Tallman M S, Gray R, Bennett J M, Variakojis D, Robert N, Wood W C, Rowe J M, Wiernik P H
Lurie Cancer Center of Northwestern University, Northwestern University Medical School, Chicago, IL 60611, USA.
J Clin Oncol. 1995 Jul;13(7):1557-63. doi: 10.1200/JCO.1995.13.7.1557.
Since large numbers of patients with early-stage breast cancer now receive adjuvant chemotherapy containing cyclophosphamide, a known leukemogenic agent, it is important to determine the risk of secondary acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). Therefore, we identified all cases of AML or MDS developing in patients treated on six clinical adjuvant chemotherapy trials conducted by the Eastern Cooperative Oncology Group (ECOG).
The patients population included 2,638 patients with previously untreated primary operable breast cancer entered onto six clinical trials conducted by the ECOG between 1978 and 1987. There are 19,200 persons-years of follow-up study and a mean follow-up duration of 7.3 years. Clinical data were obtained from flow sheets submitted to the ECOG Data Management Office.
Of 2,638 patients at risk with 19,200 person-years of follow-up study, three patients developed MDS (two with a characteristic cytogenetic abnormality). Two patients developed acute leukemia; however, one had adult T-cell leukemia associated with human T-lymphotrophic virus type 1 (HTLV-1) and a second patient developed AML after receiving additional cyclophosphamide for metastatic breast cancer. The estimated incidence rate for MDS is three per 19,200 or 16 per 100,000 person-years of follow-up study with a 95 percent confidence interval of three to 46 per 100,000 person-years. If all five patients (three MDS and two acute leukemia) are included, the estimated incidence rate is five per 19,200 or 26 per 100,000 person-years of follow-up study with a 95 percent confidence interval of eight to 61 per 100,000 person-years.
These data suggest that the risk of secondary AML or MDS among patients with early breast cancer who receive standard-dose cyclophosphamide-containing adjuvant chemotherapy is not much higher than in the general population. However, physicians must remain alert to the possible long-term consequences of alkylating agent and anthracycline-based chemotherapy.
由于大量早期乳腺癌患者现在接受含环磷酰胺(一种已知的致白血病药物)的辅助化疗,确定继发性急性髓系白血病(AML)和骨髓增生异常综合征(MDS)的风险很重要。因此,我们在东部肿瘤协作组(ECOG)开展的六项临床辅助化疗试验中,识别了接受治疗患者中发生的所有AML或MDS病例。
患者群体包括1978年至1987年间进入ECOG开展的六项临床试验的2638例既往未接受过治疗的原发性可手术乳腺癌患者。有19200人年的随访研究,平均随访时间为7.3年。临床数据来自提交给ECOG数据管理办公室的流程表。
在2638例有风险且有19200人年随访研究的患者中,3例发生MDS(2例有特征性细胞遗传学异常)。2例发生急性白血病;然而,1例患有与1型人类嗜T淋巴细胞病毒(HTLV-1)相关的成人T细胞白血病,另1例患者在接受转移性乳腺癌额外环磷酰胺治疗后发生AML。MDS的估计发病率为每19200人年3例,或每100000人年16例,95%置信区间为每100000人年3至46例。如果将所有5例患者(3例MDS和2例急性白血病)包括在内,估计发病率为每19200人年5例,或每100000人年26例,95%置信区间为每100000人年8至61例。
这些数据表明,接受含标准剂量环磷酰胺辅助化疗的早期乳腺癌患者发生继发性AML或MDS的风险并不比一般人群高很多。然而,医生必须对基于烷化剂和蒽环类药物的化疗可能产生的长期后果保持警惕。