Glucksberg H, Cheever M A, Farewell V T, Fefer A, Thomas E D
Cancer. 1983 Jul 15;52(2):198-205. doi: 10.1002/1097-0142(19830715)52:2<198::aid-cncr2820520203>3.0.co;2-a.
Thirty-nine adults with acute nonlymphoblastic leukemia (ANL) in complete remission (CR) for six months were considered for intensification therapy. All patients had received a high dose chemotherapeutic remission-induction regimen consisting of daunorubicin, cytosine arabinoside, 6-thioguanine, prednisone, and vincristine, followed by one consolidation course of the same drugs at reduced doses and then monthly maintenance course of low-dose chemotherapy. The intensification therapy consisted of the same intensive chemotherapy regimen utilized for remission induction in place of the sixth and 12th monthly courses of postremission induction chemotherapy. Twenty-three of the 39 patients received intensification therapy, whereas 16 patients refused or were not offered such therapy for medical reasons and, therefore, received only monthly therapy. The median remission duration of the 23 patients who received intensification therapy was 157 weeks, and 9 remain in continuous first remission at 176-285 weeks. The remission duration of the 16 patients who did not receive intensification therapy was 73 weeks (P = 0.03). Kaplan-Meier estimates of remission duration and survival from time of remission computed by including the patients who either relapsed or received bone marrow transplantation before the time of intensification (6 months) revealed a median remission duration and survival of 100 and 172 weeks for patients receiving intensification compared to 37 and 72 weeks, respectively, for patients not receiving intensification therapy. Since results in patients not receiving intensification therapy are consistent with our previous results in patients receiving the same induction and consolidation regimens without intensification, this nonrandomized study suggests that intensification therapy prolongs remission duration and survival in adults with ANL.
三十九名急性非淋巴细胞白血病(ANL)患者在完全缓解(CR)六个月后被考虑进行强化治疗。所有患者均接受了由柔红霉素、阿糖胞苷、6-硫鸟嘌呤、泼尼松和长春新碱组成的高剂量化疗缓解诱导方案,随后以较低剂量进行了一个相同药物的巩固疗程,然后是每月一次的低剂量化疗维持疗程。强化治疗包括使用与缓解诱导相同的强化化疗方案,取代缓解后诱导化疗的第六和第十二个月疗程。39名患者中有23名接受了强化治疗,而16名患者因医学原因拒绝或未接受此类治疗,因此仅接受每月一次的治疗。接受强化治疗的23名患者的中位缓解持续时间为157周,其中9名在176 - 285周时仍处于首次持续缓解状态。未接受强化治疗的16名患者的缓解持续时间为73周(P = 0.03)。通过纳入在强化治疗前(6个月)复发或接受骨髓移植的患者计算的Kaplan - Meier缓解持续时间和缓解后生存估计显示,接受强化治疗的患者的中位缓解持续时间和生存分别为100周和172周,而未接受强化治疗的患者分别为37周和72周。由于未接受强化治疗的患者的结果与我们之前对接受相同诱导和巩固方案但未进行强化治疗的患者的结果一致,这项非随机研究表明强化治疗可延长ANL成人患者的缓解持续时间和生存期。