Search Back New search Go to resultsDiseaseMain groupCross-Sectional, Transplantation, Cellular TherapySolid TumorsProtocol groupGastroenterologic OncologyGynecological OncologyNeuro-OncologyVisceral SurgeryDiseaseBile Duct CarcinomaFallopian Tube CarcinomaOvarian TumorPancreatic CancerPeritoneal Carcinoma, PrimaryTumor Biomarker DefinedSubgroupBRAF V600-MutationBRCA mutationClear Cell CancerepithelialMalignant Germ Cell Tumor of the OvaryICD10C24.-C24.0C24.1C24.8C24.9C25.-C48.-C48.1C56C57.0MeSHBile Duct NeoplasmsBiliary TractBiliary Tract NeoplasmsCarcinoma, Ovarian EpithelialCommon Bile Duct NeoplasmsFallopian Tube NeoplasmsNeoplasmsNeoplasms, Germ Cell and EmbryonalOvarian NeoplasmsPancreatic NeoplasmsPeritoneal NeoplasmsSequenceBEVA10/CRBP5/PGLDX30, ovarian Ca (PID2187) -|- BEVA15, maint. (PID1430)BEVA15/PACL175/CRBP5, ovarian Ca (PID1429) -|- BEVA15, maint.. (PID1430)PACL175/CRBP6/BEVA15, ovarian Ca C1 (PID498) -|- C2+ (PID499)ChemotherapyChemo-substanceBevacizumabCapecitabineCarboplatinCisplatinCyclophosphamideDabrafenibDocetaxelDoxorubicin pegylated liposomalEtoposideFluorouracilFolinic acidGemcitabineIrinotecanLetrozoleNab-paclitaxelNiraparibOlaparibOxaliplatinPaclitaxelPazopanibPembrolizumabRucaparibTopotecanTrabectedinTrametinibTreosulfanChemo-substanceBevacizumabCapecitabineCarboplatinCisplatinCyclophosphamideDabrafenibDocetaxelDoxorubicin pegylated liposomalEtoposideFluorouracilFolinic acidGemcitabineIrinotecanLetrozoleNab-paclitaxelNiraparibOlaparibOxaliplatinPaclitaxelPazopanibPembrolizumabRucaparibTopotecanTrabectedinTrametinibTreosulfanChemo-substanceBevacizumabCapecitabineCarboplatinCisplatinCyclophosphamideDabrafenibDocetaxelDoxorubicin pegylated liposomalEtoposideFluorouracilFolinic acidGemcitabineIrinotecanLetrozoleNab-paclitaxelNiraparibOlaparibOxaliplatinPaclitaxelPazopanibPembrolizumabRucaparibTopotecanTrabectedinTrametinibTreosulfanChemo-substanceBevacizumabCapecitabineCarboplatinCisplatinCyclophosphamideDabrafenibDocetaxelDoxorubicin pegylated liposomalEtoposideFluorouracilFolinic acidGemcitabineIrinotecanLetrozoleNab-paclitaxelNiraparibOlaparibOxaliplatinPaclitaxelPazopanibPembrolizumabRucaparibTopotecanTrabectedinTrametinibTreosulfanNo. Substances123 RadiotherapySupportive therapySupportive substanceBalanced Crystalloid SolutionCimetidineDexamethasoneDimetindenFosaprepitantGranisetronMagnesiumMagnesium sulfateNaCl 0.9%PegfilgrastimPotassium chloridePyridoxineSodium ThiosulfateSupportive substanceBalanced Crystalloid SolutionCimetidineDexamethasoneDimetindenFosaprepitantGranisetronMagnesiumMagnesium sulfateNaCl 0.9%PegfilgrastimPotassium chloridePyridoxineSodium ThiosulfateSupportive substanceBalanced Crystalloid SolutionCimetidineDexamethasoneDimetindenFosaprepitantGranisetronMagnesiumMagnesium sulfateNaCl 0.9%PegfilgrastimPotassium chloridePyridoxineSodium ThiosulfateSupportive substanceBalanced Crystalloid SolutionCimetidineDexamethasoneDimetindenFosaprepitantGranisetronMagnesiumMagnesium sulfateNaCl 0.9%PegfilgrastimPotassium chloridePyridoxineSodium ThiosulfateNo. Substances1234567Protocol classificationTherapy classificationalternativecurrent standardstudy analogIntensityStandard doseTherapy indicationFirst lineRelapse therapySecond lineseveral possibleThird line Therapy phaseMaintenanceTherapy intentioncurativecurative or palliativepalliativeRisksAllergic