2021
Association Between Androgen Deprivation Therapy and Mortality Among Patients With Prostate Cancer and COVID-19
Schmidt A, Tucker M, Bakouny Z, Labaki C, Hsu C, Shyr Y, Armstrong A, Beer T, Bijjula R, Bilen M, Connell C, Dawsey S, Faller B, Gao X, Gartrell B, Gill D, Gulati S, Halabi S, Hwang C, Joshi M, Khaki A, Menon H, Morris M, Puc M, Russell K, Shah D, Shah N, Sharifi N, Shaya J, Schweizer M, Steinharter J, Wulff-Burchfield E, Xu W, Zhu J, Mishra S, Grivas P, Rini B, Warner J, Zhang T, Choueiri T, Gupta S, McKay R, Desai A, Cohen A, Olszewski A, Bardia A, Daher A, Brown A, Yeh A, Hsiao A, Cheng A, Zhou A, Beeghly-Fadiel A, Morgans A, Jha A, Menendez A, Fazio A, Nizam A, Ramirez A, Kulkarni A, Verma A, Elshoury A, Rivera A, Walden A, Piper-Vallillo A, Cook A, Li A, Cantrell A, Cabal A, Nohria A, Angevine A, Gulati A, Giordano A, Kasi A, Ajmera A, Elkrief A, Kariapper A, Loaiza-Bonilla A, Jayaraj A, Thakkar A, Russ A, Bashir B, Halmos B, Logan B, Wood B, Slawik B, Dixon B, French B, Routy B, Mavromatis B, Hayes-Lattin B, Barrow McCollough B, Fleissner B, Stith B, Wicher C, Schwartz C, Thomson C, Solorzano C, Granada C, Brown C, Hennessy C, Stratton C, Castellano C, Ang C, Mandapakala C, Wang C, Jani C, Su C, Misdary C, Chapman C, McNair C, Lemmon C, Geiger C, Friese C, Su C, McKeown C, Hoppenot C, Low C, Pillainayagam C, Ferrario C, Rock C, Gonzalez Gomez C, Masson C, Mundt D, Addison D, Flora D, Stover D, Kwon D, Hausrath D, Bowles D, Reuben D, Shafer D, Bitterman D, O' Sullivan D, Mahadevan D, Sohal D, Whaley D, Slosky D, Chism D, Hershman D, Doroshow D, Ravindranathan D, Farmakiotis D, Bhutani D, Vinh D, Freeman D, Johnson D, Hatton E, Van Allen E, Griffiths E, Davis E, Nakasone E, Loggers E, Robilotti E, Levine E, Cabebe E, Hsu E, Powell E, Nemecek E, Lau E, Durbin E, Bernicker E, Small E, Cook E, Gillaspie E, Reid E, Papadopoulos E, Tadesse E, Wehbe F, Lyman G, Schwartz G, Nagaraj G, Boland G, Demetri G, Batist G, Gantt Jr. G, Kloecker G, Shaw G, Riely G, Borno H, Saker H, Dzimitrowicz H, Nelson H, Khan H, Shaikh H, Polimera H, Chen J, Stratton J, Acoba J, Patel J, Connors J, Mather J, Henderson J, Dill J, Girard J, Warner J, Graber J, Papenburg J, Altman J, Hawley J, Clement J, Park J, Campian J, Philip J, Deeken J, Riess J, Rosenberg J, Loree J, Senefeld J, Kharofa J, Garcia J, Palmer J, Lewis J, Guido J, Fu J, Wu J, Jiang J, Gainor J, Klamerus J, Steve Lo K, Patel K, de Cardenas K, Vega-Luna K, Goldsmith K, Hansen K, Huber K, Stockerl-Goldstein K, Jeffords K, Hoskins K, Reynolds K, Cerrone K, Cortez K, Enriquez K, Rosen L, Lashley