pe26 schreef op 30 september 2019 23:42:
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Uitgebreid artikel met heel veel bronnen (205?) die worden aangehaald.
ConclusionsIn summary, we are at an exciting time where several therapeutics are in advanced clinical trials for
blocking LPA signaling and inflammation (ja dat doet GLPG1690). These agents are generally well tolerated and they could be tested as novel strategies for improving the effectiveness of existing cancer therapies. These approaches should be applicable to a wide variety of cancers since they target the tumor environment, which should be relatively independent of the specific mutation in the cancer cells.
Overall, as mitigators of chronic inflammation,
inhibitors of LPA signaling could become viable therapeutic modalities for preventing cancer initiation, maintaining the efficacy of chemotherapy and radiotherapy and prolonging remission.Hoe breed gaat GLPG1690 door Gilead/Galapagos worden doorontwikkeld buiten fibrosis om..?
Als GLPG1690 de effectiviteit van chemo en radiotherapie (bestraling) kan laten voortduren en remissie kan voortzetten voor kankerbehandelingen biedt dit kansen. Zelfs verminderde kans op ontstaan van kanker wordt beschreven.
GLPG1690 in combi met YESCARTA (lymfeklierkanker/leukemie), of als aanvulling op chemo/bestraling...who knows.