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低风险HER2阳性乳腺癌治疗简化

 SIBCS 2023-02-28 发布于上海

  对于II~III期HER2阳性乳腺癌,指南推荐术后给予多西他赛+卡铂+曲妥珠单抗±帕妥珠单抗豪华套餐联合辅助治疗。不过,对于I期HER2阳性乳腺癌,术后辅助治疗能否简化?既往大样本随机对照三期临床研究极少入组此类患者,因此缺少治疗标准。2015年美国麻省医学会《新英格兰医学杂志》发表APT研究中位随访4年结果表明,紫杉醇+曲妥珠单抗辅助治疗肿瘤≤3厘米、淋巴结阴性、HER2阳性乳腺癌术后患者,3年无浸润癌生存率达98.7%。2019年美国临床肿瘤学会《临床肿瘤学杂志》发表APT研究中位随访6.5年结果表明,7年无浸润癌生存率、无复发生存率分别达93.3%、97.5%。因此,紫杉醇+曲妥珠单抗已被指南列入肿瘤较小、淋巴结阴性、HER2阳性乳腺癌术后标准治疗选择。值得注意的是,APT研究三分之二入组患者为激素受体阳性长期复发风险较高,仍需更长时间随访。

APT (NCT00542451): A Phase II Trial of Adjuvant Paclitaxel and Trastuzumab for Node-Negative HER2-Positive Breast Cancer

  2023年2月27日,英国《柳叶刀》肿瘤学分册在线发表美国哈佛大学医学院达纳法伯癌症研究院、达纳法伯布莱根癌症中心、麻省总医院、麻省理工学院和哈佛大学布罗德研究所、纽约纪念医院斯隆和凯特林癌症中心、莎拉坎农癌症中心、杜克大学癌症研究院、洛约拉大学医学中心、旧金山加利福尼亚大学、贝勒医院莱斯特和苏史密斯乳腺中心、纽约州新海德公园地区抗癌协会、霍普金斯大学悉德尼金梅尔综合癌症中心、北卡罗来纳大学医学院莱恩伯格综合癌症中心、美国临床肿瘤学会、耶鲁大学癌症中心、意大利米兰大学欧洲肿瘤研究院、西班牙巴塞罗那大学奥古斯特皮苏尼尔生物医学研究院、巴西巴西利亚医院的APT研究中位随访10.8年最终生存结局及其生物学预测指标

  该多中心非盲单组二期临床研究于2007年10月29日~2010年9月3日从从美国13个城市16个中心入组年龄≥18岁、美国东部肿瘤学协作组体力状态评分为0~1分、肿瘤≤3厘米、淋巴结阴性、HER2阳性乳腺癌患者410例,术后每周静脉注射紫杉醇(80mg/m²)+曲妥珠单抗(首次4mg/kg,随后每次2mg/kg)连续12周,再予曲妥珠单抗(每周2mg/kg或每3周6mg/kg)连续40周以完成1年曲妥珠单抗。主要终点为无浸润癌生存,次要终点包括无复发生存、总生存、乳腺癌相关生存,并采用HER2DX基因组工具进行探索性分析。

  结果,其中406例接受紫杉醇+曲妥珠单抗辅助治疗并被纳入分析,入组时平均年龄为55±10.5岁,405例(99.8%)为女性,1例(0.2%)为男性,350例(86.2%)为白人,28例(6.9%)为黑人或非洲裔美国人,272例(67.0%)为激素受体阳性

  中位随访10.8年(四分位:7.1~11.4)发生浸润癌或死亡事件31例
  • 同侧局部区域复发:6例(19.4%)
  • 对侧新发生乳腺癌:9例(29.0%)
  • 远处复发:6例(19.4%)
  • 全因死亡:10例(32.3%)
  • 10年无浸润癌生存率:91.3%
    (95%置信区间:88.3~94.4)
  • 10年无复发生存率:96.3%
    (95%置信区间:94.3~98.3)
  • 10年总生存率:94.3%
    (95%置信区间:91.8~96.8)
  • 10年乳腺癌相关生存率:98.8%
    (95%置信区间:97.6~100)



  HER2DX风险评分每增加10分
  • 浸润癌或死亡风险增加24%
    (风险比:1.24,95%置信区间:1.00~1.52,P=0.047)
  • 复发或死亡风险增加45%
    (风险比:1.45,95%置信区间:1.09~1.93,P=0.011)



  因此,该研究结果表明,对于肿瘤较小、淋巴结阴性、HER2阳性乳腺癌术后患者,紫杉醇+曲妥珠单抗是合理的治疗标准,HER2DX基因组工具可能有助于该人群的精准预后。不过,随着近十年来新药不断问世,紫杉醇+曲妥珠单抗王炸组合地位或许将被恩美曲妥珠单抗、德曲妥珠单抗等抗体缀合单药取代。

  对此,意大利都灵大学坎迪奥洛癌症研究院、米兰大学欧洲肿瘤研究院发表同期评论:低风险HER2阳性乳腺癌治疗简化

相关链接


Lancet Oncol. 2023 Mar;24(3):273-285. IF: 54.433

Adjuvant paclitaxel and trastuzumab for node-negative, HER2-positive breast cancer: final 10-year analysis of the open-label, single-arm, phase 2 APT trial.