L, Pomerantz L, Smith L, Feldman L, Fecher L, Zubiri L, Liu L, Schapira L, Tachiki L, Weissmann L, Rosenstein L, Wang L, Tomasini M, Abidi M, Khan M, Shah M, Rovito M, Gatti-Mays M, Escobedo M, Alexander M, Bonnen M, Fiala M, Lewis M, Dailey M, Reeves M, Sueyoshi M, Portes M, Salazar M, Mulcahy M, Pasquinelli M, Lustberg M, Fiebach M, Luders M, Galsky M, Weiss M, Clark M, Smits M, Accordino M, Markham M, Gurley M, Thompson M, Bar M, Wagner M, Joyner M, Glover M, Wotman M, Braccioforte M, Marcum M, Seletyn M, Huynh-Le M, Santos Dutra M, Streckfuss M, Akhtari M, Gatson N, Bahadur N, Knox N, Edwin N, Pennell N, Bouganim N, Hafez N, Venepalli N, Williams N, Balanchivadze N, Ohri N, Butt O, Panagiotou O, Serrano O, Bohachek P, Egan P, Shah P, Caimi P, LoRusso P, Weinstein P, Yu P, Lammers P, Nuzzo P, Bindal P, Peddi P, Grover P, Zaman Q, Sica R, Rosovsky R, Elias R, Zon R, Gandhi R, Belenkaya R, Rice R, Buerki R, Herbst R, Mesa R, Lynch R, Nguyen R, Monahan R, Jhawar S, Alimohamed S, Jabbour S, Del Prete S, Mahmood S, Goel S, Revankar S, Matar S, Saif S, Mushtaq S, Wall S, Croessman S, Kligerman S, McWeeney S, Goyal S, Choi S, Brouha S, Taylor S, Vinayak S, Gadgeel S, Blau S, Hallmeyer S, Reid S, Williamson S, Fry S, May S, Berg S, Duda S, Greenland S, Murdock S, Subbiah S, Shah S, Shah S, Van Loon S, Ayre S, Owenby S, Rose S, Ahmad S, Zhang S, Latif T, Bekaii-Saab T, Cronin T, Nonato T, Rhodes T, Carducci T, Halfdanarson T, Sun T, Wise-Draper T, Masters T, Topaloglu U, Koshkin V, Mico V, Karivedu V, Walters W, Miller Jr. W, Li X, Rho Y, Xie Z, Sachs Z. Association Between Androgen Deprivation Therapy and Mortality Among Patients With Prostate Cancer and COVID-19. JAMA Network Open 2021, 4: e2134330. PMID: 34767021, PMCID: PMC8590166, DOI: 10.1001/jamanetworkopen.2021.34330.Peer-Reviewed Original ResearchConceptsAndrogen deprivation therapySARS-CoV-2 infectionProstate cancerPropensity matchingDeprivation therapyCohort studyMalignant neoplasmsEastern Cooperative Oncology Group performance status scoreRole of ADTCOVID-19Androgen deprivation therapy useLarge ongoing clinical trialsPharmacologic androgen deprivation therapyCOVID-19 infection severityAndrogen-targeted therapiesBaseline steroid usePerformance status scorePrimary end pointSecond malignant neoplasmsPrimary malignant neoplasmsMonths of presentationBody mass indexOngoing clinical trialsCOVID-19 treatmentVanderbilt University Medical CenterA phase I/II study of combination olaparib and radium-223 in men with metastatic castration-resistant prostate cancer with bone metastases (COMRADE): A trial in progress.
