18F-FDG PET/CT During Neoadjuvant Targeted Therapy in Prior Unresectable Stage III Melanoma Patients Can (Early) Metabolic Imaging Predict Histopathologic Response or Recurrence?

被引:8
作者
van der Hiel, Bernies [1 ]
Blankenstein, Stephanie A. [2 ]
Aalbersberg, Else A. [1 ]
Wondergem, Maurits [1 ]
Stokkel, Marcel P. M. [1 ]
van de Wiel, Bart A. [3 ]
Klop, W. Martin C. [4 ]
van Akkooi, Alexander C. J. [2 ]
Haanen, John B. [5 ]
机构
[1] Netherlands Canc Inst Antoni Van Leeuwenhoek, Dept Nucl Med, Room C0-501,Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst Antoni Van Leeuwenhoek, Dept Surg Oncol, Amsterdam, Netherlands
[3] Netherlands Canc Inst Antoni Van Leeuwenhoek, Dept Pathol, Amsterdam, Netherlands
[4] Netherlands Canc Inst Antoni Van Leeuwenhoek, Dept Head & Neck Surg, Amsterdam, Netherlands
[5] Netherlands Canc Inst Antoni Van Leeuwenhoek, Dept Med Oncol, Amsterdam, Netherlands
关键词
PET/CT; melanoma; targeted therapy; pathologic response; recurrence; metabolic response; EMISSION-TOMOGRAPHY; BRAF INHIBITION; VEMURAFENIB; SURVIVAL;
D O I
10.1097/RLU.0000000000004217
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: The aim of this study was to investigate whether F-18-EDG PET/CT can predict histopathological response or recurrence in BRAF-mutated unresectable locally advanced stage III melanoma treated with neoadjuvant BRAF/MEK inhibition followed by resection and the value of PET in detecting early recurrence after resection. Patients and Methods: Twenty BRAF-mutated, unresectable stage III melanoma patients received BRAF/MEK inhibitors before surgery. F-18-FDG PET/CT was performed at baseline and 2 and 8 weeks after initiation of therapy. After resection, PET/CT was performed at specific time points during 5 years of follow-up. Pathological response was assessed on the dissection specimen. Response monitoring was measured with SUVmax, SUVpeak, MATV, and TLG and according to EORTC and PERCIST criteria. Results: Pathological response was assessed in 18 patients. Nine patients (50%) had a pathologic complete or near-complete response, and 9 (50%) had a pathologic partial or no response. EORTC or PERCIST response measurements did not correspond with pathologic outcome. SUVmax, SUVpeak, MATV, and TLG at all time points and absolute or percentage change among the 3 initial time points did not differ between the groups. During follow-up, 8 of 17 patients with R0 resection developed a recurrence, 6 recurrences were detected with imaging only, 4 of which with PET/CT in less than 6 months after surgery. PET parameters before surgery did not predict recurrence. Conclusions: Baseline F-18-FDG PET or PET response in previous unresectable stage III melanoma patients seems not useful to predict pathologic response after neoadjuvant BRAF/MEK inhibitors treatment. However, PET/CT seems valuable in detecting recurrence early after R0 resection.
引用
收藏
页码:583 / 589
页数:7
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