Evidence map›Paper›PMID 26228759›Full record

ReviewNature reviews. Drug discovery2015

Combination cancer immunotherapy and new immunomodulatory targets.

Kathleen M Mahoney, Paul D Rennert, Gordon J Freeman

2 registry-linked trialsAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Drug discovery, 2015. 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 698 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
698citing papers in PubMed, 4 pooled it
63.1field-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.

NCT02886897 phase1 / phase2unknown statusnot on this mapstarted 2016, after this paper: background citation

A Phase II Study of Combinations of Dendritic Cells and Cytokine-induced Killer Cell (D-CIK) Immunotherapy And Anti-Programmed Death-1 In Refractory Solid Tumors

TypeinterventionalSponsorSun Yat-sen UniversityRan2016 to 2019Enrolled50ConditionsHepatocellular Carcinoma, Renal Cell Carcinoma, Bladder Cancer, Colorectal CancerArmsD-CIK and anti-PD-1 antibody
NCT03736330 phase2unknown statusnot on this mapstarted 2018, after this paper: background citation

A Study of Anti-PD-1( Pembrolizumab) Combinations of D-CIK (Cytokine-induced Killer Cells Are Stimulated Using Mature Dendritic Cells) Immunotherapy and Axitinib in Advanced Ranal Carcinoma

TypeinterventionalSponsorSun Yat-sen UniversityRan2018 to 2021Enrolled24ConditionsRenal Cancer MetastaticArmsCombinations treatment
3 · Its place in the literature

Who cites it

698 citing papers in PubMed, 4 syntheses or guidelines pooled it, 1,325 citations in OpenAlex.

  1. Pooled it
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  14. Strategies to target PD-1/PD-L1 in the tumor microenvironment.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
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  20. Metabolic Reprogramming ofCancer communications (London, England) · 2026
    Article

638 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

3 authors at 2 institutions in 1 country.

Kathleen M Mahoney1] Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02215, USA. [2] Division of Haematology and Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA. [3].
Paul D Rennert1] SugarCone Biotech, Holliston, Massachusetts 01746, USA. [2] Videre Biotherapeutics, Watertown, Massachusetts 02472, USA. [3].
Gordon J FreemanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02215, USA.
Dana-Farber Cancer Institute · USHarvard University · US

Funding

Treating the P13-Kinase/AKTP50CA101942 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI David McDermott · 2003 to 2026
$53.4M
TIM recognition of phosphatidylserine regulates innate and adaptive immunityP01AI054456 · NIAID · STANFORD UNIVERSITY · PI UMETSU, DALE T · 2003 to 2014
$12.8M
Role of Tumor Stroma in Therapeutic Response and ResistanceU54CA163125 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CHIN, LYNDA, FLAHERTY, KEITH T · 2011 to 2015
$4.4M
TIM recognition of PtdSer on apoptotic cells and the regulation of immunityR01AI089955 · NIAID · DANA-FARBER CANCER INST · PI DEKRUYFF, ROSEMARIE H, FREEMAN, GORDON JAMES · 2010 to 2014
$2.1M
NCI NIH HHS P50CA101942NCI NIH HHS U54CA163125NIAID NIH HHS P01AI054456NIAID NIH HHS R01AI089955
6 · The paper itself

Abstract

Targeting immune checkpoints such as programmed cell death protein 1 (PD1), programmed cell death 1 ligand 1 (PDL1) and cytotoxic T lymphocyte antigen 4 (CTLA4) has achieved noteworthy benefit in multiple cancers by blocking immunoinhibitory signals and enabling patients to produce an effective antitumour response. Inhibitors of CTLA4, PD1 or PDL1 administered as single agents have resulted in durable tumour regression in some patients, and combinations of PD1 and CTLA4 inhibitors may enhance antitumour benefit. Numerous additional immunomodulatory pathways as well as inhibitory factors expressed or secreted by myeloid and stromal cells in the tumour microenvironment are potential targets for synergizing with immune checkpoint blockade. Given the breadth of potential targets in the immune system, critical questions to address include which combinations should move forward in development and which patients will benefit from these treatments. This Review discusses the leading drug targets that are expressed on tumour cells and in the tumour microenvironment that allow enhancement of the antitumour immune response.

Indexed as

AnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenCTLA-4 AntigenHumansImmunotherapyMolecular Targeted TherapyNeoplasmsProgrammed Cell Death 1 ReceptorTumor MicroenvironmentAntineoplastic AgentsB7-H1 AntigenCD274 protein, humanCTLA-4 AntigenProgrammed Cell Death 1 Receptor

Identifiers

PMID26228759
OpenAlexW1942897646

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.