Role of Cyclin-Dependent Kinase 4/6 in Metastatic Breast Cancer: Real-World Data From a Tertiary Care Institute in Eastern India

被引:0
|
作者
Majumdar, Saroj Kumar Das [1 ]
Barik, Sandip Kumar [1 ]
Pattanaik, Ashutosh [2 ]
Das, Deepak Kumar [1 ]
Parida, Kumar [1 ]
机构
[1] All India Inst Med Sci Bhubaneswar, Radiat Oncol, Bhubaneswar, India
[2] Apollo Hosp Bhubaneswar, Radiat Oncol, Bhubaneswar, India
关键词
abemaciclib; ribociclib; palbociclib; real world evidence metastatic breast cancer; cyclin dependent kinase 4/6 inhibitors; metastatic hormone positive breast cancer; INHIBITOR; PLUS; ABEMACICLIB; PALBOCICLIB; RIBOCICLIB; LETROZOLE; SURVIVAL; THERAPY; ASIA;
D O I
10.7759/cureus.52172
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction CDK4/6 inhibitors currently approved for patients with hormone-receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) metastatic breast cancer include palbociclib, ribociclib, and abemaciclib. This study aims to report on the treatment outcomes and real-world data regarding the use of CDK4/6 inhibitors in the treatment of ER+/HER2-metastatic breast cancer at a tertiary care institute in Eastern India. Materials and methods The present study is a retrospective analysis of data from patients with metastatic HR+/HER2-breast cancer who were treated with CDK4/6 inhibitors at a tertiary care institute in Eastern India between 2015 and 2022. The data were collected from online records in the departmental files and analyzed for the primary baseline characteristics of the patients, tumors, and response rates, including partial response (PR), complete response (CR), progressive disease (PD), and stable disease (SD), as defined by the Response Evaluation Criteria in Solid Tumors (RECIST) criteria version 1.1. The treatment administered, progression-free survival (PFS), and toxicity were also evaluated. Results From 2015 to 2022, 24 eligible patients were treated with CDK4/6 inhibitors for metastatic HR+/HER2-breast cancer. The average duration of follow-up was 25 months. Out of the 24 patients, 15 (62.5%) were taking Tab. ribociclib, six (25%) were taking Tab. palbociclib, and three (12.5%) were taking Tab. abemaciclib. CDK4/6 was used as a first-line therapy for 16 patients, while eight patients received it as a second-line treatment. Out of the total number of patients, six (25%) had stable disease, 13 (54.2%) had a partial response, and four (16.7%) had progressive disease. In total, of the eligible patients, five (20.8%) had grade I neutropenia, seven (29.2%) had grade II neutropenia, and four (16.7%) had grade III neutropenia. At five years, the PFS rate estimated by the Kaplan-Meier method was 50% (95% CI: 47.89-69.31). Conclusion Ribociclib and palbociclib have improved PFS in patients with metastatic HR+/HER2-breast cancer. Both drugs have well-tolerated toxicity, allowing patients to continue taking them for an extended period of time. CDK4/6 inhibitors have a higher response rate than the other agents.
引用
收藏
页数:10
相关论文
共 50 条
  • [21] Cyclin-Dependent Kinase 4/6 Inhibitors for the Treatment of Breast Cancer: A Review of Preclinical and Clinical Data
    Vidula, Neelima
    Rugo, Hope S.
    CLINICAL BREAST CANCER, 2016, 16 (01) : 8 - 17
  • [22] Non-Inflammatory skin involvement in Breast Cancer (T4b): Real-world Data from a Tertiary care centre in Eastern India
    Deepika, S.
    Jain, P.
    Saha, P.
    Sultania, M.
    Kar, M.
    Majumdar, S.
    Barik, S.
    Sable, M.
    Mishra, P.
    Muduly, D.
    EUROPEAN JOURNAL OF CANCER, 2022, 175 : S72 - S73
  • [23] Eribulin in heavily pretreated metastatic breast cancer: A real-world data from India
    Mandal, T. K.
    Bajpai, J.
    Kapoor, A.
    Kumar, A.
    Ghosh, J.
    Gulia, S.
    Rath, S.
    Gupta, S.
    ANNALS OF ONCOLOGY, 2020, 31 : S1264 - S1264
  • [24] A real-world data analysis: The first United Kingdom experience of cyclin-dependent kinase 4/6 inhibitor in advanced breast cancer in the National Health Service within an access program
    Palmieri, C.
    Musson, A.
    Harper-Wynne, C.
    Wheatley, D.
    Bertelli, G.
    MacPherson, I.
    Nathan, M.
    Verrill, M.
    Eva, J.
    Doody, C.
    Chowdhury, R.
    ANNALS OF ONCOLOGY, 2021, 32 : S464 - S464
  • [25] Real-world Outcomes of Cyclin-dependent Kinase Inhibitors Continued Beyond First Disease Progression in Hormone Receptor-positive Metastatic Breast Cancer
    Eziokwu, Akaolisa Samuel
    Varella, Leticia
    Kruse, Megan Lynn
    Jia, Xuefei
    Moore, Halle C. F.
    Budd, George Thomas
    Abraham, Jame
    Montero, Alberto J.
    CLINICAL BREAST CANCER, 2021, 21 (03) : 205 - 209
  • [26] Thromboembolism profiles associated with cyclin-dependent kinase 4/6 inhibitors: a real-world pharmacovigilance study and a systematic review
    Gao, Siyuan
    Li, Yu
    He, Zhichao
    Zhu, Jianhong
    Liang, Dan
    Yang, Shan
    Mo, Jiayao
    Lam, Kakei
    Yu, Xiaoxia
    Huang, Ming
    Wu, Junyan
    EXPERT OPINION ON DRUG SAFETY, 2023, 22 (07) : 599 - 609
  • [27] Clinical outcome and toxicity data in patients with advanced breast cancer treated with cyclin-dependent kinase 4/6 (CDK4/6) inhibitors combined with endocrine therapy in a real-world clinical setting
    Fountzilas, E.
    Koliou, G. -A.
    Rapti, V.
    Nikolakopoulos, A.
    Christopoulou, A.
    Moirogiorgou, E.
    Binas, I.
    Aravantinos, G.
    Kostadima, L.
    Nikolaidi, A.
    Karteri, S.
    Zagouri, F.
    Saridaki, Z.
    Molfeta, A.
    Oikonomopoulou, P.
    Res, E.
    Tryfonopoulos, D.
    Koumakis, G.
    Fountzilas, G.
    Razis, E.
    ANNALS OF ONCOLOGY, 2019, 30
  • [28] Cyclin-dependent kinase 4/6 inhibitors in breast cancer: palbociclib, ribociclib, and abemaciclib
    Dorota Kwapisz
    Breast Cancer Research and Treatment, 2017, 166 : 41 - 54
  • [29] Cyclin-dependent kinase 4/6 inhibitors in breast cancer: palbociclib, ribociclib, and abemaciclib
    Kwapisz, Dorota
    BREAST CANCER RESEARCH AND TREATMENT, 2017, 166 (01) : 41 - 54
  • [30] Differences of cyclin-dependent kinase 4/6 inhibitor, palbociclib and abemaciclib, in breast cancer
    Tamura, Kenji
    JAPANESE JOURNAL OF CLINICAL ONCOLOGY, 2019, 49 (11) : 993 - 998