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Lynparza is feasible as oral tablets marketed and was started indicated as a maintenance treatment or monotherapy for the therapy of adult patients with relapsed epithelial ovarian, fallopian tube or primary peritoneal cancer
Lynparza is a prescription drug which used under the supervision of medical practioners
Lynparza is used for the treatment in patients with advanced ovarian cancer
Lynparza is used for the treatment in patients with HER2 – negative metastatic breast cancer.
PARP is small for Poly (ADP-ribose) polymerase. It is a protein whichproduced damaged cells to repair themselves. Olaparib blocks PARP working.
Some cancer cells commit on PARP to keep their DNA healthy. This contains cancer cells with a convert in the BRCA gene. So, when Olaparib blocks PARP from repairing DNA injury, the cancer cells die.
This kind of drug is called a cancer growth blocker.
Absorption: Maximum plasma concentration 1 to 3 hours
Distribution: volume of distribution 167 +/-196 L, plasma protein binding is 82%
Metabolism: Primarily metabolised by CYP3A4
Elimination: Excreted through the urine 44% and 42% through the feces.
Half – life of Lynparza 11.9 hours
Maintenance treatment of recurrent ovarian cancer
The tablet recommended dose is 300mg (two 150mg – mg tablets) PO BID
Continue treatment until disease progression or unacceptable toxicity
Monotherapy for advanced BRCA – mutated ovarian cancer
The tablet recommended dose is 300mg (two 150mg – mg tablets) PO BID
The capsules recommended dose is 400mg (eight 50mg- mg capsules) PO BID
Continue treatment until disease progression or unacceptable toxicity.
Maintenance treatment for advanced BRCA-mutated ovarian cancer
The tablet recommended dose is 300mg (two 150mg – mg tablets) PO BID
Follow the treatment until disease progression, undesirable toxicity or completion of 2 years of treatment
Finishing of 2 years of treatment
When Lynparza co administrationwith myelosuppressive anticancer agents contains DNA damaging agents, indicate a potentiation and prolongation of myelosuppressive toxicity.
Interaction of strong CYP3A inhibitors (itraconazole, telithromycin, clarithromycin,) will increase Olaparib plasma concentration.
Co administration of strong CYP3A inducers (itraconazole, telithromycin, clarithromycin,) will decrease Olaparib plasma concentration.
None
Haematological toxicity will be resulted in patientsincluding diagnoses or findings of commonly mild or moderate anaemia, neutropenia, thrombocytopenia and lymphopenia.
When Lynparza monotherapy administrated to patient the incidence of myelodysplastic syndrome will occur.
On basis of mechanism of action (PARP inhibition), Lynparza could cause risk to fetal when administered to a pregnant woman.
Lynparza combination with strong or moderate CYP3A inhibitors is not recommended.
Based on Lynparza mechanism of action, the drug causes risk to the fetal may occur when administrated to a pregnant woman.
No data available on the presence of Lynparza in human milk, hence avoid breast feeding during the treatment.
Store at 200C to 250C
If dose is failed, then have the dose as soon as possible before next dose timing reaches or skip the missed dose and continue the regular schedule.
Must Consult doctors regarding missed dose.