Lanreotida

Lanreotida Uses, Dosage, Side Effects, Food Interaction and all others data.

Lanreotida is a drug employed in the management of acromegaly (a hormonal condition caused by excess growth hormone) in addition to symptoms caused by neuroendocrine tumors, especially carcinoid syndrome. This drug is a long-acting analog of the drug somatostatin, a growth hormone inhibitor. Lanreotida is manufactured by the company, Ipsen Pharmaceuticals as lanreotide acetate, and marketed as Somatuline. It is approved in several countries worldwide, including the United Kingdom, Australia, and Canada. Lanreotida was first approved for use in the United States by the FDA on August 30, 2007.

Lanreotida exhibits antisecretory effects through cAMP suppression, and activation of ion currents such as K+ and Ca2+ which leads to hyperpolarization of the membrane and inhibition of Ca2+ mediated depolarization.Furthermore, through direct and indirect mechanisms, Lanreotida has potent antiproliferative effects.

Trade Name Lanreotida
Availability Prescription only
Generic Lanreotide
Lanreotide Other Names Lanreotida, Lanreotide
Related Drugs octreotide, bromocriptine, everolimus, Sandostatin, Afinitor, Somatuline Depot, Parlodel, Zortress, Lutathera, lutetium lu 177 dotatate
Type
Formula C54H69N11O10S2
Weight Average: 1096.33
Monoisotopic: 1095.467029814
Groups Approved
Therapeutic Class
Manufacturer
Available Country
Last Updated: September 19, 2023 at 7:00 am
Lanreotida
Lanreotida

Uses

Lanreotida is a somatostatin analog used for the treatment of unresectable, well- or moderately-differentiated, locally advanced or metastatic gastroenteropancreatic neuroendocrine tumors and acromegaly.

Lanreotida is a somatostatin analog approved for treatment of neuroendocrine tumours and acromegaly.

Lanreotida is also used to associated treatment for these conditions: Acromegaly, Unresectable, locally advanced enteropancreatic neuroendocrine tumors, Unresectable, locally advanced gastroenteropancreatic neuroendocrine tumors, Unresectable, metastatic enteropancreatic neuroendocrine tumors, Unresectable, metastatic gastroenteropancreatic neuroendocrine tumors

How Lanreotida works

Lanreotida is a somatostatin analogue (SSA) and has mainly inhibitory effects which are mediated via somatostatin receptors (SSTRs) 2 and 5 and include inhibition of growth hormone release in the brain. Tumor SSTR activation induces downstream cell cycle arrest and/or apoptosis, and also results in blunted production of substances that support tumor growth as well as tumor angiogenesis. This leads to the anti-proliferative effects of Lanreotida.

Toxicity

The most common adverse events are GI related, occurring in 67-84% of patients, and are typically mild to moderate. GI related effects are often transient, improve with subsequent injections, and most frequently include diarrhea and abdominal pain. Other GI symptoms such as nausea, vomiting, and abdominal distension are less common. It is not clear whether or not GI effects are dose related. Adverse effects relating to site of injection occur in 43% of patients and are more common in patients who self-inject as opposed to those who had health-care professionals administer the injection. A small number of patients report newly impaired glucose tolerance, fasting glucose or diabetes mellitus. Patients being treated for diabetes mellitus may experience hypoglycemia. After 1 year, up to 30% of patients may experience gallstone formation and the presence of sludge within the gallbladder due to inhibition of gallbladder and GI motility. This may be influenced by previous exposure to somatostatin analogues. Other adverse effects include reduction in left ventricular end-diastolic and end-systolic volumes, bradycardia, nasopharyngitis, and alopecia. Lanreotida is classified as Pregnancy Category C.

Food Interaction

No interactions found.

[Moderate] MONITOR: Due to their gastrointestinal pharmacologic effects, somatostatin analogs (e.g., octreotide, lanreotide) may variously affect the absorption of dietary nutrients and concomitantly administered oral medications.

Somatostatin analogs have been shown to prolong gastrointestinal transit time and inhibit intestinal absorption of some nutrients such as fat.

Clinical data are limited, however.

In case reports, octreotide has been reported to reduce the relative bioavailability of cyclosporine.

Transplant rejection and significant reductions in cyclosporine levels, sometimes to undetectable levels, have been reported in association with the interaction.

Vitamin K absorption was not affected when concomitantly administered with lanreotide according to the manufacturer.



MANAGEMENT: Clinicians should be aware of the potential for altered absorption of concomitantly administered oral medications during treatment with somatostatin analogs.

Blood levels and clinical response should be monitored, particularly for drugs that have a narrow therapeutic index, and the dosages adjusted as necessary.

Volume of Distribution

Estimated Volume of Distribution = 15.1 L

Elimination Route

Lanreotida forms a drug depot at the site of injection; therefore, there are 2 phases that describe the absorption of Lanreotida: 1. Initial rapid subcutaneous release during the first few days of treatment where drug that has not precipitated is rapidly absorbed.
2. Slow release of drug from the depot via passive diffusion. Absorption is independent of body weight, gender, and dosage.

Half Life

Half-life is approximately 22 days

Clearance

Estimated Clearance = 23.1 L/h

Elimination Route

<5% of lanreotide is excreted in urine, and less than 0.5% is excreted unchanged in the feces suggesting biliary excretion involvement.

Innovators Monograph

You find simplified version here Lanreotida

*** Taking medicines without doctor's advice can cause long-term problems.
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