Surveillance imaging with FDG-PET/CT in the post-operative follow-up of stage 3 melanoma

被引:44
|
作者
Lewin, J. [1 ,2 ]
Sayers, L. [3 ]
Kee, D. [1 ]
Walpole, I. [1 ]
Sanelli, A. [1 ]
te Marvelde, L. [4 ]
Herschtal, A. [4 ]
Spillane, J. [5 ]
Gyorki, D. [5 ,6 ]
Speakman, D. [5 ]
Estall, V. [7 ]
Donahoe, S. [5 ]
Pohl, M. [5 ]
Pope, K. [7 ]
Chua, M. [7 ]
Sandhu, S. [1 ]
McArthur, G. A. [1 ,8 ]
McCormack, C. J. [9 ]
Henderson, M. [5 ,6 ]
Hicks, R. J. [6 ,10 ]
Shackleton, M. [1 ,3 ,8 ,11 ,12 ]
机构
[1] Peter MacCallum Canc Ctr, Dept Canc Med, Melbourne, Vic, Australia
[2] Princess Margaret Canc Ctr, Toronto, ON, Canada
[3] Peter MacCallum Canc Ctr, Canc Treatment & Dev Lab, Melbourne, Vic, Australia
[4] Peter MacCallum Canc Ctr, Ctr Biostat & Clin Trials, Melbourne, Vic, Australia
[5] Peter MacCallum Canc Ctr, Dept Surg, Melbourne, Vic, Australia
[6] St Vincents Hosp, Dept Surg, Melbourne, Vic, Australia
[7] Peter MacCallum Canc Ctr, Dept Radiat Oncol, Melbourne, Vic, Australia
[8] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Melbourne, Vic 3010, Australia
[9] Peter MacCallum Canc Ctr, Dept Canc Imaging, Melbourne, Vic, Australia
[10] Univ Melbourne, Dept Pathol, Melbourne, Vic, Australia
[11] Alfred Hosp, Melbourne, Vic, Australia
[12] Monash Univ, Cent Clin Sch, Fac Med Nursing & Allied Hlth, Clayton, Vic 3800, Australia
关键词
surveillance; PET; melanoma; stage; 3; EMISSION-TOMOGRAPHY; INITIAL RECURRENCE; III MELANOMA; HIGH-RISK; DISEASE; METASTASECTOMY; VEMURAFENIB; PATIENT; UTILITY;
D O I
10.1093/annonc/mdy124
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: As early detection of recurrent melanoma maximizes treatment options, patients usually undergo post-operative imaging surveillance, increasingly with FDG-PET/CT (PET). To assess this, we evaluated stage 3 melanoma patients who underwent prospectively applied and sub-stage-specific schedules of PET surveillance. Patients and methods: From 2009, patients with stage 3 melanoma routinely underwent PET +/- MRI brain scans via defined schedules based on sub-stage-specific relapse probabilities. Data were collected regarding patient characteristics and outcomes. Contingency analyses were carried out of imaging outcomes. Results: One hundred and seventy patients (stage 3A: 34; 3B: 93; 3C: 43) underwent radiological surveillance. Relapses were identified in 65 (38%) patients, of which 45 (69%) were asymptomatic. False-positive imaging findings occurred in 7%, and 6% had treatable second (non-melanoma) malignancies. Positive predictive values (PPV) of individual scans were 56%-83%. Negative scans had predictive values of 89%-96% for true non-recurrence [negative predictive values (NPV)] until the next scan. A negative PET at 18 months had NPVs of 80%-84% for true non-recurrence at any time in the 47-month (median) follow-up period. Sensitivity and specificity of the overall approach of sub-stage-specific PET surveillance were 70% and 87%, respectively. Of relapsed patients, 33 (52%) underwent potentially curative resection and 10 (16%) remained disease-free after 24months (median). Conclusions: Application of sub-stage-specific PET in stage 3 melanoma enables asymptomatic detection of most recurrences, has high NPVs that may provide patient reassurance, and is associated with a high rate of detection of resectable and potentially curable disease at relapse.
引用
收藏
页码:1569 / 1574
页数:6
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