Evidence map›Paper›PMID 32162057›Full record

ReviewEuropean archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery2020

CDK4/6 inhibitors in P16/HPV16-negative squamous cell carcinoma of the head and neck.

Camelia Billard-Sandu, Yun-Gan Tao, Marie-Paule Sablin, Gabriela Dumitrescu, David Billard, Eric Deutsch

Abstract readReview
PubMed Publisher
In one paragraph

Review in European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 40 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Camelia Billard-SanduDepartment of Oncology-Radiotherapy, Gustave Roussy Cancer Campus, 114 Rue Edouard Vaillant, 94805, Villejuif, France. camelia.billard@gustaveroussy.fr.
Yun-Gan TaoDepartment of Oncology-Radiotherapy, Gustave Roussy Cancer Campus, 114 Rue Edouard Vaillant, 94805, Villejuif, France.
Marie-Paule SablinDepartment of Drug Development and Innovation (D3i), Institut Curie, Paris, France.
Gabriela DumitrescuDepartment of Oncology-Radiotherapy, Gustave Roussy Cancer Campus, 114 Rue Edouard Vaillant, 94805, Villejuif, France.
David BillardOncology Unit, André Mignot Hospital, Versailles, France.
Eric DeutschDepartment of Oncology-Radiotherapy, Gustave Roussy Cancer Campus, 114 Rue Edouard Vaillant, 94805, Villejuif, France.
Institut Gustave Roussy · FRHôpital André Mignot · FRInstitut Curie · FR

Funding

Not applicable 0
6 · The paper itself

Abstract

purposeAddition of CDK4/6 inhibitors to a variety of established treatments in squamous cell carcinoma of the head and neck (SCCHN) has the potential to improve responses to other therapies and may help overcome treatment resistance. The SCCHN is a heterogeneous group of cancers of the oral cavity, the pharynx and the larynx with poor prognosis despite the aggressive multimodal therapies. In the past decade, significant advances were made in understanding of the molecular and genetic abnormalities leading to oncogenesis in SCCHN. RECENT

findingsBesides EGFR targeting agents, antiangiogenic agents have been shown to produce antitumor activity in these tumors. The cyclin D-cyclin-dependent kinase (CDK) 4/6-inhibitor of CDK4 (INK4)-retinoblastoma (Rb) pathway regulates cellular proliferation by controlling the G1 to S cell cycle checkpoint. In SCCHN, the Rb pathway is frequently altered through amplification of CCND1 (cyclin D1) or deletion of CDKN2A (cyclin-dependent kinase inhibitor 2A) coding for p16INK4A, and thus promoting proliferation. This article summarizes what we actually know of the place of CDK4/6 inhibitors in the therapeutic arsenal of SCCHN. CDK4/6 inhibitors could serve as a method to target these tumors, and both p16 loss and CCND1 amplification could be investigated as biomarkers.

Indexed as

Carcinoma, Squamous CellCyclin-Dependent Kinase 4Head and Neck NeoplasmsSquamous Cell Carcinoma of Head and NeckCyclin-Dependent Kinase Inhibitor p16HumansCDK4 protein, humanCyclin-Dependent Kinase 4Cyclin-Dependent Kinase Inhibitor p16AbemaciclibCCND1 amplificationCDK4/6 inhibitorsP16/HPV16-negative squamous cell carcinoma of the head and neckPalbociclibRibociclib

Identifiers

PMID32162057
OpenAlexW3011865075

What OpenQuestion holds

Textmetadata
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.