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乳腺癌内分泌治疗耐药及其逆转的研究进展

孙文婧 胡曼婷 李娜 葛菲 陈文林 刘洋

孙文婧, 胡曼婷, 李娜, 葛菲, 陈文林, 刘洋. 乳腺癌内分泌治疗耐药及其逆转的研究进展[J]. 昆明医科大学学报, 2021, 42(7): 143-149. doi: 10.12259/j.issn.2095-610X.S20210724
引用本文: 孙文婧, 胡曼婷, 李娜, 葛菲, 陈文林, 刘洋. 乳腺癌内分泌治疗耐药及其逆转的研究进展[J]. 昆明医科大学学报, 2021, 42(7): 143-149. doi: 10.12259/j.issn.2095-610X.S20210724
Wen-jing SUN, Man-ting HU, Na LI, Fei GE, Wen-lin CHEN, Yang LIU. Progress in Clinical Research on Drug Resistance and Reversal of Endocrine Therapy in Breast Cancer[J]. Journal of Kunming Medical University, 2021, 42(7): 143-149. doi: 10.12259/j.issn.2095-610X.S20210724
Citation: Wen-jing SUN, Man-ting HU, Na LI, Fei GE, Wen-lin CHEN, Yang LIU. Progress in Clinical Research on Drug Resistance and Reversal of Endocrine Therapy in Breast Cancer[J]. Journal of Kunming Medical University, 2021, 42(7): 143-149. doi: 10.12259/j.issn.2095-610X.S20210724

乳腺癌内分泌治疗耐药及其逆转的研究进展

doi: 10.12259/j.issn.2095-610X.S20210724
基金项目: 国家自然科学基金资助项目(82060538);云南省卫生健康委员会医学学科带头人培养计划(D-2018002)
详细信息
    作者简介:

    孙文婧(1995~),女,江西九江人,在读硕士研究生,主要从事乳腺肿瘤基础研究工作

    通讯作者:

    陈文林,E-mail:chenwenlin@aliyun.com

  • 中图分类号: R737.9

Progress in Clinical Research on Drug Resistance and Reversal of Endocrine Therapy in Breast Cancer

  • 摘要: 激素受体阳性HR + 乳腺癌临床治疗初始阶段依靠内分泌治疗常取得较好的预后,但一旦出现复发和转移,总的预后并不理想,因此近年来内分泌治疗的疗效因耐药性的产生而受到各种限制,内分泌耐药的逆转被认为是让早期激素受体阳性乳腺癌回归慢性疾病治疗的新的方法和希望,延缓和逆转内分泌耐药的策略也逐渐受到临床和科研工作密切的关注。对延缓和逆转内分泌治疗以及应对策略的研究进展作一综述。
  • 图  1  内分泌治疗的经典药物和联合靶向药物的相关通路和作用位点

    Figure  1.  Related pathways and action sites of classical drugs and combined targeted drugs in endocrine therapy

    表  1  HR+乳腺癌的内分泌联合治疗

    Table  1.   Endocrine combined therapy for HR + breast cancer

    药物类别/靶点药物名称临床研究研究设计无进展生存时间/月
    EGFR inhibitors Gefitinib NCT00229697[2] Tamoxifen + Gefitinib vs placebo 10.9 vs 8.8
    NCT00057941[5] Gefitinib + Anastrozole vs
    Gefitinib + Fulvestrant
    5.3 vs 5.2
    Molecular targeted agents Trastuzumab TAnDEM-3[3] Trastuzumab + Anastrozole vs anastrozole 4.8 vs 2.4
    5.6 vs 3.8
    Margetuximab SOPHIA-3[4] Margetuximab + chemotherapy vs
    Trastuzumab+ chemotherapy
    6.9 vs 5.1
    CDK4/6 inhibitors Abemaciclib MONARCH-3[7] Abemaciclib/placebo+
    non-steroidal drugs
    28.18 vs 14.76
    palbociclib NCT02549430[8] Palbociclib + ET vs palbociclib 10.8 vs 6.5
    Ribociclib MalAlESA-2[9] Ribociclib + Letrozole vs
    ribociclib + placebo
    25.3 vs 16.0
    PI3K/AKT/mTOR inhibitors buparlisib BELLE-2[10] Buparlisib + Fulvestrant vs placebo 6.9 vs 5.0;
    6.8 vs 4.5;
    6.8 vs 4.0
    Pictilisib NCT01437566[11] Pictilisib + Fulvestrant vs placebo 6.5 vs 5.1
    Alpelisib BYL719-1b[12] Alpelisib + Letrozole vs placebo -N/A
    MK-2206 NCT01344031[14] MK-2206 + Fulvestrant vs placebo N/A-
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  • 收稿日期:  2021-05-09
  • 网络出版日期:  2021-07-19
  • 刊出日期:  2021-07-21

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