Evidence map›Paper›PMID 30100909›Full record

ReviewFrontiers in immunology2018

Combining Immune Checkpoint Inhibitors With Conventional Cancer Therapy.

Yiyi Yan, Anagha Bangalore Kumar, Heidi Finnes, Svetomir N Markovic, Sean Park, Roxana S Dronca, Haidong Dong

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 3 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

131 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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71 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

7 authors.

Yiyi YanDivision of Medical Oncology, Mayo Clinic, Rochester, MN, United States.
Anagha Bangalore KumarDepartment of Immunology, Mayo Clinic, Rochester, MN, United States.
Heidi FinnesDepartment of Pharmacy, Mayo Clinic, Rochester, MN, United States.
Svetomir N MarkovicDivision of Medical Oncology, Mayo Clinic, Rochester, MN, United States.
Sean ParkDepartment of Radiation Oncology, Mayo Clinic, Rochester, MN, United States.
Roxana S DroncaDivision of Hematology and Medical Oncology, Mayo Clinic, Jacksonville, FL, United States.
Haidong DongDepartment of Immunology, Mayo Clinic, Rochester, MN, United States.

Funding

Maternal Morbidity and Mortality: Risk Factors, Early Detection and Personalized InterventionUL1TR001409 · NCATS · GEORGETOWN UNIVERSITY · PI GONDRE-LEWIS, MARJORIE C, MELLMAN, THOMAS A · 2015 to 2024
$37.8M
Paul Calabresi Program in Clinical/Translational Research at Mayo ClinicK12CA090628 · NCI · MAYO CLINIC ROCHESTER · PI WEROHA, SARAVUT · 2001 to 2025
$19.7M
TRAINING GRANT IN CLINICAL PHARMACOLOGYT32GM008685 · NIGMS · MAYO CLINIC ROCHESTER · PI Liewei Wang · 1998 to 2026
$8.2M
Functional B7-H1 expressed by T cellsR01AI095239 · NIAID · MAYO CLINIC ROCHESTER · PI DONG, HAIDONG · 2014 to 2018
$2.0M
A Phase II Evaluation of SABR in Oligometastatic Castration-Refractory Prostate Cancer and Immunogenicity of SABRR01CA200551 · NCI · MAYO CLINIC ROCHESTER · PI DONG, HAIDONG, PARK, SEAN S · 2016 to 2018
$739k
Role of Bim and soluble B7-H1 in monitoring T cell responses to anti-PD-1 therapy in melanomaR21CA197878 · NCI · MAYO CLINIC ROCHESTER · PI DONG, HAIDONG, DRONCA, ROXANA S · 2015 to 2016
$374k
NCATS NIH HHS UL1 TR001409NCI NIH HHS K12 CA090628NCI NIH HHS R01 CA200551NCI NIH HHS R21 CA197878NIAID NIH HHS R01 AI095239NIGMS NIH HHS T32 GM008685
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) have recently revolutionized cancer treatment, providing unprecedented clinical benefits. However, primary or acquired therapy resistance can affect up to two-thirds of patients receiving ICIs, underscoring the urgency to elucidate the mechanisms of treatment resistance and to design more effective therapeutic strategies. Conventional cancer treatments, including cytotoxic chemotherapy, radiation therapy, and targeted therapy, have immunomodulatory effects in addition to direct cancer cell-killing activities. Their clinical utilities in combination with ICIs have been explored, aiming to achieve synergetic effects with improved and durable clinical response. Here, we will review the immunomodulatory effects of chemotherapy, targeted therapy, and radiation therapy, in the setting of ICI, and their clinical implications in reshaping modern cancer immunotherapy.

Indexed as

Combined Modality TherapyAnimalsAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorClinical Trials as TopicHumansImmunomodulationImmunotherapyMolecular Targeted TherapyNeoplasmsRadiotherapyTreatment OutcomeAntineoplastic Agents, ImmunologicalBiomarkers, Tumorchemotherapycombination therapyimmunotherapyradiotherapytargeted therapy

Identifiers

PMID30100909
PMCPMC6072836

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.