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Pasireotide

Детермінований перегляд YAML-сутності з джерельної бази. Клінічний авторитет лишається за вказаними source ID та статусом клінічного sign-off.

IDDRUG-PASIREOTIDE
ТипПрепарат
Синоніми
SigniforSignifor LARПасиреотид
Статуспереглянуто 2026-07-11 | очікує клінічного підпису
ХворобиDIS-PITUITARY-ADENOMA
ДжерелаSRC-NCCN-CNS-2025

Дані про препарат

КласSomatostatin analogue (multi-receptor SSTR1/2/3/5, high SSTR5 affinity)
Механізм діїCyclohexapeptide somatostatin analogue binding SSTR1, SSTR2, SSTR3, and particularly SSTR5 — the receptor subtype most highly expressed on corticotroph adenomas — distinguishing pasireotide from the largely SSTR2-selective first-generation SSAs (octreotide, lanreotide). Suppresses ACTH secretion from corticotroph adenomas (Cushing disease) and, via SSTR2/SSTR5, GH/IGF-1 secretion from somatotroph adenomas (acromegaly), including tumors with an inadequate response to first-generation SSA. Two formulations: subcutaneous (short-acting, Cushing disease) and long-acting release (LAR, intramuscular monthly — acromegaly and surgery-ineligible/persistent Cushing disease).
Типове дозуванняCushing disease: pasireotide SC starting dose 0.6 mg subcutaneously twice daily, titrated per cortisol response and tolerability (product-label range approximately 0.3-0.9 mg SC BID); long-acting pasireotide LAR 10 mg IM every 4 weeks is an alternative for Cushing disease not amenable to surgery, titrated per response. Acromegaly: pasireotide LAR starting dose 40 mg IM every 4 weeks, titrated up to 60 mg IM q4w per IGF-1 response, typically reserved for inadequate response to first-generation SSA (octreotide/lanreotide). Confirm exact titration schedule with treating endocrinology team.
Зареєстровано в УкраїніFalse
Відшкодовується НСЗУFalse
Остання перевірка для України2026-07-11

Нотатки

STUB pending clinical co-lead signoff (CHARTER §6.1 — dev-mode-exempted, safe to merge as draft content, not published/verified clinical advice). Pasireotide is the medical option named in the Disease narrative for Cushing disease and is also listed among acromegaly SSA options. Modeled here as a single Drug entity covering both SC (Cushing) and LAR (acromegaly + surgery-ineligible Cushing) formulations, consistent with how this KB models other multi-formulation drugs. Steroidogenesis inhibitors named alongside pasireotide in the Cushing narrative (ketoconazole, metyrapone, osilodrostat) are not separately authored as Drug entities in this pass — see DIS-PITUITARY-ADENOMA proposal notes.

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