Taghian A, de Vathaire F, Terrier P, Le M, Auquier A, Mouriesse H, Grimaud E, Sarrazin D, Tubiana M
Department of Radiation Therapy, Institut Gustave Roussy, Villejuif, France.
Int J Radiat Oncol Biol Phys. 1991 Jul;21(2):361-7. doi: 10.1016/0360-3016(91)90783-z.
Between 1954 and 1983, 7620 patients were treated for breast carcinoma at Institut Gustave Roussy (France). Of these patients, 6919 were followed for at least 1 year. Out of these, 11 presented with sarcomas thought to be induced by irradiation, 2 of which were Steward-Treves Syndrome, and 9 of which were sarcomas within the irradiated fields. All histological slides were reviewed and a comparison with those of breast cancer was done. The sites of these sarcomas were: parietal wall, 1 case; second costal cartilage, 1 case; infraclavicular region, 1 case; supraclavicular region, 2 cases; internal third of the clavicle, 2 cases; axillary region 2 cases; and the internal side of the upper arm (Stewart-Treves syndrome), 2 cases. The median age of these 11 patients at the diagnosis of sarcomas was 65.8 (49-83). The mean latent period was 9.5 years (4-24). Three patients underwent radical mastectomy and nine modified radical mastectomy. Only one patient received chemotherapy. The radiation doses received at the site of the sarcoma were 45 Gy/18 fr. for 10 cases and 90-100 Gy for 1 case (due to overlapping between two fields). The histology was as follows: malignant fibrous histiocytoma, 5 cases; fibrosarcoma, 3 cases; lymphangiosarcoma, 2 cases; and osteochondrosarcoma, 1 case. The median survival following diagnosis of sarcoma was 2.4 years (4 months-9 years). Two patients are still alive: one with recurrence of her breast cancer, the other in complete remission, with 7 and 3 years follow-up, respectively. All other patients died from their sarcomas. The cumulative incidence of sarcoma following irradiation of breast cancer was 0.2% (0.09-0.47) at 10 years. The standardized incidence ratio (SIR) of sarcoma (observed n# of cases (Obs)/expected n# of cases (Exp) computed from the Danish Cancer Registry for the same period) was 1.81 (CI 0.91-3.23). This is significantly higher than one, with a p = 0.03 (One Tailed Exact Test). The mean annual excess (Obs-Exp)/100.000 person-years at risk during the same period/(100,000) was 9.92. This study suggests that patients treated by radiation for breast cancer have a risk of subsequent sarcomas that is higher than the general population. However, the benefit from adjuvant radiation therapy in the treatment of breast cancer exceeds the risk of second cancer; therefore, the potential of radiation-induced sarcomas should not be a factor in the selection of treatment for patients with breast cancer.
1954年至1983年间,法国古斯塔夫·鲁西研究所对7620例乳腺癌患者进行了治疗。其中,6919例患者接受了至少1年的随访。在这些患者中,有11例出现了被认为是由放疗诱发的肉瘤,其中2例为斯图尔特 - 特里夫斯综合征,9例为放疗区域内的肉瘤。所有组织学切片均经过复查,并与乳腺癌切片进行了对比。这些肉瘤的发病部位如下:胸壁,1例;第二肋软骨,1例;锁骨下区域,1例;锁骨上区域,2例;锁骨内三分之一处,2例;腋窝区域,2例;上臂内侧(斯图尔特 - 特里夫斯综合征),2例。这11例患者诊断为肉瘤时的中位年龄为65.8岁(49 - 83岁)。平均潜伏期为9.5年(4 - 24年)。3例患者接受了根治性乳房切除术,9例接受了改良根治性乳房切除术。只有1例患者接受了化疗。肉瘤部位接受的放射剂量为:10例患者为45 Gy/18次分割,1例患者为90 - 100 Gy(由于两个照射野重叠)。组织学类型如下:恶性纤维组织细胞瘤,5例;纤维肉瘤,3例;淋巴管肉瘤,2例;骨软骨肉瘤,1例。肉瘤诊断后的中位生存期为2.4年(4个月 - 9年)。2例患者仍存活:1例乳腺癌复发,另1例完全缓解,分别随访了7年和3年。所有其他患者均死于肉瘤。乳腺癌放疗后肉瘤的累积发病率在10年时为0.2%(0.09 - 0.47)。肉瘤的标准化发病比(SIR,观察到的病例数(Obs)/同期丹麦癌症登记处计算出的预期病例数(Exp))为1.81(95%置信区间为0.91 - 3.23)。这显著高于1,p = 0.03(单尾精确检验)。同期平均每年每10万人年的超额发病数(Obs - Exp)/100,000为9.92。本研究表明,接受放疗的乳腺癌患者发生后续肉瘤的风险高于一般人群。然而,辅助放疗在乳腺癌治疗中的益处超过了发生第二原发癌的风险;因此,放疗诱发肉瘤的可能性不应成为乳腺癌患者治疗选择的一个因素。