Polatuzumab vedotin, an anti-CD79b antibody-drug conjugate for the treatment of relapsed/refractory diffuse large B-cell lymphoma

被引:11
作者
Camus, Vincent [1 ,2 ]
Tilly, Herve [1 ,2 ]
机构
[1] Univ Rouen, Ctr Henri Becquerel, INSERM, U1245, Rouen, France
[2] Univ Rouen, Ctr Henri Becquerel, Dept Clin Hematol, Rouen, France
关键词
antibody-drug conjugate; CD79b; diffuse large B-cell lymphoma; polatuzumab vedotin; INDUCED PERIPHERAL NEUROPATHY; NON-HODGKIN-LYMPHOMA; PLUS RITUXIMAB; PHASE-II; BENDAMUSTINE; GEMCITABINE; OXALIPLATIN; LEUKEMIA; OUTCOMES;
D O I
10.2217/fon-2020-0675
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lay abstract Polatuzumab vedotin is a new compound with an innovative construction. It combines an antibody which targets the surface of lymphoma cells and a drug killing these cells. The binding of this compound to the cancer cell allows for specific delivery of the drug to the cell. It avoids the side effects of usual chemotherapy. This compound is now approved in combination with chemotherapy for the treatment of some lymphomas. This review presents the characteristics, advantages and limitations of this compound. Refractory/relapsed diffuse large B-cell lymphoma remains a major unmet medical need with poor outcome, especially for patients considered ineligible for stem cell transplant. Polatuzumab vedotin (PV) is a first-in-class anti-CD79b antibody-drug conjugate that contains the microtubule inhibitor monomethyl auristatin E. The development of PV is currently very active. This drug was US FDA approved in 2019 in combination with bendamustine and rituximab for the treatment of refractory/relapsed diffuse large B-cell lymphoma in third line and more, after demonstrating relevant efficacy and acceptable safety in a pivotal randomized Phase II trial. This review summarizes the features of this new drug with the primary focus on the clinical work supporting efficacy, relevance and tolerability of PV.
引用
收藏
页码:127 / 136
页数:10
相关论文
共 35 条
[1]  
Committee for Medicinal Products for Human Use (CHMP), 2019, EMACHMP6907482019
[2]   Outcomes in refractory diffuse large B-cell lymphoma: results from the international SCHOLAR-1 study [J].
Crump, Michael ;
Neelapu, Sattva S. ;
Farooq, Umar ;
Van den Neste, Eric ;
Kuruvilla, John ;
Westin, Jason ;
Link, Brian K. ;
Hay, Annette ;
Cerhan, James R. ;
Zhu, Liting ;
Boussetta, Sami ;
Feng, Lei ;
Maurer, Matthew J. ;
Navale, Lynn ;
Wiezorek, Jeff ;
Go, William Y. ;
Gisselbrecht, Christian .
BLOOD, 2017, 130 (16) :1800-1808
[3]   High metabolic tumor volume is associated with decreased efficacy of axicabtagene ciloleucel in large B-cell lymphoma [J].
Dean, Erin A. ;
Mhaskar, Rahul S. ;
Lu, Hong ;
Mousa, Mina S. ;
Krivenko, Gabriel S. ;
Lazaryan, Aleksandr ;
Bachmeier, Christina A. ;
Chavez, Julio C. ;
Nishihori, Taiga ;
Davila, Marco L. ;
Khimani, Farhad ;
Liu, Hien D. ;
Pinilla-Ibarz, Javier ;
Shah, Bijal D. ;
Jain, Michael D. ;
Balagurunathan, Yoganand ;
Locke, Frederick L. .
BLOOD ADVANCES, 2020, 4 (14) :3268-3276
[4]   Therapeutic potential of an anti-CD79b antibody-drug conjugate, anti-CD79b-vc-MMAE, for the treatment of non-Hodgkin lymphoma [J].
Dornan, David ;
Bennett, Fiona ;
Chen, Yvonne ;
Dennis, Mark ;
Eaton, Dan ;
Elkins, Kristi ;
French, Dorothy ;
Go, Mary Ann T. ;
Jack, Andrew ;
Junutula, Jagath R. ;
Koeppen, Hartmut ;
Lau, Jeffrey ;
McBride, Jacqueline ;
Rawstron, Andy ;
Shi, Xiaoyan ;
Yu, Nancy ;
Yu, Shang-Fan ;
Yue, Peng ;
Zheng, Bing ;
Ebens, Allen ;
Polson, Andrew G. .
BLOOD, 2009, 114 (13) :2721-2729
[5]   Anti-CD22 and anti-CD79b antibody-drug conjugates preferentially target proliferating B cells [J].
Fuh, Franklin K. ;
Looney, Caroline ;
Li, Dongwei ;
Poon, Kirstena ;
Dere, Randall C. ;
Danilenko, Dimitry M. ;
McBride, Jacqueline ;
Reed, Chae ;
Chung, Shan ;
Zheng, Bing ;
Mathews, William Rodney ;
Polson, Andrew ;
Prabhu, Saileta ;
Williams, Marna .
BRITISH JOURNAL OF PHARMACOLOGY, 2017, 174 (08) :628-640
[6]  
Han Tae H, 2014, Drug Metab Dispos, V42, P1914, DOI 10.1124/dmd.114.058586
[7]   Investigational Antibody-Drug Conjugates for Treatment of B-lineage Malignancies [J].
Herrera, Alex F. ;
Molina, Arturo .
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2018, 18 (07) :452-+
[8]   T cell senescence and CAR-T cell exhaustion in hematological malignancies [J].
Kasakovski, Dimitri ;
Xu, Ling ;
Li, Yangqiu .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2018, 11
[9]   Current Approaches for Absorption, Distribution, Metabolism, and Excretion Characterization of Antibody-Drug Conjugates: An Industry White Paper [J].
Kraynov, Eugenia ;
Kamath, Amrita V. ;
Walles, Markus ;
Tarcsa, Edit ;
Deslandes, Antoine ;
Iyer, Ramaswamy A. ;
Datta-Mannan, Amita ;
Sriraman, Priya ;
Bairlein, Michaela ;
Yang, Johnny J. ;
Barfield, Matthew ;
Xiao, Guangqing ;
Escandon, Enrique ;
Wang, Weirong ;
Rock, Dan A. ;
Chemuturi, Nagendra V. ;
Moore, David J. .
DRUG METABOLISM AND DISPOSITION, 2016, 44 (05) :617-623
[10]   Impact of rituximab on treatment outcomes of patients with diffuse large b-cell lymphoma: a population-based analysis [J].
Lee, Linda ;
Crump, Michael ;
Khor, Sara ;
Hoch, Jeffrey S. ;
Luo, Jin ;
Bremner, Karen ;
Krahn, Murray ;
Hodgson, David C. .
BRITISH JOURNAL OF HAEMATOLOGY, 2012, 158 (04) :481-488