Ollila Thomas A, Olszewski Adam J, Butera James N, Quesenberry Matthew I, Quesenberry Peter J, Reagan John L
Division of Hematology and Oncology, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI.
Division of Hematology and Oncology, Rhode Island Hospital, The Warren Alpert Medical School of Brown University, Providence, RI.
Clin Lymphoma Myeloma Leuk. 2018 Mar;18(3):204-209. doi: 10.1016/j.clml.2018.01.007. Epub 2018 Jan 31.
Induction chemotherapy for acute myeloid leukemia (AML) is based on the "7+3" cytarabine/anthracycline regimen. A nonhypocellular day 14 (D14) bone marrow sample with a blast count > 5% to 10% is suggestive of residual leukemia, for which a second course of induction chemotherapy has been recommended. Although the prognostic value of D14 bone marrow findings has been established, its use as a decision point is controversial because the benefit of repeat induction has been questioned.
In the present single-center retrospective study of 113 patients with newly diagnosed AML, we evaluated the role of cellularity on the clinical outcomes of patients with residual morphologic leukemia (blasts ≥ 5%). Among 64 patients with D14 bone marrow samples, 31 had residual morphologic leukemia.
The complete remission (CR) rates were greater for the hypocellular (11 of 16) than for the nonhypocellular (4 of 15) patients (P = .03). The median overall survival (OS) for the hypocellular D14 patients was longer than that for the nonhypocellular patients (17 vs. 8 months; P = .02). No significant difference between the receipt of reinduction therapy and CR or OS was found on logistic or survival model analysis. The specificity for residual leukemia on D14 bone marrow samples was better for cellularity ≥ 20% and blasts ≥ 20% than for blasts ≥ 5%.
The results of our study have shown that patients with < 20% cellularity and < 20% blasts on the D14 bone marrow assessment should continue observation until recovery rather than receive additional immediate therapy.
急性髓系白血病(AML)的诱导化疗基于“7 + 3”阿糖胞苷/蒽环类药物方案。第14天(D14)骨髓样本细胞不减少且原始细胞计数>5%至10%提示存在残留白血病,对此推荐进行第二个疗程的诱导化疗。尽管D14骨髓检查结果的预后价值已得到确立,但其作为决策点存在争议,因为重复诱导的益处受到质疑。
在本项针对113例新诊断AML患者的单中心回顾性研究中,我们评估了细胞密度对残留形态学白血病(原始细胞≥5%)患者临床结局的作用。在64例有D14骨髓样本的患者中,31例存在残留形态学白血病。
细胞减少的患者(16例中的11例)完全缓解(CR)率高于细胞未减少的患者(15例中的4例)(P = .03)。细胞减少的D14患者的中位总生存期(OS)长于细胞未减少的患者(17个月对8个月;P = .02)。在逻辑回归或生存模型分析中,再次诱导治疗与CR或OS之间未发现显著差异。D14骨髓样本中残留白血病的特异性,细胞密度≥20%且原始细胞≥20%时优于原始细胞≥5%时。
我们的研究结果表明,D14骨髓评估时细胞密度<20%且原始细胞<20%的患者应继续观察直至恢复,而非立即接受额外治疗。