Evidence map›Paper›PMID 31658994›Full record

Trial reportCancer immunology research2019

Phase II Trial of Ipilimumab with Stereotactic Radiation Therapy for Metastatic Disease: Outcomes, Toxicities, and Low-Dose Radiation-Related Abscopal Responses.

James W Welsh, Chad Tang, Patricia de Groot, Aung Naing, Kenneth R Hess, John V Heymach, Vassiliki A Papadimitrakopoulou, Taylor R Cushman, Vivek Subbiah, Joe Y Chang and 21 more

2 registry-linked trialsAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Cancer immunology research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 91 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 2 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.

NCT02239900 phase1completednot on this map

Phase I/II Trial of Ipilimumab (Immunotherapy) and Hypofractionated Stereotactic Radiation Therapy in Patients With Advanced Solid Malignancies

TypeinterventionalSponsorM.D. Anderson Cancer CenterRan2014 to 2019Enrolled143ConditionsLiver Cancer, Lung CancerArmsIpilimumab, Stereotactic Body Radiation Therapy (SBRT)
NCT06349837 phase1recruitingnot on this mapstarted 2024, after this paper: background citation

Safety and Tolerability of Low Dose Radiotherapy Plus Concurrent Partial Stereotactic Ablative Radiotherapy (Eclipse-RT) and Tislelizumab in Patients With Bulky Tumors

TypeinterventionalSponsorSichuan UniversityRan2024 to 2028Enrolled24ConditionsSolid TumorArmsTislelizumab, Low Dose Radiotherapy, Stereotactic Ablative Radiotherapy
3 · Its place in the literature

Who cites it

91 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  7. Review
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  9. Timing matters: how mechanism-guided sequencing shapes the efficacy of radiotherapy-immunotherapy combinations : A systematic review.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2026
    Review
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  18. Observational
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31 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

31 authors.

James W Welsh *Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas. jwelsh@mdanderson.org.
Chad Tang *Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Patricia de GrootDepartment of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-6552-4644
Aung NaingDepartment of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-4803-8513
Kenneth R HessDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
John V HeymachDepartment of Thoracic and Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-9068-8942
Vassiliki A PapadimitrakopoulouDepartment of Thoracic and Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Taylor R CushmanDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Vivek SubbiahDepartment of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Joe Y ChangDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
George R SimonDepartment of Thoracic and Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Rishab RamapriyanDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Hampartsoum B BarsoumianDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Hari MenonDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Maria Angelica CortezDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Erminia MassarelliDepartment of Thoracic and Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Quynh NguyenDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Padmanee SharmaDepartment of Genitouirinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
James P AllisonDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-8980-5697
Adi DiabDepartment of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Vivek VermaDepartment of Radiation Oncology, Allegheny General Hospital, Pittsburgh, Pennsylvania.
Uma RajuDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Sherif G ShaabanDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ramona DaduDepartment of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Maria E CabanillasDepartment of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-5124-1811
Kelvin WangDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Clark AndersonDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Daniel R GomezDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Stephen HahnDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Ritsuko KomakiDepartment of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
David S HongDepartment of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-8721-1609

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Convalescent Plasma to Limit Coronavirus Associated ComplicationsUL1TR003167 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KARP, DANIEL D, MCPHERSON, DAVID D · 2019 to 2023
$45.3M
NCATS NIH HHS UL1 TR003167NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Ipilimumab is effective for patients with melanoma, but not for those with less immunogenic tumors. We report a phase II trial of ipilimumab with concurrent or sequential stereotactic ablative radiotherapy to metastatic lesions in the liver or lung (NCT02239900). Ipilimumab (every 3 weeks for 4 doses) was given with radiotherapy begun during the first dose (concurrent) or 1 week after the second dose (sequential) and delivered as 50 Gy in 4 fractions or 60 Gy in 10 fractions to metastatic liver or lung lesions. In total, 106 patients received ≥1 cycle of ipilimumab with radiation. Median follow-up was 10.5 months. Median progression-free survival time was 2.9 months (95% confidence interval, 2.45-3.40), and median overall survival time was not reached. Rates of clinical benefit of nonirradiated tumor volume were 26% overall, 28% for sequential versus 20% for concurrent therapy (

Indexed as

AdultAgedAged, 80 and overAntineoplastic Agents, ImmunologicalCombined Modality TherapyFemaleHumansIpilimumabLiver NeoplasmsLung NeoplasmsMaleMiddle AgedRadiosurgerySurvival AnalysisYoung AdultAntineoplastic Agents, ImmunologicalIpilimumab

Identifiers

PMID31658994
PMCPMC6891218

What OpenQuestion holds

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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.