Synonym |
LAN-1444 |
Species |
Human |
Protein Accession |
P30872 |
Purity |
Greater than 98% as determined by SDS-PAGE |
Endotoxin Level |
Less than 0.1 ng/µg (1EU/µg) |
Biological Activity |
The ED50 is 0.2-1.7 ng/mL |
Expression System |
E. coli |
Fusion Tag |
None |
Predicted Molecular Mass |
10.3 kDa |
Formulation |
Lyophilized from a 0.2 µm filtered solution of 20mM PB, 150mM NaCl, pH 7.2 |
Reconstitution |
We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the
bottom. Reconstitute in 10mM HCl to a concentration of 0.1-1.0 mg/mL. Stock solutions should be
apportioned into working aliquots and stored at ≤ -20°C. Further dilutions should be made in
appropriate buffered solutions. |
Storage & Stability |
The lyophilized protein is stable for at least 2 years from date of receipt at -20°C. Upon
reconstitution, this cytokine can be stored in working aliquots at 2°C - 8°C for one month, or
at -20°C for six months, with a carrier protein without detectable loss of activity. |
FAQ
What is Lanreotide Acetate and how does it work in the body?
Lanreotide Acetate is a medication
that belongs to a class of drugs known as somatostatin analogs. It is primarily used to treat
acromegaly, a condition characterized by excessive growth hormone production, and may also be used to
treat certain types of neuroendocrine tumors. The drug mimics the action of somatostatin, a hormone that
inhibits the secretion of several other hormones in the body, most notably growth hormone from the
pituitary gland. It accomplishes this by binding to specific receptors on the surface of the cells,
leading to a reduction in hormone secretion. This action helps to control symptoms associated with
hormone overproduction, such as growth abnormalities or tumor progression.
The mechanism of
Lanreotide Acetate involves reducing the levels of circulating growth hormone and insulin-like growth
factor-1 (IGF-1), substances that promote abnormal tissue growth and metabolic disturbances. By doing
so, Lanreotide Acetate alleviates symptoms such as joint pain, headache, and abnormalities in facial or
hand structures that are frequently observed in patients with acromegaly. Moreover, for patients with
neuroendocrine tumors, Lanreotide Acetate aids in slowing down disease progression and controlling
symptoms related to hormone secretion by the tumors, such as flushing and diarrhea.
Lanreotide
Acetate is administered as a deep subcutaneous injection, usually once every four weeks. Its long-acting
formulation ensures sustained drug presence in the body, optimizing its therapeutic effects while
minimizing the frequency of administration. The medication's delivery system has been finely tuned to
release the active substance gradually, maintaining effective hormone suppression over the treatment
period. While the primary focus of Lanreotide Acetate's action is on the inhibition of growth hormone
and IGF-1, the drug also impacts other hormones and growth factors, thereby offering a broader scope of
utility, particularly in conditions associated with neuroendocrine activity.
Like all
medications, Lanreotide Acetate may cause side effects, including gastrointestinal disturbances such as
diarrhea, abdominal pain, and nausea. Some patients may experience reactions at the injection site,
including pain or redness. Despite these potential side effects, Lanreotide Acetate is generally
well-tolerated, and dose adjustments or specific management strategies can be employed to mitigate
adverse effects, ensuring that patients derive maximum benefit from the treatment.
Who should
consider using Lanreotide Acetate and what are the main conditions it treats?
Lanreotide Acetate
is specifically indicated for the management of acromegaly and certain neuroendocrine tumors.
Individuals diagnosed with acromegaly, a condition resulting from excessive secretion of growth hormone
usually due to a pituitary adenoma, are prime candidates for Lanreotide Acetate, particularly when
surgery or other initial treatments are not feasible or have proven ineffective. This condition, if left
untreated, can lead to severe health issues, including diabetes, cardiovascular disease, and
osteoarthritis due to the ongoing abnormal growth patterns in bones and tissues. Lanreotide Acetate, by
effectively reducing growth hormone and insulin-like growth factor-1 levels, helps manage these risks
and symptoms.
The medication is also beneficial for patients with neuroendocrine tumors,
particularly those of gastrointestinal origin, sometimes referred to as gastroenteropancreatic
neuroendocrine tumors (GEP-NETs). These tumors can either secrete hormones that cause severe
physiological symptoms or remain non-functional yet potentially malignant with the risk of metastasis.
