Graham C H, Rivers J, Kerbel R S, Stankiewicz K S, White W L
Cancer Research Division, Sunnybrook Health Science Centre, Reichmann Research Institute, Toronto, Ontario, Canada.
Am J Pathol. 1994 Sep;145(3):510-4.
Angiogenesis in malignant melanoma (MM) was evaluated by comparing mean vessel number (MVN) in Spitz's nevi (SN), thick and thin MMs that metastasized, and thick and thin MMs with > or = 10-year survival. Vessels were identified with antibodies against factor VIII-related antigen (FVIII) and CD34 in 37 MMs (17 < or = 1.9 mm and 20 > or = 4.0 mm) with > or = 10-year follow-up and 10 SN from children (< or = 9 years old). Fields (x250) with the highest vessel density were counted by independent observers blinded to clinical outcome. There were no differences in MVN between SN versus MMs (P = 1.0), but the distribution of vessels was much more uniform in SN. Seven MM pairs (> or = 5.5 mm) and five pairs (< or = 0.75 mm) were matched by sex, age, site, stage, and primary treatment (paired t-test). In the pairs > or = 5.5 mm, there was no correlation with MVN with either metastasis or death (FVIII P = 0.98; CD34 P = 0.85). Among the thin paired lesions, high MVN (FVIII = 46, CD34 = 39) was significantly related not only to metastasis (FVIII P = 0.04, CD34 P = 0.03) but also to death (FVIII P = 0.04, CD34 P = 0.05). MVN does not separate SN versus MM nor predict outcome in thick (> or = 4.0 mm) MMs; however, high MVN (> or = 42 average) is predictive of metastasis and death in MMs < or = 0.75 mm. Larger matched studies are indicated to confirm this observation.
通过比较斯皮茨痣(SN)、发生转移的厚皮和薄皮恶性黑色素瘤(MM)以及生存时间≥10年的厚皮和薄皮MM中的平均血管数(MVN),对恶性黑色素瘤中的血管生成进行评估。在37例随访时间≥10年的MM(17例≤1.9mm,20例≥4.0mm)和10例儿童(≤9岁)的SN中,用抗VIII因子相关抗原(FVIII)和CD34抗体识别血管。由对临床结果不知情的独立观察者对血管密度最高的视野(×250)进行计数。SN和MM之间的MVN没有差异(P = 1.0),但SN中的血管分布更均匀。7对MM(≥5.5mm)和5对(≤0.75mm)按性别、年龄、部位、分期和初始治疗进行匹配(配对t检验)。在≥5.5mm的配对中,MVN与转移或死亡均无相关性(FVIII P = 0.98;CD34 P = 0.85)。在薄皮配对病变中,高MVN(FVIII = 46,CD34 = 39)不仅与转移显著相关(FVIII P = 0.04,CD34 P = 0.03),而且与死亡显著相关(FVIII P = 0.04,CD34 P = 0.05)。MVN不能区分SN和MM,也不能预测厚皮(≥4.0mm)MM的预后;然而,高MVN(≥42平均)可预测≤0.75mm的MM发生转移和死亡。需要进行更大规模的匹配研究来证实这一观察结果。