Emerging New Targets in Systemic Therapy for Malignant Pleural Mesothelioma

被引:5
作者
Yun, Karen M. [1 ]
Bazhenova, Lyudmila [1 ]
机构
[1] UC San Diego Hlth, Moores Canc Ctr, Div Hematol Oncol, La Jolla, CA 92093 USA
关键词
BAP1; malignant pleural mesothelioma; mesothelin; NF2; targeted therapy; ARGININOSUCCINATE SYNTHETASE; PROGNOSTIC-SIGNIFICANCE; ANETUMAB RAVTANSINE; OPEN-LABEL; PHASE-II; T-CELLS; CANCER; GENE; BAP1; OVEREXPRESSION;
D O I
10.3390/cancers16071252
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Malignant pleural mesothelioma is an aggressive cancer that is not surgically resectable for the majority of patients diagnosed with it. Chemotherapy or immunotherapy is the current standard of care for patients with advanced malignant pleural mesothelioma. Cancer drugs that specifically target genetic alterations in mesothelioma have not yet been approved. In this clinical review, we discuss the promising molecular targets and progress made in precision medicine in malignant pleural mesothelioma.Abstract Malignant pleural mesothelioma (MPM) is a heterogeneous cancer composed of distinct molecular and pathologic subtypes. Unfortunately, MPM is aggressive, and current therapies for advanced, unresectable disease remain limited to cytotoxic chemotherapy and immunotherapy. Our understanding of the genomic landscape of MPM is steadily growing, while the discovery of effective targeted therapies in MPM has advanced more slowly than in other solid tumors. Given the prevalence of alterations in tumor suppressor genes in MPM, it has been challenging to identify actionable targets. However, efforts to characterize the genetic signatures in MPM over the last decade have led to a range of novel targeted therapeutics entering early-phase clinical trials. In this review, we discuss the advancements made thus far in targeted systemic therapies in MPM and the future direction of targeted strategies in patients with advanced MPM.
引用
收藏
页数:13
相关论文
共 73 条
[1]   A Phase I Trial of Regional Mesothelin-Targeted CAR T-cell Therapy in Patients with Malignant Pleural Disease, in Combination with the Anti-PD-1 Agent Pembrolizumab [J].
Adusumilli, Prasad S. ;
Zauderer, Marjorie G. ;
Riviere, Isabelle ;
Solomon, Stephen B. ;
Rusch, Valerie W. ;
O'Cearbhaill, Roisin E. ;
Zhu, Amy ;
Cheema, Waseem ;
Chintala, Navin K. ;
Halton, Elizabeth ;
Pineda, John ;
Perez-Johnston, Rocio ;
Tan, Kay See ;
Daly, Bobby ;
Araujo Filho, Jose A. ;
Ngai, Daniel ;
McGee, Erin ;
Vincent, Alain ;
Diamonte, Claudia ;
Sauter, Jennifer L. ;
Modi, Shanu ;
Sikder, Devanjan ;
Senechal, Brigitte ;
Wang, Xiuyan ;
Travis, William D. ;
Gonen, Mithat ;
Rudin, Charles M. ;
Brentjens, Renier J. ;
Jones, David R. ;
Sadelain, Michel .
CANCER DISCOVERY, 2021, 11 (11) :2748-2763
[2]   Efficacy of CDK4/6 inhibitors in preclinical models of malignant pleural mesothelioma [J].
Aliagas, Elisabet ;
Alay, Ania ;
Martinez-Iniesta, Maria ;
Hernandez-Madrigal, Miguel ;
Cordero, David ;
Gausachs, Mireia ;
Pros, Eva ;
Saigi, Maria ;
Busacca, Sara ;
Sharkley, Annabel J. ;
Dawson, Alan ;
Palmero, Ramon ;
Ruffinelli, Jose C. ;
Padrones, Susana ;
Aso, Samantha ;
Escobar, Ignacio ;
Ramos, Ricard ;
Llatjos, Roger ;
Vidal, August ;
Dorca, Eduard ;
Varela, Mar ;
Sanchez-Cespedes, Montse ;
Fennell, Dean ;
Munoz-Pinedo, Cristina ;
Villanueva, Alberto ;
Sole, Xavi ;
Nadal, Ernest .
