Joensuu H, Ristamäki R, Söderström K O, Jalkanen S
Department of Oncology, University of Turku, Finland.
J Clin Oncol. 1994 Oct;12(10):2167-75. doi: 10.1200/JCO.1994.12.10.2167.
To investigate the prognostic value of cell proliferation rate in non-Hodgkin's lymphoma, study its association with histologic classification, and investigate whether its predictive value is influenced by the type of treatment given.
The S-phase fraction (SPF) size was determined by DNA flow cytometry from paraffin-embedded tissue obtained at diagnosis from 490 patients with non-Hodgkin's lymphoma, diagnosed in a defined geographic area from 1970 to 1991. Clinical data were collected from hospital records and the files of the Finnish Cancer Registry.
SPF size correlated well with histologic grading performed either according to the Working Formulation or Kiel classification (P < .0001 for both). The mean SPFs of low-, intermediate-, and high-grade malignant lymphomas were 4.9% (95% confidence interval [CI], 4.2% to 5.5%), 10.3% (95% CI, 9.3% to 11.4%), and 15.5% (95% CI, 14.0% to 16.9%), respectively. Lymphomas with an SPF lower than the median (7.9%) had a 58% 5-year and 44% 15-year survival rate, whereas those with an SPF larger than the median had a 44% 5-year and 40% 15-year survival rate (P < .0001). SPF size was not significantly associated with prognosis in some subgroups, such as among patients treated primarily with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) (n = 114) or cyclophosphamide, vincristine, and prednisone (COP) (n = 124) with or without radiotherapy (P > .05), whereas a stronger association was found among patients with stage I or II lymphoma treated with radiotherapy only (n = 100; P = .003) and among patients with stage III or IV lymphoma who did not receive chemotherapy (n = 44; P < .0001). In multivariate analyses that included the factors used to construct the International Prognostic Index, SPF had independent prognostic value both in low-grade and intermediate- or high-grade lymphomas, but not in the subset of patients treated with combination chemotherapy with or without radiotherapy.
Cell proliferation rate measured as SPF is closely associated with histologic grading in non-Hodgkin's lymphoma, and it has independent prognostic value. The treatment given influences considerably the prognostic value of SPF.
探讨细胞增殖率在非霍奇金淋巴瘤中的预后价值,研究其与组织学分类的关系,并研究其预测价值是否受所给予治疗类型的影响。
通过DNA流式细胞术测定1970年至1991年在特定地理区域诊断的490例非霍奇金淋巴瘤患者诊断时石蜡包埋组织中的S期细胞分数(SPF)大小。临床数据从医院记录和芬兰癌症登记处的档案中收集。
SPF大小与根据工作分类法或基尔分类法进行的组织学分级密切相关(两者P均<.0001)。低、中、高级别恶性淋巴瘤的平均SPF分别为4.9%(95%置信区间[CI],4.2%至5.5%)、10.3%(95%CI,9.3%至11.4%)和15.5%(95%CI,14.0%至16.9%)。SPF低于中位数(7.9%)的淋巴瘤5年生存率为58%,15年生存率为44%,而SPF高于中位数的淋巴瘤5年生存率为44%,15年生存率为40%(P<.0001)。在一些亚组中,SPF大小与预后无显著相关性,如主要接受环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)治疗(n = 114)或环磷酰胺、长春新碱和泼尼松(COP)治疗(n = 124)且无论有无放疗的患者(P>.05),而在仅接受放疗的I期或II期淋巴瘤患者(n = 100;P =.003)和未接受化疗的III期或IV期淋巴瘤患者(n = 44;P<.0001)中发现更强的相关性。在包括用于构建国际预后指数的因素的多变量分析中,SPF在低级别和中或高级别淋巴瘤中均具有独立的预后价值,但在接受联合化疗且无论有无放疗的患者亚组中则不然。
以SPF衡量的细胞增殖率与非霍奇金淋巴瘤的组织学分级密切相关,且具有独立的预后价值。所给予的治疗对SPF的预后价值有相当大的影响。