Röllig Christoph, Schäfer-Eckardt Kerstin, Hänel Matthias, Kramer Michael, Schaich Markus, Thiede Christian, Oelschlägel Uta, Mohr Brigitte, Wagner Thomas, Einsele Hermann, Krause Stefan W, Bodenstein Heinrich, Martin Sonja, Stuhlmann Reingard, Ho Antony D, Bornhäuser Martin, Ehninger Gerhard, Schuler Ulrich, Platzbecker Uwe
Medizinische Klinik und Poliklinik I, Universitätsklinikum Dresden, Fetscherstraße 74, 01307, Dresden, Germany.
Ann Hematol. 2015 Apr;94(4):557-63. doi: 10.1007/s00277-014-2242-6. Epub 2014 Nov 5.
The combination of all-trans retinoic acid (ATRA) and idarubicin (AIDA) for induction therapy followed by three cycles of risk-adapted consolidation cycles is considered standard of care for patients with acute promyelocytic leukemia (APL). We report the outcome of 141 patients (median age 51 years; range, 19-82, 31 % ≥60 years) enrolled into the prospective Study Alliance Leukemia (SAL)-AIDA2000 trial, which comprised AIDA-based induction followed by only two courses of risk-adapted consolidation (daunorubicin or mitoxantrone ± cytarabine) followed by 2-year maintenance treatment. The early death rate was 7 % (median age 66 years), and additional 9 % stopped further treatment after induction. The estimated 6-year disease-free survival (DFS) was 80 % in all patients, 84 % in patients ≤60 and 72 % in patients >60 years (p = 0.140). No significant survival differences were observed between the high-risk and the non-high-risk patients (6-year OS 78 vs. 81 %, p = 0.625). Our results confirm the efficacy of a risk-adapted approach in APL patients. Furthermore, long-term outcomes are comparable to the results obtained with three cycles of consolidation. A modification of the number and intensity of conventional consolidation treatment may be a less toxic but equally effective approach and should be considered for further evaluation in randomized clinical trials in APL.
全反式维甲酸(ATRA)与伊达比星(AIDA)联合用于诱导治疗,随后进行三个周期的风险适应性巩固治疗,被认为是急性早幼粒细胞白血病(APL)患者的标准治疗方案。我们报告了141例患者(中位年龄51岁;范围19 - 82岁,31%≥60岁)的治疗结果,这些患者参加了前瞻性研究联盟白血病(SAL)- AIDA2000试验,该试验包括以AIDA为基础的诱导治疗,随后仅进行两个疗程的风险适应性巩固治疗(柔红霉素或米托蒽醌±阿糖胞苷),然后进行2年的维持治疗。早期死亡率为7%(中位年龄66岁),另有9%的患者在诱导治疗后停止进一步治疗。所有患者的估计6年无病生存率(DFS)为80%,≤60岁患者为84%,>60岁患者为72%(p = 0.140)。高危和非高危患者之间未观察到显著的生存差异(6年总生存率78%对81%,p = 0.625)。我们的结果证实了风险适应性治疗方法在APL患者中的疗效。此外,长期结果与三个周期巩固治疗所获得的结果相当。对传统巩固治疗的次数和强度进行调整可能是一种毒性较小但同样有效的方法,应考虑在APL的随机临床试验中进行进一步评估。