在费城阴性B细胞前体急性淋巴细胞白血病老年患者中,通过实际应用微小残留病(MRD)监测进行强化化疗后获得满意结果:一项基于瑞典登记处的研究
Satisfactory outcome after intensive chemotherapy with pragmatic use of minimal residual disease (MRD) monitoring in older patients with Philadelphia-negative B cell precursor acute lymphoblastic leukaemia: a Swedish registry-based study.
作者信息
Bergfelt Emma, Kozlowski Piotr, Ahlberg Lucia, Hulegårdh Erik, Hägglund Hans, Karlsson Karin, Markuszewska-Kuczymska Alicja, Tomaszewska-Toporska Beata, Smedmyr Bengt, Åström Maria, Amini Rose-Marie, Hallböök Heléne
机构信息
Department of Medical Sciences, Haematology, Uppsala University, Uppsala, Sweden,
出版信息
Med Oncol. 2015 Apr;32(4):135. doi: 10.1007/s12032-015-0582-2. Epub 2015 Mar 22.
The introduction of minimal residual disease (MRD) monitoring, in the Swedish national guidelines for acute lymphoblastic leukaemia, was evaluated in 35 patients aged 46-79 years (median 61), who were diagnosed from 2007 to 2011 and treated with high-intensity, block-based chemotherapy (ABCDV/VABA induction). Both a high complete remission rate (91 %) and acceptable overall survival (OS) rate (47 %) at 5 years were achieved. MRD by flow cytometry was measured in 73 % of the patients reaching complete remission after the first course, but was omitted by the clinicians for eight patients who were either over 70 years of age or already met conventional high-risk criteria. Factors negatively influencing OS were age over 65 years and WHO status ≥2. MRD < 0.1 % after induction had positive impact on continuous complete remission but not on OS. Only five patients were allocated to allogeneic haematopoietic stem cell transplantation in first remission, mainly due to conventional high risk factors. Thus, use of intensive remission induction therapy is effective in a selection of older patients. In a population for whom the possibilities of treatment escalation are limited, the optimal role of MRD monitoring remains to be determined.
在瑞典急性淋巴细胞白血病国家指南中引入微小残留病(MRD)监测,对2007年至2011年诊断的35例年龄在46 - 79岁(中位年龄61岁)的患者进行了评估,这些患者接受了高强度的、基于疗程的化疗(ABCDV/VABA诱导方案)。5年时达到了较高的完全缓解率(91%)和可接受的总生存率(OS,47%)。73%达到首次疗程后完全缓解的患者进行了流式细胞术MRD检测,但临床医生未对8例年龄超过70岁或已符合传统高危标准的患者进行检测。对总生存率有负面影响的因素是年龄超过65岁和世界卫生组织(WHO)状态≥2。诱导后MRD<0.1%对持续完全缓解有积极影响,但对总生存率无影响。仅5例患者在首次缓解期接受了异基因造血干细胞移植,主要是由于传统高危因素。因此,强化缓解诱导治疗在部分老年患者中有效。在治疗升级可能性有限的人群中,MRD监测的最佳作用仍有待确定。