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EVA treatment for recurrent or unresponsive Hodgkin's disease
Cancer Chemotherapy and Pharmacology
|January 1, 1986
Summary
This study shows that the etoposide, vincristine, and adriamycin (EVA) chemotherapy regimen achieved clinical remission in 58% of patients with recurrent Hodgkin
Area of Science:
- Oncology
- Hematology
- Clinical Pharmacology
Background:
- Hodgkin's disease is a cancer of the lymphatic system.
- Recurrent or unresponsive Hodgkin's disease often requires salvage chemotherapy.
- Previous standard treatments include mustine, vinblastine, prednisolone, and procarbazine (MVPP or ChlVPP).
Purpose of the Study:
- To evaluate the efficacy and safety of the etoposide, vincristine, and adriamycin (EVA) combination chemotherapy.
- To assess EVA's effectiveness in patients with recurrent or unresponsive Hodgkin's disease previously treated with MVPP or ChlVPP.
- To determine if EVA exhibits cross-resistance with prior chemotherapy regimens.
Main Methods:
- Nineteen patients with recurrent or unresponsive Hodgkin's disease were enrolled.
- Patients had previously received MVPP or ChlVPP chemotherapy.
- Treatment consisted of etoposide, vincristine, and adriamycin (EVA) combination therapy.
Main Results:
- Eleven out of nineteen patients (58%) achieved clinical remission (complete or good partial).
- Remission rates were comparable between patients who previously responded well and those who responded poorly to chemotherapy.
- Myelosuppression was the primary toxicity, generally manageable.
Conclusions:
- The EVA regimen demonstrated potential non-cross-resistance with MVPP and ChlVPP.
- EVA shows promise as a salvage chemotherapy option for Hodgkin's disease.
- While not curative for treatment failures, EVA may be valuable for previously untreated patients.