One Cup of Coffee a Day Keeps AF Away? Insights from the DECAF Trial
November 10, 2025
Brand Name :
Imfinzi
(United States) [Available]Synonyms :
durvalumab
Class :
Antineoplastic agents and monoclonal antibodies
Dosage Forms & Strengths Â
SolutionÂ
120 mg/2.4 ml Â
500 mg/10 ml Â
10
mg/kg
Intravenous (IV)
every 2 weeks
or 1500 mg IV every 4 weeks for 12 months
1500
mg
Intravenous (IV)
every 4 weeks
for 4 cycles in combination with etoposide and carboplatin/cisplatin
 Dosage Forms & Strengths Â
SolutionÂ
120 mg/2.4 ml Â
500 mg/10 ml Â
10
mg/kg
Intravenous (IV)
every 2 weeks
12
months
or continue until disease progression or severe health side effects
Initial dose:
20
mg/kg
Intravenous (IV)
every 3 weeks
for 4 cycles in combination with etoposide and carboplatin or cisplatin
Maintenance dose:
10
mg
Intravenous (IV)
every 2 weeks
or continue until disease progression or severe health side effects
Dose Adjustments
Dose adjustment for hepatic impairment: Terminate the therapy temporarily if AST or ALT >3 up to 8 Ă— ULN or total bilirubin >1.5 up to 3 Ă— ULN Discontinue the treatment permanently if AST or ALT >8 Ă— ULN or total bilirubin >3 Ă— ULN
Refer to adult dosingÂ
it may increase the hyponatremic effect of desmopressin
it may reduce the therapeutic efficacy of Fc receptor-binding agents
it may increase the hepatotoxic effects of ketoconazole
Actions and spectrum:Â Â
Durvalumab inhibits the interaction of PD-L1 with CD 80 and PD-1 that inhibits the immune responses without causing cell-mediated toxicity which is antibody dependent. Â
Frequency defined:Â Â
>10%:Â Â
Pruritis Â
Skin rash  Â
Hyperglycemia  Â
Diarrhea Â
Fatigue    Â
1%-10%Â Â
Dermatitis Â
Night sweatsÂ
Abdominal pain Â
Colitis Â
<1%:Â Â
Myocarditis Â
Vasculitis Â
Type 1 diabetes mellitusÂ
Â
Black Box Warning  Â
None Â
Â
Contraindication/Caution:Â Â
None
Pregnancy Warnings:Â
Pregnancy category: N/AÂ
Lactation: Excretion of the drug into the human breast milk is unknownÂ
Pregnancy categories:Â
Category A: Satisfactory and well-controlled studies show no evidence of risk to the fetus in the first trimester or in the later trimester.Â
Category B: No evidence of risk to fetus found in animal reproduction studies and there are not enough studies on pregnant women.Â
Category C: Adverse effects on the fetus found with evidence in animal reproduction studies and no adequate evidence for an effect in humans, care must be taken for potential risks in pregnant women.Â
Category D: There is adequate data available with sufficient evidence of human fetal risk from various platforms, but despite potential risks may be used only in emergency cases for potential benefits.Â
Category X: Drugs listed in this category clearly outweigh risks over benefits. These category drugs should be prohibited for pregnant women.Â
Category N: There is no data available for the drug under this category.Â
Pharmacology:Â Â
Durvalumab is an antineoplastic agent and inhibits PD-L1 used to treat advanced urothelial carcinoma. Â
Pharmacodynamics:Â Â
Durvalumab stimulates immune cell-mediated antitumor responses. It blocks PD-L1 from acting, which increases the activation of T cells and improves tumor cell ablation and detection.  Â
Pharmacokinetics:Â Â
Limited information is available on ADME. Â
Administration:Â Â
It is administered as an intravenous infusion.Â
Generic Name: durvalumabÂ
Pronunciation: dur-VAL-yoo-mabÂ
Why do we use durvalumab?Â
Durvalumab (Imfinzi) is an immunotherapy used to treat several cancers, including non-small cell lung cancer (NSCLC), extensive-stage small cell lung cancer (ES-SCLC), bile duct and gallbladder cancers, unresectable liver cancer, advanced or recurrent dMMR endometrial cancer, and certain cases of muscle-invasive bladder cancer (MIBC). It works by boosting the immune system’s ability to detect and attack cancer cells, helping to slow cancer growth, reduce tumor size, and improve survival.Â