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Bendamustine

Non-platinum based Alkylating Agents

MECHANISM OF ACTION

Bendamustine is an alkylating agent (nitrogen mustard derivative) with a benzimidazole ring (purine analog) which demonstrates only partial cross-resistance (in vitro) with other alkylating agents. It leads to cell death via single and double strand DNA cross-linking. Bendamustine is active against quiescent and dividing cells.

Elimination
Feces (~25%); urine (~50%; ~3% as active parent drug).

MECHANISM OF KIDNEY INJURY

increase in serum Cr

CLINICAL KIDNEY SYNDROME

Pseudo AKI (false elevation in Cr), BLE edema, UTI , TLS

CARDIOVASCULAR ADVERSE EFFECTS

edema, HTN exacerbation, tachycardia, chest pain, A fib ( can cause hypotension too)

LYTE ABNORMALITIES

increase Cr

RISK FACTORS

CrCl <30 mL/minute: Use is not recommended

MITIGATION STRATEGIES

CrCl <30 mL/minute: Use is not recommended

SUGGESTIONS 

If pseudo AKI, hold drug to see improvement Cr

NOTES/COMMENTS

PHARMACOKINETICS

Molecular Weight

Volume of Distribution

Plasma Protein Binding

Metabolism

Bioavailability

Half-life elimination

Time to peak

Excretion

Dialyzable?

Unknown

REF:

https://www.cdc.gov/niosh/docs/2016-161/.
Treanda (bendamustine) [prescribing information]. North Wales, PA: Teva Pharmaceuticals USA Inc; June 2021.

PATHOLOGY SLIDES:

ENTRY UPDATES:

Kartik Kalra

United States

Sep 25, 2022

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