ReactionAlopeciaAnemia Hb below 8g/dlArthalgiaAstheniaBleedingCardiotoxicityConstipationDiarrheaDyspneaEdemaElectrolyte DisturbanceEmetogenicity (ASCO)Emetogenicity (MASCC/ESMO)FatigueFebrile NeutropeniaGastrointestinal ToxicityHand-Foot SyndromeHeadacheHematotoxicityHemorrhageHepatotoxicityHypertensionHypomagnesemiaHyponatremiaIncrease Alkaline PhosphataseIncrease AminotransferasesInfectionsLeukopeniaLymphopeniaMucositisMyalgiasNephrotoxicityNeuropathyNeurotoxicityNeutropeniaOral MucositisPainProteinuriaPyrexiaRashRenal FailureThrombocytopenia below 50 000/µlThromboembolic EventVomiting only studiesPublicationAuthorAghajanian CBell JBurger RAColeman RColombo NConteduca VDu Bois AFerrandina GFriedlander MGonzález Martín A Gordon ANHandolias DKatsumata NMarkman MMirza MMonk BJMoore K / Pujade-Lauraine EMorgan RDMutch DGPapadimitriou CAPerren TJPfisterer JPignata SPujade-Lauraine ERaspagliesi FRay-Coquard I Salama AKSSehouli CSehouli JSugiyama T Tanyi JTillmanns Tvan Driel WVasey PVasey PAWilliams SDZsiros RDiseaseDysgerminom, Stadium IB-III, nach kompletter Resektion, bei Patientinnen, die keine hohe Toxizität tolerieren könnenFortgeschrittenes oder metastasiertes Ovarialkarzinom, Rezidivtherapie, ECOG 0-2Fortgeschrittenes oder metastasiertes Ovarialkarzinom, Rezidivtherapie, platinresistent, ECOG 0-1frühes Ovarial-Ca, Stadium I und II, ErstlinieKlarzelliges Ovarialkarzinom, max. 6 Wochen nach der Operation, ECOG 0-1Lokal fortgeschrittene oder metastasierte Karzinome, BRAF V600E mutiert, Progress nach der Erstlinientherapie, ECOG 0-2Neudiagnostiziertes Ovarial-Ca, Eileiter-Ca oder Peritoneal-Ca, Stadium III mit neoadjuvanter Therapie, ECOG 0-2neudiagnostiziertes Ovarial-Ca, Stadium III/IV, Erstlinienbehandlung mit Platin-/Taxan-/Bevacizumabtherapie, ECOG 0-1Ovarial-Ca, FIGO Ic–IV, postoperativ, ECOG 0-2, keine vorausgegangene Chemotherapie oder RadiatioOvarial-Ca, fortgeschritten, nach Debulking-OP, ECOG 0-2Ovarial-Ca, inkompl. resekt. Stadium III oder jedes Stadium IV, ErstlinieOvarial-Ca, nach OP, high-risk early stage oder fortgeschritten, ECOG 0-2Ovarial-Ca, Rezidiv, platinsensitiv, Zweitlinie, BRCA Mutation, ECOG 0-1Ovarial-Ca, Rezidiv innerhalb von 6 Monaten nach platinbasierter ErstlinieOvarial-Ca, Rezidiv innerhalb von 6 Monaten nach platinbasierter Erstlinie/ZweitlinieOvarial-Ca, Rezidiv nach oder refraktär nach/unter platinbasierter Erstlinie.Ovarial-Ca, Rezidiv nach oder refraktär nach/unter platinbasierter Erstlinie innerhalb von 12 Monaten, ECOG 0-2Ovarial-Ca fortgeschritten, Stadium II-IVOvarial-Ca Rezidiv, mehr als 6 Monate nach Komplettierung der Platinum-basierten Erst- oder Zweitlinie (Platinum-sensitives Rez.), Taxan-Vorhterapie, ECOG 0-2Ovarial-Ca Rezidiv, mehr als 6 Monate nach Komplettierung der Platinum-basierten Erstlinie (Platinum-sensitives Rez.), ECOG 0-1Ovarial-Ca Rezidiv, mehr als 6 Monate nach Komplettierung der Platinum-basierten Erstlinie (Platinum-sensitives Rez.), ECOG 0-2Ovarial-Ca Rezidiv, nach Platinum-basierter Erstlinie, Progress innerhalb und nach mehr als 6 Monaten (Platinumresistent und -sensibel; Platinumrefraktäre Patienten waren ausgeschlossen), ECOG 0-2Ovarialkarzinom, Erstlinie, ECOG 0-2Ovarialkarzinom, Peritonealkarzinom, Karzinom der Eileiter, Rezidivtherapie, >6 Monate Erstlinie mit Platin, ECOG 0-2Ovarialkarzinom, Rezidiv nach oder refraktär