For functional tumors that lead to carcinoid syndrome, symptoms like diarrhea, flushing, wheezing, and
heart valve issues can be debilitating. Lanreotide Acetate helps control these symptoms by inhibiting
hormone release and may also have an anti-proliferative effect that slows tumor growth.
Though
Lanreotide Acetate is primarily targeted toward these conditions, eligibility for its use should always
be carefully evaluated by a healthcare professional. Evaluation typically involves comprehensive medical
history review, diagnosis confirmation via appropriate imaging and laboratory tests, and consideration
of the patient's overall health status, including other medical conditions and concomitant medications.
Patients with gallbladder disease, heart disease, or diabetes may require closer monitoring and dose
adjustments to avoid exacerbating these conditions while on Lanreotide Acetate.
It's crucial to
have a thorough discussion with a healthcare provider to understand the potential benefits and risks
associated with Lanreotide Acetate treatment. Patient education should also cover aspects such as
potential side effects, the importance of adhering to the injection schedule, and the necessity of
periodic follow-up tests to monitor hormone levels and adjust treatment as necessary. This informed and
collaborative approach ensures that patients can maximize therapeutic outcomes from Lanreotide Acetate
while minimizing risks.
What are the potential side effects of Lanreotide Acetate and how can
they be managed?
Lanreotide Acetate, while effective in managing conditions like acromegaly and
neuroendocrine tumors, can be associated with a range of side effects, though not everyone experiences
them. Understanding these side effects and knowing how to manage them is important for anyone
considering or currently undergoing treatment with this medication.
Among the most common side
effects are gastrointestinal issues, such as diarrhea, nausea, vomiting, abdominal pain, and flatulence.
These effects are often due to the medication's influence on digestive hormones, and while they can be
uncomfortable, they are typically manageable. Patients experiencing these symptoms are encouraged to
maintain hydration and may find relief through dietary adjustments, such as smaller, more frequent meals
and avoiding foods that trigger symptoms. Over-the-counter medications can also be considered to manage
symptoms like diarrhea, but it's important to consult a healthcare provider before taking additional
medications.
Injection site reactions are another potential side effect, usually presenting as
pain, redness, or lumps where the medication was administered. To minimize these reactions, rotating the
injection site each time can be helpful. Patients are advised to allow the medication to reach room
temperature before injection and to use the proper technique to reduce discomfort. Should these
reactions persist or cause significant discomfort, discussing alternative injection techniques or
interventions with a healthcare provider is advisable.
Some patients might experience
gallbladder-related issues, such as the formation of gallstones due to the drug's inhibitory effects on
bile secretions. Regular monitoring through ultrasound or other imaging techniques may be recommended,
especially for patients with a history of gallbladder disease. In cases where gallstones become
symptomatic, medical or surgical management may be necessary.
Metabolic changes can also occur,
including hyperglycemia or hypoglycemia, especially in patients with diabetes or prediabetes. Regular
monitoring of blood glucose levels and appropriate adjustments in anti-diabetic medications can help
maintain blood sugar control. It is essential for patients to report any signs of dizziness, confusion,
or excessive sweating, which could indicate blood sugar fluctuations.
Other less common side
effects include thyroid dysfunction and bradycardia (slowed heart rate). Routine thyroid function tests
and heart rate monitoring may be advised, and any significant abnormalities should be addressed promptly
with a healthcare provider.
Overall, while the side effects of Lanreotide Acetate can impact
daily living, working closely with healthcare professionals to monitor and manage these effects ensures
that the benefits of treatment are maximized. Patients should be proactive in communicating any concerns
and maintaining scheduled follow-ups, which are integral to optimizing the therapeutic regimen and
enhancing quality of life.
How does Lanreotide Acetate compare to other treatments available for
acromegaly and neuroendocrine tumors?
Lanreotide Acetate offers distinct advantages that set it
apart from other treatment options for acromegaly and neuroendocrine tumors, though its suitability
depends on individual patient circumstances. Understanding its role in the broader spectrum of therapies
is integral to making an informed decision about treatment.
For acromegaly, the first-line
treatment is often surgery to remove the pituitary tumor responsible for excess growth hormone
production. However, in cases where surgery is not possible or fails to normalize hormone levels,
medical therapy becomes necessary. Lanreotide Acetate serves as a crucial option in this scenario. It
effectively reduces growth hormone and IGF-1 levels, helping manage symptoms and complications when
surgical outcomes are suboptimal. Compared to another somatostatin analog, octreotide, Lanreotide
Acetate offers the convenience of less frequent dosing, usually as a deep subcutaneous injection every
four weeks. This aspect can be significantly beneficial in terms of adherence and lifestyle integration
for many patients.
