Macdougall L G, Jankowitz P, Cohn R, Bernstein R
Am J Pediatr Hematol Oncol. 1986 Spring;8(1):43-51. doi: 10.1097/00043426-198608010-00009.
Acute childhood leukemia was found to be less common in black children than in white children in the Johannesburg area of South Africa. Of 195 consecutive patients, 78 were black and 117 white. The annual incidence was 0.8/100,000 black children and 3.3/100,000 white. The low incidence in black children was due to the very low incidence of acute lymphoblastic leukemia (ALL), which was 0.41/100,000 black children compared with 2.73/100,000 white children. The incidence of acute nonlymphoblastic leukemia (ANLL) was approximately the same for both ethnic groups; 0.38/100,000 black children and 0.57/100,000 white children. Remission rates for black children with ALL were lower than for white children and the cumulative proportion of black patients surviving at 60 months was only 32% compared with 72% of white patients (p = 0.0001). The most significant poor prognostic factors in ALL were ethnic group and age (p = 0.0006), CNS disease at onset (p = 0.006), FAB L2 and L3 morphology (p = 0.05), and irregular clinic attendance during maintenance therapy (p = 0.05). In ANLL, remission and survival rates were less favorable than in ALL but there were no significant differences between black and white patients. Black patients exhibited certain clinical features rarely seen in white patients, including chloromata, oropharyngeal lesions, and CNS involvement at onset. Karyotypic abnormalities were common. The most significant poor prognostic factors in ANLL were CNS disease at onset (p = 0.03), generalized lymphadenopathy (p = 0.0001), and FAB morphology classification M3-M6 (p = 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
在南非约翰内斯堡地区,发现患急性儿童白血病的黑人儿童比白人儿童少见。在连续的195例患者中,78例为黑人,117例为白人。黑人儿童的年发病率为0.8/10万,白人儿童为3.3/10万。黑人儿童发病率低是由于急性淋巴细胞白血病(ALL)发病率极低,黑人儿童为0.41/10万,而白人儿童为2.73/10万。急性非淋巴细胞白血病(ANLL)在两个种族中的发病率大致相同,黑人儿童为0.38/10万,白人儿童为0.57/10万。患ALL的黑人儿童的缓解率低于白人儿童,60个月时存活的黑人患者累积比例仅为32%,而白人患者为72%(p = 0.0001)。ALL中最显著的不良预后因素是种族和年龄(p = 0.0006)、发病时的中枢神经系统疾病(p = 0.006)、FAB L2和L3形态(p = 0.05)以及维持治疗期间不定期就诊(p = 0.05)。在ANLL中,缓解率和生存率不如ALL,但黑人和白人患者之间没有显著差异。黑人患者表现出一些白人患者罕见的临床特征,包括绿色瘤、口咽病变和发病时的中枢神经系统受累。染色体核型异常很常见。ANLL中最显著的不良预后因素是发病时的中枢神经系统疾病(p = 0.03)、全身淋巴结肿大(p = 0.0001)和FAB形态学分类M3 - M6(p = 0.05)。(摘要截短至250字)