BRITISH JOURNAL OF CANCER, 2021, 125 (10) :1365-1376
[3]   HPN536, a T cell-engaging, mesothelin/CD3-specific TriTAC for the treatment of solid tumors [J].
Austin, Richard ;
Aaron, Wade ;
Baeuerle, Patrick ;
Barath, Manasi ;
Jones, Adrie ;
Jones, Susan D. ;
Law, Che-Leung ;
Kwant, Kathryn ;
Lemon, Bryan ;
Muchnik, Anna ;
Sexton, Kenneth ;
Tatalick, Laurie ;
Wesche, Holger ;
Yu, Timothy .
CANCER RESEARCH, 2018, 78 (13)
[4]   First-line nivolumab plus ipilimumab in unresectable malignant pleural mesothelioma (CheckMate 743): a multicentre, randomised, open-label, phase 3 trial [J].
Baas, Paul ;
Scherpereel, Arnaud ;
Nowak, Anna K. ;
Fujimoto, Nobukazu ;
Peters, Solange ;
Tsao, Anne S. ;
Mansfield, Aaron S. ;
Popat, Sanjay ;
Jahan, Thierry ;
Antonia, Scott ;
Oulkhouir, Youssef ;
Bautista, Yolanda ;
Cornelissen, Robin ;
Greillier, Laurent ;
Grossi, Francesco ;
Kowalski, Dariusz ;
Rodriguez-Cid, Jeronimo ;
Aanur, Praveen ;
Oukessou, Abderrahim ;
Baudelet, Christine ;
Zalcman, Gerard .
LANCET, 2021, 397 (10272) :375-386
[5]   Mesothelin-Specific Chimeric Antigen Receptor mRNA-Engineered T Cells Induce Antitumor Activity in Solid Malignancies [J].
Beatty, Gregory L. ;
Haas, Andrew R. ;
Maus, Marcela V. ;
Torigian, Drew A. ;
Soulen, Michael C. ;
Plesa, Gabriela ;
Chew, Anne ;
Zhao, Yangbing ;
Levine, Bruce L. ;
Albelda, Steven M. ;
Kalos, Michael ;
June, Carl H. .
CANCER IMMUNOLOGY RESEARCH, 2014, 2 (02) :112-120
[6]   Mesothelin is not required for normal mouse development or reproduction [J].
Bera, TK ;
Pastan, I .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (08) :2902-2906
[7]   Targeting AXL in mesothelioma: From functional characterization to clinical implication [J].
Bhadresha, Kinjal ;
Mirza, Sheefa ;
Penny, Clement ;
Mughal, Muhammed Jameel .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2023, 188
[8]   Combined Inhibition of CDK4/6 and PI3K/AKT/mTOR Pathways Induces a Synergistic Anti-Tumor Effect in Malignant Pleural Mesothelioma Cells [J].
Bonelli, Mara A. ;
Digiacomo, Graziana ;
Fumarola, Claudia ;
Alfieri, Roberta ;
Quainia, Federico ;
Falco, Angela ;
Madeddu, Denise ;
La Monica, Silvia ;
Cretella, Daniele ;
Ravelli, Andrea ;
Ulivi, Paola ;
Tebaldi, Michela ;
Calistri, Daniele ;
Delmonte, Angelo ;
Ampollini, Luca ;
Carbognani, Paolo ;
Tiseo, Marcello ;
Cavazzoni, Andrea ;
Petronini, Pier Giorgio .
NEOPLASIA, 2017, 19 (08) :637-648
[9]   Clinical significance of histologic subtyping of malignant pleural mesothelioma [J].
Brcic, Luka ;
Kern, Izidor .
TRANSLATIONAL LUNG CANCER RESEARCH, 2020, 9 (03) :924-933
[10]  
Briggs KJ, 2022, CANCER RES, V82