核心概念
Patients with multiple myeloma who have undetectable residual disease can safely discontinue maintenance therapy without compromising progression-free survival.
要約
The content discusses research presented at the American Society of Clinical Oncology (ASCO) 2024 annual meeting, which showed that most patients with multiple myeloma can safely discontinue maintenance therapy if they have undetectable residual disease.
The key findings are:
- 85% of patients with undetectable residual disease at baseline were progression-free 3 years after discontinuing maintenance therapy.
- This percentage improved to 93% when using a more sensitive test to detect measurable residual disease (MRD).
- Absence of MRD, coupled with ongoing monitoring for disease reemergence, seems to be the key to safely discontinuing maintenance therapy.
- Patients who were clear of disease down to a sensitivity of 10^-7 (no cancer cells among 10,000,000 normal cells) had better 3-year progression-free survival and MRD-free survival compared to those clear only to a sensitivity of 10^-6.
- High-risk cytogenetics was associated with worse MRD-free survival.
- Discontinuing maintenance therapy improved patients' quality of life and resulted in significant cost savings.
- However, there are still patients at risk for disease reemergence even with MRD negativity, such as those with high-risk cytogenetics, stage III disease, and late achievement of MRD clearance.
統計
85% of patients with undetectable residual disease at baseline were progression-free 3 years after discontinuing maintenance therapy.
93% of patients clear of disease down to a sensitivity of 10^-7 were progression-free 3 years after discontinuing maintenance therapy.
78% of patients who were 10^-7 negative at baseline had 3-year MRD-free survival.
33% of patients who were 10^-7 positive at baseline had 3-year MRD-free survival.
引用
"MRD negativity does not mean cure, MRD-guided treatment individualization may offer long treatment-free intervals with improved quality of life and help in cost savings."
"There are patients at risk for disease reemergence even with MRD negativity, including those with high-risk cytogenetics, stage III disease, and late achievement of MRD clearance."