The Effects of Anlotinib Combined with Chemotherapy following Progression on Cyclin-Dependent Kinase 4/6 Inhibitor in Hormone Receptor-Positive Metastatic Breast Cancer

被引:0
|
作者
Xu, Ting [1 ]
Xiong, Weili [1 ]
Zhang, Lili [2 ]
Yuan, Yuan [2 ]
机构
[1] Nanjing Med Univ, Affiliated Canc Hosp, Dept Oncol, Nanjing, Peoples R China
[2] Nanjing Med Univ, Jiangsu Canc Hosp, Affiliated Canc Hosp, Jiangsu Inst Canc Res,Dept Chemotherapy, Nanjing, Peoples R China
来源
BREAST JOURNAL | 2024年 / 2024卷
关键词
PALBOCICLIB;
D O I
10.1155/2024/5396107
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose. Endocrine therapy combined with cyclin-dependent kinase (CDK) 4/6 inhibitors (CDK4/6i) is the preferred treatment for hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer (MBC). However, there are currently no recommendations for therapeutic strategies after progression on CDK4/6i-based treatment. This study aimed to examine the efficacy and safety of anlotinib plus chemotherapy in HR+/HER2- MBC after progression on CDK4/6 inhibitors. Methods. We collected data from 32 patients with HR+/HER2- MBC treated with anlotinib plus chemotherapy after progressing on CDK4/6i at Jiangsu Cancer Hospital from March 2020 to October 2023. The median follow-up was 9.1 months (range, 2.0-19.7 months) as of the data cutoff date in October 2023. The primary endpoint was median progression-free survival (PFS); secondary endpoints included objective response rate (ORR), disease control rate (DCR), and adverse events. Results. The median PFS (mPFS) of all patients was 7.6 months (95% confidence interval (CI), 5.75-9.45). There was no significant difference in mPFS between patients who responded to prior CDK4/6i treatment and those who did not (8.3 months vs. 6.8 months, p=0.580). Besides, the ORR was 34.4% and DCR was 93.8%. The most frequently observed adverse events were anemia (50.0%), neutropenia (40.6%), thrombocytopenia (34.4%), and epistaxis (34.4%). Dose interruption or reductions due to adverse events occurred in 2 (6.3%) and 5 (15.6%) patients, respectively. Conclusions. The study preliminarily demonstrates that anlotinib combined with chemotherapy may be an optional recommendation for patients with HR+/HER2- metastatic breast cancer who have progressed after CDK4/6i.
引用
收藏
页数:8
相关论文
共 50 条
  • [21] The Association of ERBB2-Low Expression With the Efficacy of Cyclin-Dependent Kinase 4/6 Inhibitor in Hormone Receptor-Positive, ERBB2-Negative Metastatic Breast Cancer
    Bao, Kelvin K. H.
    Sutanto, Leone
    Tse, Shirley S. W.
    Man Cheung, Ka
    Chan, Jeffrey C. H.
    JAMA NETWORK OPEN, 2021, 4 (11)
  • [22] Abemaciclib, a potent cyclin-dependent kinase 4 and 6 inhibitor, for treatment of ER-positive metastatic breast cancer
    Lee, Karla A.
    Shepherd, Scott T. C.
    Johnston, Stephen R. D.
    FUTURE ONCOLOGY, 2019, 15 (29) : 3309 - 3326
  • [23] Cyclin-Dependent Kinase 4/6 Inhibitors Combined With Radiotherapy for Patients With Metastatic Breast Cancer
    Ratosa, Ivica
    Orazem, Miha
    Scoccimarro, Erika
    Steinacher, Mateja
    Dominici, Luca
    Aquilano, Michele
    Cerbai, Cecilia
    Desideri, Isacco
    Ribnikar, Domen
    Marinko, Tanja
    Livi, Lorenzo
    Meattini, Icro
    CLINICAL BREAST CANCER, 2020, 20 (06) : 495 - 502
  • [24] Does toxicity of cyclin-dependent kinase 4/6 inhibitor predict treatment response in metastatic hormone-positive breast cancer patients?
    Gulbagci, Burcu
    Demirci, Ayse
    Celebi, Abdussamet
    Firat, Sedat Tarik
    Gokmen, Ivo
    Ugurlu, Irem
    Ilce, Huri Tilla
    Cakir, Emre
    Hacibekiroglu, Ilhan
    ONCOLOGY IN CLINICAL PRACTICE, 2025,
  • [25] Therapy after cyclin-dependent kinase inhibition in metastatic hormone receptor-positive breast cancer: Resistance mechanisms and novel treatment strategies
    Sharifi, Marina N.
