Refining Immuno-Oncology Approaches in Metastatic Prostate Cancer: Transcending Current Limitations

被引:12
作者
Wong, Risa L. [1 ,2 ]
Yu, Evan Y. [1 ,2 ]
机构
[1] Univ Washington, Div Oncol, Dept Med, 825 Eastlake Ave E,G4830, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Clin Res Div, 1100 Fairview Ave N,D5-100, Seattle, WA 98109 USA
关键词
Immunotherapy; Immuno-oncology; Prostate cancer; Immune checkpoint inhibitors; Bispecific antibodies; CAR-T; ACETATE PLUS PREDNISONE; RANDOMIZED PHASE-II; SIPULEUCEL-T; PD-L1; EXPRESSION; KEYNOTE-365; COHORT; PATIENTS PTS; DOUBLE-BLIND; PRETREATED PATIENTS; ENZALUTAMIDE ENZA; TUMOR-CELLS;
D O I
10.1007/s11864-020-00808-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Opinion statementDue to its immunosuppressive tumor microenvironment, prostate cancer has historically been difficult to treat with immuno-oncology approaches. Other than pembrolizumab, which is now regulatory-approved for all microsatellite instability (MSI)-high and tumor mutational burden (TMB)-high advanced solid tumors, sipuleucel-T is the only immunotherapeutic agent approved by the US Food and Drug Administration (FDA) for prostate cancer. However, sipuleucel-T efficacy is optimal for select patients with indolent metastatic castration-resistant prostate cancer. Although manipulation of immune regulation by blocking immune checkpoints has led to substantial benefit in many cancers, experience with single-agent CTLA-4 and PD-1 or PD-L1 antibodies has shown limited effect for the majority of patients with prostate cancer, especially when administered as monotherapy. Combination therapies are now being attempted, in addition to enrichment strategies employing patient clinicopathologic and biologic characteristics that may heighten responses to immuno-oncology treatment, such as PD-L1 expression, TMB, MSI status, and alterations in CDK12. More work is needed to overcome the immune-exclusive barriers in prostate cancer, such as relatively low TMB, increased activity of myeloid-derived suppressor cells (MDSCs) and regulatory T cells, and defects in major histocompatibility complex (MHC) class I expression and interferon (IFN)-1 signaling. A promising approach and the likely next step in immuno-oncology for prostate cancer involves forced direction to markers expressed by prostate cancer tumor cells, such as prostate-specific membrane antigen (PSMA), that bypass the typical requirements for MHC class I interaction. The future will incorporate bispecific antibodies and chimeric antigen receptor (CAR)-T cells, potentially targeted towards phenotypic markers identified by next-generation PET imaging as part of the next wave of "precision medicine" in prostate cancer. Ultimately, we believe that the immune-exclusive prostate cancer tumor microenvironment can be overcome, and that patient outcomes can be enhanced through these more refined immuno-oncology approaches.
引用
收藏
页数:18
相关论文
共 98 条
[1]  
Agarwal N, 2020, J CLIN ONCOL, V38
[2]  
[Anonymous], 2020, EXELIXIS NEWS RELEAS
[3]  
Antonarakis ES, 2020, JCO PRECIS ONCOL, V4, P370, DOI [10.1200/PO.19.00399, 10.1200/po.19.00399]
[4]   Pembrolizumab for Treatment-Refractory Metastatic Castration-Resistant Prostate Cancer: Multicohort, Open-Label Phase II KEYNOTE-199 Study [J].
Antonarakis, Emmanuel S. ;
Piulats, Josep M. ;
Gross-Goupil, Marine ;
Goh, Jeffrey ;
Ojamaa, Kristiina ;
Hoimes, Christopher J. ;
Vaishampayan, Ulka ;
Berger, Ranaan ;
Sezer, Ahmet ;
Alanko, Tuomo ;
de Wit, Ronald ;
Li, Chunde ;
Omlin, Aurelius ;
Procopio, Giuseppe ;
Fukasawa, Satoshi ;
Tabata, Ken-ichi ;
Park, Se Hoon ;
Feyerabend, Susan ;
Drake, Charles G. ;
Wu, Haiyan ;
Qiu, Ping ;
Kim, Jeri ;
Poehlein, Christian ;
de Bono, Johann Sebastian .
JOURNAL OF CLINICAL ONCOLOGY, 2020, 38 (05)
[5]   Immune Characterization of the Programmed Death Receptor Pathway in High Risk Prostate Cancer [J].
Baas, Wesley ;
Gershburg, Svetlana ;
Dynda, Danuta ;
Delfino, Kristin ;
Robinson, Kathy ;
Nie, Daotai ;
Yearley, Jennifer Holmes ;
Alanee, Shaheen .
CLINICAL GENITOURINARY CANCER, 2017, 15 (05) :577-581
[6]   Preclinical evaluation of AMG 160, a next-generation bispecific T cell engager (BiTE) targeting the prostate-specific membrane antigen PSMA for metastatic castration-resistant prostate cancer (mCRPC). [J].
Bailis, Julie ;
Deegen, Petra ;
Thomas, Oliver ;
Bogner, Pamela ;
Wahl, Joachim ;
Liao, Mike ;
Li, Shyun ;
Matthes, Katja ;
Naegele, Virginie ;
Rau, Doris ;
Rattel, Benno ;
Raum, Tobias ;
Kufer, Peter ;
Coxon, Angela .
JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (07)
[7]   Targeting STEAP1 Protein in Human Cancer: Current Trends and Future Challenges [J].
Barroca-Ferreira, J. ;
Pais, J. P. ;
Santos, M. M. ;
Goncalves, A. M. ;
Gomes, I. M. ;
Sousa, I. ;
Rocha, S. M. ;
Passarinha, L. A. ;
Maia, C. J. .
CURRENT CANCER DRUG TARGETS, 2018, 18 (03) :222-230
[8]   Randomized, Double-Blind, Phase III Trial of Ipilimumab Versus Placebo in Asymptomatic or Minimally Symptomatic Patients With Metastatic Chemotherapy-Naive Castration-Resistant Prostate Cancer [J].
Beer, Tomasz M. ;
Kwon, Eugene D. ;
Drake, Charles G. ;
Fizazi, Karim ;
Logothetis, Christopher ;
Gravis, Gwenaelle ;
Ganju, Vinod ;
Polikoff, Jonathan ;
Saad, Fred ;
Humanski, Piotr ;
Piulats, Josep M. ;
Gonzalez Mella, Pablo ;
Ng, Siobhan S. ;
Jaeger, Dirk ;
Parnis, Francis X. ;
Franke, Fabio A. ;
Puente, Javier ;
Carvajal, Roman ;
Sengelov, Lisa ;
McHenry, M. Brent ;
Varma, Arvind ;
van den Eertwegh, Alfonsus J. ;
Gerritsen, Winald .
JOURNAL OF CLINICAL ONCOLOGY, 2017, 35 (01) :40-+
[9]  
Berry WR, 2020, J CLIN ONCOL, V38
[10]   PD-L1 is highly expressed in Enzalutamide resistant prostate cancer [J].
Bishop, Jennifer L. ;
Sio, Alexander ;
Angeles, Arkhjamil ;
Roberts, Morgan E. ;
Azad, Arun A. ;
Chi, Kim N. ;
Zoubeidi, Amina .
ONCOTARGET, 2015, 6 (01) :234-242