Sancho Juan-Manuel, Ribera Josep-Maria, Xicoy Blanca, Morgades Mireia, Oriol Albert, Tormo Mar, del Potro Eloy, Debén Guillermo, Abella Eugenia, Bethencourt Concepción, Ortín Xavier, Brunet Salut, Ortega-Rivas Fernando, Novo Andrés, López Ramón, Hernández-Rivas Jesús-María, Sanz Miguel-Angel, Feliu Evarist
Clinical Hematology Department, Institut Catalá d'Oncologia-Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
Eur J Haematol. 2007 Feb;78(2):102-10. doi: 10.1111/j.1600-0609.2006.00778.x. Epub 2006 Nov 6.
Only 20-30% of elderly patients with acute lymphoblastic leukemia (ALL) are enrolled in clinical trials because of co-morbid disorders or poor performance status. We present the results of treatment of Philadelphia chromosome-negative (Ph-) ALL patients over 55 yr treated in the PETHEMA ALL-96 trial.
From 1996 to 2006, 33 patients > or = 55 yr with Ph- ALL were included. Induction therapy was vincristine, daunorubicin, prednisone, asparaginase, and cyclophosphamide over 5 weeks. Central nervous system (CNS) prophylaxis involved triple intrathecal (IT) therapy, 14 doses over the first year. Consolidation-1 included mercaptopurine, methotrexate, teniposide and cytarabine, followed by one consolidation-2 cycle similar to the induction cycle. Maintenance consisted of mercaptopurine and methotrexate up to 2 yr in complete remission (CR) with monthly reinduction cycles (vincristine, prednisone and asparaginase) during the first year.
Median (range) age was 65 yr (56-77). Phenotype (30 patients): early-pre-B 7, common/pre-B 18, T 5. Cytogenetics (28 patients): normal 12, complex 10, t(4;11) 2 and other 4. CR was achieved in 19/33 (57.6%) patients, early death occurred in 12 (36.4%) and 2 (6%) were resistant. Overall survival and disease-free survival probabilities (2 yr, 95% CI) were 39% (21%-57%) and 46% (22%-70%), respectively (median follow up of 24 months). Removal of asparaginase and cyclophosphamide from the induction decreased induction death (OR 0.119, CI 95% 0.022-0.637, P = 0.013) and increased survival (20% vs. 52%, P = 0.05).
The prognosis of elderly Ph- ALL patients is poor. In this study, less intensive induction decreased toxic death, allowing delivery of planned consolidation therapy and increased survival probability.
由于合并症或身体状况不佳,仅有20%-30%的老年急性淋巴细胞白血病(ALL)患者参与临床试验。我们展示了在PETHEMA ALL-96试验中治疗的55岁以上费城染色体阴性(Ph-)ALL患者的治疗结果。
1996年至2006年,纳入了33例年龄≥55岁的Ph- ALL患者。诱导治疗为在5周内使用长春新碱、柔红霉素、泼尼松、天冬酰胺酶和环磷酰胺。中枢神经系统(CNS)预防包括鞘内三联治疗,第一年14剂。巩固治疗-1包括巯嘌呤、甲氨蝶呤、替尼泊苷和阿糖胞苷,随后进行一个与诱导周期相似的巩固治疗-2周期。维持治疗包括在完全缓解(CR)状态下使用巯嘌呤和甲氨蝶呤长达2年,第一年每月进行再诱导周期(长春新碱、泼尼松和天冬酰胺酶)。
中位(范围)年龄为65岁(56-77岁)。表型(30例患者):早前B细胞型7例,普通/前B细胞型18例,T细胞型5例。细胞遗传学(28例患者):正常12例,复杂核型10例,t(4;11) 2例,其他4例。19/33(57.6%)例患者达到CR,12例(36.4%)早期死亡,2例(6%)耐药。总生存和无病生存概率(2年,95%CI)分别为39%(21%-57%)和46%(22%-70%)(中位随访24个月)。诱导治疗中去除天冬酰胺酶和环磷酰胺可降低诱导期死亡(OR 0.119,CI 95% 0.022-0.637,P = 0.013)并提高生存率(20%对52%,P = 0.05)。
老年Ph- ALL患者预后较差。在本研究中,强度较低的诱导治疗降低了毒性死亡,使计划的巩固治疗得以进行并提高了生存概率。