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Published on: May 15, 2019
[Adverse effects of PAD and VAD regimens in multiple myeloma patients]
1Department of Heamatology, Chinese PLA General Hospital, Beijing 100853, China. zhaoyu301@yahoo.com.cn
Abstract:
The study was aimed to evaluate the adverse effects of PAD (bortezomib + adriamycin + dexamethasone) and VAD (vincristine + adriamycin + dexamethasone) as chemotherapy regimens in multiple myeloma patients. 27 and 30 patients with multiple myeloma (MM) were enrolled in PAD and VAD groups respectively. MM patients accepted 3 - 5 cycles of VAD or PAD regimens. The type, degree and occurrence time of adverse reactions during the treatment were observed. The results showed that the rash was found in two patients only in PAD group, leucocytopenia, thrombocytopenia, peripheral neuropathy, infection, fatigue, nausea, constipation, and adverse effects of cortex hormone (hypertension, glycemia, hypokalemia, hyponatremia and acne) were found in the both two groups. The thrombosis was not observed in both two groups during treatment. Although statistical analysis indicated that only the incidence of thrombocytopenia was higher in PAD group than in VAD group with statistical difference but the incidence of leucocytopenia, peripheral neuropathy and infection in PAD group were higher than those in VAD group. Rash, constipation, peripheral neuropathy could be found in the first course of chemotherapy, while the others mostly emerged after 3 courses of treatment. The main reasons for the patients who's treatment was stopped include infection and intolerable peripheral neuropathy. Although peripheral neuropathy could be found in the two groups, but the chemotherapy was stopped only in 2 patients of PAD group after 3 cycles of treatment. It is concluded that compared with conventional VAD chemotherapy, PAD may improve therapeutic effect, but it may bring more severe toxicities to the patients with multiple myeloma.
Insights
The PAD chemotherapy regimen for multiple myeloma patients showed increased risks of thrombocytopenia and other toxicities compared to VAD. While potentially effective, PAD requires careful monitoring for adverse effects.
Area of Science:
- Oncology
- Pharmacology
- Hematology
Background:
- Multiple myeloma (MM) is a hematologic malignancy.
- Chemotherapy regimens like bortezomib + adriamycin + dexamethasone (PAD) and vincristine + adriamycin + dexamethasone (VAD) are used for MM treatment.
- Evaluating the comparative adverse effects of different chemotherapy regimens is crucial for patient management.
Purpose of the Study:
- To compare the adverse effects of PAD and VAD chemotherapy regimens in multiple myeloma patients.
- To identify specific toxicities associated with each regimen and their incidence.
- To assess the impact of these adverse events on treatment continuation.
Main Methods:
- A comparative study involving 27 patients in the PAD group and 30 patients in the VAD group.
- Patients received 3-5 cycles of either PAD or VAD chemotherapy.
- Adverse reactions, their type, severity, and timing were systematically observed and recorded.
Main Results:
- Both PAD and VAD regimens caused adverse effects including leucocytopenia, thrombocytopenia, peripheral neuropathy, infection, fatigue, nausea, and corticosteroid-related effects.
- Rash was observed exclusively in the PAD group.
- The incidence of thrombocytopenia was statistically higher in the PAD group. Higher incidences of leucocytopenia, peripheral neuropathy, and infection were also noted in the PAD group compared to VAD.
- Treatment discontinuation was primarily due to infection and peripheral neuropathy, with more cases in the PAD group.
Conclusions:
- The PAD regimen may offer improved therapeutic effects for multiple myeloma but is associated with potentially more severe toxicities than the VAD regimen.
- Adverse effects like rash, constipation, and peripheral neuropathy can occur early in treatment, while others emerge later.
- Careful monitoring and management of toxicities are essential when using the PAD regimen in multiple myeloma patients.
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