Singh Neha, Alexander Nora A, Lachance Kristina, Lewis Christopher W, McEvoy Aubriana, Akaike Gensuke, Byrd David, Behnia Sanaz, Bhatia Shailender, Paulson Kelly G, Nghiem Paul
Department of Medicine, Division of Dermatology, University of Washington, Seattle, Washington.
Department of Medicine, Division of Dermatology, University of Washington, Seattle, Washington; Department of Physical Medicine and Rehabilitation, Northwestern University, Evanston, Illinois.
J Am Acad Dermatol. 2021 Feb;84(2):330-339. doi: 10.1016/j.jaad.2020.07.065. Epub 2020 Jul 21.
Merkel cell carcinoma (MCC) guidelines derive from melanoma and do not recommend baseline cross-sectional imaging for most patients. However, MCC is more likely to have metastasized at diagnosis than melanoma.
To determine how often baseline imaging identifies clinically occult MCC in patients with newly diagnosed disease with and without palpable nodal involvement.
Analysis of 584 patients with MCC with a cutaneous primary tumor, baseline imaging, no evident distant metastases, and sufficient staging data.
Among 492 patients with clinically uninvolved regional nodes, 13.2% had disease upstaged by imaging (8.9% in regional nodes, 4.3% in distant sites). Among 92 patients with clinically involved regional nodes, 10.8% had disease upstaged to distant metastatic disease. Large (>4 cm) and small (<1 cm) primary tumors were both frequently upstaged (29.4% and 7.8%, respectively). Patients who underwent positron emission tomography-computed tomography more often had disease upstaged (16.8% of 352), than those with computed tomography alone (6.9% of 231; P = .0006).
This was a retrospective study.
In patients with clinically node-negative disease, baseline imaging showed occult metastatic MCC at a higher rate than reported for melanoma (13.2% vs <1%). Although imaging is already recommended for patients with clinically node-positive MCC, these data suggest that baseline imaging is also indicated for patients with clinically node-negative MCC because upstaging is frequent and markedly alters management and prognosis.
默克尔细胞癌(MCC)的诊疗指南源自黑色素瘤,并不建议大多数患者进行基线横断面成像检查。然而,MCC在确诊时比黑色素瘤更易发生转移。
确定基线成像在新诊断的、有无可触及淋巴结受累的患者中发现临床隐匿性MCC的频率。
分析584例患有皮肤原发性肿瘤、接受基线成像检查、无明显远处转移且有足够分期数据的MCC患者。
在492例临床区域淋巴结未受累的患者中,13.2%的患者因成像检查而上调分期(区域淋巴结为8.9%,远处部位为4.3%)。在92例临床区域淋巴结受累的患者中,10.8%的患者上调分期为远处转移性疾病。大(>4 cm)、小(<1 cm)原发性肿瘤均常有分期上调情况(分别为29.4%和7.8%)。接受正电子发射断层扫描-计算机断层扫描的患者比仅接受计算机断层扫描的患者更常出现分期上调(352例中的16.8%对比231例中的6.9%;P = 0.0006)。
这是一项回顾性研究。
在临床淋巴结阴性的患者中,基线成像显示隐匿性转移性MCC的发生率高于黑色素瘤报告的发生率(13.2%对比<1%)。尽管已建议对临床淋巴结阳性的MCC患者进行成像检查,但这些数据表明,临床淋巴结阴性的MCC患者也应进行基线成像检查,因为分期上调很常见,且会显著改变治疗和预后。