Schouten H C, Sanger W G, Weisenburger D D, Armitage J O
Department of Internal Medicine, University Hospital Maastricht, The Netherlands.
Cancer Genet Cytogenet. 1990 Jul 1;47(1):73-82. doi: 10.1016/0165-4608(90)90265-c.
Several cytogenetic abnormalities involving chromosome 6 occurring in non-Hodgkin's lymphoma (NHL) have been described. We report 34 newly diagnosed patients with NHL who had an abnormal chromosome 6 on initial biopsy. Monosomies (n = 5), trisomies (n = 6), deletions of 6q (n = 13), and isochromosomes 6p (n = 9) were frequently observed and translocations were rare. As compared with 70 other NHL patients with cytogenetic abnormalities, the patients with an abnormal chromosome 6 had a higher frequency of immunoblastic lymphoma (p less than 0.001). These patients also were more likely to have B symptoms (p = 0.02). Patients with a breakpoint at 6q11-16 all had a deletion of the distal portion and also were more likely to have B symptoms (p less than 0.001). Most patients with breakpoints at 6q21-25 had a deletion associated with a lower frequency of stage IV disease (p = 0.03) and a higher complete remission (CR) rate (p = 0.03). The patients with an i(6p) had a lower frequency of stage IV disease (p = 0.03), and the patients with a trisomy 6 had a shorter median survival (p = 0.005). Our results suggest that chromosome 6, especially the long arm, carries important information for the clinical behavior of NHL. Future studies are necessary to resolve the molecular defects.
已描述了非霍奇金淋巴瘤(NHL)中发生的几种涉及6号染色体的细胞遗传学异常。我们报告了34例新诊断的NHL患者,他们在初次活检时6号染色体异常。常见的有单体(n = 5)、三体(n = 6)、6q缺失(n = 13)和6号染色体短臂等臂染色体(n = 9),而染色体易位罕见。与其他70例有细胞遗传学异常的NHL患者相比,6号染色体异常的患者免疫母细胞淋巴瘤发生率更高(p < 0.001)。这些患者也更易出现B症状(p = 0.02)。6q11 - 16有断点的患者均有远端部分缺失,也更易出现B症状(p < 0.001)。大多数6q21 - 25有断点的患者存在与IV期疾病较低发生率(p = 0.03)和较高完全缓解(CR)率(p = 0.03)相关的缺失。6号染色体短臂等臂染色体(i(6p))的患者IV期疾病发生率较低(p = 0.03),6号染色体三体的患者中位生存期较短(p = 0.005)。我们的结果表明,6号染色体,尤其是长臂,携带着NHL临床行为的重要信息。未来有必要开展研究以解决分子缺陷问题。