Karmiris T, Rohatiner A Z, Love S, Carter M, Ganjoo R K, Amess J, Norton A J, Lister T A
ICRF Department of Medical Oncology, St. Bartholomew's Hospital, London, UK.
Hematol Oncol. 1994 Jan-Feb;12(1):29-39. doi: 10.1002/hon.2900120105.
Over a 24-year period, 137 patients were referred for management of newly diagnosed chronic lymphocytic leukemia. One hundred and nineteen patients have been reviewed in terms of response to therapy and prognostic factors for survival; 18 patients were excluded either because lymph node biopsy was not compatible with the diagnosis of CLL (11 patients), or because the lymphocyte count at presentation was < 5 x 10(9)/l (seven patients). Patients were staged retrospectively according to both the Rai and Binet Classifications. Forty-eight per cent (57/119) were deemed not to be in need of any treatment at presentation, 36 per cent (43/119) have never received any specific therapy. The majority of patients received chlorambucil alone, at a dose of 10 mg daily given for 6 weeks, followed by a 2-week interval, followed by three, 2-week cycles. The overall response rate (complete+partial remission) was 38 per cent. In terms of survival, there was a trend in favour of patients who responded to treatment in comparison with those who did not but this did not reach statistical significance (P = 0.07). Correlations with stage were highly significant, the median survivals for patients with stage A, B and C disease (Binet) were 12.5, 8 and 3.5 years respectively. On univariate analysis, the absolute lymphocyte count at presentation was the most significant prognostic factor for survival, patients presenting with an absolute lymphocyte count above 50 x 10(9)/l having a less favourable prognosis (P = 0.002). However, on multivariate analysis, older age, a low hemoglobin, low platelet count, and the presence of lymphadenopathy and fever at presentation correlated adversely with survival. Overall, 40 patients died as a consequence of CLL or from disease-related causes, 34/40 dying of infection. Twenty-one patients developed second cancers. With a median follow-up of 13 years, these results confirm that the two staging systems can separate patients into prognostic groups, however in practice, there is heterogeneity of outcome within stage. New approaches are urgently needed.
在24年的时间里,137例新诊断的慢性淋巴细胞白血病患者被转诊接受治疗。对119例患者的治疗反应和生存预后因素进行了评估;18例患者被排除,其中11例是因为淋巴结活检结果与慢性淋巴细胞白血病的诊断不符,7例是因为就诊时淋巴细胞计数<5×10⁹/L。根据Rai和Binet分类法对患者进行回顾性分期。48%(57/119)的患者在就诊时被认为无需任何治疗,36%(43/119)的患者从未接受过任何特异性治疗。大多数患者仅接受苯丁酸氮芥治疗,剂量为每日10mg,持续6周,随后间隔2周,接着是三个2周的疗程。总缓解率(完全缓解+部分缓解)为38%。在生存方面,与未对治疗产生反应的患者相比,对治疗有反应的患者有生存优势的趋势,但未达到统计学显著性(P = 0.07)。与分期的相关性非常显著,A、B和C期(Binet分类)患者的中位生存期分别为12.5年、8年和3.5年。单因素分析显示,就诊时的绝对淋巴细胞计数是生存的最显著预后因素,就诊时绝对淋巴细胞计数高于50×10⁹/L的患者预后较差(P = 0.002)。然而,多因素分析显示,年龄较大、血红蛋白水平低、血小板计数低以及就诊时存在淋巴结病和发热与生存呈负相关。总体而言,40例患者死于慢性淋巴细胞白血病或与疾病相关的原因,其中34/40死于感染。21例患者发生了第二肿瘤。中位随访13年,这些结果证实这两种分期系统可以将患者分为不同的预后组,但在实际中,各期内的结局存在异质性。迫切需要新的方法。