Evidence map›Paper›PMID 31700993›Full record

ReviewNPJ breast cancer2019

If we build it they will come: targeting the immune response to breast cancer.

Margaret E Gatti-Mays, Justin M Balko, Sofia R Gameiro, Harry D Bear, Sangeetha Prabhakaran, Jami Fukui, Mary L Disis, Rita Nanda, James L Gulley, Kevin Kalinsky and 7 more

Open access · goldAbstract readReview
In one paragraph

Review in NPJ breast cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
139citing papers in PubMed, 1 pooled it
11.4field-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.

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

139 citing papers in PubMed, 1 synthesis or guideline pooled it, 198 citations in OpenAlex.

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79 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

17 authors at 14 institutions in 2 countries.

Margaret E Gatti-Mays1Laboratory of Tumor Immunology and Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD USA.
Justin M Balko2Department of Medicine and Breast Cancer Research Program, Vanderbilt University Medical Center, Nashville, TN USA.ORCID 0000-0002-4263-5974
Sofia R Gameiro1Laboratory of Tumor Immunology and Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD USA.ORCID 0000-0002-2392-8122
Harry D Bear3Division of Surgical Oncology and the Massey Cancer Center, Virginia Commonwealth University, Richmond, VA USA.
Sangeetha Prabhakaran4Division of Surgical Oncology, Department of Surgery, University of New Mexico; University of New Mexico Comprehensive Cancer Center, Albuquerque, NM USA.
Jami Fukui5University of Hawaii Cancer Center, Honolulu, HI USA.
Mary L Disis6University of Washington, Seattle, WA USA.
Rita Nanda7The University of Chicago, Chicago, IL USA.
James L Gulley8Genitourinary Malignancies Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD USA.
Kevin Kalinsky9Columbia University Irving Medical Center, New York, NY USA.
Houssein Abdul Sater8Genitourinary Malignancies Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD USA.
Joseph A SparanoDepartment of Medical Oncology, Montefiore Medical Center, Albert Einstein Cancer Center, Albert Einstein College of Medicine, Bronx, NY USA.
David Cescon11Division of Medical Oncology and Hematology, Department of Medicine, Princess Margaret Cancer Centre, University Health Network and University of Toronto, Toronto, ON Canada.ORCID 0000-0002-1080-0998
David B Page12Providence Cancer Institute, Earle A. Chiles Research Institute, Portland, OR USA.
Heather McArthur13Cedars Sinai Medical Center, Los Angeles, CA USA.
Sylvia Adams14Perlmutter Cancer Center, NYU School of Medicine, New York, NY USA.
Elizabeth A Mittendorf15Division of Breast Surgery, Department of Surgery, Brigham and Women's Hospital, Boston, MA USA.
National Institutes of Health · USAlbert Einstein College of Medicine · USBreast Cancer Research Foundation · USBrigham and Women's Hospital · USCedars-Sinai Medical Center · USColumbia University Irving Medical Center · USNYU Langone’s Laura and Isaac Perlmutter Cancer CenterProvidence Portland Medical Center · USUniversity Health Network · CAUniversity of Chicago · USUniversity of Hawaiʻi at Mānoa · USUniversity of New Mexico · USUniversity of Washington · USVirginia Commonwealth University · US

Funding

TISSUE CoreP50CA098131 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PARK, BEN HO, PIETENPOL, JENNIFER A · 2003 to 2024
$48.7M
NCI NIH HHS P50 CA098131
6 · The paper itself

Abstract

Historically, breast cancer tumors have been considered immunologically quiescent, with the majority of tumors demonstrating low lymphocyte infiltration, low mutational burden, and modest objective response rates to anti-PD-1/PD-L1 monotherapy. Tumor and immunologic profiling has shed light on potential mechanisms of immune evasion in breast cancer, as well as unique aspects of the tumor microenvironment (TME). These include elements associated with antigen processing and presentation as well as immunosuppressive elements, which may be targeted therapeutically. Examples of such therapeutic strategies include efforts to (1) expand effector T-cells, natural killer (NK) cells and immunostimulatory dendritic cells (DCs), (2) improve antigen presentation, and (3) decrease inhibitory cytokines, tumor-associated M2 macrophages, regulatory T- and B-cells and myeloid derived suppressor cells (MDSCs). The goal of these approaches is to alter the TME, thereby making breast tumors more responsive to immunotherapy. In this review, we summarize key developments in our understanding of antitumor immunity in breast cancer, as well as emerging therapeutic modalities that may leverage that understanding to overcome immunologic resistance.

Indexed as

Breast cancerTumour immunology

Identifiers

PMID31700993
PMCPMC6820540
OpenAlexW2982449517

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.