Shaya J, Xie W, Saraiya B, Parikh M, Folefac E, Olson A, Choudhury A, Einstein D, Heath E, Parikh R, Kunos C, Ivy S, LoRusso P, Kurzrock R, Shapiro G, McKay R. A phase I/II study of combination olaparib and radium-223 in men with metastatic castration-resistant prostate cancer with bone metastases (COMRADE): A trial in progress. Journal Of Clinical Oncology 2021, 39: tps182-tps182. DOI: 10.1200/jco.2021.39.6_suppl.tps182.Peer-Reviewed Original ResearchMetastatic castration-resistant prostate cancerPhase 2 componentCastration-resistant prostate cancerPhase 1 componentBone metastasesRadium-223PARP inhibitorsPrimary endpointOverall survivalProstate cancerPhase I/II studyRadiographic progression-free survivalFirst skeletal eventKey exclusion criteriaMore bone metastasesNon-bone metastasisPhase 2 doseStratification of responsePhase 1/2 studyPrior radiation therapyPhase 1/2 trialProgression-free survivalDose-escalation designTumor immune microenvironmentPlasma cell-free DNA
2019
First-in-Human Study of Mivebresib (ABBV-075), an Oral Pan-Inhibitor of Bromodomain and Extra Terminal Proteins, in Patients with Relapsed/Refractory Solid Tumors
Piha-Paul SA, Sachdev JC, Barve M, LoRusso P, Szmulewitz R, Patel SP, Lara PN, Chen X, Hu B, Freise KJ, Modi D, Sood A, Hutti JE, Wolff J, O'Neil BH. First-in-Human Study of Mivebresib (ABBV-075), an Oral Pan-Inhibitor of Bromodomain and Extra Terminal Proteins, in Patients with Relapsed/Refractory Solid Tumors. Clinical Cancer Research 2019, 25: 6309-6319. PMID: 31420359, DOI: 10.1158/1078-0432.ccr-19-0578.Peer-Reviewed Original ResearchConceptsTreatment-emergent adverse eventsDose escalationSolid tumorsStable diseaseSafety profileProstate cancerCommon grade 3/4 treatment-emergent adverse eventsGrade 3/4 treatment-emergent adverse eventsHuman studiesMost common treatment-emergent adverse eventsCommon treatment-emergent adverse eventsMedian progression-free survivalTolerable safety profilePhase II doseAdvanced solid tumorsProgression-free survivalRefractory solid tumorsPreliminary antitumor activityMalignant solid tumorsAminotransferase elevationEvaluable patientsDose expansionExpansion cohortGastrointestinal bleedAdverse events
2017
A Phase I/Ib Study of Enzalutamide Alone and in Combination with Endocrine Therapies in Women with Advanced Breast Cancer
Schwartzberg LS, Yardley D, Elias A, Patel M, LoRusso P, Burris HA, Gucalp A, Peterson A, Blaney M, Steinberg J, Gibbons J, Traina TA. A Phase I/Ib Study of Enzalutamide Alone and in Combination with Endocrine Therapies in Women with Advanced Breast Cancer. Clinical Cancer Research 2017, 23: 4046-4054. PMID: 28280092, DOI: 10.1158/1078-0432.ccr-16-2339.Peer-Reviewed Original ResearchMeSH KeywordsAdultAgedAnastrozoleAntineoplastic Agents, HormonalAntineoplastic Combined Chemotherapy ProtocolsAromatase InhibitorsBenzamidesBreast NeoplasmsCytochrome P-450 CYP3ADose-Response Relationship, DrugDrug-Related Side Effects and Adverse ReactionsFemaleHumansMiddle AgedNeoplasm StagingNitrilesPhenylthiohydantoinPostmenopauseReceptors, EstrogenReceptors, ProgesteroneTriazolesConceptsEndocrine therapyEnzalutamide monotherapyBreast cancerEstrogen receptor-positive/progesterone receptor-positive breast cancerProgesterone receptor-positive breast cancerCytochrome P450 3A4 inducerRandomized phase II studyReceptor-positive breast cancerDose-expansion cohortsEffect of enzalutamidePhase II studyAdvanced breast cancerAndrogen receptor signalingBreast cancer modelClin Cancer ResDose modificationII studyPharmacokinetic interactionsPreclinical dataProstate cancerIb studyAdditional cohortMonotherapyCancer modelExemestane
2012
MDV3100-08: A phase I open-label, dose-escalation study evaluating the safety, tolerability, and pharmacokinetics of MDV3100 in women with incurable breast cancer.
Elias A, Richer J, LoRusso P, Peterson A, Steinberg J, Mordenti J, Lopez C, Hudis C, Traina T. MDV3100-08: A phase I open-label, dose-escalation study evaluating the safety, tolerability, and pharmacokinetics of MDV3100 in women with incurable breast cancer. Journal Of Clinical Oncology 2012, 30: tps668-tps668. DOI: 10.1200/jco.2012.30.15_suppl.tps668.Peer-Reviewed Original ResearchPhase 2 doseIncurable breast cancerBreast cancerAndrogen receptorDay 1PK samplesDay 8Dose-escalation stageOverall survival benefitDose-escalation studyPhase 1 studyAR nuclear translocationInhibition of androgenPotential therapeutic strategyPK samplingAdverse eventsDaily dosingSurvival benefitAR expressionHistologic subtypeDiscontinuation criteriaPreclinical activityProstate cancerTumor assessmentMDV3100