Tucker M A, Fraumeni J F
Epidemiology and Biostatistics Program, National Cancer Institute, Bethesda, Maryland 20892.
Cancer. 1987 Oct 15;60(8 Suppl):2117-22. doi: 10.1002/1097-0142(19901015)60:8+<2117::aid-cncr2820601525>3.0.co;2-0.
Second malignancies are one of the known complications of cancer treatment. Several recent studies which have quantified the risk of treatment-induced cancers following gynecologic malignancies are reviewed. After cervical cancer, there is a 9% excess risk of second cancers, of which only 5% could be attributed to radiation therapy. Most of the treatment-related malignancies after cervical or endometrial cancer are solid tumors occurring within the radiation field. Following both cervical and endometrial cancer, there is a small increased risk of leukemia associated with radiation therapy. In contrast, after ovarian cancer, there is significantly increased risk of leukemia related to treatment with alkylating agents, which varies by drug type and total dose. The cumulative risk of leukemia and preleukemia following single agent melphalan is 11.2% +/- 2.6% at ten years; the risk after cyclophosphamide is 5.4% +/- 3.2%. Overall, the risk of second malignancies following treatment of gynecologic cancers is small.
第二原发性恶性肿瘤是癌症治疗已知的并发症之一。本文综述了近期几项对妇科恶性肿瘤治疗后诱发癌症风险进行量化的研究。宫颈癌治疗后,患第二原发性癌症的风险增加9%,其中只有5%可归因于放射治疗。宫颈癌或子宫内膜癌治疗后发生的大多数与治疗相关的恶性肿瘤是发生在放射野内的实体瘤。宫颈癌和子宫内膜癌治疗后,与放射治疗相关的白血病风险略有增加。相比之下,卵巢癌治疗后,与烷化剂治疗相关的白血病风险显著增加,这因药物类型和总剂量而异。单药美法仑治疗后十年白血病和白血病前期的累积风险为11.2%±2.6%;环磷酰胺治疗后的风险为5.4%±3.2%。总体而言,妇科癌症治疗后发生第二原发性恶性肿瘤的风险较小。