Linker C A, Levitt L J, O'Donnell M, Forman S J, Ries C A
Department of Medicine, University of California, San Francisco.
Blood. 1991 Dec 1;78(11):2814-22.
We treated 109 patients with adult acute lymphoblastic leukemia (ALL) diagnosed by histochemical and immunologic techniques. Patients were excluded only for age greater than 50 years and Burkitt's leukemia. Treatment included a four-drug remission induction phase followed by alternating cycles of noncrossresistant chemotherapy and prolonged oral maintenance therapy. Eighty-eight percent of patients entered complete remission. With a median follow-up of 77 months (range, 48 to 111 months), 42% +/- 6% (SEM) of patients achieving remission are projected to remain disease-free at 5 years, and disease-free survival for all patients entered on study is 35% +/- 5%. Failure to achieve remission within the first 4 weeks of therapy and the presence of the Philadelphia chromosome are associated with a 100% risk of relapse. Remission patients with neither of these adverse features have a 48% +/- 6% probability of remaining in continuous remission for 5 years. Patients with T-cell phenotype have a favorable prognosis with 59% +/- 13% of patients achieving remission remaining disease-free compared with 31% +/- 7% of CALLA-positive patients. Intensive chemotherapy may produce prolonged disease-free survival in a sizable fraction of adults with ALL. Improved therapy is needed, especially for patients with adverse prognostic features.
我们对109例经组织化学和免疫技术诊断的成人急性淋巴细胞白血病(ALL)患者进行了治疗。仅因年龄大于50岁和伯基特白血病而排除患者。治疗包括一个四药缓解诱导期,随后是交替进行的非交叉耐药化疗周期和长期口服维持治疗。88%的患者进入完全缓解期。中位随访77个月(范围48至111个月),预计缓解的患者中有42%±6%(标准误)在5年时仍无疾病,所有纳入研究的患者的无病生存率为35%±5%。治疗的前4周内未达到缓解以及存在费城染色体与100%的复发风险相关。没有这些不良特征的缓解患者有48%±6%的概率持续缓解5年。T细胞表型的患者预后良好,达到缓解的患者中有59%±13%仍无疾病,而CALLA阳性患者为31%±7%。强化化疗可能使相当一部分成人ALL患者获得延长的无病生存期。需要改进治疗方法,尤其是针对具有不良预后特征的患者。