F. Vicini, R. Cecchini, J. White, T. Julian, D. Arthur, R. Rabinovitch, R. Kuske, D. Parda, P. Ganz, M. Scheier, K. Winter, S. Paik, H. Kuerer, L. Vallow, L. Pierce, E. Mamounas, J. Costantino, H. Bear, I. Germaine, G. Gustafson, L. Grossheim, I. Petersen, R. Hudes, W. Curran, N. Wolmark
{"title":"GS4-04: NSABP B-39/RTOG 0413 (NRG Oncology)的主要结果:一项随机III期研究,对0、I、II期乳腺癌女性进行常规全乳照射(WBI)与部分乳房照射(PBI)的比较","authors":"F. Vicini, R. Cecchini, J. White, T. Julian, D. Arthur, R. Rabinovitch, R. Kuske, D. Parda, P. Ganz, M. Scheier, K. Winter, S. Paik, H. Kuerer, L. Vallow, L. Pierce, E. Mamounas, J. Costantino, H. Bear, I. Germaine, G. Gustafson, L. Grossheim, I. Petersen, R. Hudes, W. Curran, N. Wolmark","doi":"10.1158/1538-7445.SABCS18-GS4-04","DOIUrl":null,"url":null,"abstract":"Background: Conventional WBI after lumpectomy for early-stage breast cancer decreases ipsilateral breast tumor recurrence (IBTR), yielding comparable results to mastectomy. Accelerated PBI appears effective in reducing IBTR by treating only the tumor bed area. As the majority of IBTR occur at or in the vicinity of the tumor bed, we hypothesized that PBI would be as effective as WBI in controlling IBTR. The primary aim of NSABP B-39/RTOG 0413 was to determine if PBI provides equivalent local tumor control post lumpectomy compared to WBI in pts with early-stage breast cancer. The equivalency test was based on a 50% margin of increase in the hazard ratio (HR=1.5). Secondary endpoints included: overall survival (OS), recurrence-free interval (RFI), distant disease-free interval (DDFI), and toxicity. Methods: Eligible pts had lumpectomy with histologically-free margins and 0-3 positive axillary nodes. Pts were stratified by stage, menopausal status, hormone receptor status, and intent to receive chemotherapy and then randomized to PBI or WBI. PBI was 10 fractions of 3.4-3.85 Gy, given twice daily with either brachytherapy or 3D external beam radiation. WBI was 50 Gy in 2 Gy fractions given daily with a sequential boost to the surgical cavity. Follow-up was every 6 mos for 5 yrs and then annually. All analyses were by intent-to-treat. Results: From 3-21-05 to 4-16-13, 4216 pts were randomized: 2107 PBI; 2109 WBI. 61% were postmenopausal; 81% were hormone receptor-positive; 29% intended to receive chemotherapy. Stage distribution was: DCIS, 24%; invasive pN0, 65%; invasive pN1, 10%. As of 7-31-18, median follow-up was 10.2 yrs. There were 161 IBTRs as first events: 90 PBI v 71 WBI (HR 1.22; 90%CI 0.94-1.58). Per protocol-defined margin, to declare PBI and WBI equivalent regarding IBTR risk, the 90% CI for the observed HR had to lie entirely between 0.667 and 1.5. The percent of pts IBTR-free at 10 yrs was 95.2% PBI v 95.9% WBI. A statistically significant difference in the 10-yr RFI rate favored WBI (91.9% PBI v 93.4% WBI; HR 1.32; 95%CI 1.04-1.68; p=0.02). No statistically significant differences existed between PBI and WBI in DDFI (HR 1.31; 95%CI 0.91-1.91; p=0.15), OS (HR 1.10; 95%CI 0.90-1.35; p=0.35), or DFS (HR 1.12; 95%CI 0.98-1.29; p=0.11). Grade 3 toxicity was 9.6% PBI v 7.1% WBI, and grade 4-5 toxicity was 0.5% v 0.3%, respectively. Discussion: PBI did not meet the criteria for equivalence to WBI in controlling IBTR based on the upper limit of the hazard ratio confidence interval. However, the absolute difference in 10-yr rate of IBTR was Support: U10CA180868, -180822, UG1CA189867. Citation Format: Vicini FA, Cecchini RS, White JR, Julian TB, Arthur DW, Rabinovitch RA, Kuske RR, Parda DS, Ganz PA, Scheier MF, Winter KA, Paik S, Kuerer HM, Vallow LA, Pierce LJ, Mamounas EP, Costantino JP, Bear HD, Germaine I, Gustafson G, Grossheim L, Petersen IA, Hudes