Evidence map›Paper›PMID 32576627›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2020

Integrating Immunotherapy and Targeted Therapy in Cancer Treatment: Mechanistic Insights and Clinical Implications.

Johann S Bergholz, Qiwei Wang, Sheheryar Kabraji, Jean J Zhao

Abstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Johann S Bergholz *Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts. jean_zhao@dfci.harvard.edu johann_bergholz@dfci.harvard.edu.
Qiwei Wang *Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Sheheryar KabrajiDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Jean J ZhaoDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts. jean_zhao@dfci.harvard.edu johann_bergholz@dfci.harvard.edu.

Funding

Targeting the Vasular SystemP50CA165962 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DAPHNE A. HAAS-KOGAN · 2013 to 2026
$33.5M
Tissue and Pathology CoreP50CA168504 · NCI · DANA-FARBER CANCER INST · PI JUDY E. GARBER · 2013 to 2026
$30.1M
Integrating targeted therapy and immunotherapy to break through cancerR35CA210057 · NCI · DANA-FARBER CANCER INST · PI Jean Zhao · 2016 to 2026
$10.8M
NCI NIH HHS P50 CA165962NCI NIH HHS P50 CA168504NCI NIH HHS R35 CA210057
6 · The paper itself

Abstract

Small-molecule targeted therapies have demonstrated outstanding potential in the clinic. These drugs are designed to minimize adverse effects by selectively attacking cancer cells while exerting minimal damage to normal cells. Although initial response to targeted therapies may be high, yielding positive response rates and often improving survival for an important percentage of patients, resistance often limits long-term effectiveness. On the other hand, immunotherapy has demonstrated durable results, yet for a limited number of patients. Growing evidence indicates that some targeted agents can modulate different components of the antitumor immune response. These include immune sensitization by inhibiting tumor cell-intrinsic immune evasion programs or enhancing antigenicity, as well as direct effects on immune effector and immunosuppressive cells. The combination of these two approaches, therefore, has the potential to result in synergistic and durable outcomes for patients. In this review, we focus on the latest advances on integrating immunotherapy with small-molecule targeted inhibitors. In particular, we discuss how specific oncogenic events differentially affect immune response, and the implications of these findings on the rational design of effective combinations of immunotherapy and targeted therapies.

Indexed as

ImmunotherapyMolecular Targeted TherapyAntineoplastic AgentsHumansImmunologic FactorsNeoplasmsSmall Molecule LibrariesTumor EscapeTumor MicroenvironmentAntineoplastic AgentsImmunologic FactorsSmall Molecule Libraries

Identifiers

PMID32576627
PMCPMC7641965

What OpenQuestion holds

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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.