Evidence map›Paper›PMID 30413527›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2019

The Reciprocity between Radiotherapy and Cancer Immunotherapy.

Yifan Wang, Zhi-Gang Liu, Hengfeng Yuan, Weiye Deng, Jing Li, Yuhui Huang, Betty Y S Kim, Michael D Story, Wen Jiang

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05798845 (Exploratory Phase II Clinical Study of Toripalimab Plus Radiotherapy Versus Toripalimab Plus Chemotherapy for the Neoadjuvant Treatment of Operable Stage II-IIIA), which is not on this map. Cited by 116 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed, 3 pooled it
3.4field-weighted citation impact, top 5% 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.

NCT05798845 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

Exploratory Phase II Clinical Study of Toripalimab Plus Radiotherapy Versus Toripalimab Plus Chemotherapy for the Neoadjuvant Treatment of Operable Stage II-IIIA (N+) Non-small Cell Lung Cancer (NSCLC)

TypeinterventionalSponsorShanghai Chest HospitalRan2025 to 2026Enrolled124ConditionsNSCLCArmsSBRT+LDRT, Toripalimab, Chemotherapy drug
3 · Its place in the literature

Who cites it

116 citing papers in PubMed, 3 syntheses or guidelines pooled it, 175 citations in OpenAlex.

  1. Pooled it
  2. Effect ofFrontiers in pharmacology · 2025
    Pooled it
  3. Pooled it
  4. Camrelizumab, Apatinib, and Radiotherapy in Locally Advanced, Unresectable Hepatocellular Carcinoma: A Phase II Study.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Trial
  5. Trial
  6. Article
  7. Observational
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. A Review on Melanoma Brain Metastases.Current pharmaceutical design · 2026
    Review
  18. Article
  19. Article
  20. Article

56 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

9 authors at 6 institutions in 2 countries.

Yifan Wang *Department of Radiation Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas.ORCID 0000-0001-7387-0654
Zhi-Gang Liu *Department of Radiotherapy, Hunan Cancer Hospital, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, China.
Hengfeng YuanDepartment of Orthopedics, Zhongshan Hospital, Fudan University, Shanghai, China.
Weiye DengDepartment of Radiation Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas.
Jing LiDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Yuhui HuangCyrus Tang Hematology Center, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, China.ORCID 0000-0002-6226-2028
Betty Y S KimDepartment of Neurosurgery, Cancer Biology and Neurosciences, Mayo Clinic, Jacksonville, Florida.
Michael D StoryDepartment of Radiation Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas.
Wen JiangDepartment of Radiation Oncology, The University of Texas Southwestern Medical Center, Dallas, Texas. wen.jiang@utsouthwestern.edu.
The University of Texas Southwestern Medical Center · USThe University of Texas MD Anderson Cancer Center · USCentral South University · CNFudan University · CNJacksonville College · USSoochow University · CN

Funding

Therapeutic modulation of the phagocytosis axis as a novel glioblastoma immunotherapyR01NS104315 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KIM, BETTY · 2018 to 2022
$1.7M
NINDS NIH HHS R01 NS104315
6 · The paper itself

Abstract

The clinical success of immune checkpoint inhibitors in treating metastatic and refractory cancers has generated significant interest in investigating their role in treating locally advanced diseases, thus requiring them to be combined with standard treatments in the hope of producing synergistic antitumor responses. Radiotherapy, in particular, has long been hypothesized to have actions complementary to those of immune checkpoint blockade, and a growing body of evidence indicates that cancer immunotherapy may also have radiosensitizing effects, which would provide unique benefit for locoregional treatments. Recent studies have demonstrated that when immune cells are activated by immunotherapeutics, they can reprogram the tumor microenvironment in ways that may potentially increase the radiosensitivity of the tumor. In this review, we highlight the evidence that supports reciprocal interactions between cancer immunotherapy and radiotherapy, where in addition to the traditional notion that radiation serves to enhance the activation of antitumor immunity, an alternative scenario also exists in which T-cell activation by cancer immunotherapy may sensitize tumors to radiation treatment through mechanisms that include normalization of the tumor vasculature and tissue hypoxia. We describe the empirical observations from preclinical models that support such effects and discuss their implications for future research and trial design.

Indexed as

AnimalsAntineoplastic Agents, ImmunologicalCell Line, TumorClinical Trials as TopicCombined Modality TherapyCostimulatory and Inhibitory T-Cell ReceptorsDisease Models, AnimalHumansImmunotherapyNeoplasmsRadiation ToleranceRadiotherapyResearch DesignT-LymphocytesTumor EscapeTumor MicroenvironmentAntineoplastic Agents, ImmunologicalCostimulatory and Inhibitory T-Cell Receptors

Identifiers

PMID30413527
PMCPMC6420874
OpenAlexW2899706009

What OpenQuestion holds

Textmetadata
LicenceTDM
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.