Sara M Tolaney, Paolo Tarantino, Noah Graham, Nabihah Tayob, Laia Parè, Guillermo Villacampa, Chau T Dang, Denise A Yardley, Beverly Moy, P Kelly Marcom, Kathy S Albain, Hope S Rugo, Matthew J Ellis, Iuliana Shapira, Antonio C Wolff, Lisa A Carey, Romualdo Barroso-Sousa, Patricia Villagrasa, Michelle DeMeo, Molly DiLullo, Jorge Gomez Tejeda Zanudo, Jakob Weiss, Nikhil Wagle, Ann H Partridge, Adrienne G Waks, Clifford A Hudis, Ian E Krop, Harold J Burstein, Aleix Prat, Eric P Winer.

Dana-Farber Cancer Institute, Boston, MA, USA; Dana-Farber Brigham Cancer Center, Boston, MA, USA; Harvard Medical School, Boston, MA, USA; Massachusetts General Hospital, Boston, MA, USA; Broad Institute of MIT and Harvard, Boston, MA, USA; Memorial Sloan Kettering Cancer Center, New York, NY, USA; Sarah Cannon Cancer Center, Nashville, TN, USA; Duke Cancer Institute, Durham, NC, USA; Loyola University Medical Center, Maywood, IL, USA; University of California, San Francisco, CA, USA; Baylor Clinic Lester and Sue Smith Breast Center, Houston, TX, USA; Regional Cancer Care Associates, New Hyde Park, New York, NY, USA; Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA; Lineberger Comprehensive Cancer Center, University of North Carolina School of Medicine, Chapel Hill, NC, USA; American Society of Clinical Oncology, Alexandria, VA, USA; Yale Cancer Center, New Haven, CT, USA; University of Milan, Milan, Italy; European Institute of Oncology IRCCS, Milan, Italy; Reveal Genomics, Barcelona, Spain; August Pi I Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain; University of Barcelona, Barcelona, Spain; Brasilia Hospital, Diagnósticos da América SA (DASA), Brasília, Brazil.

BACKGROUND: We aimed to report on long-term outcomes of patients with small, node-negative, HER2-positive breast cancer treated with adjuvant paclitaxel and trastuzumab and to establish potential biomarkers to predict prognosis.

METHODS: In this open-label, single-arm, phase 2 study, patients aged 18 years or older, with small (≤3 cm), node-negative, HER2-positive breast cancer, and an Eastern Cooperative Oncology Group performance status of 0-1, were recruited from 16 institutions in 13 cities in the USA. Eligible patients were given intravenous paclitaxel (80 mg/m2) with intravenous trastuzumab (loading dose of 4 mg/kg, subsequent doses 2 mg/kg) weekly for 12 weeks, followed by trastuzumab (weekly at 2 mg/kg or once every 3 weeks at 6 mg/kg) for 40 weeks to complete a full year of trastuzumab. The primary endpoint was 3-year invasive disease-free survival. Here, we report 10-year survival outcomes, assessed in all participants who received protocol-defined treatment, with exploratory analyses using the HER2DX genomic tool. This study is registered on ClinicalTrials.gov, NCT00542451, and is closed to accrual.

FINDINGS: Between Oct 29, 2007, and Sept 3, 2010, 410 patients were enrolled and 406 were given adjuvant paclitaxel and trastuzumab and included in the analysis. Mean age at enrolment was 55 years (SD 10.5), 405 (99.8%) of 406 patients were female and one (0.2%) was male, 350 (86.2%) were White, 28 (6.9%) were Black or African American, and 272 (67.0%) had hormone receptor-positive disease. After a median follow-up of 10.8 years (IQR 7.1-11.4), among 406 patients included in the analysis population, we observed 31 invasive disease-free survival events, of which six (19.4%) were locoregional ipsilateral recurrences, nine (29.0%) were new contralateral breast cancers, six (19.4%) were distant recurrences, and ten (32.3%) were all-cause deaths. 10-year invasive disease-free survival was 91.3% (95% CI 88.3-94.4), 10-year recurrence-free interval was 96.3% (95% CI 94.3-98.3), 10-year overall survival was 94.3% (95% CI 91.8-96.8), and 10-year breast cancer-specific survival was 98.8% (95% CI 97.6-100). HER2DX risk score as a continuous variable was significantly associated with invasive disease-free survival (hazard ratio [HR] per 10-unit increment 1.24 [95% CI 1.00-1.52]; p=0.047) and recurrence-free interval (1.45 [1.09-1.93]; p=0.011).

INTERPRETATION: Adjuvant paclitaxel and trastuzumab is a reasonable treatment standard for patients with small, node-negative, HER2-positive breast cancer. The HER2DX genomic tool might help to refine the prognosis for this population.

FUNDING: Genentech.

DOI: 10.1016/S1470-2045(23)00051-7



Lancet Oncol. 2023 Mar;24(3):200-201. IF: 54.433

De-escalation in low-risk, HER2-positive breast cancer.

Elena Geuna, Giuseppe Curigliano, Filippo Montemurro.

Candiolo Cancer Institute, Candiolo, Italy; European Institute of Oncology, Milan, Italy; University of Milan, Milan, Italy.

DOI: 10.1016/S1470-2045(23)00064-5

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