Cobben David C P, Jager Piet L, Elsinga Philip H, Maas Bram, Suurmeijer Albert J H, Hoekstra Harald J
PET Center and Department of Surgical Oncology, Groningen University Hospital, Groningen, The Netherlands.
J Nucl Med. 2003 Dec;44(12):1927-32.
In this study, the feasibility of 3'-(18)F-fluoro-3'-deoxy-L-thymidine PET ((18)F-FLT PET) for staging patients with clinical stage III melanoma was investigated.
Ten patients with melanoma and metastases to the locoregional draining lymph nodes, clinical stage III-based on physical examination, chest radiography, lactate dehydrogenase, and histopathologic confirmation-underwent a whole-body (18)F-FLT PET scan 1 h after injection of a median 400-MBq dose (range, 185-430 MBq) of (18)F-FLT. All (18)F-FLT PET lesions were verified using the American Joint Committee on Cancer Staging System, which includes physical examination, spiral CT, ultrasound, chest radiography, and histopathologic examinations. Size and mitotic rate of metastatic lymph nodes and skin metastases were determined.
All histopathologic samples and (18)F-FLT PET lesions were categorized over anatomic regions and correlated. All locoregional metastases were correctly visualized by (18)F-FLT PET. Region-based sensitivity for detection of lymph node metastatic disease was 88%. There were 3 true-negative and 2 false-positive lesions. The detection limit for lymph node metastases appeared to be approximately 6 mm or a mitotic rate of 9 mitoses per 2 mm(2). Two patients were upstaged by (18)F-FLT PET, which was confirmed by CT. In 3 patients, (18)F-FLT PET detected a total of 3 additional lesions with therapeutic consequences, without influencing staging. These lesions were initially missed by clinical staging.
(18)F-FLT PET seems promising for (re)staging purposes in clinical stage III melanoma. Further research is needed, in which (18)F-FLT PET should be compared with (18)F-FDG PET.
在本研究中,探讨了3'-(18)F-氟-3'-脱氧-L-胸腺嘧啶正电子发射断层显像((18)F-FLT PET)用于临床III期黑色素瘤患者分期的可行性。
10例黑色素瘤伴局部区域引流淋巴结转移的患者,基于体格检查、胸部X线、乳酸脱氢酶及组织病理学确诊为临床III期,在注射中位剂量400MBq(范围185 - 430MBq)的(18)F-FLT后1小时接受全身(18)F-FLT PET扫描。所有(18)F-FLT PET病变均使用美国癌症联合委员会分期系统进行验证,该系统包括体格检查、螺旋CT、超声、胸部X线及组织病理学检查。测定转移淋巴结及皮肤转移灶的大小和有丝分裂率。
所有组织病理学样本及(18)F-FLT PET病变按解剖区域分类并进行相关性分析。所有局部区域转移灶均被(18)F-FLT PET正确显示。基于区域的淋巴结转移疾病检测敏感性为88%。有3例假阴性和2例假阳性病变。淋巴结转移的检测限似乎约为6mm或每2mm²有9个有丝分裂。2例患者经(18)F-FLT PET分期上调,CT证实。在3例患者中,(18)F-FLT PET共检测到3个有治疗意义的额外病变,未影响分期。这些病变最初被临床分期漏诊。
(18)F-FLT PET在临床III期黑色素瘤的(重新)分期方面似乎很有前景。需要进一步研究,将(18)F-FLT PET与(18)F-FDG PET进行比较。