Smith Roy E
National Surgical Adjuvant Breast and Bowel Project, Pittsburgh, PA 15212, USA.
Clin Breast Cancer. 2003 Oct;4(4):273-9. doi: 10.3816/cbc.2003.n.032.
Regimens of adjuvant chemotherapy for early-stage breast cancer commonly include alkylating agents and anthracyclines. These agents have been associated with treatment-related acute myelocytic leukemia (AML) or myelodysplastic syndrome (MDS). This article reviews the medical literature concerning the incidence, causes, and natural history of treatment-related AML/MDS, with emphasis on the association of these factors with alkylating agents, topoisomerase inhibitors, growth factors, and radiation treatment. Data from 6 completed adjuvant National Surgical Adjuvant Breast and Bowel Project trials that tested regimens containing doxorubicin and cyclophosphamide were reviewed to characterize the incidence of treatment-related AML/MDS. The regimens differed in cyclophosphamide intensity, cumulative cyclophosphamide dose, and the presence or absence of mandated prophylactic support with growth factor and ciprofloxacin. Rates were compared across regimens, by patient age, and by treatment with or without adjuvant in-breast radiation therapy (RT). The relative risk (RR) for the development of treatment-related AML/MDS was greater for patients undergoing the more-intense regimens than for those undergoing standard AC (doxorubicin/cyclophosphamide) regimens (RR, 6.16; P<0.0001). Risk correlated more closely with dose intensity than with cumulative dose, and the data suggested that granulocyte colony-stimulating factor (G-CSF) dose may also be independently correlated with increased risk. Patients who received in-breast RT experienced more secondary AML/MDS than those who did not (RR, 2.38; P=0.006). Patients treated with AC with intensified doses of cyclophosphamide requiring G-CSF support had increased rates of treatment-related AML/MDS, even though the incidence was slight relative to breast cancer relapse. In-breast RT appeared to be associated with an increased risk of AML/MDS.
早期乳腺癌的辅助化疗方案通常包括烷化剂和蒽环类药物。这些药物与治疗相关的急性髓细胞白血病(AML)或骨髓增生异常综合征(MDS)有关。本文回顾了有关治疗相关AML/MDS的发病率、病因和自然史的医学文献,重点关注这些因素与烷化剂、拓扑异构酶抑制剂、生长因子和放射治疗的关联。回顾了6项已完成的国家外科辅助乳腺和肠道项目试验的数据,这些试验测试了含阿霉素和环磷酰胺的方案,以确定治疗相关AML/MDS的发病率。这些方案在环磷酰胺强度、累积环磷酰胺剂量以及是否有生长因子和环丙沙星的强制性预防性支持方面存在差异。比较了不同方案、患者年龄以及接受或未接受辅助性乳腺内放射治疗(RT)患者的发病率。接受更强方案治疗的患者发生治疗相关AML/MDS的相对风险(RR)高于接受标准AC(阿霉素/环磷酰胺)方案的患者(RR,6.16;P<0.0001)。风险与剂量强度的相关性比与累积剂量的相关性更密切,数据表明粒细胞集落刺激因子(G-CSF)剂量也可能与风险增加独立相关。接受乳腺内放疗的患者比未接受放疗的患者发生继发性AML/MDS的情况更多(RR,2.38;P=0.006)。接受需要G-CSF支持的强化剂量环磷酰胺的AC治疗的患者,治疗相关AML/MDS的发生率增加,尽管相对于乳腺癌复发而言发生率较低。乳腺内放疗似乎与AML/MDS风险增加有关。