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PI3K 抑制剂为转移性乳腺化生性癌提供持久缓解:BELLE-4 研究中的一颗隐藏瑰宝。

PI3K inhibitor provides durable response in metastatic metaplastic carcinoma of the breast: A hidden gem in the BELLE-4 study.

机构信息

Department of Oncology, National Taiwan University Hospital, Taiwan; Department of Oncology, National Taiwan University Cancer Center, Taiwan.

Department of Oncology, National Taiwan University Hospital, Taiwan; Department of Oncology, National Taiwan University Cancer Center, Taiwan; Graduate Institute of Oncology, National Taiwan University, Taiwan.

出版信息

J Formos Med Assoc. 2019 Sep;118(9):1333-1338. doi: 10.1016/j.jfma.2018.12.004. Epub 2018 Dec 18.


DOI:10.1016/j.jfma.2018.12.004
PMID:30577988
Abstract

PURPOSE: Metaplastic carcinoma of the breast (MCB) is a rare cancer characterized by the histologic presence of two or more histological cell types originating from epithelial and mesenchymal stem cells. Patients with metastatic MCB have a low response rate to conventional chemotherapy and poor survival. Optimal treatment strategies for metastatic MCB are urgently needed. METHODS: We retrospectively reviewed a patient who had enrolled in the phase II/III seamless study, BELLE-4 (NCT01572727). The patient's response to the study drug assessed by an investigator per protocol and clinical course were examined and compared with those of the main cohorts in the BELLE-4 study. RESULTS: Our patient exhibited metastatic MCB and received systemic chemotherapy, paclitaxel (70 mg/m/week) and buparlisib (80 mg/day), a pan-class I phosphatidylinositol-3 kinase (PI3K) inhibitor. The optimal response was a confirmed partial response for 17 months in total. During the compassionated use program period, the tumor regrew when buparlisib was stop because of toxicity, and responded to the treatment again after resumed the buparlisib treatment. The overall survival of the patient after the development of metastatic MCB was 42 months. She experienced grade 3 hyperglycemia similar to that observed in the main cohort. CONCLUSION: Buparlisib plus weekly paclitaxel might be a new treatment option for patients with metastatic MCB harboring a PIK3CA mutation. Additional prospective studies for investigating the efficacy of the proposed combination are warranted.

摘要

目的:乳腺化生性癌(MCB)是一种罕见的癌症,其特征为组织学上存在两种或多种来源于上皮和间充质干细胞的组织学细胞类型。转移性 MCB 患者对常规化疗的反应率低,生存预后差。迫切需要为转移性 MCB 制定最佳的治疗策略。

方法:我们回顾性分析了一名入组 BELLE-4 (NCT01572727)二期/三期无缝研究的患者。根据方案评估研究者和临床过程评估了患者对研究药物的反应,并与 BELLE-4 研究的主要队列进行了比较。

结果:我们的患者患有转移性 MCB,并接受了系统化疗,紫杉醇(70mg/m/周)和 buparlisib(80mg/天),一种全类 I 磷脂酰肌醇-3 激酶(PI3K)抑制剂。最佳反应是完全缓解,总缓解持续时间为 17 个月。在同情用药期间,由于毒性停止使用 buparlisib 后肿瘤再次生长,重新使用 buparlisib 治疗后肿瘤再次缓解。该患者发生转移性 MCB 后的总生存期为 42 个月。她经历了与主要队列观察到的类似的 3 级高血糖。

结论:buparlisib 联合每周紫杉醇可能是一种治疗携带 PIK3CA 突变的转移性 MCB 患者的新选择。需要进行额外的前瞻性研究来评估该联合方案的疗效。

相似文献

[1]
PI3K inhibitor provides durable response in metastatic metaplastic carcinoma of the breast: A hidden gem in the BELLE-4 study.

