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Vulvar and vaginal squamous cell carcinoma · line 1 · Cisplatin radiosensitization (concurrent with EBRT + brachytherapy)

Vue déterministe de l'entité source de la LJAM. L'autorité clinique demeure avec les ID de la source cités et l'état d'approbation de l ́examinateur.

Contenu clinique provisoire : il ne s'agit pas d'une ordonnance. Un oncologue doit vérifier les sources originales, l'applicabilité et le statut de révision.

Source YAML: dossier complet

Ligne thérapeutique1
Voiestandard
Régime liéREG-CISPLATIN-RADIOSENS
IDIND-VULVAR-VAGINAL-SCC-LA-1L-CISPLATIN-RT
TypeIndication
Étatreviewed 2026-07-11 | pending_clinical_signoff
MaladiesDIS-VULVAR-VAGINAL-SCC
SourcesSRC-NCCN-CERVICAL-2025

Notes

STUB pending clinical co-lead signoff (CHARTER §6.1; dev-mode-exempted per CHARTER §8.3 — draft content only, NOT published/verified clinical advice). PARTIAL — RT dose/field not modellable per KNOWLEDGE_SCHEMA_SPECIFICATION §17, mirrors the IND-CERVICAL-LOCALLY- ADVANCED-CRT pattern exactly. REG-CISPLATIN-RADIOSENS is reused UNCHANGED (no existing file was modified) — its own notes/notes_ua describe cervical FIGO IB3-IVA dosing context, but the weekly- cisplatin component dose (40 mg/m², cap 70mg) is the identical radiosensitizing backbone applied here; RT field/dose for vulvar/vaginal SCC (primary + groin ± pelvic nodes) is planned by radiation oncology, distinct from the cervical pelvic RT + brachytherapy field. No vulvar/vaginal-specific pivotal chemoradiation RCT was found — evidence is extrapolated from cervical (GOG-120) and anal (ACT II) chemoradiation paradigms; flagged as an open evidentiary gap rather than asserting invented response-rate numbers for this specific disease.

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