Wazer D E, Morr J, Erban J K, Schmid C H, Ruthazer R, Schmidt-Ullrich R K
Department of Radiation Oncology, New England Medical Center, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
Cancer. 1997 Aug 15;80(4):732-40. doi: 10.1002/(sici)1097-0142(19970815)80:4<732::aid-cncr12>3.0.co;2-u.
The aim of this study was to evaluate the impact on disease recurrence and cosmetic outcome of tamoxifen treatment initiated after breast-conserving therapy (BCT).
Between 1982 and 1994, 498 women (509 breasts) were treated with BCT in accordance with a highly standardized institutional protocol. Adjuvant tamoxifen was administered to 130 patients (134 breasts), beginning 1-6 weeks after irradiation. The median ages and duration of follow-up for groups who received tamoxifen (TAM+) and no tamoxifen (TAM-) were 62.5 years/56 months and 53 years/60 months, respectively. The members of the TAM+ group were significantly older (P = 0.0001) and had increased incidences of positive axillary lymph nodes or undissected axilla (P = 0.001). There was a significant (P = 0.001) difference between the TAM+ and TAM- groups in the distribution of histopathologic subtypes; this reflected an increased proportion of associated ductal carcinoma in situ in the TAM- group. More extensive regional lymphatic irradiation was administered to the TAM+ group. Chemotherapy was administered to 15% of TAM+ and 28% (P = 0.003) of TAM- patients. There were no significant differences between the groups with respect to tumor size, reexcision, total excised tissue volume, final margin status, total radiation dose, or use of interstitial implant boost.
There was no significant difference between the TAM+ and TAM- groups in the overall distribution of cosmetic scores (P = 0.18). The 5-, 7-, and 10-year actuarial local failure rates for TAM+ versus TAM- patients were 0% versus 3.1%, 1.9% versus 5.4%, and 1.9% versus 8.4%, respectively. Multivariate regression analyses of potentially confounding variables revealed no significant associations between tamoxifen and either cosmetic outcome or local failure.
Radiotherapy followed by tamoxifen has no adverse interactive effect on cosmesis, and tamoxifen is associated with a trend toward enhanced 5-year local control probability.
本研究旨在评估保乳治疗(BCT)后开始使用他莫昔芬治疗对疾病复发和美容效果的影响。
1982年至1994年间,498名女性(509个乳房)按照高度标准化的机构方案接受了保乳治疗。130名患者(134个乳房)在放疗后1 - 6周开始接受辅助性他莫昔芬治疗。接受他莫昔芬治疗(TAM +)和未接受他莫昔芬治疗(TAM -)组的中位年龄和随访时间分别为62.5岁/56个月和53岁/60个月。TAM +组的成员年龄显著更大(P = 0.0001),腋窝淋巴结阳性或腋窝未清扫的发生率更高(P = 0.001)。TAM +组和TAM -组在组织病理学亚型分布上存在显著差异(P = 0.001);这反映出TAM -组原位导管癌相关比例增加。TAM +组接受了更广泛的区域淋巴照射。15%的TAM +患者和28%(P = 0.003)的TAM -患者接受了化疗。两组在肿瘤大小、再次切除、总切除组织体积、最终切缘状态、总放射剂量或间质植入物增强使用方面无显著差异。
TAM +组和TAM -组在美容评分的总体分布上无显著差异(P = 0.18)。TAM +组与TAM -组患者的5年、7年和10年精算局部失败率分别为0%对3.1%、1.9%对5.4%和1.9%对8.4%。对潜在混杂变量的多因素回归分析显示,他莫昔芬与美容效果或局部失败之间无显著关联。
放疗后使用他莫昔芬对美容效果无不良交互作用,且他莫昔芬与5年局部控制概率提高的趋势相关。