Product image of Octreoscan (Indium In-111 Pentetreotide) supplied by GNH India

Octreoscan

Active Ingredient:
Indium In-111 Pentetreotide
Origin:
EU

Octreoscan (Indium In-111 Pentetreotide)

Indium In-111 pentetreotide, the active ingredient in Octreoscan, is a somatostatin analog presented as a radiopharmaceutical for intravenous use. It is employed in diagnostic imaging to locate neuroendocrine tumors and assess disease extent in adult patients. GNH India supplies Octreoscan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and oncology centres worldwide.

GNH India supplies Octreoscan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and oncology centres worldwide.

Manufacturer / TM Owner

Curium Netherlands B.V.

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Indications & Clinical Uses

Octreoscan is a radiolabeled somatostatin analogue that targets somatostatin receptor‑positive neuroendocrine tumors.

  • Gastroenteropancreatic neuroendocrine tumors: helps detect the presence and anatomical distribution of disease.
  • Carcinoid syndrome tumors: assists in staging and therapeutic planning by visualising receptor‑positive lesions.
  • Medullary thyroid carcinoma: aids in identifying metastatic sites for surgical or systemic treatment decisions.
  • Small‑cell lung cancer (rare indication for imaging research).

How It Works

  • Indium In-111 pentetreotide binds selectively to somatostatin receptor subtype 2 (SSTR2) on the surface of neuroendocrine tumor cells. After intravenous injection, the radiolabelled peptide circulates, attaches to SSTR2‑expressing cells, and emits gamma photons that are captured by a gamma camera, producing high‑resolution images of tumor location and burden.

Side Effects

Adverse reactions are generally related to the radiopharmaceutical and the injection process.

Common Side Effects

  • Nausea: mild to moderate, often transient.
  • Flushing: brief erythema and warmth, usually self‑limiting.
  • Headache: mild discomfort occurring shortly after administration.
  • Injection site pain: localized tenderness at the venous access point.
  • Transient hypotension: brief drop in blood pressure during or after injection.

Serious or Rare Side Effects

  • Severe allergic reaction (anaphylaxis): rapid onset of airway swelling, hives, or circulatory collapse.
  • Significant radiation‑induced organ toxicity: especially to kidneys or bone marrow with high cumulative exposure.
  • Persistent hypotension requiring medical intervention.
  • Acute hemolysis or hematuria.
  • Development of secondary malignancies (theoretical risk with high cumulative doses).

Precautions & Warnings

Octreoscan should be used only under the supervision of physicians experienced in nuclear medicine imaging.

  • Pregnancy testing: perform before administration because radiation may affect fetal development.
  • Breastfeeding: discontinue nursing for an appropriate period after dosing due to possible radiotracer excretion.
  • Renal function: assess baseline kidney function; adjust or avoid in severe impairment.
  • Concomitant radiopharmaceuticals: avoid simultaneous use to prevent overlapping radiation exposure.
  • Allergic history: verify no prior severe reaction to somatostatin analogues or indium‑based agents.
  • Store at 2‑8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Octreoscan may interact with other agents that influence radiation exposure or somatostatin receptor activity.

Major Interactions (Avoid)

  • Concurrent radiopharmaceuticals: may lead to additive radiation dose and increased toxicity.
  • High‑dose somatostatin analog therapy (e.g., octreotide infusion): can compete for receptor binding and reduce imaging quality.

Moderate Interactions (Monitor Closely)

  • Nephrotoxic drugs (e.g., aminoglycosides, NSAIDs): may exacerbate renal radiation exposure.
  • Diuretics: can alter renal clearance of the tracer, affecting dosimetry.
  • Antihistamines or steroids: may mask mild allergic reactions, delaying recognition.
  • Chemotherapy agents: consider timing to avoid overlapping toxicity.
  • Contrast agents used in CT: schedule appropriately to prevent image artefacts.

Frequently Asked Questions

Octreoscan is a radiolabeled somatostatin analogue used in nuclear medicine to locate and stage somatostatin receptor‑positive neuroendocrine tumours, including gastro‑intestinal and pancreatic NETs, as well as certain carcinoid and medullary thyroid cancers.

Indium In-111 pentetreotide binds to somatostatin receptor subtype 2 on tumour cells. The indium‑111 isotope emits gamma photons that are detected by a gamma camera, creating detailed images that reveal the distribution of receptor‑positive lesions throughout the body.

The administered activity of Octreoscan is determined by the prescribing physician based on the patient’s weight, the imaging protocol and regulatory guidelines. Dosage is individualized and should not be altered without medical direction.

Octreoscan involves ionising radiation and is generally contraindicated in pregnancy. Women of child‑bearing potential should undergo pregnancy testing before administration, and breastfeeding should be paused for a period advised by the treating physician.

To request Octreoscan, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if needed) and import documentation.

Octreoscan (Indium‑111) is a well‑established SSTR2‑targeted tracer offering high‑resolution planar and SPECT imaging. Newer agents such as Ga‑68‑DOTATATE provide PET imaging with higher sensitivity and faster acquisition, but Octreoscan remains a validated option where PET facilities are unavailable.

Octreoscan must be stored at 2‑8 °C, protected from light, and kept in its original container. It should not be frozen or shaken, and any vial opened for patient use should be discarded according to local radiation safety regulations.

Octreoscan is administered intravenously by a qualified nuclear medicine professional. After injection, imaging is typically performed 24 hours later to allow optimal tumour uptake and background clearance.

Serious risks include severe allergic reactions (anaphylaxis), significant radiation‑induced organ toxicity—particularly to the kidneys and bone marrow—and rare cases of secondary malignancy with high cumulative radiation exposure.

Octreoscan is contraindicated in patients with known hypersensitivity to indium‑111 pentetreotide or other somatostatin analogues, in pregnant women, and in individuals with severe renal impairment where radiation dose cannot be safely managed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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