Evidence map›Paper›PMID 26598942›Full record

ReviewNature reviews. Clinical oncology2016

Combination cancer immunotherapies tailored to the tumour microenvironment.

Mark J Smyth, Shin Foong Ngiow, Antoni Ribas, Michele W L Teng

2 registry-linked trialsAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Clinical oncology, 2016. 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 502 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
502citing papers in PubMed, 2 pooled it
35.6field-weighted citation impact, top 1% 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.

NCT04211168 phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

Toripalimab Plus Lenvatinib as Second-line Treatment in Advanced Biliary Tract Cancers: a Single-arm, Non-randomized, Single-center Clinical Trial and Biomarker Study

TypeinterventionalSponsorPeking Union Medical College HospitalRan2020 to 2024Enrolled44ConditionsAdvanced Biliary Tract CancerArmsToripalimab plus Lenvatinib
NCT05504252 phase2active not recruitingnot on this mapstarted 2022, after this paper: background citation

METIMMOX-2: Metastatic pMMR/MSS Colorectal Cancer - Shaping Anti-Tumor Immunity by Oxaliplatin

TypeinterventionalSponsorUniversity Hospital, AkershusRan2022 to 2028Enrolled80ConditionsColorectal Adenocarcinoma, Mucinous Adenocarcinoma, Signet Ring Cell AdenocarcinomaArmsNivolumab, Oxaliplatin
3 · Its place in the literature

Who cites it

502 citing papers in PubMed, 2 syntheses or guidelines pooled it, 965 citations in OpenAlex.

  1. Pooled it
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  12. Tumor cell intrinsic mechanisms of immune escape.Cell communication and signaling : CCS · 2026
    Review
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442 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

4 authors at 2 institutions in 2 countries.

Mark J SmythImmunology in Cancer and Infection Laboratory, QIMR Berghofer Medical Research Institute, Herston 4006, Queensland, Australia.
Shin Foong NgiowImmunology in Cancer and Infection Laboratory, QIMR Berghofer Medical Research Institute, Herston 4006, Queensland, Australia.
Antoni RibasDepartment of Medicine, Division of Haematology/Oncology, Jonsson Comprehensive Cancer Center at UCLA, Los Angeles, California 90095, USA.
Michele W L TengCancer Immunoregulation and Immunotherapy Laboratory QIMR Berghofer Medical Research Institute, Herston, 4006 Queensland, Australia.
QIMR Berghofer Medical Research Institute · AUUniversity of California, Los Angeles · US

Funding

Next Generation Cancer Immunotherapies to Defeat MelanomaR35CA197633 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ANTONI RIBAS · 2015 to 2026
$10.4M
NCI NIH HHS R35 CA197633
6 · The paper itself

Abstract

Evidence suggests that cancer immunotherapy will be a major part of the combination treatment plan for many patients with many cancer types in the near future. There are many types of immune processes involving different antitumour and tumour-promoting leucocytes, and tumour cells use many strategies to evade the immune response. The tumour microenvironment can help determine which immune suppressive pathways become activated to restrain antitumour immunity. This includes immune checkpoint receptors on effector T-cells and myeloid cells, and release of inhibitory cytokines and metabolites. Therapeutic approaches that target these pathways, particularly immune-checkpoint receptors, can induce durable antitumour responses in patients with advanced-stage cancers, including melanoma. Nevertheless, many patients do not have a good response to monotherapy approaches and alternative strategies are required to achieve optimal therapeutic benefit. These strategies include eliminating the bulk of tumour cells to provoke tumour-antigen release and antigen-presenting cell (APC) function, using adjuvants to enhance APC function, and using agents that enhance effector-cell activity. In this Review, we discuss the stratification of the tumour microenvironment according to tumour-infiltrating lymphocytes and PD-L1 expression in the tumour, and how this stratification enables the design of optimal combination cancer therapies tailored to target different tumour microenvironments.

Indexed as

Adjuvants, ImmunologicAnimalsAntibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenHumansImmunotherapyMolecular Targeted TherapyNeoplasmsSignal TransductionTreatment OutcomeTumor EscapeTumor MicroenvironmentAdjuvants, ImmunologicAntibodies, MonoclonalB7-H1 AntigenCD274 protein, human

Identifiers

PMID26598942
OpenAlexW2257916459

What OpenQuestion holds

Textmetadata
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.