pubmed-article:7540220 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7540220 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
pubmed-article:7540220 | lifeskim:mentions | umls-concept:C0079459 | lld:lifeskim |
pubmed-article:7540220 | lifeskim:mentions | umls-concept:C0023467 | lld:lifeskim |
pubmed-article:7540220 | lifeskim:mentions | umls-concept:C0001143 | lld:lifeskim |
pubmed-article:7540220 | lifeskim:mentions | umls-concept:C0010711 | lld:lifeskim |
pubmed-article:7540220 | lifeskim:mentions | umls-concept:C0015133 | lld:lifeskim |
pubmed-article:7540220 | lifeskim:mentions | umls-concept:C0026259 | lld:lifeskim |
pubmed-article:7540220 | lifeskim:mentions | umls-concept:C1707455 | lld:lifeskim |
pubmed-article:7540220 | lifeskim:mentions | umls-concept:C0205195 | lld:lifeskim |
pubmed-article:7540220 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:7540220 | pubmed:dateCreated | 1995-7-14 | lld:pubmed |
pubmed-article:7540220 | pubmed:abstractText | We used a new chemotherapy regimen for the treatment of 18 consecutive patients with relapsed AML. The regimen consisted of low-dose cytosine arabinoside (Ara-C), low-dose aclarubicin and concurrent use of G-CSF (CAG regimen). Fifteen out of 18 patients (83%) achieved complete remission (CR). Median CR duration and median survival were 6 months and 15 months, respectively. These results were similar to those of previously reported salvage therapies for relapsed AML including intensive chemotherapy consisting of intermediate-dose Ara-C and sequential mitoxantrone with or without etoposide (MC/MEC), which we previously adopted. Myelosuppression and non-hematological toxicities were apparently lower and less frequent compared to MC/MEC. The CAG regimen seems promising for the treatment of relapsed AML with its low toxicity contributing to a high quality of life for the patient. | lld:pubmed |
pubmed-article:7540220 | pubmed:language | jpn | lld:pubmed |
pubmed-article:7540220 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7540220 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:7540220 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7540220 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7540220 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7540220 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7540220 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7540220 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7540220 | pubmed:month | Mar | lld:pubmed |
pubmed-article:7540220 | pubmed:issn | 0485-1439 | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:SaitoKK | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:ArimuraHH | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:NoguchiMM | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:YamadaKK | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:FurusawaSS | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:KoikeTT | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:SakumaHH | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:AoyagiAA | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:WagaKK | lld:pubmed |
pubmed-article:7540220 | pubmed:author | pubmed-author:YamatoHH | lld:pubmed |
pubmed-article:7540220 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7540220 | pubmed:volume | 36 | lld:pubmed |
pubmed-article:7540220 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7540220 | pubmed:authorsComplete | N | lld:pubmed |
pubmed-article:7540220 | pubmed:pagination | 165-74 | lld:pubmed |
pubmed-article:7540220 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:7540220 | pubmed:year | 1995 | lld:pubmed |
pubmed-article:7540220 | pubmed:articleTitle | [Comparison of low-dose cytosine arabinoside and aclarubicin in combination with granulocyte colony-stimulating factor to intermediate-dose cytosine arabinoside and mitoxantrone with or without etoposide in the treatment of relapsed acute myeloid leukemia]. | lld:pubmed |
pubmed-article:7540220 | pubmed:affiliation | Third Department of Internal Medicine, Dokkyo University School of Medicine. | lld:pubmed |
pubmed-article:7540220 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7540220 | pubmed:publicationType | Clinical Trial | lld:pubmed |
pubmed-article:7540220 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:7540220 | pubmed:publicationType | English Abstract | lld:pubmed |