Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1991-8-16
pubmed:abstractText
Forty-five patients with metastatic neuroendocrine tumors were treated with a regimen of etoposide 130 mg/m2/d for 3 days plus cisplatin 45 mg/m2/d on days 2 and 3. Both drugs were given by continuous intravenous infusion. Among 27 patients with well-differentiated carcinoid tumors or islet cell carcinomas, only two partial objective tumor regressions were observed (7%). Among 18 patients prospectively classified as having anaplastic neuroendocrine carcinomas, however, there were nine partial regressions and three complete regressions, an overall regression rate of 67%. For anaplastic disease, the median duration of regression was 8 months (range to 21 months). Tumor response was unrelated to primary site, endocrine hyperfunction, or prior therapy experience. The median survival of all patients with anaplastic tumors was 19 months; this seemed favorable when considering the small experiences with these rare tumors reported in the literature. Toxicity, which was severe for most patients, consisted primarily of vomiting, leukopenia, thrombocytopenia, anemia, alopecia, and neuropathy. The anaplastic neuroendocrine tumor is strongly responsive to therapy with combined etoposide and cisplatin. Patients with undifferentiated carcinomas, originating in typical neuroendocrine tumor sites (small and large bowel, pancreas, and stomach) or of unknown origin, who have consistent histologic findings by light microscopy should be evaluated for this possibility with appropriate immune staining or electron microscopy.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0008-543X
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
68
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
227-32
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:1712661-Adenoma, Islet Cell, pubmed-meshheading:1712661-Adult, pubmed-meshheading:1712661-Aged, pubmed-meshheading:1712661-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:1712661-Carcinoid Tumor, pubmed-meshheading:1712661-Carcinoma, pubmed-meshheading:1712661-Cisplatin, pubmed-meshheading:1712661-Etoposide, pubmed-meshheading:1712661-Female, pubmed-meshheading:1712661-Gastrins, pubmed-meshheading:1712661-Glucagon, pubmed-meshheading:1712661-Humans, pubmed-meshheading:1712661-Hydroxyindoleacetic Acid, pubmed-meshheading:1712661-Male, pubmed-meshheading:1712661-Middle Aged, pubmed-meshheading:1712661-Pancreatic Neoplasms, pubmed-meshheading:1712661-Prospective Studies, pubmed-meshheading:1712661-Remission Induction, pubmed-meshheading:1712661-Survival Rate
pubmed:year
1991
pubmed:articleTitle
Treatment of neuroendocrine carcinomas with combined etoposide and cisplatin. Evidence of major therapeutic activity in the anaplastic variants of these neoplasms.
pubmed:affiliation
Department of Oncology, Mayo Clinic, Rochester, Minnesota 55905.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.