Alternatively, pegvisomant, a growth hormone receptor antagonist, directly
lowers IGF-1 levels by blocking the effects of growth hormone on cells. However, it does not reduce
growth hormone levels themselves. The choice between these medications often depends on individual
patient response, side effect profile, and specific health considerations. Lanreotide Acetate's proven
ability to provide symptom control and its administration route and schedule are strong factors in its
favor for many patients.
In the context of neuroendocrine tumors, particularly those producing
excess hormones, Lanreotide Acetate is used not only for symptom control but also for its
antiproliferative effects that can slow disease progression. While surgical resection of tumors remains
the primary curative approach when feasible, medical therapies play a vital role in managing inoperable
or metastatic cases. Other treatments like peptide receptor radionuclide therapy (PRRT) or targeted
therapies such as everolimus and sunitinib are options, particularly for advanced stages. Lanreotide
Acetate's ability to control tumor symptoms, alongside its potential to delay progression, provides a
complementary approach that can be combined with these treatments based on the patient's disease
profile.
Combination therapy may also involve chemotherapy in some cases, depending on the
tumor's grade and progression. The relatively mild side effect profile of Lanreotide Acetate, when
compared to chemotherapy's more pronounced adverse effects, represents an additional advantage for
patient quality of life.
Ultimately, the choice of Lanreotide Acetate over other treatments is a
decision that should be taken through detailed consultation with healthcare providers, considering the
specific nature of the disease, previous treatments, patient preferences, and overall health. By
aligning patient needs with the unique benefits of Lanreotide Acetate, optimal treatment outcomes can be
achieved.
What lifestyle modifications are recommended for patients on Lanreotide Acetate to
enhance treatment outcomes?
Lifestyle modifications can play a crucial role in enhancing the
efficacy and tolerability of Lanreotide Acetate treatment for patients with acromegaly and
neuroendocrine tumors. Implementing specific lifestyle changes complements the therapeutic effects of
the medication and can contribute to overall well-being and improved quality of life.
Firstly,
maintaining a balanced diet is essential, particularly in the management of gastrointestinal side
effects commonly associated with Lanreotide Acetate. Patients are encouraged to eat smaller, more
frequent meals that are low in fat and high in fiber. Foods that are easily digestible can help mitigate
issues such as diarrhea and abdominal discomfort. Additionally, staying well-hydrated is vital to
counteract potential dehydration resulting from gastrointestinal symptoms. Consulting a dietitian can
provide personalized dietary advice tailored to the individual's health status and treatment side
effects.
Regular physical activity is another crucial component of lifestyle management for
patients on Lanreotide Acetate. Engaging in moderate exercises such as walking, swimming, or cycling can
help maintain a healthy weight, improve mood, and reduce the risk of cardiovascular complications
associated with acromegaly. Exercise can also aid in managing the long-term effects of muscle weakness
or joint pain resulting from the condition. However, it's important for patients to consult their
healthcare provider before starting any new exercise regimen to ensure it is safe and appropriate for
their health status.
Stress management techniques, including mindfulness, meditation, or yoga,
can be particularly beneficial in supporting emotional well-being. These practices help cope with the
anxiety or mood changes that may accompany chronic health conditions and their treatments. Involvement
in support groups or counseling may provide additional emotional support and practical tips from others
undergoing similar experiences.
Regular follow-up appointments with healthcare providers are
imperative for monitoring treatment progress and adjusting lifestyle recommendations as needed. Blood
tests and imaging studies help in assessing hormone levels and tumor status, allowing timely
interventions that complement medication and lifestyle management.
Patients with comorbid
conditions such as diabetes or cardiovascular issues should work closely with their healthcare team to
coordinate care and manage these conditions alongside their primary treatment. This comprehensive
approach helps ensure that all health issues are addressed holistically and that the impact on treatment
efficacy is minimized.
Lastly, adherence to the administration schedule of Lanreotide Acetate is
crucial. Patients should be educated about proper injection techniques if self-administering, to
minimize injection site reactions and ensure optimal drug delivery. Setting reminders or utilizing apps
designed for medication management can help maintain consistency in the treatment
schedule.
Ultimately, an integrated approach combining Lanreotide Acetate with lifestyle
modifications fosters a supportive environment for the patient's health journey, maximizing therapeutic
benefits and enhancing the overall treatment experience.