RS, Curran, Jr. WJ, Wolmark N. Primary results of NSABP B-39/RTOG 0413 (NRG Oncology): A randomized phase III study of conventional whole breast irradiation (WBI) versus partial breast irradiation (PBI) for women with stage 0, I, or II breast cancer [abstract]. In: Proceedings of the 2018 San Antonio Breast Cancer Symposium; 2018 Dec 4-8; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2019;79(4 Suppl):Abstract nr GS4-04.","PeriodicalId":12697,"journal":{"name":"General Session Abstracts","volume":"12 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-02-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"45","resultStr":"{\"title\":\"Abstract GS4-04: Primary results of NSABP B-39/RTOG 0413 (NRG Oncology): A randomized phase III study of conventional whole breast irradiation (WBI) versus partial breast irradiation (PBI) for women with stage 0, I, or II breast cancer\",\"authors\":\"F. Vicini, R. Cecchini, J. White, T. Julian, D. Arthur, R. Rabinovitch, R. Kuske, D. Parda, P. Ganz, M. Scheier, K. Winter, S. Paik, H. Kuerer, L. Vallow, L. Pierce, E. Mamounas, J. Costantino, H. Bear, I. Germaine, G. Gustafson, L. Grossheim, I. Petersen, R. Hudes, W. Curran, N. 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Per protocol-defined margin, to declare PBI and WBI equivalent regarding IBTR risk, the 90% CI for the observed HR had to lie entirely between 0.667 and 1.5. The percent of pts IBTR-free at 10 yrs was 95.2% PBI v 95.9% WBI. A statistically significant difference in the 10-yr RFI rate favored WBI (91.9% PBI v 93.4% WBI; HR 1.32; 95%CI 1.04-1.68; p=0.02). No statistically significant differences existed between PBI and WBI in DDFI (HR 1.31; 95%CI 0.91-1.91; p=0.15), OS (HR 1.10; 95%CI 0.90-1.35; p=0.35), or DFS (HR 1.12; 95%CI 0.98-1.29; p=0.11). Grade 3 toxicity was 9.6% PBI v 7.1% WBI, and grade 4-5 toxicity was 0.5% v 0.3%, respectively. Discussion: PBI did not meet the criteria for equivalence to WBI in controlling IBTR based on the upper limit of the hazard ratio confidence interval. However, the absolute difference in 10-yr rate of IBTR was Support: U10CA180868, -180822, UG1CA189867. 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引用次数: 45
摘要
背景:早期乳腺癌乳房肿瘤切除术后常规WBI可降低同侧乳房肿瘤复发率(IBTR),其结果与乳房切除术相当。加速PBI似乎通过仅治疗肿瘤床区来有效降低IBTR。由于大多数IBTR发生在肿瘤床或肿瘤床附近,我们假设PBI在控制IBTR方面与WBI一样有效。NSABP B-39/RTOG 0413的主要目的是确定在早期乳腺癌患者中,与WBI相比,PBI是否能在乳房肿瘤切除术后提供同等的局部肿瘤控制。等效性检验以风险比增加50%为基础(HR=1.5)。次要终点包括:总生存期(OS)、无复发间期(RFI)、远端无病间期(DDFI)和毒性。方法:符合条件的患者行无组织学边缘和0-3个阳性腋窝淋巴结的乳房肿瘤切除术。患者按分期、绝经状态、激素受体状态和接受化疗的意向分层,然后随机分为PBI组或WBI组。PBI为10次,3.4-3.85 Gy,每日两次,近距离治疗或3D外束放疗。WBI为50gy,每天给予2gy的剂量,连续增加到手术腔。每6个月随访一次,持续5年,然后每年随访一次。所有分析均按意向治疗进行。结果:从3-21-05到4-16-13,4216名患者被随机分配:2107名PBI;2109 WBI。61%为绝经后;激素受体阳性占81%;29%的人打算接受化疗。分期分布为:DCIS占24%;侵袭性pN0, 65%;侵袭性pN1, 10%。截至7-31-18,中位随访时间为10.2年。有161例ibtr作为首发事件:90例PBI vs 71例WBI (HR 1.22;90%可信区间0.94 - -1.58)。根据方案定义的边际,为了宣布PBI和WBI在IBTR风险方面相等,观察到的HR的90% CI必须完全介于0.667和1.5之间。10年无ibtr患者的百分比为95.2% PBI vs 95.9% WBI。10年RFI率对WBI有显著的统计学差异(91.9%的PBI vs 93.4%的WBI;人力资源1.32;95%可信区间1.04 - -1.68;p = 0.02)。PBI和WBI在DDFI中的差异无统计学意义(HR 1.31;95%可信区间0.91 - -1.91;p=0.15), OS (HR 1.10;95%可信区间0.90 - -1.35;p=0.35)或DFS (HR 1.12;95%可信区间0.98 - -1.29;p = 0.11)。3级毒性分别为9.6% PBI vs 7.1% WBI, 4-5级毒性分别为0.5% v 0.3%。讨论:基于风险比置信区间上限,PBI在控制IBTR方面不符合与WBI等效的标准。而10年期IBTR的绝对差值为:Support: U10CA180868, -180822, UG1CA189867。引用格式:Vicini FA, Cecchini RS, White JR, Julian TB, Arthur DW, Rabinovitch RA, Kuske RR, Parda DS, Ganz PA, Scheier MF, Winter KA, Paik S, Kuerer HM, Vallow LA, Pierce LJ, Mamounas EP, Costantino JP, Bear HD, Germaine I, Gustafson G, Grossheim L, Petersen IA, Hudes RS, Curran, JR . WJ, Wolmark N. NSABP B-39/RTOG 0413 (NRG Oncology)的主要结果:传统全乳照射(WBI)与部分乳房照射(PBI)对0、I、II期乳腺癌患者的随机III期研究[摘要]。2018年圣安东尼奥乳腺癌研讨会论文集;2018年12月4-8日;费城(PA): AACR;癌症杂志,2019;79(4增刊):摘要nr GS4-04。
