Long-Term Outcomes of Invasive Ipsilateral Breast Tumor Recurrences After Lumpectomy in NSABP B-17 and B-24 Randomized Clinical Trials for DCIS

被引:578
作者
Wapnir, Irene L. [1 ,2 ,5 ]
Dignam, James J. [2 ,3 ,5 ]
Fisher, Bernard [4 ]
Mamounas, Eleftherios P. [2 ,5 ,6 ]
Anderson, Stewart J. [2 ,5 ,7 ]
Julian, Thomas B. [2 ,5 ,8 ]
Land, Stephanie R. [2 ,5 ,7 ]
Margolese, Richard G. [2 ,5 ,9 ]
Swain, Sandra M. [10 ]
Costantino, Joseph P. [2 ,5 ,7 ]
Wolmark, Norman [2 ,5 ,8 ]
机构
[1] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA
[2] Natl Surg Adjuvant Breast & Bowel Project NSABP, Operat Ctr, Pittsburgh, PA USA
[3] Univ Chicago, Dept Hlth Studies, Chicago, IL 60637 USA
[4] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA
[5] Natl Surg Adjuvant Breast & Bowel Project NSABP, Ctr Biostat, Pittsburgh, PA USA
[6] NE Ohio State Univ, Aultman Canc Ctr, Canton, OH USA
[7] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Biostat, Pittsburgh, PA 15261 USA
[8] Allegheny Gen Hosp, Dept Human Oncol, Pittsburgh, PA 15212 USA
[9] McGill Univ, Jewish Gen Hosp, Dept Oncol, Montreal, PQ H3T 1E2, Canada
[10] Washington Canc Inst, Washington, DC USA
关键词
CARCINOMA-IN-SITU; SURGICAL ADJUVANT BREAST; INTRADUCTAL-CARCINOMA; PATHOLOGICAL FINDINGS; RADIATION-THERAPY; PROTOCOL B-17; LOCOREGIONAL RECURRENCES; FOLLOW-UP; CANCER; WOMEN;
D O I
10.1093/jnci/djr027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ipsilateral breast tumor recurrence (IBTR) is the most common failure event after lumpectomy for ductal carcinoma in situ (DCIS). We evaluated invasive IBTR (I-IBTR) and its influence on survival among participants in two National Surgical Adjuvant Breast and Bowel Project (NSABP) randomized trials for DCIS. In the NSABP B-17 trial (accrual period: October 1, 1985, to December 31, 1990), patients with localized DCIS were randomly assigned to the lumpectomy only (LO, n = 403) group or to the lumpectomy followed by radiotherapy (LRT, n = 410) group. In the NSABP B-24 double-blinded, placebo-controlled trial (accrual period: May 9, 1991, to April 13, 1994), all accrued patients were randomly assigned to LRT+ placebo, (n=900) or LRT + tamoxifen (LRT + TAM, n = 899). Endpoints included I-IBTR, DCIS-IBTR, contralateral breast cancers (CBC), overall and breast cancer-specific survival, and survival after I-IBTR. Median follow-up was 207 months for the B-17 trial (N = 813 patients) and 163 months for the B-24 trial (N = 1799 patients). Of 490 IBTR events, 263 (53.7%) were invasive. Radiation reduced I-IBTR by 52% in the LRT group compared with LO (B-17, hazard ratio [HR] of risk of I-IBTR = 0.48, 95% confidence interval [CI] = 0.33 to 0.69, P < .001). LRT + TAM reduced I-IBTR by 32% compared with LRT + placebo (B-24, HR of risk of I-IBTR = 0.68, 95% CI = 0.49 to 0.95, P = .025). The 15-year cumulative incidence of I-IBTR was 19.4% for LO, 8.9% for LRT (B-17), 10.0% for LRT + placebo (B-24), and 8.5% for LRT + TAM. The 15-year cumulative incidence of all contralateral breast cancers was 10.3% for LO, 10.2% for LRT (B-17), 10.8% for LRT + placebo (B-24), and 7.3% for LRT + TAM. I-IBTR was associated with increased mortality risk (HR of death = 1.75, 95% CI = 1.45 to 2.96, P < .001), whereas recurrence of DCIS was not. Twenty-two of 39 deaths after I-IBTR were attributed to breast cancer. Among all patients (with or without I-IBTR), the 15-year cumulative incidence of breast cancer death was 3.1% for LO, 4.7% for LRT (B-17), 2.7% for LRT + placebo (B-24), and 2.3% for LRT + TAM. Although I-IBTR increased the risk for breast cancer-related death, radiation therapy and tamoxifen reduced I-IBTR, and long-term prognosis remained excellent after breast-conserving surgery for DCIS.
引用
收藏
页码:478 / 488
页数:11
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