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Br J Cancer ; 95(10): 1326-33, 2006 Nov 20.
Article in English | MEDLINE | ID: mdl-17088915

ABSTRACT

To retrospectively evaluate the incidence of tumour cell contamination of peripheral blood stem cell (PBSC) collections and to correlate these data with the clinical outcome after high-dose chemotherapy (HDCT) with stem cell rescue in patients with a high-risk Ewing tumour. Peripheral blood stem cell collections obtained from 171 patients were analysed. Tumour contamination was assessed by reverse transcriptase-polymerase chain reaction (RT-PCR). The files of 88 patients who underwent HDCT followed by PBSC reinfusion were reviewed in detail, and their outcome compared to the PBSC RT-PCR results. Seven of 88 PBSC collections (8%) contained tumour cells as detected by RT-PCR. Peripheral blood stem cells were collected after a median of five cycles of chemotherapy. No clinical factor predictive of tumour cell contamination of PBSC harvest could be identified. Event-free survival (EFS) and overall survival (OS) of the whole study population were 45.3 % and 51.8 % at 3 years from the date of the graft, respectively. Forty-five patients relapsed with a median time of 15 months after graft, only four of whom had tumour cell contamination of the PBSC harvest. Tumour cell contamination of PBSC collection is rare and does not seem to be associated with a significantly poorer EFS or OS in this high-risk population.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Hematopoietic Stem Cell Mobilization/methods , Hematopoietic Stem Cell Transplantation/methods , Oncogene Proteins, Fusion/genetics , Reverse Transcriptase Polymerase Chain Reaction/standards , Sarcoma, Ewing/pathology , Transcription Factors/genetics , Adolescent , Adult , Antigens, CD34/analysis , Bone Marrow Neoplasms/genetics , Bone Marrow Neoplasms/secondary , Child , Child, Preschool , Disease-Free Survival , Female , Granulocyte Colony-Stimulating Factor/therapeutic use , Humans , Infant , Leukapheresis , Male , Oncogene Proteins, Fusion/metabolism , Proto-Oncogene Protein c-fli-1 , RNA, Messenger/analysis , RNA-Binding Protein EWS , Retrospective Studies , Reverse Transcriptase Polymerase Chain Reaction/methods , Sarcoma, Ewing/genetics , Sensitivity and Specificity , Survival Rate , Transcription Factors/metabolism , Treatment Outcome
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