Bartelink Harry, Horiot Jean-Claude, Poortmans Philip M, Struikmans Henk, Van den Bogaert Walter, Fourquet Alain, Jager Jos J, Hoogenraad Willem J, Oei S Bing, Wárlám-Rodenhuis Carla C, Pierart Marianne, Collette Laurence
Department of Radiation Oncology, the Netherlands Cancer Institute, Amsterdam, the Netherlands.
J Clin Oncol. 2007 Aug 1;25(22):3259-65. doi: 10.1200/JCO.2007.11.4991. Epub 2007 Jun 18.
To investigate the long-term impact of a boost radiation dose of 16 Gy on local control, fibrosis, and overall survival for patients with stage I and II breast cancer who underwent breast-conserving therapy.
A total of 5,318 patients with microscopically complete excision followed by whole-breast irradiation of 50 Gy were randomly assigned to receive either a boost dose of 16 Gy (2,661 patients) or no boost dose (2,657 patients), with a median follow-up of 10.8 years.
The median age was 55 years. Local recurrence was reported as the first treatment failure in 278 patients with no boost versus 165 patients with boost; at 10 years, the cumulative incidence of local recurrence was 10.2% versus 6.2% for the no boost and the boost group, respectively (P < .0001). The hazard ratio of local recurrence was 0.59 (0.46 to 0.76) in favor of the boost, with no statistically significant interaction per age group. The absolute risk reduction at 10 years per age group was the largest in patients <or= 40 years of age: 23.9% to 13.5% (P = .0014). As a result, the number of salvage mastectomies has been reduced by 41%. Severe fibrosis was statistically significantly increased (P < .0001) in the boost group, with a 10-year rate of 4.4% versus 1.6% in the no boost group (P < .0001). Survival at 10 years was 82% in both arms.
After a median follow-up period of 10.8 years, a boost dose of 16 Gy led to improved local control in all age groups, but no difference in survival.
探讨16 Gy的追加放疗剂量对接受保乳治疗的Ⅰ�治疗的I期和II期乳腺癌患者局部控制、纤维化及总生存期的长期影响。
共有5318例患者在显微镜下完全切除后接受50 Gy的全乳照射,随机分为两组,一组接受16 Gy的追加剂量(2661例患者),另一组不接受追加剂量(2657例患者),中位随访时间为10.8年。
中位年龄为55岁。278例未接受追加剂量的患者和165例接受追加剂量的患者报告局部复发为首次治疗失败;10年时,未接受追加剂量组和接受追加剂量组的局部复发累积发生率分别为10.2%和6.2%(P<0.0001)。局部复发的风险比为0.59(0.46至0.76),有利于追加剂量组,各年龄组之间无统计学显著的相互作用。每个年龄组10年时的绝对风险降低在年龄≤40岁的患者中最大:从23.9%降至13.5%(P = 0.0014)。结果,挽救性乳房切除术的数量减少了41%。追加剂量组的严重纤维化在统计学上显著增加(P<0.0001),10年发生率在追加剂量组为4.4%,未接受追加剂量组为1.6%(P<0.0001)。两组10年生存率均为82%。
中位随访10.8年后,16 Gy的追加剂量可改善所有年龄组的局部控制,但生存期无差异。