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HOW CAN THE TREATMENT PARADIGM OF cGVHD BE OPTIMIZED?

The lack of standardized treatment and response biomarkers, as well as the variability of the disease from person to person, impedes the goals of extending survival and improving QOL.1

First-line therapy

with systemic corticosteroids, with or without CNIs, is well established in patients with chronic graft-versus-host disease.2-4

Second-line therapy

Second-line therapy
may be required for approximately
70%
of patients with cGVHD.5

Third-line therapy

may be required for approximately
50%
of those patients, with many progressing to later lines of therapy.5

Both corticosteroids and CNIs may provide effective initial therapy for cGVHD. However, prolonged systemic use of either can cause significant toxicities.2

Toxicities associated with prolonged corticosteroid use include2

  • Weight gain
  • Bone loss 
  • Myopathy
  • Diabetes 
  • Hypertension
  • Mood swings
  • Cataract formation
  • Increased risk of infection

Toxicities associated with prolonged CNI use include6

  • Nephrotoxicity
  • Neurotoxicity
  • Metabolic abnormalities

Corticosteroids should be tapered to allow for the lowest dose that adequately controls cGVHD. Once cGVHD is controlled, corticosteroids should be withdrawn, followed by withdrawal of CNIs.2 For these patients who are unable to tolerate prolonged exposure, a more targeted approach may be required.3,4,6,7

As patients progress to later lines of therapy, the focus of treatment becomes stabilizing the condition while limiting AEs and maintaining QOL.6,8

A treatment paradigm that allows for the right treatment for the right patient at the right time may better address the manifestations of cGVHD.

If initial therapy is not enough, what is the next step?

MAT-SA-2300860/v2/March2024