    Anandan, Apoorva
    Grogan, Patrick
    O'Regan, Ruth M.
    CANCER, 2020, 126 (15) : 3400 - 3416
  • [26] Safety of cyclin-dependent kinase4/6 inhibitor combined with palliative radiotherapy in patients with metastatic breast cancer
    Kim, Kristine N.
    Shah, Payal
    Clark, Amy
    Freedman, Gary M.
    Dastgheyb, Sana
    Barsky, Andrew R.
    Dreyfuss, Alexandra D.
    Taunk, Neil K.
    BREAST, 2021, 60 : 163 - 167
  • [27] PACE: A Randomized Phase II Study of Fulvestrant, Palbociclib, and Avelumab After Progression on Cyclin-Dependent Kinase 4/6 Inhibitor and Aromatase Inhibitor for Hormone Receptor-Positive/Human Epidermal Growth Factor Receptor-Negative Metastatic Breast Cancer
    Mayer, Erica L.
    Ren, Yue
    Wagle, Nikhil
    Mahtani, Reshma
    Ma, Cynthia
    DeMichele, Angela
    Cristofanilli, Massimo
    Meisel, Jane
    Miller, Kathy D.
    Abdou, Yara
    Riley, Elizabeth C.
    Qamar, Rubina
    Sharma, Priyanka
    Reid, Sonya
    Sinclair, Natalie
    Faggen, Meredith
    Block, Caroline C.
    Ko, Naomi
    Partridge, Ann H.
    Chen, Wendy Y.
    Demeo, Michelle
    Attaya, Victoria
    Okpoebo, Amanda
    Alberti, Jillian
    Liu, Yuan
    Gauthier, Eric
    Burstein, Harold J.
    Regan, Meredith M.
    Tolaney, Sara M.
    JOURNAL OF CLINICAL ONCOLOGY, 2024, 42 (17) : 2050 - 2060
  • [28] Evaluation of cyclin-dependent kinase 4/6 inhibitor-induced serum creatinine elevations in patients with hormone receptor positive breast cancer
    Ly, Emily
    Howard, Frederick Matthew
    Chen, Nan
    Hahn, Olwen Mary
    Fleming, Gini F.
    Nanda, Rita
    Patel, Shivani
    Thimothy, Lida
    Yang, Heng
    JOURNAL OF CLINICAL ONCOLOGY, 2024, 42 (16)
  • [29] Evaluation of cyclin-dependent kinase 4/6 inhibitor-induced serum creatinine elevations in patients with hormone receptor positive breast cancer
    Ly, Emily
    Howard, Frederick M.
    Chen, Nan
    Hahn, Olwen
    Fleming, Gini F.
    Nanda, Rita
    Patel, Shivani
    Thimothy, Lida
    Yang, Heng
    JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2024,
  • [30] NeoPalAna: Neoadjuvant Palbociclib, a Cyclin-Dependent Kinase 4/6 Inhibitor, and Anastrozole for Clinical Stage 2 or 3 Estrogen Receptor-Positive Breast Cancer
    Ma, Cynthia X.
    Gao, Feng
    Luo, Jingqin
    Northfelt, Donald W.
    Goetz, Matthew
    Forero, Andres
    Hoog, Jeremy
    Naughton, Michael
    Ademuyiwa, Foluso
    Suresh, Rama
    Anderson, Karen S.
    Margenthaler, Julie
    Aft, Rebecca
    Hobday, Timothy
    Moynihan, Timothy
    Gillanders, William
    Cyr, Amy
    Eberlein, Timothy J.
    Hieken, Tina
    Krontiras, Helen
    Guo, Zhanfang
    Lee, Michelle V.
    Spies, Nicholas C.
    Skidmore, Zachary L.
    Griffith, Obi L.
    Griffith, Malachi
    Thomas, Shana
    Bumb, Caroline
    Vij, Kiran
    Bartlett, Cynthia Huang
    Koehler, Maria
    Al-Kateb, Hussam
    Sanati, Souzan
    Ellis, Matthew J.
    CLINICAL CANCER RESEARCH, 2017, 23 (15) : 4055 - 4065