Primary vs nodal site PET/CT response as a prognostic marker in oropharyngeal squamous cell carcinoma treated with intensity-modulated radiation therapy.

Oropharyngeal squamous cell carcinoma (OPSCC) PET/CT response assessment head and neck cancers (HNC) human papilloma virus (HPV) intensity-modulated radiation therapy (IMRT) positron emission tomography/computed tomography (PET/CT)

Journal

Head & neck
ISSN: 1097-0347
Titre abrégé: Head Neck
Pays: United States
ID NLM: 8902541

Informations de publication

Date de publication:
09 2020
Historique:
received: 10 11 2019
revised: 05 04 2020
accepted: 22 04 2020
pubmed: 12 5 2020
medline: 28 5 2021
entrez: 12 5 2020
Statut: ppublish

Résumé

Positron emission tomography/computed tomography (PET/CT) in staging of advanced oropharyngeal squamous cell carcinoma (OPSCC) and at 3 months posttreatment (PETpost) is often utilized to assess response. The significance of lymph node vs primary site treatment response is incompletely understood. We reviewed 230 patients treated with radiation therapy. PETpost response was graded at primary and nodal sites and correlated with survival. Median age was 58, and 83% were p16-positive. Median follow-up was 24.3 months. Nodal response at PETpost predicted improved 2-year local recurrence-free survival (LRFS) (93% vs 72%, P =.004), 2-year disease-free survival (DFS) (80% vs 61.3%, P =.021), and 2-year overall survival (OS) (89% vs 83%, P =.051), while primary response only predicted improved 2-year LRFS (91% vs 76% P = .035). In OPSCC patients, both nodal and primary response at 3 months on PET/CT predicted for improved LRFS, but only nodal response predicted DFS and OS.

Sections du résumé

BACKGROUND
Positron emission tomography/computed tomography (PET/CT) in staging of advanced oropharyngeal squamous cell carcinoma (OPSCC) and at 3 months posttreatment (PETpost) is often utilized to assess response. The significance of lymph node vs primary site treatment response is incompletely understood.
METHODS
We reviewed 230 patients treated with radiation therapy. PETpost response was graded at primary and nodal sites and correlated with survival.
RESULTS
Median age was 58, and 83% were p16-positive. Median follow-up was 24.3 months. Nodal response at PETpost predicted improved 2-year local recurrence-free survival (LRFS) (93% vs 72%, P =.004), 2-year disease-free survival (DFS) (80% vs 61.3%, P =.021), and 2-year overall survival (OS) (89% vs 83%, P =.051), while primary response only predicted improved 2-year LRFS (91% vs 76% P = .035).
CONCLUSION
In OPSCC patients, both nodal and primary response at 3 months on PET/CT predicted for improved LRFS, but only nodal response predicted DFS and OS.

Identifiants

pubmed: 32391626
doi: 10.1002/hed.26242
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2405-2413

Informations de copyright

© 2020 Wiley Periodicals, Inc.

Références

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Auteurs

Jacob Matthew Eckstein (JM)

Department of Radiation Medicine, Northwell Health, New Hyde Park, New York, USA.

Nicole Nolan (N)

Department of Radiation Oncology, Methodist Health System, Omaha, Nebraska, USA.

Erin Healy (E)

Department of Radiation Oncology, The Ohio State Univ, Columbus, Ohio, USA.

Chadwick Lewis Wright (CL)

Department of Radiation Oncology, The Ohio State Univ, Columbus, Ohio, USA.

Angita Jain (A)

Kasturba Medical College, Mangalore, India.

Christian Louis Barney (CL)

Department of Radiation Oncology, Methodist Health System, Omaha, Nebraska, USA.

Iman Washington (I)

Department of Radiation Oncology, Moffitt Cancer Center, Tampa, Florida, USA.

Joseph Paul McElroy (JP)

Department of Radiation Oncology, The Ohio State Univ, Columbus, Ohio, USA.

John Christopher Grecula (JC)

Department of Radiation Oncology, The Ohio State Univ, Columbus, Ohio, USA.

Jessica Lynn Wobb (JL)

Department of Radiation Oncology, Fort Hamilton Hospital, Kettering Medical Center, Ohio, USA.

Darrion Luther Mitchell (DL)

Department of Radiation Oncology, The Ohio State Univ, Columbus, Ohio, USA.

Eric Miller (E)

Department of Radiation Oncology, The Ohio State Univ, Columbus, Ohio, USA.

Mauricio Gamez (M)

Department of Radiation Oncology, The Ohio State Univ, Columbus, Ohio, USA.

Dukagjin Blakaj (D)

Department of Radiation Oncology, The Ohio State Univ, Columbus, Ohio, USA.

Virginia Diavolitsis (V)

Department of Radiation Oncology, OhioHealth, Columbus, Ohio, USA.

Aashish Bhatt (A)

Department of Radiation Oncology, University Hospitals/Seidman Cancer Center at Case Western Reserve Univ, Cleveland, Ohio, USA.

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