Curtis R E, Boice J D, Stovall M, Bernstein L, Greenberg R S, Flannery J T, Schwartz A G, Weyer P, Moloney W C, Hoover R N
Radiation Epidemiology Branch, National Cancer Institute, Bethesda, Md. 20892.
N Engl J Med. 1992 Jun 25;326(26):1745-51. doi: 10.1056/NEJM199206253262605.
Few studies have evaluated the late effects of adjuvant chemotherapy for breast cancer. Moreover, the relation between the risk of leukemia and the amount of drug given and the interaction of chemotherapy with radiotherapy have not been described in detail.
We conducted a case-control study in a cohort of 82,700 women given a diagnosis of breast cancer from 1973 to 1985 in five areas of the United States. Detailed information about therapy was obtained for 90 patients with leukemia and 264 matched controls. The dose of radiation to the active marrow was estimated from individual radiotherapy records (mean dose, 7.5 Gy).
The risk of acute nonlymphocytic leukemia was significantly increased after regional radiotherapy alone (relative risk, 2.4), alkylating agents alone (relative risk, 10.0), and combined radiation and drug therapy (relative risk, 17.4). Dose-dependent risks were observed after radiotherapy and treatment with melphalan and cyclophosphamide. Melphalan was 10 times more leukemogenic than cyclophosphamide (relative risk, 31.4 vs. 3.1). There was little increase in the risk associated with total cyclophosphamide doses of less than 20,000 mg.
Although leukemia occurs in few patients with breast cancer, significantly elevated risks were linked to treatments with regional radiation and alkylating agents. Melphalan is a more potent leukemogen than cyclophosphamide or radiotherapy. Low risks were associated with the levels of cyclophosphamide in common use today. Systemic drug therapy combined with radiotherapy that delivers high doses to the marrow appears to enhance the risk of leukemia.
很少有研究评估乳腺癌辅助化疗的远期影响。此外,白血病风险与给药剂量之间的关系以及化疗与放疗的相互作用尚未得到详细描述。
我们在美国五个地区对1973年至1985年期间被诊断为乳腺癌的82700名女性队列进行了一项病例对照研究。获得了90例白血病患者和264例匹配对照的详细治疗信息。根据个体放疗记录估算对活跃骨髓的辐射剂量(平均剂量,7.5 Gy)。
单纯区域放疗后急性非淋巴细胞白血病风险显著增加(相对风险,2.4),单纯烷化剂治疗后(相对风险,10.0),以及放疗与药物联合治疗后(相对风险,17.4)。放疗以及美法仑和环磷酰胺治疗后观察到剂量依赖性风险。美法仑致白血病的可能性比环磷酰胺高10倍(相对风险,31.4对3.1)。环磷酰胺总剂量低于20000 mg时,相关风险几乎没有增加。
虽然乳腺癌患者中白血病发生率较低,但区域放疗和烷化剂治疗与显著升高的风险相关。美法仑比环磷酰胺或放疗更易致白血病。当今常用的环磷酰胺剂量相关风险较低。全身药物治疗联合对骨髓给予高剂量放疗似乎会增加白血病风险。