Evidence map›Paper›PMID 41182431›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2026

Facts and Hopes in Radioimmunotherapy for Localized Stages of Cancer.

Carlo Bosi, Alice Y Ho, Fabiana Gregucci, Silvia C Formenti

Abstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

4 authors.

Carlo BosiDepartment of Radiation Oncology, New York-Presbyterian/Weill Cornell Medicine, New York, New York.ORCID 0000-0002-7719-8428
Alice Y HoDepartment of Radiation Oncology, Duke University Medical Center, Durham, North Carolina.ORCID 0000-0002-6812-4187
Fabiana GregucciDepartment of Radiation Oncology, New York-Presbyterian/Weill Cornell Medicine, New York, New York.ORCID 0000-0002-9947-9650
Silvia C FormentiDepartment of Radiation Oncology, New York-Presbyterian/Weill Cornell Medicine, New York, New York.ORCID 0000-0002-8227-8924

Funding

Radiation Effect on Immune Cells and the MicrobiomeU54CA274291 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI Encouse Golden · 2022 to 2026
$9.1M
Immunomodulation of breast cancer via TLR7 agonist imiquimod and radiotherapy.R01CA161891 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI ADAMS, SYLVIA, FORMENTI, SILVIA C. · 2011 to 2015
$1.7M
American-Italian Cancer Foundation (AICF)NCI NIH HHS R01 CA161891NCI NIH HHS U54 CA274291Transformative Breast Cancer Consortium Award BC201085P3U.S. Department of Defense (DOD) BC180476P1U.S. Department of Defense (DOD) BC180595
6 · The paper itself

Abstract

Radiotherapy (RT) has emerged as a promising partner to immunotherapy, owing to its capacity to induce immunogenic tumor cell death, modulate the tumor microenvironment, and prime systemic antitumor immunity. Preclinical studies demonstrate that focal RT elicits a variety of immunologic effects, recruiting both the innate and adaptive immune system, that enable it to function as an in situ vaccine. Translational work has underscored the relevance of RT fractionation, timing, and field choice to enhance synergy with immune checkpoint inhibitors. In this review, we examine the clinical rationale and translational progress underpinning RT-immunotherapy combinations in the localized, nonmetastatic setting of cancer. We summarize the results of pivotal trials that have tested the immunogenic use of RT across multiple disease sites in combination with immune checkpoint inhibitors and propose interpretations for the results of these trials. Finally, we highlight emerging opportunities to optimize radiation-immunotherapy through rational treatment sequencing, the choice of the immunotherapy partner for combinations, and the emerging development of a biomarker-informed patient selection. We conclude by emphasizing the importance of better understanding, in human specimens, how irradiated cancers and normal tissues shape local and systemic immune responses to inform a more rational design of the next generation of RT-immunotherapy clinical trials.

Indexed as

NeoplasmsRadioimmunotherapyAnimalsClinical Trials as TopicCombined Modality TherapyHumansImmune Checkpoint InhibitorsImmunotherapyNeoplasm StagingTumor MicroenvironmentImmune Checkpoint Inhibitors

Identifiers

PMID41182431
PMCPMC12938856

What OpenQuestion holds

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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.