Ерлотиниб: Өкпе және қарын безі ісігіне қарсы емдік дәрі

Medication for treatment of non small cell lung cancer

Erlotinib in unresectable non small cell lung cancer when added to chemotherapy improves overall survival by 19%, and improved progression free survival (PFS) by 29%, when compared to chemotherapy alone. The U. S. Food and Drug Administration (FDA) approved erlotinib for the treatment of locally advanced or metastatic non small cell lung cancer that has failed at least one prior chemotherapy regimen. In lung cancer, erlotinib has been shown to be effective in patients with or without EGFR mutations, but appears to be more effective in patients with EGFR mutations. Overall survival, progression free survival and one year survival are similar to standard second line therapy (docetaxel or pemetrexed). Overall response rate is about 50% better than standard second line chemotherapy.

In November 2005, the FDA approved erlotinib in combination with gemcitabine for treatment of locally advanced, unresectable, or metastatic pancreatic cancer.

As with other ATP competitive small molecule tyrosine kinase inhibitors, such as imatinib in CML, patients rapidly develop resistance. In the case of erlotinib this typically occurs 8–12 months from the start of treatment. Over 50% of resistance is caused by a mutation in the ATP binding pocket of the EGFR kinase domain involving substitution of a small polar threonine residue with a large nonpolar methionine residue (T790M). Approximately 20% of drug resistance is caused by amplification of the hepatocyte growth factor receptor, which drives ERBB3 dependent activation of PI3K.

Erlotinib is not a substrate for either of hepatic OATPs (OATP1B1 or OATP1B3). Also, erlotinib is not an inhibitor of OATP 1B1 or OATP 1B3 transporter. Erlotinib is mainly metabolized by the liver enzyme CYP3A4. Compounds which induce this enzyme (i. e. stimulate its production), such as St John's wort, can lower erlotinib concentrations, while inhibitors can increase concentrations.

Erlotinib is an epidermal growth factor receptor inhibitor (EGFR inhibitor). The drug follows Iressa (gefitinib), which was the first drug of this type. Erlotinib specifically targets the epidermal growth factor receptor (EGFR) tyrosine kinase, which is highly expressed and occasionally mutated in various forms of cancer. It binds in a reversible fashion to the adenosine triphosphate (ATP) binding site of the receptor. For the signal to be transmitted, two EGFR molecules need to come together to form a homodimer. These then use the molecule of ATP to trans phosphorylate each other on tyrosine residues, which generates phosphotyrosine residues, recruiting the phosphotyrosine binding proteins to EGFR to assemble protein complexes that transduce signal cascades to the nucleus or activate other cellular biochemical processes. When erlotinib binds to EGFR, formation of phosphotyrosine residues in EGFR is not possible and the signal cascades are not initiated.

It is marketed in the United States by Genentech and elsewhere by Roche. The drug's U. S. patent expired in 2020. In May 2012, the US District Court of Delaware passed an order in favor of OSI Pharmaceutical LLC against Mylan Pharmaceuticals upholding the validity of the patent for Erlotinib. In India, generic pharmaceutical firm Cipla is battling with Roche against the Indian patent for this drug.