nach/unter platinbasierter ErstlinieOvarialkarzinom, Rezidiv nach oder refraktär nach/unter platinbasierter Erstlinie, ECOG 0-2Ovarialkarzinom, Stadium IC-IV, ECOG 0-2platinsensitives Ovarial-Ca oder primäre Peritonealkarzinose, Drittlinie, ECOG 0-1Rezidiv. Ovarial-Ca, mind. 6 Mo krankheitsfreies Intervall nach letzter Cisplatingabe und Ansprechen auf mind. 3 Zyklen Cisplatin in der Erstlinie, ECOG 0-2rezidivierendes, platinsensitives Ovarialkarzinom, Rezidivtherapie, ECOG 0-1rezidivierendes Ovarialkarzinom, Drittlinie, Karnofsky > 70%rezidivierendes Ovarialkarzinom, fallopian tube or primary peritoneal cancer, ECOG 0-1rezidivierendes Ovarialkarzinom, nach platinbasierter Erstlinie, ECOG 0-2Rezidiviertes fortgeschrittenes oder metastasiertes OvarialkarzinomRezidiviertes fortgeschrittenes oder metastasiertes Ovarialkarzinom, nach platinhaltiger Therapie, ECOG 0-1Rezidiviertes fortgeschrittenes oder metastasiertes Ovarialkarzinom, Zweitlinierezidiviertes Ovarialkarzinom, Eileiterkarzinom oder primäres Peritonealkarzinom, Cisplatin-sensitiv, Drittlinie, ECOG 0-1rezidiviertes Ovarialkarzinom, nach platinbasierter Erstlinie, ECOG 0-2wiederkehrendes oder fortschreitendes Ovarial-Ca/Peritoneal-Ca, Stadium I-IV, nach Platintherapie, ECOG 0-1OriginAGO-OVAR, NCIC CTG, EORTC GCGArbeitsgemeinschaft Gynaekologische Onkologie (AGO) Study Group and Gynaecologic Oncology Center, Kiel, Germany, AGO-OVAR 2.21/ENGOT-ov 18 InvestigatorsBeatson Oncology Centre, Western Infirmary, Glasgow, UKCentre Léon Bérard, France, PAOLA-1 TrialsCharité University Medical Center and Center for Clinical Research, Berlin, NOGGODepartment of Clinical Therapeutics, Alexandra Hospital, Athens University School of Medicine, AthensDepartment of Gynecologic Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, New YorkDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas, Houston, USA, GOG-0213Department of Gynecology, Netherlands Cancer Institute, AmsterdamDepartment of Medical Oncology, Glasgow, U.K.Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas, USADepartment of Oncology, Catholic University, Campobasso, ItalienDepartment of Oncology, Rigshospitalet–Copenhagen University Hospital, ENGOT-OV16/NOVA InvestigatorsDuke University, Durham, NC, NCI-MATCH Trial Subprotocol HEuropean Institute of Oncology, Milan, ItalyGCIG, GINECO, AGO, NSGO, ANZGOG, NCIC-CTG, EORTC, MITO, MaNGO; CALYPSO StudieGynecology and Gynecologic Oncology, Charité University Medicine Campus Virchow, Berlin, Germany, NOGGOHorst Schmidt Klinik, Wiesbaden, DeutschlandIndiana University Cancer Center, Indianapolis, USAIstituto Nazionale per lo Studio e la Cura dei Tumori, Fondazione G Pascale, IRCCS, Napoli, Italy, MITO-7 trialIstituto Nazionale per lo Studio e la Cura dei Tumori, MilanoIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS, Meldola, ItalyJapanese Gynecologic Oncology Group, JGOG 3016 StudieManchester Cancer Research Centre, University of Manchester, UKMD Anderson Cancer Center Spain, Madrid, Spain, ICON7 investigatorsMemorial Sloan Kettering Cancer Center, New York, USA; OCEANS StudiePrince of Wales Hospital, Randwick, Sydney, AustraliaRoyal Women's Hospital, Melbourne, Victoria, AustraliaStevenson Cancer Center, University of Oklahoma, SOLO2/ENGOT-Ov21 investigatorsThe Gynecologic Oncology GroupThe Gynecologic Oncology Group; GOG-0218 