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Multiple myeloma treated with high dose intravenous melphalan
British Journal of Haematology
|May 1, 1987
Summary
High dose melphalan (HDM) shows promise for multiple myeloma, achieving complete remission in 27% of previously untreated patients. While effective, HDM causes significant side effects and early deaths, necessitating careful management and further research.
Area of Science:
- Hematology
- Oncology
- Clinical Pharmacology
Background:
- Multiple myeloma is a hematologic malignancy characterized by uncontrolled proliferation of plasma cells.
- Current treatment strategies for multiple myeloma aim to induce remission and prolong survival.
Purpose of the Study:
- To evaluate the efficacy and safety of high-dose melphalan (HDM) in patients with multiple myeloma.
- To assess the impact of adding high-dose methylprednisolone to HDM therapy.
Main Methods:
- A study involving 58 patients under 63 years with multiple myeloma treated with HDM (140 mg/m2 i.v.).
- A subsequent study added high-dose methylprednisolone (1 g/m2 daily for 5 d) to HDM.
- Patient response was assessed by complete remission (CR) and partial remission (PR) criteria.
Main Results:
- In previously untreated patients, HDM achieved 27% CR and 51% PR, with a median remission duration of 19 months.
- In patients who failed prior chemotherapy, the response rate was 66%, but all relapsed within 1 year.
- Adding methylprednisolone to HDM showed similar response rates with a significant reduction in early deaths.
Conclusions:
- HDM is an effective treatment for multiple myeloma, inducing significant remission rates.
- HDM is associated with substantial toxicities, including myelosuppression and gastrointestinal side effects.
- Further research, including a prospective MRC trial, is warranted to compare HDM with and without steroids against conventional therapy.