Olson John A, Budd G Thomas, Carey Lisa A, Harris Lyndsay A, Esserman Laura J, Fleming Gini F, Marcom Paul K, Leight George S, Giuntoli Therese, Commean Paul, Bae Kyongtae, Luo Jingqin, Ellis Matthew J
Department of Surgery, Duke Comprehensive Cancer Center, Durham, NC, USA.
J Am Coll Surg. 2009 May;208(5):906-14; discussion 915-6. doi: 10.1016/j.jamcollsurg.2009.01.035.
Neoadjuvant aromatase inhibitor therapy has been reported to improve surgical outcomes for postmenopausal women with clinical stage II or III hormone receptor-positive breast cancer. A multicenter phase II clinical trial was conducted to investigate the value of this approach for US surgical practice.
One hundred fifteen postmenopausal women with >2 cm, estrogen receptor (ER) or progesterone receptor (PgR)-positive breast cancer were enrolled in a trial of 16 to 24 weeks of letrozole 2.5 mg daily before operation.
One hundred six patients were eligible for primary analysis, 96 underwent operations, 7 received chemotherapy after progressive disease, and 3 did not undergo an operation. Baseline surgical status was marginal for breast-conserving surgery (BCS) in 48 (45%), 47 were definitely ineligible for BCS (44%), and 11 were inoperable by standard mastectomy (10%). Overall Response Evaluation Criteria In Solid Tumors clinical response rate in the breast was 62%, with 12% experiencing progressive disease. Fifty percent underwent BCS, including 30 of 46 (65%) patients who were initially marginal for BCS and 15 of 39 (38%) patients who were initially ineligible for BCS. All 11 inoperable patients successfully underwent operations, including 3 (27%) who had BCS. Nineteen percent of patients undergoing mastectomy had a pathologic T1 tumor, suggesting that some highly responsive tumors were overtreated surgically.
Neoadjuvant aromatase inhibitor improves operability and facilitates BCS, but there was considerable variability in responsiveness. Better techniques to predict response, determine residual tumor burden before operation, and greater willingness to attempt BCS in responsive patients could additionally improve the rate of successful BCS.
据报道,新辅助芳香化酶抑制剂治疗可改善临床II期或III期激素受体阳性绝经后乳腺癌女性的手术结局。开展了一项多中心II期临床试验,以研究这种方法在美国外科手术实践中的价值。
115例绝经后、肿瘤直径大于2 cm、雌激素受体(ER)或孕激素受体(PgR)阳性的乳腺癌女性患者纳入试验,术前每日口服来曲唑2.5 mg,持续16至24周。
106例患者符合初步分析条件,96例接受了手术,7例疾病进展后接受了化疗,3例未接受手术。保乳手术(BCS)的基线手术状态为边缘可手术的有48例(45%),47例绝对不符合BCS条件(44%),11例无法进行标准乳房切除术(10%)。实体瘤疗效评价标准中乳房的临床缓解率为62%,疾病进展的为12%。50%的患者接受了BCS,包括46例最初边缘可手术的患者中的30例(65%)和39例最初不符合BCS条件的患者中的15例(38%)。所有11例无法手术的患者均成功接受了手术,其中3例(27%)接受了BCS。接受乳房切除术的患者中有19%的患者病理检查为T1期肿瘤,这表明一些高反应性肿瘤接受了过度的手术治疗。
新辅助芳香化酶抑制剂可提高手术可操作性并促进BCS,但反应性存在相当大的差异。更好的预测反应、术前确定残余肿瘤负荷的技术,以及在反应性患者中更愿意尝试BCS,可能会进一步提高BCS的成功率。