Checkpoint inhibitor therapy for metastatic triple-negative breast cancer

被引:85
作者
Heeke, Arielle L. [1 ]
Tan, Antoinette R. [1 ]
机构
[1] Atrium Hlth, Levine Canc Inst, Charlotte, NC 28203 USA
关键词
Triple-negative breast cancer; Metastatic; Immunotherapy; Checkpoint inhibitor; Review; TUMOR-INFILTRATING LYMPHOCYTES; T-CELL; SUPPRESSOR-CELLS; ANTITUMOR IMMUNITY; PLUS CHEMOTHERAPY; PD-L1; EXPRESSION; OPEN-LABEL; PEMBROLIZUMAB; IMMUNOTHERAPY; CYCLOPHOSPHAMIDE;
D O I
10.1007/s10555-021-09972-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunotherapy has become a mainstay of cancer treatment in many malignancies, though its application in breast cancer remains limited. Of the breast cancer subtypes, triple-negative breast cancers (TNBCs) are characterized by immune activation and infiltration and more commonly express biomarkers associated with response to immunotherapy. Checkpoint inhibitor therapy has shown promising activity in metastatic TNBC. In 2019, the US FDA granted accelerated approval of atezolizumab, a programmed death-ligand 1 (PD-L1) inhibitor, in combination with nab-paclitaxel for unresectable locally advanced or metastatic PD-L1-positive TNBC, based on the results of the phase III IMpassion130 trial. In 2020, the FDA also granted accelerated approval of pembrolizumab, a PD-1 inhibitor, in combination with chemotherapy for locally recurrent unresectable and metastatic PD-L1-positive TNBC, based on results of the phase III KEYNOTE-355 trial. Additional combination strategies are being explored in the treatment of metastatic TNBC, with the goal of augmenting antitumor activity. In this review, the clinical development of checkpoint inhibitors in the treatment of metastatic TNBC will be discussed, including clinical outcomes with monotherapy and combination therapy regimens, biomarkers that may predict for benefit, and future directions in the field.
引用
收藏
页码:537 / 547
页数:11
相关论文
共 73 条
[41]   Tumor infiltrating lymphocytes are prognostic in triple negative breast cancer and predictive for trastuzumab benefit in early breast cancer: results from the FinHER trial [J].
Loi, S. ;
Michiels, S. ;
Salgado, R. ;
Sirtaine, N. ;
Jose, V. ;
Fumagalli, D. ;
Kellokumpu-Lehtinen, P-L ;
Bono, P. ;
Kataja, V. ;
Desmedt, C. ;
Piccart, M. J. ;
Loibl, S. ;
Denkert, C. ;
Smyth, M. J. ;
Joensuu, H. ;
Sotiriou, C. .
ANNALS OF ONCOLOGY, 2014, 25 (08) :1544-1550
[42]  
Loi S, ANN ONCOL, V30, pIII1
[43]   RAS/MAPK Activation Is Associated with Reduced Tumor-Infiltrating Lymphocytes in Triple-Negative Breast Cancer: Therapeutic Cooperation Between MEK and PD-1/PD-L1 Immune Checkpoint Inhibitors [J].
Loi, Sherene ;
Dushyanthen, Sathana ;
Beavis, Paul A. ;
Salgado, Roberto ;
Denkert, Carsten ;
Savas, Peter ;
Combs, Susan ;
Rimm, David L. ;
Giltnane, Jennifer M. ;
Estrada, Monica V. ;
Sanchez, Violeta ;
Sanders, Melinda E. ;
Cook, Rebecca S. ;
Pilkinton, Mark A. ;
Mallal, Simon A. ;
Wang, Kai ;
Miller, Vincent A. ;
Stephens, Phil J. ;
Yelensky, Roman ;
Doimi, Franco D. ;
Gomez, Henry ;
Ryzhov, Sergey V. ;
Darcy, Phillip K. ;
Arteaga, Carlos L. ;
Balko, Justin M. .
CLINICAL CANCER RESEARCH, 2016, 22 (06) :1499-1509
[44]   Analysis of the Association Between Adverse Events and Outcome in Patients Receiving a Programmed Death Protein 1 or Programmed Death Ligand 1 Antibody [J].
Maher, V. Ellen ;
Fernandes, Laura L. ;
Weinstock, Chana ;
Tang, Shenghui ;
Agarwal, Sundeep ;
Brave, Michael ;
Ning, Yang-min ;
Singh, Harpreet ;
Suzman, Daniel ;
Xu, James ;
Goldberg, Kirsten B. ;
Sridhara, Rajeshwari ;
Ibrahim, Amna ;
Theoret, Marc ;
Beaver, Julia A. ;
Pazdur, Richard .
JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (30) :2730-+
[45]   Neoantigens and genome instability: impact on immunogenomic phenotypes and immunotherapy response [J].
Mardis, Elaine R. .
GENOME MEDICINE, 2019, 11 (01)
[46]   Primary results from IMpassion131, a double-blind placebo-controlled randomised phase III trial of first- line paclitaxel (PAC) ± atezolizumab (atezo) for unresectable locally advanced/metastatic triple-negative breast cancer (mTNBC) [J].
Miles, D. W. ;
Gligorov, J. ;
Andre, F. ;
Cameron, D. ;
Schneeweiss, A. ;
Barrios, C. H. ;
Xu, B. ;
Wardley, A. M. ;
Kaen, D. ;
Andrade, L. ;
Semiglazov, V. ;
Reinisch, M. ;
Patre, M. ;
Morales, L. ;
Russell, K. ;
Donica, M. ;
O'Shaughnessy, J. .
ANNALS OF ONCOLOGY, 2020, 31 :S1147-S1148
[47]   PD-L1 Expression in Triple-Negative Breast Cancer [J].
Mittendorf, Elizabeth A. ;
Philips, Anne V. ;
Meric-Bernstam, Funda ;
Qiao, Na ;
Wu, Yun ;
Harrington, Susan ;
Su, Xiaoping ;
Wang, Ying ;
Gonzalez-Angulo, Ana M. ;
Akcakanat, Argun ;
Chawla, Akhil ;
Curran, Michael ;
Hwu, Patrick ;
Sharma, Padmanee ;
Litton, Jennifer K. ;
Molldrem, Jeffrey J. ;
Alatrash, Gheath .
CANCER IMMUNOLOGY RESEARCH, 2014, 2 (04) :361-370
[48]   KEYNOTE-012: Long-lasting responses in a phase Ib study of pembrolizumab for metastatic triple-negative breast cancer (mTNBC) [J].
Nanda, R. ;
Specht, J. ;
Dees, C. ;
Berger, R. ;
Gupta, S. ;
Geva, R. ;
Pusztai, L. ;
Pathiraja, K. ;
Ray, A. ;
Karantza, V. ;
Buisseret, L. .
CANCER RESEARCH, 2017, 77
[49]   Pembrolizumab in Patients With Advanced Triple-Negative Breast Cancer: Phase Ib KEYNOTE-012 Study [J].
Nanda, Rita ;
Chow, Laura Q. M. ;
Dees, E. Claire ;
Berger, Raanan ;
Gupta, Shilpa ;
Geva, Ravit ;
Pusztai, Lajos ;
Pathiraja, Kumudu ;
Aktan, Gursel ;
Cheng, Jonathan D. ;
Karantza, Vassiliki ;
Buisseret, Laurence .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (21) :2460-+
[50]  
Nio Y, 2000, ANTICANCER RES, V20, P3293