors at distant sites. Here, we investigate the use of radiation and immunogenic biomaterials (IBM) targeting only the gross tumor volume/subvolume for boosting the abscopal effect in immunologically cold tumors. METHODS AND MATERIALS: To evaluate the abscopal effect, 2 syngeneic contralateral tumors were implanted in each mouse, where only 1 tumor was treated. IBM was administered to the treated tumor with 1 fraction of radiation and results were compared, including as a function of different radiation therapy field sizes. The IBM was designed similar to fiducial markers using immunogenic polymer components loaded with anti-CD40 agonist. Tumor volumes of both treated and untreated tumors were measured over time, along with survival and corresponding immune cell responses.

resultsResults showed that radiation with IBM administered to the gross tumor subvolume can effectively boost abscopal responses in both pancreatic and prostate cancers, significantly increasing survival (P < .0001 and P < .001, respectively). Results also showed equal or superior abscopal responses when using field sizes smaller than the gross tumor volume compared with irradiating the whole tumor volume. These results were buttressed by observation of higher infiltration of cytotoxic CD8+ T-lymphocytes in the treated tumors (P < .0001) and untreated tumors (P < .0001) for prostate cancer. Significantly higher infiltration was also observed in treated tumors (P < .0001) and untreated tumors P < .01) for pancreatic cancer. Moreover, the immune responses were accompanied by a positive shift of proinflammatory cytokines in both prostate and pancreatic tumors.

conclusionsThe approach targeting gross tumor subvolumes with radiation and IBM offers opportunity for boosting the abscopal effect while significantly minimizing healthy tissue toxicity. This approach proffers a radioimmunotherapy dose-painting strategy that can be developed for overcoming current barriers of immunosuppression especially for immunologically cold tumors.

Indexed as

Biocompatible MaterialsNeoplasmsAnimalsCD8-Positive T-LymphocytesMaleMiceRadioimmunotherapyTumor BurdenTumor MicroenvironmentBiocompatible Materials

Identifiers

PMID34530092
PMCPMC8750216

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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.