OnCo

Gemcitabine + cisplatin

Checked 2026-09-09

Advanced biliary tract cancer first line (with durvalumab or pembrolizumab); cisplatin-eligible urothelial cancer

Also called GemCis.

One cycle

every 21 days × 8 · about 24 weeks in total
178141521Cisplatin: 25 mg/m² (biliary) or 70 mg/m² day 1 (urothelial), IntravenousCisplatinGemcitabine: 1,000 mg/m², IntravenousGemcitabine
21-day cycle × 8 (biliary, 24 weeks); 4-6 (urothelial) (about 24 weeks)Intravenous

Components

DrugDoseRouteDays
Cisplatin
Cytotoxic chemotherapy (platinum)
25 mg/m² (biliary) or 70 mg/m² day 1 (urothelial)IVD1, 8
Gemcitabine
Nucleoside analogue (deoxycytidine)
1,000 mg/m²IVD1, 8
Cycles
8 (biliary, 24 weeks); 4-6 (urothelial)
21-day cycle
Emetogenicity
High (>90%)
G-CSF
Not routine

Notes

  • TOPAZ-1 adds durvalumab 1,500 mg every 3 weeks for 8 cycles then every 4 weeks; KEYNOTE-966 adds pembrolizumab 200 mg every 3 weeks.
  • In urothelial cancer cisplatin is 70 mg/m² on day 1 only (von der Maase, JCO 2000).

Used in

Source

ABC-02, NEJM 2010

Reference doses for a typical adult from the cited protocol or label. Doses are adjusted for renal and hepatic function, age, performance status and prior toxicity, and institutional protocols vary. Verify against the current label and your local protocol before treating. Not medical advice.

Other regimens for these cancers