Genmab — Juni 2014
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hvad er din kommentar til dara dataene sukker?
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SAR døjer også med side effects: " although patients receiving SR650984 doses of 3 mg/kg or higher also received 100 mg of prednisone during their SAR650984 infusions to prevent infusion-related side effects."
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og hvis man ser på det link sukker delte har SAR som single agent flere bivirkning end Dara+Len+Dex sammen??
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Of the 30 patients evaluable for response, 33 percent of those treated with at least 1 mg/kg of SAR650984 every two weeks responded, and 27 percent of those treated with at least 10 mg/kg every two weeks responded. SARs responsrater i ORR er ikke høje, men flot de har CR. Virker lidt til at SAR ikke rammer så bredt som Dara men til gengæld går noget dybere`?
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Nu er det nok svært at sammenligne. Men 18 måneder follow up med Ibrutinib+Ofa er 82,5% stadig i PFS hvorimod Ibrutinib+R er 78%. Så en lille fordel til Ofa der: http://ir.pharmacyclics.com/releasedetail.cfm?ReleaseID=851587 http://www.mdanderson.org/newsroom/news-releases/2013/ibrutinib-and-rituximab-trigger.html samtidig har Ofa en 100% ORR og Rituxan 95% ORR. Ofatumumab studiet er dog lidt mudret fordi der også er SLL og PLL patienter med
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Her lidt mere fra ASH i 2013 https://ash.confex.com/ash/2013/webprogram/Paper58781.html
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http://www.esmo.org/Oncology-News/Phase-III-Study-of-Idelalisib-and-Rituximab-for-Previously-Treated-Patients-with-Chronic-Lymphocytic-Leukaemia http://www.cancer.gov/clinicaltrials/results/summary/2014/idelalisib-CLL0314 Idelalisib + Rituxan er ikke så effektiv som Ofa+Ibrutinib mens patienterne var vidst også mere syge i det studie....
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Men vi kan ihvetfald snart sammenligne Ofa+Idelalisib. Det studie bliver mega spændende
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Det er vel ikke udelukket. Men bl.a dette forsøg et GSK 2 år bagud http://clinicaltrials.gov/ct2/show?term=Ibrutinib+rituxan&rank=9
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