Evidence map›Paper›PMID 33069764›Full record

ArticleRadiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology2021

CT and FDG-PET radiologic biomarkers in p16+ oropharyngeal squamous cell carcinoma patients treated with definitive chemoradiotherapy.

Benjamin S Rosen, Joel R Wilkie, Yilun Sun, Mohannad Ibrahim, Keith A Casper, Jessa E Miller, Thong Chotchutipan, Chaz L Stucken, Carol Bradford, Mark E P Prince and 13 more

Open access · greenAbstract read
In one paragraph

Article in Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Initial Feasibility and Acute Toxicity Outcomes From a Phase 2 Trial ofInternational journal of radiation oncology, biology, physics · 2023
    Trial
  4. Early HPV ctDNA Kinetics and Imaging Biomarkers Predict Therapeutic Response in p16+ Oropharyngeal Squamous Cell Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Trial
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
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

23 authors at 5 institutions in 2 countries.

Benjamin S RosenDepartment of Radiation Oncology, Michigan Medicine, Ann Arbor, United States. Electronic address: rosenbs@med.umich.edu.
Joel R WilkieDepartment of Radiation Oncology, Michigan Medicine, Ann Arbor, United States.
Yilun SunDepartment of Radiation Oncology, Michigan Medicine, Ann Arbor, United States; Department of Biostatistics, University of Michigan, Ann Arbor, MI, Uninet States.
Mohannad IbrahimDepartment of Radiology, Division of Neuroradiology, Michigan Medicine, Ann Arbor, United States.
Keith A CasperDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Jessa E MillerDepartment of Head and Neck Surgery, UCLA, Los Angeles, United States.
Thong ChotchutipanDepartment of Radiation Oncology, Chulabhorn Hospital, HRH Princess Chulabhorn College of Medical Science, Chulabhorn Royal Academy, Bangkok, Thailand.
Chaz L StuckenDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Carol BradfordDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Mark E P PrinceDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Andrew J RoskoDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Kelly M MalloyDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Scott A McLeanDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Steven B ChinnDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Andrew G ShumanDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Matthew E SpectorDepartment of Otolaryngology-Head and Neck Surgery, Michigan Medicine, Ann Arbor, United States.
Paul L SwiecickiDepartment of Internal Medicine, Michigan Medicine, Ann Arbor, United States; U.S. Department of Veterans Affairs, VA Center for Clinical Management Research, Ann Arbor, United States.
Francis P WordenDepartment of Internal Medicine, Michigan Medicine, Ann Arbor, United States.
Jennifer L ShahDepartment of Radiation Oncology, Michigan Medicine, Ann Arbor, United States.
Caitlin A SchonewolfDepartment of Radiation Oncology, Michigan Medicine, Ann Arbor, United States.
Christina H ChapmanDepartment of Radiation Oncology, Michigan Medicine, Ann Arbor, United States; U.S. Department of Veterans Affairs, VA Center for Clinical Management Research, Ann Arbor, United States.
Avraham EisbruchDepartment of Radiation Oncology, Michigan Medicine, Ann Arbor, United States.
Michelle L MierzwaDepartment of Radiation Oncology, Michigan Medicine, Ann Arbor, United States.
Michigan Medicine · USUnited States Department of Veterans Affairs · USChulabhorn Hospital · THRoss School · USUniversity of Michigan · US

Funding

Functional imaging-directed adaptive therapy of head and neck cancerR01CA184153 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CAO, YUE · 2015 to 2019
$2.4M
Quantitative MRI models of HN Cancers for Physiological Adaption of RTU01CA183848 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CAO, YUE · 2014 to 2019
$2.0M
Integrated Analysis of Germline and Somatic Mutations in Young, Low-Risk and Older, High-Risk Oral Cavity CancerK08CA226350 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINN, STEVEN BENNETT · 2018 to 2021
$882k
NCI NIH HHS K08 CA226350NCI NIH HHS R01 CA184153NCI NIH HHS U01 CA183848
6 · The paper itself

Abstract

purposeTo assess associations between imaging biomarkers from standard of care pre-treatment CT and FDG-PET scans and locoregional (LR) and distant metastatic (DM) recurrences in patients with p16+ oropharyngeal squamous cell carcinoma (OPSCC) treated with definitive chemoradiotherapy (CRT).

methodsAn institutional database from a single NCI-designated cancer center identified 266 patients with p16+ OPSCC treated with definitive CRT in our department from 2005 to 2016 with evaluable pre-treatment FDG-PET scans. Quantitative SUV metrics and qualitative imaging metrics were determined from FDG-PET and CT scans, while clinical characteristics were abstracted from the medical record. Associations between clinical/imaging features and time to LR (TTLRF) or DM (TTDMF) failure and overall survival (OS) were assessed using univariable Cox regression and penalized stepwise regression for multivariable analyses (MVA).

resultsThere were 27 LR and 32 DM recurrences as incident failures. Imaging biomarkers were significantly associated with TTLRF, TTDMF and OS. FDG-PET metrics outperformed CT and clinical metrics for TTLRF, with metabolic tumor volume being the only significant feature selected on MVA: C-index = 0.68 (p = 0.01). Radiographic extranodal extension (rENE), positive retropharyngeal nodes (RPN+), and clinical stage were significant on MVA for TTDMF: C-index = 0.84 (p < 0.001). rENE, group stage, and RPN+ were significant on MVA for OS: C-index = 0.77 (p < 0.001).

conclusionsIn the largest study to date of uniformly treated patients with CRT to evaluate both pretreatment CT and FDG-PET, radiographic biomarkers were significantly associated with TTLRF, TTDMF and OS among patients with p16+ OPSCC treated with CRT. CT metrics performed best to predict TTDMF, while FDG-PET metrics showed improved prediction for LRRFS. These metrics may help identify candidates for treatment intensification or de-escalation of therapy. STATEMENT OF TRANSLATIONAL RELEVANCE: Pre-treatment imaging features from standard-of-care PET/CT imaging show promise for predicting long-term outcomes following HPV-associated oropharynx cancer (HPV-OPC) therapy. This study comprehensively characterizes qualitative and quantitative pre-treatment imaging metrics associated with time to pattern-specific failure in a cohort of 266 patients treated uniformly with definitive chemoradiation. Multivariate analysis (MVA) for time to locoregional failure (TTLRF), time to distant metastatic failure (TTDMF), and overall survival (OS) was performed. FDG-PET metrics outperformed CT and clinical metrics for TTLRF. CT radiographic extranodal extension, positive retropharyngeal nodes, and stage strongly predicted TTDMF (combined C-index = 0.84, log rank p < 0.001). Number of smoking pack-years complemented clinical and imaging features only in patients without radiographic extranodal extension or positive retropharyngeal nodes. Time to pattern-specific failure is important for guiding treatment de-escalation strategies, which intend to reduce treatment-related toxicity in patients with relatively long expected survival times. This study suggests that PET/CT features should play a crucial role in future de-escalation trials and management of HPV-OPC patients.

Indexed as

Carcinoma, Squamous CellHead and Neck NeoplasmsOropharyngeal NeoplasmsBiomarkersChemoradiotherapyFluorodeoxyglucose F18HumansPositron-Emission TomographyPositron Emission Tomography Computed TomographyPrognosisRetrospective StudiesSquamous Cell Carcinoma of Head and NeckTomography, X-Ray ComputedBiomarkersFluorodeoxyglucose F18Computed tomographyFDG-PETHPV cancersImaging biomarkersOropharynx

Identifiers

PMID33069764
PMCPMC10326862
OpenAlexW3092754893

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Registered trials

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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.