Abstract
Purpose
Malignant mesothelioma (MM) is an aggressive tumor of the serosal surfaces with a poor prognosis. Advances in the understanding of tumor biology have led to the development of several targeted treatments, which have been evaluated in clinical trials. This article is a comprehensive review of all clinical trials evaluating the effect of targeted treatments in MM.
Methods
An extensive literature search was performed in January 2011 using pubmed and medline. No constraints on publication date were applied.
Results
Thirty-two trials exploring 17 different targeted agents in MM were found. Treatment in first- and second-line targeted agents induced response rates ranging from 0–14% and 0–16%, respectively. The tyrosine kinase inhibitor sunitinib induced partial response in 10% and stable disease in 66% of MPM patients as second-line treatment. A preliminary analysis of a phase II/III trial suggests that addition of bevacizumab to pemetrexed and cisplatin first-line treatment significantly improves disease control (CR + PR + SD) in the bevacizumab arm (73.5%) compared with treatment with pemetrexed and cisplatin without bevacizumab (43.2%) (P = 0.010). Another phase II trial did not observe any significant clinical benefit of adding of bevacizumab to gemcitabine and cisplatin.
Conclusions
Disease stabilization is reported in some patients with several targeted treatments and might be beneficial in subgroups of patients or in combination with classic chemotherapy. None of the hitherto explored targeted treatments can currently be recommended as standard treatment in MM.
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Abbreviations
- ABL:
-
Abelson murine leukemia viral oncogene homolog
- AKT:
-
A member of the non-specific serine/threonine-protein kinase family
- ALK:
-
Anaplastic lymphoma kinase
- BCR:
-
Breakpoint cluster region
- CALGB:
-
Cancer and leukemia group B
- c-KIT:
-
V-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
- CML:
-
Chronic myeloid leukemia
- CR:
-
Complete response
- EGF:
-
Endothelial growth factor
- EGFR:
-
Endothelial growth factor receptor
- EML4:
-
Echinoderm microtubule-associated protein-like 4
- EPP:
-
Extrapleural pneumectomy
- FDG-PET:
-
Fludeoxyglucose(18F) positron emission tomography
- GIST:
-
Gastrointestinal stromal tumor
- HDAC:
-
Histone deacetylase
- HDACi:
-
Histone deacetylase inhibitor
- IFP:
-
Interstitial fluid pressure
- IGF-1:
-
Insulin-like growth factor 1
- KDR:
-
Kinase insert domain receptor
- MM:
-
Malignant mesothelioma
- MPM:
-
Malignant pleural mesothelioma
- mTOR:
-
Mammalian target of rapamycin
- NGR:
-
Asparagine–glycine–arginine
- hTNF:
-
Human tumor necrosis factor-alpha
- OS:
-
Overall survival
- PD:
-
Progression disease
- PDGF:
-
Platelet derived growth factor
- PDGFR:
-
Platelet derived growth factor receptor
- P/D:
-
Pleurectomy/decortication
- PFS:
-
Progression free survival
- PI3K:
-
Phosphatidylinositol 3-kinase
- PR:
-
Partial response
- RNA:
-
Ribonucleic acid
- SRC:
-
Sarcoma
- SD:
-
Stable disease
- TGF-alpha:
-
Tumor growth factor-alpha
- TKI:
-
Tyrosine kinase inhibitor
- VEGF:
-
Vascular endothelial growth factor
- VEGFR:
-
Vascular endothelial growth factor receptor
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Jakobsen, J.N., Sørensen, J.B. Review on clinical trials of targeted treatments in malignant mesothelioma. Cancer Chemother Pharmacol 68, 1–15 (2011). https://doi.org/10.1007/s00280-011-1655-3
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DOI: https://doi.org/10.1007/s00280-011-1655-3