Current Issues in Malignant Pleural Mesothelioma Evaluation and Management

被引:26
作者
Ai, Jing [1 ]
Stevenson, James P. [1 ]
机构
[1] Cleveland Clin Fdn, Taussig Canc Inst, Cleveland, OH 44120 USA
关键词
Mesothelioma; Pleural neoplasms; Review; Clinical trials; Asbestos adverse effects; PHASE-II TRIAL; EMISSION TOMOGRAPHY/COMPUTED TOMOGRAPHY; HISTONE DEACETYLASE INHIBITORS; PEMETREXED-PRETREATED PATIENTS; CELL LUNG-CANCER; EXTRAPLEURAL PNEUMONECTOMY; TGF-BETA; DOUBLE-BLIND; INTERNATIONAL-ASSOCIATION; ENVIRONMENTAL EXPOSURE;
D O I
10.1634/theoncologist.2014-0122
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant pleural mesothelioma (MPM) is an uncommon disease most often associated with occupational asbestos exposure and is steadily increasing in worldwide incidence. Patients typically present at an older age, with advanced clinical stage and other medical comorbidities, making management quite challenging. Despite great efforts, the prognosis of MPM remains poor, especially at progression after initial treatment. Macroscopic complete resection of MPM can be achieved through extrapleural pneumonectomy (EPP) or extended (ie, radical) pleurectomy (e-P/D) in selected patients and can result in prolonged survival when incorporated into a multimodality approach. Given the morbidity associated with surgical resection of MPM, optimizing identification of appropriate patients is essential. Unfortunately, most patients are not candidates for EPP or e-P/D due to advanced stage, age, and/or medical comorbidity. Pemetrexed and platinum combination chemotherapy has become the cornerstone of therapy for patients with unresectable disease because the combination is associated with improved survival and quality of life in treated patients. However, MPM eventually becomes resistant to initial therapy, and benefit to further lines of therapy has not been substantiated in randomized clinical trials. Translational research has provided exciting insights into tumorigenesis, biomarkers, and immune response in MPM, leading to the development of multiple novel therapeutic agents that are currently in clinical trials. These advances hold the promise of a new era in the treatment of MPM and suggest that this disease will not be left behind in the war on cancer.
引用
收藏
页码:975 / 984
页数:10
相关论文
共 123 条
[1]   Targeting the TGFβ signalling pathway in disease [J].
Akhurst, Rosemary J. ;
Hata, Akiko .
NATURE REVIEWS DRUG DISCOVERY, 2012, 11 (10) :790-811
[2]  
[Anonymous], J CLIN ONCOL
[3]   NATURAL-HISTORY AND EPIDEMIOLOGY OF MALIGNANT MESOTHELIOMA [J].
ANTMAN, KH .
CHEST, 1993, 103 (04) :S373-S376
[4]   The management of malignant pleural mesothelioma; single centre experience in 10 years [J].
Aziz, T ;
Jilaihawi, A ;
Prakash, D .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2002, 22 (02) :298-305
[5]   Activity of chemotherapy and immunotherapy on malignant mesothelioma: a systematic review of the literature with meta-analysis [J].
Berghmans, T ;
Paesmans, M ;
Lalami, Y ;
Louviaux, I ;
Luce, S ;
Mascaux, C ;
Meert, AP ;
Sculier, JP .
LUNG CANCER, 2002, 38 (02) :111-121
[6]   HIGH-FREQUENCY OF INACTIVATING MUTATIONS IN THE NEUROFIBROMATOSIS TYPE-2 GENE (NF2) IN PRIMARY MALIGNANT MESOTHELIOMAS [J].
BIANCHI, AB ;
MITSUNAGA, SI ;
CHENG, JQ ;
KLEIN, WM ;
JHANWAR, SC ;
SEIZINGER, B ;
KLEY, N ;
KLEINSZANTO, AJP ;
TESTA, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (24) :10854-10858
[7]   Immune responses and immunotherapeutic interventions in malignant pleural mesothelioma [J].
Bograd, Adam J. ;
Suzuki, Kei ;
Vertes, Eva ;
Colovos, Christos ;
Morales, Eduardo A. ;
Sadelain, Michel ;
Adusumilli, Prasad S. .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2011, 60 (11) :1509-1527
[8]   The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma [J].
Bott, Matthew ;
Brevet, Marie ;
Taylor, Barry S. ;
Shimizu, Shigeki ;
Ito, Tatsuo ;
Wang, Lu ;
Creaney, Jenette ;
Lake, Richard A. ;
Zakowski, Maureen F. ;
Reva, Boris ;
Sander, Chris ;
Delsite, Robert ;
Powell, Simon ;
Zhou, Qin ;
Shen, Ronglai ;
Olshen, Adam ;
Rusch, Valerie ;
Ladanyi, Marc .
NATURE GENETICS, 2011, 43 (07) :668-U81
[9]  
BOUTIN C, 1993, CANCER, V72, P394, DOI 10.1002/1097-0142(19930715)72:2<394::AID-CNCR2820720214>3.0.CO
[10]  
2-5