Deininger Michael W N, Cortes Jorge, Paquette Ron, Park Byung, Hochhaus Andreas, Baccarani Michele, Stone Richard, Fischer Thomas, Kantarjian Hagop, Niederwieser Dietger, Gambacorti-Passerini Carlo, So Charlene, Gathmann Insa, Goldman John M, Smith Douglas, Druker Brian J, Guilhot François
Division of Hematology and Medical Oncology, Oregon Health & Science University Cancer Institute, Portland, Oregon 97239, USA.
Cancer. 2007 Oct 1;110(7):1509-19. doi: 10.1002/cncr.22936.
Clonal cytogenetic abnormalities (CCA) were detected in Philadelphia chromosome (Ph)-negative cells in some patients with chronic myeloid leukemia (CML) who attained a cytogenetic response to imatinib mesylate. In some patients, CCA/Ph-negative status was associated with myelodysplasia or acute myeloid leukemia. The objective of the current study was to determine the prognostic impact of CCA/Ph-negative cells.
The authors compared the pretherapeutic risk factors (Kruskall-Wallis test), exposure to cytotoxic drugs (chi-square test), and overall and progression-free survival (Kaplan-Meyer and logistic regression analysis, respectively) of 515 patients with mostly chronic-phase CML who were treated with imatinib mesylate after failure of interferon-alpha according to whether they attained a major cytogenetic response (MCR) (n = 324 patients), an MCR with CCA/Ph-negative status (n = 30 patients), or no MCR (n = 161 patients).
CCA/Ph-negative status most frequently involved chromosomes Y, 8, and 7. No significant differences in pretherapeutic risk factors were detected between patients who attained an MCR with and without CCA/Ph-negative cells, except that exposure to alkylating agents was more frequent in patients with CCA/Ph-negative cells, and overall and progression-free survival were identical. With a median follow-up of 51 months, only 2 patients developed myelodysplastic syndromes (MDS).
The overall prognosis for patients who had CML with CCA/Ph-negative status was good and was driven by the CML response to imatinib mesylate. Isolated CCA/Ph-negative cells in the absence of morphologic evidence of MDS do not justify a change in therapy.
在一些对甲磺酸伊马替尼获得细胞遗传学反应的慢性髓性白血病(CML)患者的费城染色体(Ph)阴性细胞中检测到克隆性细胞遗传学异常(CCA)。在一些患者中,CCA/Ph阴性状态与骨髓发育异常或急性髓性白血病相关。本研究的目的是确定CCA/Ph阴性细胞的预后影响。
作者比较了515例主要处于慢性期的CML患者的治疗前危险因素(Kruskal-Wallis检验)、细胞毒性药物暴露情况(卡方检验)以及总生存期和无进展生存期(分别采用Kaplan-Meier法和逻辑回归分析),这些患者在α干扰素治疗失败后接受甲磺酸伊马替尼治疗,根据他们是否获得主要细胞遗传学反应(MCR)(n = 324例患者)、具有CCA/Ph阴性状态的MCR(n = 30例患者)或未获得MCR(n = 161例患者)进行分组。
CCA/Ph阴性状态最常涉及染色体Y、8和7。在获得MCR且有和没有CCA/Ph阴性细胞的患者之间,未检测到治疗前危险因素的显著差异,只是CCA/Ph阴性细胞的患者接触烷化剂的频率更高,且总生存期和无进展生存期相同。中位随访51个月时,只有2例患者发生骨髓增生异常综合征(MDS)。
具有CCA/Ph阴性状态的CML患者的总体预后良好,且由CML对甲磺酸伊马替尼的反应所驱动。在没有MDS形态学证据的情况下,孤立的CCA/Ph阴性细胞并不足以证明需要改变治疗方案。