Asou N, Adachi K, Tamura J, Kanamaru A, Kageyama S, Hiraoka A, Omoto E, Akiyama H, Tsubaki K, Saito K, Kuriyama K, Oh H, Kitano K, Miyawaki S, Takeyama K, Yamada O, Nishikawa K, Takahashi M, Matsuda S, Ohtake S, Suzushima H, Emi N, Ohno R
Kumamoto University Hospital, Japan.
J Clin Oncol. 1998 Jan;16(1):78-85. doi: 10.1200/JCO.1998.16.1.78.
We conducted a multicenter study of differentiation therapy with all-trans retinoic acid (ATRA) followed by intensive chemotherapy in patients with newly diagnosed acute promyelocytic leukemia (APL) and analyzed the prognostic factors for predicting complete remission (CR), event-free survival (EFS), and disease-free survival (DFS).
All patients received ATRA until CR. If patients had an initial leukocyte count greater than 3.0 x 10(9)/L, they received daunorubicin (DNR) and behenoyl cytarabine (BHAC). During therapy, if patients showed blast and promyelocyte counts greater than 1.0 x 10(9)/L, they received additional DNR and BHAC. After achieving CR, patients received three courses of consolidation and six courses of maintenance/intensification chemotherapy.
Of 198 registered, 196 were assessable (age range, 15 to 86 years; median, 46) and 173 (88%) achieved CR. Multivariate analysis showed that no or minor purpura at diagnosis (P = .0046) and age less than 30 years (P = .0076) were favorable factors for achievement of CR. Predicted 4-year overall survival and EFS rates were 74% and 54%, respectively, and the 4-year predicted DFS rate for 173 CR patients was 62%. Multivariate analysis showed that age less than 30 years (P = .0003) and initial leukocyte count less than 10 x 10(9)/L (P = .0296) were prognostic factors for longer EFS, and initial leukocyte count less than 10.0 x 10(9)/L was a sole significant prognostic factor for longer DFS (P = .0001).
Our results show that age, hemorrhagic diathesis, and initial leukocyte count are prognostic factors for APL treated with ATRA followed by intensive chemotherapy.
我们开展了一项多中心研究,对新诊断的急性早幼粒细胞白血病(APL)患者采用全反式维甲酸(ATRA)进行分化治疗,随后进行强化化疗,并分析预测完全缓解(CR)、无事件生存期(EFS)和无病生存期(DFS)的预后因素。
所有患者接受ATRA治疗直至CR。如果患者初始白细胞计数大于3.0×10⁹/L,则接受柔红霉素(DNR)和山嵛酰阿糖胞苷(BHAC)治疗。在治疗期间,如果患者的原始细胞和早幼粒细胞计数大于1.0×10⁹/L,则接受额外的DNR和BHAC治疗。达到CR后,患者接受三个疗程的巩固治疗和六个疗程的维持/强化化疗。
在登记的198例患者中,196例可评估(年龄范围15至86岁;中位数46岁),173例(88%)达到CR。多因素分析显示,诊断时无紫癜或仅有轻微紫癜(P = 0.0046)以及年龄小于30岁(P = 0.0076)是实现CR的有利因素。预测的4年总生存率和EFS率分别为74%和54%,173例CR患者的4年预测DFS率为62%。多因素分析显示,年龄小于30岁(P = 0.0003)和初始白细胞计数小于10×10⁹/L(P = 0.0296)是EFS较长的预后因素,而初始白细胞计数小于10.0×10⁹/L是DFS较长的唯一显著预后因素(P = 0.0001)。
我们的结果表明,年龄、出血素质和初始白细胞计数是接受ATRA治疗后再进行强化化疗的APL患者的预后因素。