Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1999-1-27
pubmed:abstractText
There is considerable interest in an autologous transplantation (AT) programme for patients with high-risk breast cancer; however, the issue of the incidence of occult bone marrow (BM) micrometastasis at diagnosis, and the cancer contamination of peripheral blood stem cell (PBSC) collections used for haematological rescue, is still debated. The presence of BM micrometastasis was evaluated in bilateral BM biopsies obtained at diagnosis of 33 patients with stage II/IIIA breast cancer using: (i) a 'nested' reverse transcriptase-polymerase chain reaction (RT-PCR) assay for cytokeratin 19 (K19) mRNA, (ii) histology, and (iii) immunohistochemistry (IHC) analysis with a panel of three monoclonal antibodies. The RT-PCR assay only was used to determine contamination of PBSC collections obtained after priming with recombinant human granulocyte-colony stimulating factor (rhG-CSF). K19 transcripts in one or both BM samples were detected in 48% of patients at diagnosis, with an overall 85% concordance with the results of IHC analysis. On the other hand, 56% of PCR- and IHC-positive BM samples were diagnosed as 'normal' on histological analysis. 57% of patients showed K19 mRNA in at least one PBSC collection; the possibility to have contaminated PBSC collections was significantly higher in patients with K19 positivity in BM at diagnosis. In four patients who had shown K19 positivity in BM and in PBSC collections, immunoselected CD34+ cells used for haematological rescue were K19-negative. There was a trend towards longer relapse free survival (RFS) in patients transplanted with K19-negative PBSC collections as compared to the others. In conclusion, a substantial proportion of patients with high-risk non-metastatic breast cancer present occult BM micrometastasis at diagnosis and also show cancer contamination of PBSC collections used for AT. These might represent a category of patients with poorer prognosis after AT, and possible candidates for more intensive and/or alternative therapeutic regimens, including AT with purged PBSCs.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0007-1048
pubmed:author
pubmed:issnType
Print
pubmed:volume
103
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
610-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9858208-Adult, pubmed-meshheading:9858208-Antigens, CD34, pubmed-meshheading:9858208-Bone Marrow Neoplasms, pubmed-meshheading:9858208-Breast Neoplasms, pubmed-meshheading:9858208-Disease-Free Survival, pubmed-meshheading:9858208-Female, pubmed-meshheading:9858208-Granulocyte Colony-Stimulating Factor, pubmed-meshheading:9858208-Hematopoietic Stem Cell Mobilization, pubmed-meshheading:9858208-Hematopoietic Stem Cell Transplantation, pubmed-meshheading:9858208-Humans, pubmed-meshheading:9858208-Immunohistochemistry, pubmed-meshheading:9858208-Keratins, pubmed-meshheading:9858208-Leukapheresis, pubmed-meshheading:9858208-Middle Aged, pubmed-meshheading:9858208-RNA, Messenger, pubmed-meshheading:9858208-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:9858208-Sensitivity and Specificity, pubmed-meshheading:9858208-Treatment Outcome
pubmed:year
1998
pubmed:articleTitle
Evaluation of breast tumour cell contamination in the bone marrow and leukapheresis collections by RT-PCR for cytokeratin-19 mRNA.
pubmed:affiliation
Division of Haematology, University of Florence, Azienda Ospedaliera di Careggi, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't