Keijzer R, Bril H, van der Loo E M, de Graaf P W
Afd. Chirurgie: hr.dr.R.Keijzer, Reinier de Graaf Groep, Reinier de Graafweg 3-11, 2625 AD Delft.
Ned Tijdschr Geneeskd. 2004 May 1;148(18):884-8.
To determine the prognostic significance of sentinel-node biopsy in patients with malignant melanoma (unlike the United States, a sentinel-node biopsy is still not routinely performed on melanoma patients in the Netherlands, as the outcomes of prospectively randomised clinical trials are being awaited).
Retrospective.
Between 1996 and 2001 a sentinel-node biopsy and a re-excision of the scar of the diagnostic biopsy were performed on all melanoma patients who had a Breslow thickness > or = 1 mm or a Clark level > or = IV. At operation the sentinel node was identified with a gamma probe and patent blue. It was removed and sent for pathological investigation for the presence of melanoma cells. If the sentinel node was tumour positive, a dissection of the regional lymph-node basin was performed. Subsequently, these patients were put forward for the European Organisation for Research and Treatment of Cancer (EORTC) peginterferon alfa(2b) adjuvant treatment study.
A sentinel-node biopsy was performed in 61 lymphnode basins in 57 patients (18 male and 39 female; median age: 45 years (range: 9-80)). The median Breslow thickness of the melanomas was 2.2 mm (range: 0.7-13 mm). In 10 of the 61 cases histological examination of the sentinel node demonstrated tumour cells. In 2 additional cases tumour cells were demonstrated only by immunohistochemical studies or complete dissection of the node. Eight regional lymph-node basins were dissected, two of which contained additional metastases. The median follow-up was 36 months (range: 1-68). During follow-up 12 of the 57 patients were found to have metastases, in 8 of these patients the sentinel-node biopsy contained tumour cells. The negative predictive value of a tumourless sentinel node with respect to the later occurrence of distant metastases was 92%.
The patients with a tumour-positive sentinel node had a poorer prognosis with respect to distant metastases than patients with a tumour-negative node. This is the main reason for performing sentinel-node biopsy: to predict the prognosis of the disease. Therefore sentinel-node biopsy should be incorporated into the treatment of patients with malignant melanoma.
确定前哨淋巴结活检对恶性黑色素瘤患者的预后意义(与美国不同,在荷兰黑色素瘤患者仍未常规进行前哨淋巴结活检,因为正在等待前瞻性随机临床试验的结果)。
回顾性研究。
1996年至2001年间,对所有Breslow厚度≥1mm或Clark分级≥IV级的黑色素瘤患者进行了前哨淋巴结活检以及对诊断性活检瘢痕的再次切除。手术中用γ探测器和专利蓝识别前哨淋巴结。将其切除并送去进行黑色素瘤细胞存在情况的病理检查。如果前哨淋巴结肿瘤阳性,则进行区域淋巴结清扫。随后,这些患者被纳入欧洲癌症研究与治疗组织(EORTC)聚乙二醇干扰素α(2b)辅助治疗研究。
对57例患者(18例男性和39例女性;中位年龄:45岁(范围:9 - 80岁))的61个淋巴结区域进行了前哨淋巴结活检。黑色素瘤的中位Breslow厚度为2.2mm(范围:0.7 - 13mm)。在61例病例中的10例,前哨淋巴结的组织学检查显示有肿瘤细胞。另外2例仅通过免疫组化研究或对淋巴结的完整清扫发现肿瘤细胞。对8个区域淋巴结进行了清扫,其中2个含有额外转移灶。中位随访时间为36个月(范围:1 - 68个月)。随访期间,57例患者中有12例发生转移,其中8例患者的前哨淋巴结活检含有肿瘤细胞。无前肿瘤前哨淋巴结对远处转移后期发生的阴性预测值为92%。
前哨淋巴结肿瘤阳性的患者与肿瘤阴性的患者相比,远处转移的预后较差。这是进行前哨淋巴结活检的主要原因:预测疾病的预后。因此,前哨淋巴结活检应纳入恶性黑色素瘤患者的治疗中。