Evidence map›Paper›PMID 41101558›Full record

Trial reportInternational journal of radiation oncology, biology, physics2026

A Phase 2 Exploratory Trial Evaluating Computed Tomography-Based Midtreatment Nodal Response to Select for De-escalated Chemoradiation Therapy in the Definitive Management of p16+ Oropharyngeal Cancer.

Joseph K Kim, Moses Tam, Sungheon Gene Kim, Eddy Solomon, Colin Hill, Jerome M Karp, Christie Hung, Cheongeun Oh, Catherine Concert, Marissa Rybstein and 10 more

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in International journal of radiation oncology, biology, physics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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

20 authors.

Joseph K KimDepartment of Radiation Oncology, New York University Long Island Grossman School of Medicine, Mineola, New York. Electronic address: joseph.kim3@nyulangone.org.
Moses TamDepartment of Radiation Oncology, New York University Long Island Grossman School of Medicine, Mineola, New York.
Sungheon Gene KimDepartment of Radiology, Weill Cornell Medical College, New York, New York.
Eddy SolomonDepartment of Radiology, Weill Cornell Medical College, New York, New York.
Colin HillDepartment of Radiation Oncology, New York University Grossman School of Medicine, New York, New York.
Jerome M KarpDepartment of Radiation Oncology, New York University Grossman School of Medicine, New York, New York.
Christie HungDepartment of Radiation Oncology, New York University Grossman School of Medicine, New York, New York.
Cheongeun OhBiostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, New York.
Catherine ConcertDepartment of Radiation Oncology, New York University Grossman School of Medicine, New York, New York.
Marissa RybsteinDepartment of Medicine, New York University Long Island Grossman School of Medicine, Mineola, New York.
Zujun LiDepartment of Otolaryngology-Head and Neck Surgery, New York University Grossman School of Medicine, New York, New York.
Elcin ZanDepartment of Nuclear Medicine, Cleveland Clinic, Cleveland, Ohio.
Judith D GoldbergBiostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, New York.
Tsivia HochmanBiostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, New York.
Adam JacobsonDepartment of Otolaryngology-Head and Neck Surgery, New York University Grossman School of Medicine, New York, New York.
Umamaheswar DuvvuriDepartment of Otolaryngology-Head and Neck Surgery, New York University Grossman School of Medicine, New York, New York.
Michael PerskyDepartment of Otolaryngology-Head and Neck Surgery, New York University Grossman School of Medicine, New York, New York.
Mark PerskyDepartment of Otolaryngology-Head and Neck Surgery, New York University Grossman School of Medicine, New York, New York.
Louis HarrisonDepartment of Radiation Oncology, Moffitt Cancer Center, Tampa, Florida.
Kenneth HuDepartment of Radiation Oncology, New York University Grossman School of Medicine, New York, New York.

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
Diffusion MRI of Treatment Response for De-escalation of Radiation TherapyUH3CA228699 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI KIM, SUNGHEON GENE · 2021 to 2023
$1.2M
NCI NIH HHS P30 CA016087NCI NIH HHS UH3 CA228699
6 · The paper itself

Abstract

purposeThis prospective, nonrandomized phase 2 single-arm pilot trial aimed to explore favorable midtreatment nodal response (FMNR) through computed tomography (CT) imaging to guide de-escalated chemoradiation therapy (CRT) in patients with favorable risk, node-positive human papillomavirus (HPV)-associated oropharyngeal cancer (OPC). METHODS AND MATERIALS: Eligible patients included p16+ OPC (AJCC 8th: cT1-3 N1 M0, <10 pack-year smokers). All patients were initially planned to receive 70 Gy with concurrent weekly cisplatin 40 mg/m

resultsOf 39 patients, 26 had FMNR and underwent de-escalated treatment. Thirteen patients had slow midtreatment nodal shrinkage and received a standard dose. At a median follow-up of 47.4 months, the 2-year PFS was 92.1% (95% CI, 0.72-0.98) for the de-escalated dose group and 92.3% for the standard dose patients (95% CI, 0.57-0.99), P = .96. With a median survival follow-up of 48.9 months (range, 16.7-77.8 months), there were no deaths or distant failures. FMNR was associated with rapid TTMV HPV DNA clearance, reduced TTMV HPV DNA flare, lower baseline and week 4 MRI diffusivity, and higher baseline and week 4 MRI diffusional kurtosis. No differences in acute or late maximum grade 3 to 4 toxicity by patient were noted. MD Anderson Dysphagia Inventory composite scores showed minimal clinically important difference in the de-escalated group at 1-month posttreatment, whereas the standard group had minimal clinically important difference up to 1-year posttreatment. No patients required feeding tube placement.

conclusionsDe-escalated CRT using CT-based midtreatment nodal response in favorable risk, node-positive HPV-associated OPC achieved excellent 2-year PFS and overall survival rates, and represents a potential approach in better selecting patients for treatment de-escalation.

Indexed as

ChemoradiotherapyLymph NodesOropharyngeal NeoplasmsTomography, X-Ray ComputedAdultAgedCisplatinFemaleHumansMaleMiddle AgedPapillomavirus InfectionsPilot ProjectsProgression-Free SurvivalProspective StudiesRadiotherapy DosageCisplatin

Identifiers

PMID41101558
PMCPMC12750345

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.