rdf:type |
|
lifeskim:mentions |
umls-concept:C0007320,
umls-concept:C0011777,
umls-concept:C0015133,
umls-concept:C0020823,
umls-concept:C0025241,
umls-concept:C0026764,
umls-concept:C0032950,
umls-concept:C0042679,
umls-concept:C0077973,
umls-concept:C0085752,
umls-concept:C0085973,
umls-concept:C0179926,
umls-concept:C0332325
|
pubmed:issue |
5
|
pubmed:dateCreated |
1991-5-28
|
pubmed:abstractText |
A patient with plasma cell myeloma refractory to both MP (melphalan-prednisolone) and VAD (vincristine-adriamycin-dexamethasone) was treated with a combination chemotherapy consisting of VP-16, ifosfamide and dexamethasone (VID). A partial remission of 12-month duration was achieved. VID combination might be considered for myeloma patients who are refractory to both MP and VAD, and not eligible for high-dose melphalan with bone marrow transplantation.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0021-5120
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
29
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
516-8
|
pubmed:dateRevised |
2006-4-24
|
pubmed:meshHeading |
pubmed-meshheading:2089176-Adult,
pubmed-meshheading:2089176-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:2089176-Dexamethasone,
pubmed-meshheading:2089176-Doxorubicin,
pubmed-meshheading:2089176-Drug Resistance,
pubmed-meshheading:2089176-Etoposide,
pubmed-meshheading:2089176-Female,
pubmed-meshheading:2089176-Humans,
pubmed-meshheading:2089176-Ifosfamide,
pubmed-meshheading:2089176-Melphalan,
pubmed-meshheading:2089176-Multiple Myeloma,
pubmed-meshheading:2089176-Prednisolone,
pubmed-meshheading:2089176-Remission Induction,
pubmed-meshheading:2089176-Vincristine
|
pubmed:articleTitle |
Etoposide and ifosfamide for MP (melphalan and prednisolone)- and VAD (vincristine, adriamycin and dexamethasone)-resistant plasma cell myeloma: a case report.
|
pubmed:affiliation |
First Department of Internal Medicine, Kagawa Medical School, Japan.
|
pubmed:publicationType |
Journal Article,
Case Reports
|