Franzke A, Probst-Kepper M, Buer J, Duensing S, Hoffmann R, Wittke F, Volkenandt M, Ganser A, Atzpodien J
Department of Hematology and Oncology, Medizinische Hochschule Hanover, Germany.
Br J Cancer. 1998 Jul;78(1):40-5. doi: 10.1038/bjc.1998.439.
Very rapid progression of disease with a median survival of 6-9 months is a common feature of metastatic cutaneous malignant melanoma. Nevertheless, substantial variability of survival suggests that metastatic cutaneous malignant melanoma can be divided into several biological subgroups. Pretreatment serum levels of soluble adhesion molecules and various clinical parameters in cutaneous metastatic malignant melanoma were evaluated to determine their prognostic value. In this study pretreatment serum levels of soluble vascular cell adhesion molecule 1 (sVCAM-1), soluble intercellular cell adhesion molecule 1 (sICAM-1), soluble endothelial leukocyte adhesion molecule 1 (sE-selectin) and multiple clinical factors were assessed in relation to overall survival of 97 consecutive patients with metastatic cutaneous malignant melanoma seen at our institution between May 1990 and April 1996. For statistical analysis, both univariate and multivariate Cox proportional-hazards models were used. Elevated pretreatment serum levels of sVCAM-1 (P < 0.005) and of lactate dehydrogenase (P < 0.002) were rendered statistically independent and were significantly associated with unfavourable outcome. Patients were assigned to one of three risk categories (low, intermediate and high) according to a cumulative risk score defined as the function of the sum of these two variables. There were significant differences in overall survival (P < 0.0001) between low- (n = 53, 5-year survival probability of 23.3%), intermediate- (n = 29, 5-year survival probability of 9.9%) and high-risk (n = 15) patients. Elevated pretreatment serum levels of sVCAM-1 and of lactate dehydrogenase correlate with poor outcome in metastatic cutaneous malignant melanoma. These data support risk stratification for future therapeutic trials and identify factors that need to be validated in prospective studies and may potentially influence decision-making in palliative management of patients with disseminated cutaneous malignant melanoma.
疾病进展极快,中位生存期为6至9个月,这是转移性皮肤恶性黑色素瘤的一个常见特征。然而,生存期的显著差异表明转移性皮肤恶性黑色素瘤可分为几个生物学亚组。为了确定其预后价值,对皮肤转移性恶性黑色素瘤患者治疗前血清可溶性黏附分子水平和各种临床参数进行了评估。在本研究中,对1990年5月至1996年4月期间在我们机构就诊的97例连续性转移性皮肤恶性黑色素瘤患者,评估了其治疗前血清可溶性血管细胞黏附分子1(sVCAM-1)、可溶性细胞间黏附分子1(sICAM-1)、可溶性内皮白细胞黏附分子1(sE-选择素)水平以及多个临床因素与总生存期的关系。为进行统计分析,使用了单变量和多变量Cox比例风险模型。治疗前血清sVCAM-1水平升高(P < 0.005)和乳酸脱氢酶水平升高(P < 0.002)具有统计学独立性,且与不良预后显著相关。根据这两个变量之和定义的累积风险评分,将患者分为三个风险类别之一(低、中、高)。低风险(n = 53,5年生存概率为23.3%)、中风险(n = 29,5年生存概率为9.9%)和高风险(n = 15)患者的总生存期存在显著差异(P < 0.0001)。治疗前血清sVCAM-1水平升高和乳酸脱氢酶水平升高与转移性皮肤恶性黑色素瘤的不良预后相关。这些数据支持未来治疗试验的风险分层,并确定了需要在前瞻性研究中验证的因素,这些因素可能会影响播散性皮肤恶性黑色素瘤患者姑息治疗的决策。