Malignant pleural mesothelioma: current treatments and emerging drugs

被引:31
作者
Belli, Carmen [1 ]
Fennell, Dean [2 ]
Giovannini, Monica [1 ]
Gaudino, Giovanni [3 ,4 ]
Mutti, Luciano [5 ]
机构
[1] Ist Sci San Raffaele, Dept Oncol, I-20132 Milan, Italy
[2] Queens Univ Belfast, Canc Res UK, Ctr Canc Res & Cell Biol, Belfast BT7 1NN, Antrim, North Ireland
[3] Univ Piemonte Orientale, DISCAFF, Novara, Italy
[4] DFB Ctr, Novara, Italy
[5] Lab Clin Oncol, Dept Med, Local Hlth Unit 11, Borgosesia Vercelli, Italy
关键词
chemotherapy; EGFR; malignant mesothelioma; mesothelin; mTOR; PDGFR; proteosoma; target therapy; VEGFR; PHASE-II TRIAL; MODULATED RADIATION-THERAPY; PEMETREXED PLUS CARBOPLATIN; PREVIOUSLY TREATED PATIENTS; RANDOMIZED-TRIAL; EXTRAPLEURAL PNEUMONECTOMY; DIFFERENTIAL EXPRESSION; CROCIDOLITE ASBESTOS; 2ND-LINE TREATMENT; IMATINIB MESYLATE;
D O I
10.1517/14728210903074563
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Malignant pleural mesothelioma (MPM) is an uncommon disease whose incidence is increasing worldwide over the past 30 years. Surgical resection and radiotherapy represent the standard treatment in patient with resectable MPM. Chemotherapy is also necessary to reduce incidence of distant metastases, but the optimal setting of treatment (neoadjuvant, adjuvant and intrapleural) is not clarified. For the patients with unresectable MPM, the combination cisplatin and pemetrexed or ralitrexed is the standard treatment as supported by a Phase III study. Better understanding of molecular pathways involved in MPM has enabled inclusion of new drugs targeted against pathways responsible for proliferation, cell survival and angiogenesis. Objective: This review discusses the current treatment option, the specific signal pathways activated in MPM and the novel agents under evaluation in clinical trials. Methods: We use for this article abstracts, papers, oral presentations from ASCO and the website http://www.clinical-trials.gov. Results/conclusion: This review summarizes the activity of chemotherapy and of new agents under evaluation in clinical trials. The better understanding of molecular pathways activated in MPM will hopefully provide new therapeutic options for these patients in the future.
引用
收藏
页码:423 / 437
页数:15
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