Evidence map›Paper›PMID 32580338›Full record

ReviewInternational journal of molecular sciences2020

Combination of Ipilimumab and Nivolumab in Cancers: From Clinical Practice to Ongoing Clinical Trials.

Omid Kooshkaki, Afshin Derakhshani, Negar Hosseinkhani, Mitra Torabi, Sahar Safaei, Oronzo Brunetti, Vito Racanelli, Nicola Silvestris, Behzad Baradaran

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 3 pooled it
6.4field-weighted citation impact, top 2% 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.

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

82 citing papers in PubMed, 3 syntheses or guidelines pooled it, 128 citations in OpenAlex.

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22 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 4 institutions in 2 countries.

Omid KooshkakiStudent Research Committee, Birjand University of Medical Sciences, Birjand 9717853577, Iran.ORCID 0000-0002-0398-6587
Afshin DerakhshaniImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 5165665811, Iran.ORCID 0000-0002-3243-233X
Negar HosseinkhaniDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz 5166614766, Iran.
Mitra TorabiStudent Research Committee, Tabriz University of Medical Sciences, Tabriz 5165665811, Iran.
Sahar SafaeiImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 5165665811, Iran.
Oronzo BrunettiNedical Oncology Unit, IRCCS IstitutoTumori "Giovanni Paolo II" of Bari, 70124 Bari, Italy.ORCID 0000-0002-7014-6828
Vito RacanelliDepartment of Biomedical Sciences and Human Oncology, University of Bari "Aldo Moro", 70124 Bari, Italy.ORCID 0000-0002-8639-1940
Nicola SilvestrisNedical Oncology Unit, IRCCS IstitutoTumori "Giovanni Paolo II" of Bari, 70124 Bari, Italy.ORCID 0000-0001-7814-7318
Behzad BaradaranImmunology Research Center, Tabriz University of Medical Sciences, Tabriz 5165665811, Iran.ORCID 0000-0002-8642-6795
Tabriz University of Medical Sciences · IRIstituto Tumori Bari · ITBirjand University of Medical Sciences · IRUniversity of Bari Aldo Moro · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) and programmed cell death protein 1 (PD-1) are inhibitory checkpoints that are commonly seen on activated T cells and have been offered as promising targets for the treatment of cancers. Immune checkpoint inhibitors (ICIs)targeting PD-1, including pembrolizumab and nivolumab, and those targeting its ligand PD-L1, including avelumab, atezolizumab, and durvalumab, and two drugs targeting CTLA-4, including ipilimumab and tremelimumab have been approved for the treatment of several cancers and many others are under investigating in advanced trial phases. ICIs increased antitumor T cells' responses and showed a key role in reducing the acquired immune system tolerance which is overexpressed by cancer and tumor microenvironment. However, 50% of patients could not benefit from ICIs monotherapy. To overcome this, a combination of ipilimumab and nivolumab is frequently investigated as an approach to improve oncological outcomes. Despite promising results for the combination of ipilimumab and nivolumab, safety concerns slowed down the development of such strategies. Herein, we review data concerning the clinical activity and the adverse events of ipilimumab and nivolumab combination therapy, assessing ongoing clinical trials to identify clinical outlines that may support combination therapy as an effective treatment. To the best of our knowledge, this paper is one of the first studies to evaluate the efficacy and safety of ipilimumab and nivolumab combination therapy in several cancers.

Indexed as

Practice Patterns, Physicians'Antineoplastic Combined Chemotherapy ProtocolsClinical Trials as TopicHumansIpilimumabNeoplasmsNivolumabPrognosisIpilimumabNivolumabcancercombination therapyimmune checkpoint inhibitorsipilimumabnivolumab

Identifiers

PMID32580338
PMCPMC7352976
OpenAlexW3036371943

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.