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  • Electronic Resource  (2)
  • 1995-1999  (2)
  • Chemistry  (1)
  • JM216  (1)
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  • Electronic Resource  (2)
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  • 1
    ISSN: 1569-8041
    Keywords: JM216 ; lung cancer ; non-small cell ; oral chemotherapy ; platinum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Background: JM216 is a new oral platinum complex with dose-limitingtoxicity myelosuppresssion, now undergoing phase II evaluation. Patients and methods: JM216 was evaluated as first line therapy innon-small-cell lung cancer. 17 patients received 120 mg/m2/dayfor five days repeated every three weeks. Results: Toxicity was manageable, the commonest side-effects being nausea,vomiting, diarrhoea, constipation and asthenia. Myelososuppression wasgenerally grade 〈2 and there were no cases of neutropenic sepsis orbleeding. Thirteen patients were fully evaluable for response. No sustainedobjective responses were reported. One patient was reported as stable diseasehad a partial response after three courses but was progressing again afterfour. An additional five patients had stable disease (46.2%). Conclusions: Although some patients may have had useful palliation, JM216did not appear to have significant antitumour activity in non-small-cell lungcancer.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: Biomaterial-associated infection results in increased morbidity and mortality, and may occur because of nonproductive premature activation of neutrophils resulting in impaired phagocyte function at the biomaterial surface in the event of bacterial challenge. To further explore the effects of this premature activation, we evaluated the supernatants of biomaterial associated neutrophils to determine whether soluble mediators were released, and the likely role of these mediators. We show that these supernatants contain a chemoattractant and thereby induce chemotaxis by fresh neutrophils. No evidence of enhanced oxidative free radical production by either unstimulated neutrophils or a primed response to other mediators occurs when neutrophils were incubated with these supernatants. We also examined the effect of adding fresh neutrophils to a biomaterial surface containing a previous inoculum of neutrophils, and observed that the fresh cells did not become stimulated to release reactive oxygen intermediates (ROI) and also exhibited impaired killing of staphylococci. These studies suggest that not only does the biomaterial surface activate the initial wave of neutrophils but that subsequent waves of neutrophils exhibit an impaired host-defense function. These results are consistent with the known impairment of host defense in the presence of biomaterials, and provide evidence for a long-term down-regulation of neutrophil function at biomaterial surfaces. © 1995 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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