False-Positive Results and Incidental Findings with Annual CT or PET/CT Surveillance in Asymptomatic Patients with Resected Stage III Melanoma.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 18 10 2018
pubmed: 27 3 2019
medline: 12 9 2019
entrez: 27 3 2019
Statut: ppublish

Résumé

The aim of this study was to quantify false-positive and incidental findings from annual surveillance imaging in asymptomatic, American Joint Committee on Cancer stage III melanoma patients. This was a cohort study of patients treated at Melanoma Institute Australia (2000-2015) with baseline computed tomography (CT) or positron emission tomography (PET)/CT imaging and at least two annual surveillance scans. False-positives were defined as findings suspicious for melanoma recurrence that were not melanoma, confirmed by histopathology, subsequent imaging, or clinical follow-up, while incidental findings were defined as non-melanoma-related findings requiring further action. Outcomes of incidental findings were classified as 'benign' if they resolved spontaneously or were not seriously harmful; 'malignant' if a second malignancy was identified; or 'other' if potentially harmful. Among 154 patients, 1022 scans were performed (154 baseline staging, 868 surveillance) during a median follow-up of 85 months (interquartile range 56-112); 57 patients (37%) developed a recurrence. For baseline and surveillance imaging, 124 false-positive results and incidental findings were identified in 81 patients (53%). The frequency of these findings was 5-14% per year, and an additional 181 tests, procedures, and referrals were initiated to investigate these findings. The diagnosis was benign in 109 findings of 124 findings (88%). Fifteen patients with a benign finding underwent an unnecessary invasive procedure. Surveillance imaging identified distant metastases in 20 patients (13%). False-positive results and incidental findings occur in at least half of all patients undergoing annual surveillance imaging, and the additional healthcare use is substantial. These findings persist over time. Clinicians need to be aware of these risks and discuss them with patients, alongside the expected benefits of surveillance imaging.

Identifiants

pubmed: 30911946
doi: 10.1245/s10434-019-07311-0
pii: 10.1245/s10434-019-07311-0
doi:

Substances chimiques

Radiopharmaceuticals 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1860-1868

Auteurs

Amanda A G Nijhuis (AAG)

Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia.
University of Utrecht, Utrecht, The Netherlands.

Mbathio Dieng (M)

NHMRC Clinical Trials Centre, University of Sydney, Level 6, Medical Foundation Building, 92-94 Parramatta Road, Camperdown, NSW, 2050, Australia.

Nikita Khanna (N)

NHMRC Clinical Trials Centre, University of Sydney, Level 6, Medical Foundation Building, 92-94 Parramatta Road, Camperdown, NSW, 2050, Australia.

Sally J Lord (SJ)

NHMRC Clinical Trials Centre, University of Sydney, Level 6, Medical Foundation Building, 92-94 Parramatta Road, Camperdown, NSW, 2050, Australia.

Jo Dalton (J)

Poche Centre, Clinical Trials, Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia.

Alexander M Menzies (AM)

Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia.
Department of Medical Oncology, Royal North Shore and Mater Hospitals, Sydney, NSW, Australia.

Robin M Turner (RM)

Biostatistics Unit, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.

Jay Allen (J)

Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia.

Robyn P M Saw (RPM)

Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia.
Sydney Medical School, The University of Sydney, Sydney, NSW, Australia.
Department of Melanoma and Surgical Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

Omgo E Nieweg (OE)

Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia.
Sydney Medical School, The University of Sydney, Sydney, NSW, Australia.
Department of Melanoma and Surgical Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

John F Thompson (JF)

Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia.
Sydney Medical School, The University of Sydney, Sydney, NSW, Australia.
Department of Melanoma and Surgical Oncology, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

Rachael L Morton (RL)

Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia. rachael.morton@ctc.usyd.edu.au.
NHMRC Clinical Trials Centre, University of Sydney, Level 6, Medical Foundation Building, 92-94 Parramatta Road, Camperdown, NSW, 2050, Australia. rachael.morton@ctc.usyd.edu.au.

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Classifications MeSH