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dc.contributor.authorGhielmini, Michele
dc.contributor.authorPettengell, Ruth
dc.contributor.authorCoutinho, Lucia H
dc.contributor.authorTesta, Nydia G
dc.contributor.authorCrowther, Derek
dc.date.accessioned2010-04-06T11:18:56Z
dc.date.available2010-04-06T11:18:56Z
dc.date.issued1996-04
dc.identifier.citationThe effect of the GM-CSF/IL-3 fusion protein PIXY321 on bone marrow and circulating haemopoietic cells of previously untreated patients with cancer. 1996, 93 (1):6-12 Br. J. Haematol.en
dc.identifier.issn0007-1048
dc.identifier.pmid8611477
dc.identifier.doi10.1046/j.1365-2141.1996.4731015.x
dc.identifier.urihttp://hdl.handle.net/10541/95698
dc.description.abstractThis is a phase I/II study of the GM-CSF/IL-3 fusion protein (PIXY321. Patients were treated with PIXY321 at a daily subcutaneous dose of 500, 750 and 1000 micrograms/m2 for 14 d. Side-effects were mild and consisted mainly of injection-site reactions and constitutional symptoms. A biphasic modest increase of white blood count (2-5-fold) and platelets (1-1.5 fold) was seen, accompanied by an increased bone marrow cellularity and an increase in circulating progenitors. Colony-forming cells in the blood rose to a median of 184 granulocyte/macrophage-colony forming cells (GM-CFC)/ml, eight Mix-CFC/ml, 250 burst forming units-erythroid (BFU-E)/ml and 140 CFU-mega-karyocytes/ml, corresponding to a 10-, 2.5, 8- and 30-fold increase respectively. When seeded for long-term culture on irradiated bone marrow stroma, the mobilized cells were not able to sustain haemopoiesis in vitro to the same degree as bone marrow. Taken together these results indicate that PIXY321 has a biological effect in humans more similar to that of IL-3 than to that of GM-CSF.
dc.language.isoenen
dc.subjectHaematopoietic Stem Cellsen
dc.subjectOvarian Canceren
dc.subject.meshAdult
dc.subject.meshCell Count
dc.subject.meshCell Movement
dc.subject.meshFemale
dc.subject.meshGranulocyte-Macrophage Colony-Stimulating Factor
dc.subject.meshHematopoietic Stem Cells
dc.subject.meshHodgkin Disease
dc.subject.meshHumans
dc.subject.meshInterleukin-3
dc.subject.meshLeukocyte Count
dc.subject.meshLymphoma
dc.subject.meshLymphoma, Non-Hodgkin
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshOvarian Neoplasms
dc.subject.meshPlatelet Count
dc.subject.meshRecombinant Fusion Proteins
dc.titleThe effect of the GM-CSF/IL-3 fusion protein PIXY321 on bone marrow and circulating haemopoietic cells of previously untreated patients with cancer.en
dc.typeArticleen
dc.contributor.departmentCRC Department of Medical Oncology, Christie Hospital, Manchester.en
dc.identifier.journalBritish Journal of Haematologyen
html.description.abstractThis is a phase I/II study of the GM-CSF/IL-3 fusion protein (PIXY321. Patients were treated with PIXY321 at a daily subcutaneous dose of 500, 750 and 1000 micrograms/m2 for 14 d. Side-effects were mild and consisted mainly of injection-site reactions and constitutional symptoms. A biphasic modest increase of white blood count (2-5-fold) and platelets (1-1.5 fold) was seen, accompanied by an increased bone marrow cellularity and an increase in circulating progenitors. Colony-forming cells in the blood rose to a median of 184 granulocyte/macrophage-colony forming cells (GM-CFC)/ml, eight Mix-CFC/ml, 250 burst forming units-erythroid (BFU-E)/ml and 140 CFU-mega-karyocytes/ml, corresponding to a 10-, 2.5, 8- and 30-fold increase respectively. When seeded for long-term culture on irradiated bone marrow stroma, the mobilized cells were not able to sustain haemopoiesis in vitro to the same degree as bone marrow. Taken together these results indicate that PIXY321 has a biological effect in humans more similar to that of IL-3 than to that of GM-CSF.


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