1989
DOI: 10.1016/s0140-6736(89)91549-3
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Infusion of Vincristine and Doxorubicin With Oral Dexamethasone as First-Line Therapy for Multiple Myeloma

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Cited by 179 publications
(114 citation statements)
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“…12 Different combination regimens have been used for induction therapy in these patients, the most common one being the combination of vincristine, doxorubicin, and dexamethasone (VAD), which was initially introduced in the mid eighties. 17,18 Given that dexamethasone is the most active component in the combination and based on reports of efficacy of dexamethasone used alone in myeloma, [19][20][21] as well as the known adverse effects with VAD, we treated a group of patients with single agent dexamethasone as induction therapy.…”
Section: Discussionmentioning
confidence: 99%
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“…12 Different combination regimens have been used for induction therapy in these patients, the most common one being the combination of vincristine, doxorubicin, and dexamethasone (VAD), which was initially introduced in the mid eighties. 17,18 Given that dexamethasone is the most active component in the combination and based on reports of efficacy of dexamethasone used alone in myeloma, [19][20][21] as well as the known adverse effects with VAD, we treated a group of patients with single agent dexamethasone as induction therapy.…”
Section: Discussionmentioning
confidence: 99%
“…13,17,18 Adverse events seen with VAD include myelosuppression, increased risk of deep vein thrombosis, neuropathy due to vincristine, sepsis and thrombotic phenomena from indwelling catheter, as well as potential cardiotoxicity due to doxorubicin. 17,18,22 In addition, it involves continuous infusion of adriamycin and vincristine over 4 days necessitating central venous access and possible hospitalization. The concept behind the VAD combination was the dose responsiveness of myeloma to dexamethasone as well as targeting of the slow cycling plasma cells with continuous infusion of doxorubicin and vincristine.…”
Section: Discussionmentioning
confidence: 99%
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“…Aggressive chemotherapy has been shown to be associated with a greater likelihood of achieving an initial 'plateau' phase (70-80%) but is associated with only a marginal survival advantage compared to less intensive chemotherapy. 2 High-dose chemoradiotherapy supported with autologous bone marrow transplantation (ABMT) has been shown, in a randomised multicentre trial, to improve complete remission (CR) rates and survival when compared to standard-dose chemotherapy. 3 Based on this observation high-dose therapy is being increasingly utilised as first-line therapy in younger (age Ͻ70 years) MM patients.…”
Section: Introductionmentioning
confidence: 99%
“…Although the remissions induced are no more durable than those following other types of conventional chemotherapy, the responses are rapid (Samson et al, 1989;Salmon & Crowley, 1992), and the use of these treatments for cytoreduction prior to high-dose treatment with alkylating agents has the theoretical advantage of non-crossresistance.…”
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confidence: 99%