Evidence map›Paper›PMID 42850183›Full record

ReviewTrends in pharmacological sciences2026

The emerging landscape for next-generation HNSCC treatment.

Kailey N Jackett, Meghri Katerji, Kiranya Arnold, Kyunghee Burkitt, Andrew Gennaro, Vassiliki Saloura, John Brognard

Abstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Kailey N JackettDepartment of Surgery, Pharmacology, and Biochemistry and Molecular Biology, Upstate Medical University, Syracuse, NY 13210, USA; Cancer Therapeutics Program, Upstate Medical University, Syracuse, NY 13210, USA.
Meghri KaterjiDepartment of Surgery, Pharmacology, and Biochemistry and Molecular Biology, Upstate Medical University, Syracuse, NY 13210, USA; Cancer Therapeutics Program, Upstate Medical University, Syracuse, NY 13210, USA.
Kiranya ArnoldCancer Therapeutics Program, Upstate Medical University, Syracuse, NY 13210, USA; Department of Otolaryngology and Communication Sciences, Upstate Medical University, Syracuse, NY 13210, USA.
Kyunghee BurkittDepartment of Oncology, Cleveland Clinic, Cleveland, OH 44195, USA.
Andrew GennaroDepartment of Surgery, Pharmacology, and Biochemistry and Molecular Biology, Upstate Medical University, Syracuse, NY 13210, USA; Cancer Therapeutics Program, Upstate Medical University, Syracuse, NY 13210, USA.
Vassiliki SalouraThoracic and GI Malignancies Branch, National Cancer Institute, Bethesda, MD 20892, USA. Electronic address: valia.saloura@nih.gov.
John BrognardDepartment of Surgery, Pharmacology, and Biochemistry and Molecular Biology, Upstate Medical University, Syracuse, NY 13210, USA; Cancer Therapeutics Program, Upstate Medical University, Syracuse, NY 13210, USA. Electronic address: brognarj@upstate.edu.

Funding

The Role of WHSC1L1 in Squamous Cell Carcinoma of the Head and NeckZIABC011831 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI SALOURA, VASSILIKI · 2018 to 2025
$7.6M
Intramural NIH HHS ZIA BC011831
6 · The paper itself

Abstract

Head and neck squamous cell carcinoma (HNSCC) is a biologically complex malignancy in which durable responses to standard multimodal therapies, targeted therapies, and immune checkpoint inhibitors remain limited. Therapeutic resistance arises from interconnected oncogenic signaling, tumor plasticity, heterogeneity, and immune evasion, which enable tumors to bypass inhibition of individual pathways. These mechanisms also differ across biologically distinct HNSCC subsets, including human papillomavirus (HPV)-positive and HPV-negative disease. Emerging therapeutic platforms in preclinical and clinical development, including targeted protein degraders, engineered antibodies, cellular and vaccine-based immunotherapies, photoimmunotherapy, and epigenetic modulators, provide new opportunities to target these interconnected vulnerabilities. In this review, we examine how these pharmacological strategies may overcome resistance in HNSCC and discuss their integration into biomarker-guided, mechanism-driven combination regimens.

Indexed as

combination strategiesHNSCCprecision oncology

Identifiers

PMID42850183
PMCPMC13693649

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.