J Formos Med Assoc. 2018-12-18

[2]
A randomized adaptive phase II/III study of buparlisib, a pan-class I PI3K inhibitor, combined with paclitaxel for the treatment of HER2- advanced breast cancer (BELLE-4).

Ann Oncol. 2017-2-1

[3]
Buparlisib plus fulvestrant versus placebo plus fulvestrant in postmenopausal, hormone receptor-positive, HER2-negative, advanced breast cancer (BELLE-2): a randomised, double-blind, placebo-controlled, phase 3 trial.

Lancet Oncol. 2017-7

[4]
A Phase I Trial of the PI3K Inhibitor Buparlisib Combined With Capecitabine in Patients With Metastatic Breast Cancer.

Clin Breast Cancer. 2017-10-28

[5]
Buparlisib plus fulvestrant in postmenopausal women with hormone-receptor-positive, HER2-negative, advanced breast cancer progressing on or after mTOR inhibition (BELLE-3): a randomised, double-blind, placebo-controlled, phase 3 trial.

Lancet Oncol. 2017-12-7

[6]
Buparlisib and paclitaxel in patients with platinum-pretreated recurrent or metastatic squamous cell carcinoma of the head and neck (BERIL-1): a randomised, double-blind, placebo-controlled phase 2 trial.

Lancet Oncol. 2017-1-26

[7]
Stand up to cancer phase Ib study of pan-phosphoinositide-3-kinase inhibitor buparlisib with letrozole in estrogen receptor-positive/human epidermal growth factor receptor 2-negative metastatic breast cancer.

J Clin Oncol. 2014-3-24

[8]
Phase 2 study of buparlisib (BKM120), a pan-class I PI3K inhibitor, in patients with metastatic triple-negative breast cancer.

Breast Cancer Res. 2020-11-2

[9]
A phase 1b dose expansion study of the pan-class I PI3K inhibitor buparlisib (BKM120) plus carboplatin and paclitaxel in PTEN deficient tumors and with dose intensified carboplatin and paclitaxel.

Invest New Drugs. 2017-3-9

[10]
Buparlisib plus fulvestrant versus placebo plus fulvestrant for postmenopausal, hormone receptor-positive, human epidermal growth factor receptor 2-negative, advanced breast cancer: Overall survival results from BELLE-2.

Eur J Cancer. 2018-9-18

引用本文的文献

[1]
Translational Aspects in Metaplastic Breast Carcinoma.

Cancers (Basel). 2024-4-7

[2]
Case report: Successful treatment of a rare HER2-positive advanced breast squamous cell carcinoma.

Front Pharmacol. 2024-2-22

[3]
Discrepancy between Tumor Size Assessed by Full-Field Digital Mammography or Ultrasonography (cT) and Pathology (pT) in a Multicenter Series of Breast Metaplastic Carcinoma Patients.

Cancers (Basel). 2023-12-30

[4]
Outcomes of Metaplastic Breast Cancer Versus Triple-Negative Breast Cancer: A Propensity Score Matching Analysis.

World J Surg. 2023-12

[5]
Rare subtypes of triple negative breast cancer: Current understanding and future directions.

NPJ Breast Cancer. 2023-6-23

[6]
Metaplastic Carcinoma of the Breast: Case Series of a Single Institute and Review of the Literature.

Med Sci (Basel). 2023-5-19

[7]
Metaplastic Breast Cancer: Current Understanding and Future Directions.

Clin Breast Cancer. 2023-12

[8]
Clinical characteristics and overall survival prognostic nomogram for metaplastic breast cancer.

Front Oncol. 2023-3-2

[9]
Long noncoding RNA-mediated activation of PROTOR1/PRR5-AKT signaling shunt downstream of PI3K in triple-negative breast cancer.

Proc Natl Acad Sci U S A. 2022-10-25

[10]
TERT promoter hotspot mutations and gene amplification in metaplastic breast cancer.

NPJ Breast Cancer. 2021-4-16

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