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曲妥珠单抗治疗后 HER2 阳性转移性乳腺癌的疗效:一项网络荟萃分析。

Efficacy of tucatinib for HER2-positive metastatic breast cancer after HER2-targeted therapy: a network meta-analysis.

机构信息

Global Health Economics Outcome Research, Seagen Inc., Bothell, WA 98021, USA.

RTI Health Solutions, Towers Business Park, Wilmslow Road, Didsbury, Manchester, M20 2LS, UK.

出版信息

Future Oncol. 2021 Nov;17(33):4635-4647. doi: 10.2217/fon-2021-0742. Epub 2021 Aug 31.


DOI:10.2217/fon-2021-0742
PMID:34463120
Abstract

A systematic literature review and network meta-analysis of randomized controlled trials in patients receiving therapy for HER2+ unresectable/metastatic breast cancer after ≥1 HER2-directed therapy was conducted to compare progression-free survival (PFS) and overall survival (OS). Hazard ratios (HRs) and relative differences from fractional polynomials (FPs) for PFS and OS were assessed by Bayesian network meta-analyses. For PFS, surface under the cumulative rankogram (SUCRA) ranked tucatinib plus trastuzumab with capecitabine as highest in both HR and FP analyses, followed by T-DM1 monotherapy and neratinib plus capecitabine. For OS, SUCRA ranked tucatinib plus trastuzumab with capecitabine as highest in both HR and FP analyses, followed by pertuzumab plus trastuzumab with capecitabine and T-DM1 monotherapy, with similar scores. Tucatinib plus trastuzumab with capecitabine, and T-DM1 monotherapy, consistently showed improved PFS and OS versus lapatinib/trastuzumab plus capecitabine and non-targeted treatments.

摘要

对接受过≥1 种曲妥珠单抗靶向治疗的 HER2+不可切除/转移性乳腺癌患者的治疗进行了系统文献回顾和网络荟萃分析,以比较无进展生存期(PFS)和总生存期(OS)。采用贝叶斯网络荟萃分析评估 PFS 和 OS 的风险比(HR)和来自分数多项式(FP)的相对差异。对于 PFS,累积等级排序曲线下面积(SUCRA)排名曲妥珠单抗联合卡培他滨的 tucatinib 在 HR 和 FP 分析中均为最高,其次是 T-DM1 单药治疗和 neratinib 联合卡培他滨。对于 OS,曲妥珠单抗联合卡培他滨的 tucatinib 在 HR 和 FP 分析中均为最高,其次是曲妥珠单抗联合卡培他滨的 pertuzumab 和 T-DM1 单药治疗,得分相似。曲妥珠单抗联合卡培他滨的 tucatinib 和 T-DM1 单药治疗与 lapatinib/trastuzumab 联合卡培他滨和非靶向治疗相比,始终显示出改善的 PFS 和 OS。

相似文献

[1]
Efficacy of tucatinib for HER2-positive metastatic breast cancer after HER2-targeted therapy: a network meta-analysis.

Future Oncol. 2021-11

[2]
Preservation of quality of life in patients with human epidermal growth factor receptor 2-positive metastatic breast cancer treated with tucatinib or placebo when added to trastuzumab and capecitabine (HER2CLIMB trial).

Eur J Cancer. 2021-8

[3]
Neratinib: an option for HER2-positive metastatic breast cancer.

Clin Adv Hematol Oncol. 2020-9

[4]
Impact of the line of treatment on progression-free survival in patients treated with T-DM1 for metastatic breast cancer.

BMC Cancer. 2021-11-11

[5]
Targeting HER2 in Breast Cancer: Latest Developments on Treatment Sequencing and the Introduction of Biosimilars.

Drugs. 2020-11

[6]
Tucatinib, Trastuzumab, and Capecitabine for HER2-Positive Metastatic Breast Cancer.

N Engl J Med. 2019-12-11

[7]
Lapatinib plus capecitabine in patients with HER2-positive metastatic breast cancer: A systematic review
.

Int J Clin Pharmacol Ther. 2018-2

[8]
Evaluating the clinical effectiveness and safety of various HER2-targeted regimens after prior taxane/trastuzumab in patients with previously treated, unresectable, or metastatic HER2-positive breast cancer: a systematic review and network meta-analysis.

Breast Cancer Res Treat. 2020-2-25

[9]
T-DM1 Efficacy in Patients With HER2-positive Metastatic Breast Cancer Progressing After a Taxane Plus Pertuzumab and Trastuzumab: An Italian Multicenter Observational Study.

Clin Breast Cancer. 2020-4

[10]
Alliance A011801 (compassHER2 RD): postneoadjuvant T-DM1 + tucatinib/placebo in patients with residual HER2-positive invasive breast cancer.

Future Oncol. 2021-12

引用本文的文献

[1]
Mechanism of miRNAs and miRNA-mRNA Regulatory Networks in Modulating Drug Resistance in HER2-Positive Breast Cancer: An Integrative Bioinformatics Approach.

Cancers (Basel). 2024-11-26

[2]
A Cell-Penetrating Peptide Improves Anti-HER2 Single-Chain Variable Fragment Internalization and Antitumor Activity against HER2-Positive Breast Cancer In Vitro and In Vivo.

Molecules. 2024-3-11

[3]
miRNAs as biomarkers of therapeutic response to HER2-targeted treatment in breast cancer: A systematic review.

Biochem Biophys Rep. 2023-11-28

[4]
Tyrosine kinase inhibitors and human epidermal growth factor receptor-2 positive breast cancer.

World J Clin Oncol. 2023-5-24

[5]
Prognostic Factors Influencing Progression-Free Survival in HER2-Positive Metastatic Breast Cancer Patients Who Were Treated With A Combination of Lapatinib and Capecitabine.

Eur J Breast Health. 2023-4-1

[6]
The Value of Tucatinib in Metastatic HER2-Positive Breast Cancer Patients: An Italian Cost-Effectiveness Analysis.

Cancers (Basel). 2023-2-12

[7]
Prognostic impact of body mass index (BMI) in HER2+ breast cancer treated with anti-HER2 therapies: from preclinical rationale to clinical implications.

Ther Adv Med Oncol. 2022-3-8

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