Patient-reported outcomes, physician-reported toxicities, and treatment outcomes in a modern cohort of patients with sinonasal cancer treated using proton beam therapy.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
07 2020
Historique:
received: 03 02 2020
revised: 20 04 2020
accepted: 07 05 2020
pubmed: 18 5 2020
medline: 15 4 2021
entrez: 18 5 2020
Statut: ppublish

Résumé

To report physician-assessed toxicities (PATs) and patient-reported outcomes (PROs) in a prospective cohort of patients treated using proton beam therapy (PBT). From 2011 to 2019, PBT-treated patients with a sinonasal malignancy were enrolled with a primary endpoint of toxicity assessment. PATs and PROs were assessed at baseline, acute (during PBT), subacute (within 90 days after PBT), and chronic time points. PATs were graded with the Common Terminology Criteria for Adverse Events V4.0. PROs were assessed with the Xerostomia-Related Quality-of-Life Scale (XeQoLS), MD Anderson Dysphagia Inventory (MDADI), and Functional Assessment of Cancer Therapy (FACT). PRO changes from baseline to follow-up were defined as significantly different based on a paired t-test plus a minimal clinically important difference. Sixty-four patients had a median follow-up time of 33 months (interquartile range: 10-52 months). The most common histology was olfactory neuroblastoma (28%) and most patients had T4 disease (46%). One acute G3 neurologic PAT (blurred vision) resolved, and no late G3-4 neurologic PATs were observed. Feeding tube placement occurred in 6% of patients. No significant changes were noted in PROs from baseline to the chronic period. Significant worsening from baseline was noted in the XeQoLS acute-subacute physical functioning, pain, personal/psychological distress, and social function; acute-subacute MDADI physical function; and acute-subacute FACT head/neck subscale. The 3-year local control, disease-free survival, and overall survival rates were 88%, 76%, and 82%, respectively. We demonstrate low grade ≥3 toxicity and encouraging disease outcomes with PBT. PROs suggest significant changes in the acute-subacute period but no chronic sequelae.

Sections du résumé

BACKGROUND AND PURPOSE
To report physician-assessed toxicities (PATs) and patient-reported outcomes (PROs) in a prospective cohort of patients treated using proton beam therapy (PBT).
METHODS AND MATERIALS
From 2011 to 2019, PBT-treated patients with a sinonasal malignancy were enrolled with a primary endpoint of toxicity assessment. PATs and PROs were assessed at baseline, acute (during PBT), subacute (within 90 days after PBT), and chronic time points. PATs were graded with the Common Terminology Criteria for Adverse Events V4.0. PROs were assessed with the Xerostomia-Related Quality-of-Life Scale (XeQoLS), MD Anderson Dysphagia Inventory (MDADI), and Functional Assessment of Cancer Therapy (FACT). PRO changes from baseline to follow-up were defined as significantly different based on a paired t-test plus a minimal clinically important difference.
RESULTS
Sixty-four patients had a median follow-up time of 33 months (interquartile range: 10-52 months). The most common histology was olfactory neuroblastoma (28%) and most patients had T4 disease (46%). One acute G3 neurologic PAT (blurred vision) resolved, and no late G3-4 neurologic PATs were observed. Feeding tube placement occurred in 6% of patients. No significant changes were noted in PROs from baseline to the chronic period. Significant worsening from baseline was noted in the XeQoLS acute-subacute physical functioning, pain, personal/psychological distress, and social function; acute-subacute MDADI physical function; and acute-subacute FACT head/neck subscale. The 3-year local control, disease-free survival, and overall survival rates were 88%, 76%, and 82%, respectively.
CONCLUSIONS
We demonstrate low grade ≥3 toxicity and encouraging disease outcomes with PBT. PROs suggest significant changes in the acute-subacute period but no chronic sequelae.

Identifiants

pubmed: 32417351
pii: S0167-8140(20)30260-7
doi: 10.1016/j.radonc.2020.05.007
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

258-266

Subventions

Organisme : NIBIB NIH HHS
ID : R25 EB025787
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA214825
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA225190
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Dario Pasalic (D)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Ethan B Ludmir (EB)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Pamela K Allen (PK)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Nikhil G Thaker (NG)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Bhavana V Chapman (BV)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Ehab Y Hanna (EY)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Shirley Y Su (SY)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Renata Ferrarotto (R)

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Bonnie S Glisson (BS)

Department of Thoracic/Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Jay P Reddy (JP)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

G Brandon Gunn (G)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

C David Fuller (CD)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Jack Phan (J)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

David I Rosenthal (DI)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

William H Morrison (WH)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Adam S Garden (AS)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States.

Steven J Frank (SJ)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States. Electronic address: sjfrank@mdanderson.org.

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