Abstract GS4-04: Primary results of NSABP B-39/RTOG 0413 (NRG Oncology): A randomized phase III study of conventional whole breast irradiation (WBI) versus partial breast irradiation (PBI) for women with stage 0, I, or II breast cancer
Background: Conventional WBI after lumpectomy for early-stage breast cancer decreases ipsilateral breast tumor recurrence (IBTR), yielding comparable results to mastectomy. Accelerated PBI appears effective in reducing IBTR by treating only the tumor bed area. As the majority of IBTR occur at or in the vicinity of the tumor bed, we hypothesized that PBI would be as effective as WBI in controlling IBTR. The primary aim of NSABP B-39/RTOG 0413 was to determine if PBI provides equivalent local tumor control post lumpectomy compared to WBI in pts with early-stage breast cancer. The equivalency test was based on a 50% margin of increase in the hazard ratio (HR=1.5). Secondary endpoints included: overall survival (OS), recurrence-free interval (RFI), distant disease-free interval (DDFI), and toxicity. Methods: Eligible pts had lumpectomy with histologically-free margins and 0-3 positive axillary nodes. Pts were stratified by stage, menopausal status, hormone receptor status, and intent to receive chemotherapy and then randomized to PBI or WBI. PBI was 10 fractions of 3.4-3.85 Gy, given twice daily with either brachytherapy or 3D external beam radiation. WBI was 50 Gy in 2 Gy fractions given daily with a sequential boost to the surgical cavity. Follow-up was every 6 mos for 5 yrs and then annually. All analyses were by intent-to-treat. Results: From 3-21-05 to 4-16-13, 4216 pts were randomized: 2107 PBI; 2109 WBI. 61% were postmenopausal; 81% were hormone receptor-positive; 29% intended to receive chemotherapy. Stage distribution was: DCIS, 24%; invasive pN0, 65%; invasive pN1, 10%. As of 7-31-18, median follow-up was 10.2 yrs. There were 161 IBTRs as first events: 90 PBI v 71 WBI (HR 1.22; 90%CI 0.94-1.58). Per protocol-defined margin, to declare PBI and WBI equivalent regarding IBTR risk, the 90% CI for the observed HR had to lie entirely between 0.667 and 1.5. The percent of pts IBTR-free at 10 yrs was 95.2% PBI v 95.9% WBI. A statistically significant difference in the 10-yr RFI rate favored WBI (91.9% PBI v 93.4% WBI; HR 1.32; 95%CI 1.04-1.68; p=0.02). No statistically significant differences existed between PBI and WBI in DDFI (HR 1.31; 95%CI 0.91-1.91; p=0.15), OS (HR 1.10; 95%CI 0.90-1.35; p=0.35), or DFS (HR 1.12; 95%CI 0.98-1.29; p=0.11). Grade 3 toxicity was 9.6% PBI v 7.1% WBI, and grade 4-5 toxicity was 0.5% v 0.3%, respectively. Discussion: PBI did not meet the criteria for equivalence to WBI in controlling IBTR based on the upper limit of the hazard ratio confidence interval. However, the absolute difference in 10-yr rate of IBTR was Support: U10CA180868, -180822, UG1CA189867. Citation Format: Vicini FA, Cecchini RS, White JR, Julian TB, Arthur DW, Rabinovitch RA, Kuske RR, Parda DS, Ganz PA, Scheier MF, Winter KA, Paik S, Kuerer HM, Vallow LA, Pierce LJ, Mamounas EP, Costantino JP, Bear HD, Germaine I, Gustafson G, Grossheim L, Petersen IA, Hudes RS, Curran, Jr. WJ, Wolmark N. Primary results of NSABP B-39/RTOG 0413 (NRG Oncology): A randomized phase III study of conventional whole breast irradiation (WBI) versus partial breast irradiation (PBI) for women with stage 0, I, or II breast cancer [abstract]. In: Proceedings of the 2018 San Antonio Breast Cancer Symposium; 2018 Dec 4-8; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2019;79(4 Suppl):Abstract nr GS4-04.