2006
Pharmacokinetic and safety study of weekly irinotecan and oral capecitabine in patients with advanced solid cancers
Goel S, Desai K, Karri S, Gollamudi R, Chaudhary I, Bulgaru A, Kaubisch A, Goldberg G, Einstein M, Camacho F, Baker S, Mani S. Pharmacokinetic and safety study of weekly irinotecan and oral capecitabine in patients with advanced solid cancers. Investigational New Drugs 2006, 25: 237-245. PMID: 17195945, DOI: 10.1007/s10637-006-9028-1.Peer-Reviewed Original ResearchMeSH KeywordsAdministration, OralAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsArea Under CurveCamptothecinCapecitabineCarboxylesteraseDeoxycytidineDose-Response Relationship, DrugDrug Administration ScheduleDrug InteractionsFemaleFluorouracilHumansInfusions, IntravenousIrinotecanMaleMiddle AgedNeoplasmsNeutropeniaTreatment OutcomeConceptsDrug-drug interactionsDay 1Day 8Open-label phase ISN-38Potential drug-drug interactionsConversion of irinotecanGrade 3 diarrheaCycles of chemotherapyAdvanced solid cancersAdvanced solid tumorsDose level 5Diarrhea/vomitingWarrants further evaluationSynergistic anti-cancer activitySN-38GWarrants further studyFatal neutropeniaOral capecitabineAnti-cancer activityDose cohortsEvaluable patientsEscalation trialNegative sepsisMin infusion
2003
A safety study of a mixed-backbone oligonucleotide (GEM231) targeting the type I regulatory subunit alpha of protein kinase A using a continuous infusion schedule in patients with refractory solid tumors.
Goel S, Desai K, Bulgaru A, Fields A, Goldberg G, Agrawal S, Martin R, Grindel M, Mani S. A safety study of a mixed-backbone oligonucleotide (GEM231) targeting the type I regulatory subunit alpha of protein kinase A using a continuous infusion schedule in patients with refractory solid tumors. Clinical Cancer Research 2003, 9: 4069-76. PMID: 14519628.Peer-Reviewed Original Research