S
Sujata Arora
Researcher at Eisai
Publications - 41
Citations - 1621
Sujata Arora is an academic researcher from Eisai. The author has contributed to research in topics: Rolapitant & Chemotherapy-induced nausea and vomiting. The author has an hindex of 13, co-authored 40 publications receiving 1172 citations.
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Journal ArticleDOI
Single-Arm Phases 1 and 2 Trial of Niraparib in Combination With Pembrolizumab in Patients With Recurrent Platinum-Resistant Ovarian Carcinoma
Panagiotis A. Konstantinopoulos,Steven E. Waggoner,Gregory A. Vidal,Monica M. Mita,John W. Moroney,Robert W. Holloway,Linda Van Le,Jasgit C. Sachdev,Eloise Chapman-Davis,Gerardo Colon-Otero,Richard T. Penson,Ursula A. Matulonis,Young B. Kim,Kathleen N. Moore,Kathleen N. Moore,Elizabeth M. Swisher,Anniina Färkkilä,Alan D. D'Andrea,Erica Stringer-Reasor,Jing Wang,Nathan Buerstatte,Sujata Arora,Julie R. Graham,Dmitri Bobilev,Bruce J. Dezube,Pamela N. Munster +25 more
TL;DR: Niraparib in combination with pembrolizumab is tolerable, with promising antitumor activity for patients with ovarian carcinoma who have limited treatment options regardless of platinum status, biomarker status, or prior treatment with bevacizumabs.
Journal ArticleDOI
Multicenter Study of Decitabine Administered Daily for 5 Days Every 4 Weeks to Adults With Myelodysplastic Syndromes: The Alternative Dosing for Outpatient Treatment (ADOPT) Trial
David P. Steensma,Maria R. Baer,James L. Slack,Rena Buckstein,Lucy A. Godley,Guillermo Garcia-Manero,Maher Albitar,Julie S. Larsen,Sujata Arora,Michael T. Cullen,Hagop M. Kantarjian +10 more
TL;DR: It is suggested that decitabine can be administered in an outpatient setting with comparable efficacy and safety to the United States Food and Drug Administration-approved inpatient regimen.
Journal ArticleDOI
Open-label Clinical Trial of Niraparib Combined With Pembrolizumab for Treatment of Advanced or Metastatic Triple-Negative Breast Cancer.
Shaveta Vinayak,Shaveta Vinayak,Sara M. Tolaney,Lee S. Schwartzberg,Monica M. Mita,Georgia A. McCann,Antoinette R. Tan,Andrea E. Wahner-Hendrickson,Andres Forero,Carey K. Anders,Gerburg M. Wulf,Patrick M. Dillon,Filipa Lynce,Corrine Zarwan,John K. Erban,Yinghui Zhou,Nathan Buerstatte,Julie R. Graham,Sujata Arora,Bruce J. Dezube,Melinda L. Telli +20 more
TL;DR: Combination niraparib plus pembrolizumab provides promising antitumor activity in patients with advanced or metastatic TNBC, with numerically higher response rates in those with tumor BRCA mutations.
Journal ArticleDOI
Safety and efficacy of rolapitant for prevention of chemotherapy-induced nausea and vomiting after administration of cisplatin-based highly emetogenic chemotherapy in patients with cancer: two randomised, active-controlled, double-blind, phase 3 trials
Bernardo Leon Rapoport,Martin Chasen,Cesare Gridelli,Laszlo Urban,Manuel Modiano,Ian D. Schnadig,Allen Poma,Sujata Arora,Vikram Kansra,Lee S. Schwartzberg,Rudolph M. Navari +10 more
TL;DR: Rlapitant, an NK-1 receptor antagonist, was aimed to assess for prevention of chemotherapy-induced nausea and vomiting in patients with cancer after administration of cisplatin-based highly emetogenic chemotherapy.
Journal ArticleDOI
Safety and efficacy of rolapitant for prevention of chemotherapy-induced nausea and vomiting after administration of moderately emetogenic chemotherapy or anthracycline and cyclophosphamide regimens in patients with cancer: a randomised, active-controlled, double-blind, phase 3 trial.
Lee S. Schwartzberg,Manuel Modiano,Bernardo Leon Rapoport,Martin Chasen,Cesare Gridelli,Laszlo Urban,Allen Poma,Sujata Arora,Rudolph M. Navari,Ian D. Schnadig +9 more
TL;DR: Rolapitant in combination with a 5-HT3 receptor antagonist and dexamethasone is well tolerated and shows superiority over active control for the prevention of chemotherapy-induced nausea and vomiting during the 5-day at-risk period after administration of moderately emetogenic chemotherapy or regimens containing an anthracycline and cyclophosphamide.