RVD – Regimen Overview

RVD stands for:

R – Revlimid (lenalidomide)

V – Velcade (bortezomib)

D – Dexamethasone

It is a standard triplet regimen used in multiple myeloma for both:

  • Induction therapy (newly diagnosed, transplant-eligible or ineligible patients)
  • Relapsed/refractory disease

Components & Mechanisms

Drug Mechanism of Action Route Key Toxicities
Lenalidomide Immunomodulatory (IMiD), anti-angiogenic, induces apoptosis PO Myelosuppression (neutropenia, thrombocytopenia), risk of thromboembolism, rash
Bortezomib Proteasome inhibitor (reversible 26S proteasome inhibition) SC or IV Peripheral neuropathy, thrombocytopenia, GI upset, herpes zoster reactivation
Dexamethasone Corticosteroid, anti-inflammatory, cytotoxic to plasma cells PO/IV Hyperglycemia, insomnia, mood changes, infection risk

Typical Dosing (Example – Induction)

Lenalidomide: 25 mg PO daily on days 1–21 of a 28-day cycle

Bortezomib: 1.3 mg/m² SC or IV on days 1, 4, 8, 11 of a 21-day cycle (or weekly in some regimens)

Dexamethasone: 20–40 mg PO weekly or divided doses

Dose modifications are made for renal impairment, age, or toxicity.

Supportive Measures

  • Antiviral prophylaxis: Acyclovir (to prevent herpes zoster reactivation from bortezomib)
  • Thromboprophylaxis: Aspirin, LMWH, or DOAC depending on VTE risk
  • Growth factor support if neutropenia occurs

Clinical Notes

  • RVD is highly effective for newly diagnosed multiple myeloma.
  • RVD-lite regimens exist for frail or elderly patients.
  • Can be used pre-transplant as induction before autologous HSCT.
  • Monitoring: CBC, renal function, neuropathy, blood glucose, infection risk.