Perel Yves, Auvrignon Anne, Leblanc Thierry, Vannier Jean-Pierre, Michel Gerard, Nelken Brigitte, Gandemer Virginie, Schmitt Claudine, Lamagnere Jean-Pierre, De Lumley Lionel, Bader-Meunier Brigitte, Couillaud Gerard, Schaison Gerard, Landman-Parker Judith, Thuret Isabelle, Dalle Jean-Hugues, Baruchel Andre, Leverger Guy
Unité d'Onco-Hématologie, Département de Pédiatrie, Hôpital des Enfants, Groupe Hospitalier Pellegrin, Centres Hospitalo-Universitaires de Bordeaux, France.
J Clin Oncol. 2002 Jun 15;20(12):2774-82. doi: 10.1200/JCO.2002.07.300.
To determine whether the use of maintenance therapy (MT) delivered after intensive induction and consolidation therapy confers any advantage in childhood acute myeloid leukemia (AML).
A total of 268 children with AML were registered in the Leucámie Aiquë Myéloïde Enfant (LAME) 89/91 protocol. This regimen included an intensive induction phase (mitoxantrone plus cytarabine) and, for patients without allograft, two consolidation courses, one containing timed-sequential high-dose cytarabine, asparaginase, and amsacrine. In the LAME 89 pilot study, patients were given an additional MT consisting of mercaptopurine and cytarabine for 18 months. In the LAME 91 trial, patients were randomized to receive or not receive MT.
A total of 241 (90%) of 268 patients achieved a complete remission. The overall survival and event-free survival at 6 years were 60% +/- 6% and 48% +/- 6%, respectively. For the complete responders after consolidation therapy, the 5-year disease-free survival was not significantly different in MT-negative and in MT-positive randomized patients (respectively, 60% +/- 19% v 50% +/- 15%; P =.25), whereas the 5-year overall survival was significantly better in MT-negative randomized patients (81% +/- 13% v 58% +/- 15%; P =.04) due to a higher salvage rate after relapse.
More than 50% of patients can be cured of AML in childhood. Either drug intensity or each of the induction and postremission phases may have contributed to the outstanding improvement in outcome. Low-dose MT is not recommended. Exposure to this low-dose MT may contribute to clinical drug resistance and treatment failure in patients who experience relapse.
确定在强化诱导和巩固治疗后使用维持治疗(MT)是否对儿童急性髓系白血病(AML)有任何益处。
共有268例儿童AML患者登记入Leucámie Aiquë Myéloïde Enfant(LAME)89/91方案。该方案包括强化诱导期(米托蒽醌加阿糖胞苷),对于未进行同种异体移植的患者,有两个巩固疗程,其中一个疗程包含序贯大剂量阿糖胞苷、天冬酰胺酶和安吖啶。在LAME 89试点研究中,患者接受了为期18个月的由巯嘌呤和阿糖胞苷组成的额外MT。在LAME 91试验中,患者被随机分组以接受或不接受MT。
268例患者中有241例(90%)实现完全缓解。6年时的总生存率和无事件生存率分别为60%±6%和48%±6%。对于巩固治疗后的完全缓解者,MT阴性和MT阳性随机分组患者的5年无病生存率无显著差异(分别为60%±19%对50%±15%;P = 0.25),而MT阴性随机分组患者的5年总生存率显著更高(81%±13%对58%±15%;P = 0.04),这是由于复发后的挽救率更高。
超过50%的儿童AML患者可被治愈。药物强度或诱导期及缓解后各阶段可能都对结果的显著改善有所贡献。不推荐低剂量MT。经历复发的患者接触这种低剂量MT可能导致临床耐药和治疗失败。