StudieThe ICON7 Investigators, ICON7 StudieThe Jikei University School of Medicine, Tokyo, Japan, JGOG3017/GCIG TrialThe Nordic Society of Gynecological Oncology (NSGO) and Rigshospitalet, Copenhagen, Denmark, ENGOT-OV24 / AVANOVA1The Texas Ocology Professional Association, Dallas Texas, USAThe University of Texas MD Anderson Cancer Center, ARIEL3 StudieThe West Clinic, Memphis, USAUniversite Paris Descartes, Hopitaux Universitaires Paris Centre, AURELIAUniversity of California at Irvine and UCI Medical Center, Orange, CA, USAWashington University School of Medicine, USAProtocols in Revision 48 protocols foundProtocols under revision.Bevacizumab 10 / Carboplatin 5 / Doxorubicin Pegylated Liposomal 30, Ovarian Ca. (PID2187)Bevacizumab 15 / Gemcitabine 1000 / Carboplatin 4, Ovarian ca (PID126)Bevacizumab 15 / Paclitaxel 175 / Carboplatin 5, Ovarian ca (PID1429)Bevacizumab 15, Ovarian Carcinoma (PID495)Bevacizumab 15, Ovarian Carcinoma, maintenance. (PID1430)Bevacizumab 7.5, Ovarian Carcinoma (PID501)Capecitabine 1250, Ovarian Carcinoma (PID2191)Carboplatin 5, Ovarian ca (PID1332)Carboplatin 6 / Etoposide 120, Ovarian Tumor (PID2188)Carboplatin 7, Ovarian ca (PID1428)Cisplatin 35 / Gemcitabine 1000, Ovarian Carcinoma (PID2190)Cyclophosphamide 150, Ovarian Carcinoma (PID2192)Dabrafenib 150 / Trametinib 2, Tumor Biomarker Defined (PID2197)Docetaxel 75 / Carboplatin 5, Ovarian ca (PID1421)Gemcitabine 1000 / Carboplatin 4, Ovarian ca (PID493)Gemcitabine 1000, Ovarian Carcinoma (PID504)Gemcitabine 1000, Ovarian ca, variant 1 (PID505)GemOx - Gemcitabine 1000 / Oxaliplatin 130, Ovarian Carcinoma (PID2195)HIPEC - Cisplatin 100, Ovarian ca (PID108)Irinotecan 60 / Cisplatin 60, Ovarian Carcinoma (PID2194)Letrozole 2.5, Ovarian Carcinoma (PID2200)Nab-Paclitaxel 100 / Bevacizumab 10, Ovarian ca (PID900)Niraparib 300 / Bevacizumab 15, Ovarian ca, maintenance (PID487)Niraparib 300, ovarian carcinoma, maintenance (PID477)Olaparib 300 / Bevacizumab 15, Ovarian ca, maintenance (PID1351)Olaparib 300, Ovarian ca, maintenance (PID531)Oxaliplatin 85 / Folinic Acid 200 / Fluorouracil 600, Ovarian Carcinoma. (PID2196)Paclitaxel 175 / Carboplatin 5 / Bevacizumab 7.5, Ovarian Carcinoma (PID500)Paclitaxel 175 / Carboplatin 5, Ovarian ca (PID497)Paclitaxel 175 / Carboplatin 6 / Bevacizumab 15, Ovarian Carcinoma cycle 1 (PID498)Paclitaxel 175 / Carboplatin 6 / Bevacizumab 15, Ovarian Carcinoma cycle 2+ (PID499)Paclitaxel 175 / Carboplatin 7.5, Ovarian ca, adjuvant (PID1335)Paclitaxel 60 / Carboplatin 2, Ovarian Carcinoma (PID2429)Paclitaxel 80 / Bevacizumab 10, Ovarian ca (PID1366)Paclitaxel 80 / Carboplatin 6, Ovarian ca (PID91)Paclitaxel 80, Ovarian Carcinoma (PID508)Pazopanib 800, Ovarian Carcinoma (PID2193)Pegylated liposomal Doxorubicin 30 / Carboplatin 5, Ovarian Ca (PID494)Pegylated Liposomal Doxorubicin 30 / Trabectedin 1,1, Ovarian Carcinoma (PID496)Pegylated liposomal Doxorubicin 40 / Bevacizumab 10, Ovarian ca (PID1367)Pegylated Liposomal Doxorubicin 40, Ovarian ca (PID913)Pegylated Liposomal Doxorubicin 50, Ovarian Carcinoma (PID502)Pembrolizumab 200 / Bevacizumab 15 / Cyclophosphamide 50, Ovarian ca (PID1109)Rucaparib 600, Ovarian ca, maintenance (PID1501)Topotecan 1.25 / Bevacizumab 15, Ovarian ca (PID1368)Topotecan 1.5, Ovarian Carcinoma (PID503)Topotecan 4, Ovarian ca (PID860)Treosulfan 7, Ovarian ca (PID863)