Pharmacology-based ranking of anti-cancer drugs to guide clinical development of cancer immunotherapy combinations

被引:34
作者
Lemaire, Vincent [1 ]
Shemesh, Colby S. [1 ]
Rotte, Anand [2 ]
机构
[1] Genentech Inc, Dept Clin Pharmacol, 1 DNA Way, San Francisco, CA 94080 USA
[2] Arcellx, Clin & Regulatory Affairs, Gaithersburg, MD USA
关键词
Clinical trials; Cancer immunotherapy; Combination development; Cancer; Pharmacology; CELL LUNG-CANCER; PACLITAXEL PLUS CARBOPLATIN; IMMUNE CHECKPOINT BLOCKADE; DESIGN TASK-FORCE; OPEN-LABEL; PHASE-I; ANTIBODY CP-870,893; MONOCLONAL-ANTIBODY; 1ST-LINE TREATMENT; COMBINED NIVOLUMAB;
D O I
10.1186/s13046-021-02111-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The success of antibodies targeting Programmed cell death protein 1 (PD-1) and its ligand L1 (PD-L1) in cancer treatment and the need for improving response rates has led to an increased demand for the development of combination therapies with anti-PD-1/PD-L1 blockers as a backbone. As more and more drugs with translational potential are identified, the number of clinical trials evaluating combinations has increased considerably and the demand to prioritize combinations having potential for success over the ones that are unlikely to be successful is rising. This review aims to address the unmet need to prioritize cancer immunotherapy combinations through comprehensive search of potential drugs and ranking them based on their mechanism of action, clinical efficacy and safety. As lung cancer is one of the most frequently studied cancer types, combinations that showed potential for the treatment of lung cancer were prioritized. A literature search was performed to identify drugs with potential in combination with PD-1/PD-L1 blockers and the drugs were ranked based on their mechanism of action and known clinical efficacy. Nineteen drugs or drug classes were identified from an internal list of lead molecules and were scored for their clinical potential. Efficacy and safety data from pivotal studies was summarized for the selected drugs. Further, overlap of mechanisms of action and adverse events was visualized using a heat map illustration to help screen drugs for combinations. The quantitative scoring methodology provided in this review could serve as a template for preliminary ranking of novel combinations.
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页数:17
相关论文
共 102 条
[1]   Mechanism-based treatment of cancer with immune checkpoint inhibitor therapies [J].
Abdou, Yara ;
Pandey, Manu ;
Sarma, Maithreyi ;
Shah, Shrunjal ;
Baron, Jeffrey ;
Ernstoff, Marc S. .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2020, 86 (09) :1690-1702
[2]   IMMUNOTHERAPY TRIALS LACK A BIOMARKER FOR INCLUSION: IMPLICATIONS FOR DRUG DEVELOPMENT [J].
Adashek, Jacob ;
Goloubev, Alexey ;
Kato, Shumei ;
Kurzrock, Razelle .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2020, 8 :A106-A106
[3]  
[Anonymous], FDA approves nivolumab plus ipilimumab and chemotherapy for first-line treatment of metastatic NSCLC | FDA
[4]   The great debate at "Immunotherapy Bridge 2018", Naples, November 29th, 2018 [J].
Ascierto, Paolo A. ;
Butterfield, Lisa H. ;
Demaria, Sandra ;
Ferris, Robert L. ;
Freeman, Gordon J. ;
Lo, Roger S. ;
Mantovani, Alberto ;
Nathan, Paul ;
Hamid, Omid ;
Politi, Katerina ;
Puzanov, Igor .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2019, 7 (01)
[5]   Long-term outcomes of a phase I study of agonist CD40 antibody and CTLA-4 blockade in patients with metastatic melanoma [J].
Bajor, David L. ;
Mick, Rosemarie ;
Riese, Matthew J. ;
Huang, Alex C. ;
Sullivan, Brendan ;
Richman, Lee P. ;
Torigian, Drew A. ;
George, Sangeeth M. ;
Stelekati, Erietta ;
Chen, Fang ;
Melenhorst, J. Joseph ;
Lacey, Simon F. ;
Xu, Xiaowei ;
Wherry, E. John ;
Gangadhar, Tara C. ;
Amaravadi, Ravi K. ;
Schuchter, Lynn M. ;
Vonderheide, Robert H. .
ONCOIMMUNOLOGY, 2018, 7 (10)
[6]   A Phase I Study of an Agonist CD40 Monoclonal Antibody (CP-870,893) in Combination with Gemcitabine in Patients with Advanced Pancreatic Ductal Adenocarcinoma [J].
Beatty, Gregory L. ;
Torigian, Drew A. ;
Chiorean, E. Gabriela ;
Saboury, Babak ;
Brothers, Alex ;
Alavi, Abass ;
Troxel, Andrea B. ;
Sun, Weijing ;
Teitelbaum, Ursina R. ;
Vonderheide, Robert H. ;
O'Dwyer, Peter J. .
CLINICAL CANCER RESEARCH, 2013, 19 (22) :6286-6295
[7]   Current Panorama and Challenges for Neoadjuvant Cancer Immunotherapy [J].
Benitez, Jose Carlos ;
Remon, Jordi ;
Besse, Benjamin .
CLINICAL CANCER RESEARCH, 2020, 26 (19) :5068-5077
[8]  
Bhandaru M, 2019, METHODS MOL BIOL, V1904, P83, DOI 10.1007/978-1-4939-8958-4_4
[9]  
Caruso C, 2020, CANCER DISCOV, V10, P1086, DOI 10.1158/2159-8290.CD-NB2020-063
[10]  
Cecchini M, 2019, AACR ANN M