Management of Adverse Events Following Treatment With Anti‐Programmed Death‐1 Agents
dc.contributor.author | Weber, Jeffrey S. | |
dc.contributor.author | Postow, Michael | |
dc.contributor.author | Lao, Christopher D. | |
dc.contributor.author | Schadendorf, Dirk | |
dc.date.accessioned | 2017-12-15T16:49:14Z | |
dc.date.available | 2017-12-15T16:49:14Z | |
dc.date.issued | 2016-10 | |
dc.identifier.citation | Weber, Jeffrey S.; Postow, Michael; Lao, Christopher D.; Schadendorf, Dirk (2016). "Management of Adverse Events Following Treatment With Anti‐Programmed Death‐1 Agents." The Oncologist 21(10): 1230-1240. | |
dc.identifier.issn | 1083-7159 | |
dc.identifier.issn | 1549-490X | |
dc.identifier.uri | https://hdl.handle.net/2027.42/140047 | |
dc.publisher | AlphaMed Press | |
dc.publisher | Wiley Periodicals, Inc. | |
dc.subject.other | Drug‐related side effects and adverse reactions | |
dc.subject.other | Melanoma | |
dc.subject.other | Pembrolizumab | |
dc.subject.other | Nivolumab | |
dc.subject.other | Programmed cell death 1 receptor | |
dc.title | Management of Adverse Events Following Treatment With Anti‐Programmed Death‐1 Agents | |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | |
dc.subject.hlbsecondlevel | Hematology and Oncology | |
dc.subject.hlbtoplevel | Health Sciences | |
dc.description.peerreviewed | Peer Reviewed | |
dc.contributor.affiliationum | Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA | |
dc.contributor.affiliationother | University Hospital Essen, Essen, Germany | |
dc.contributor.affiliationother | Laura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York, USA | |
dc.contributor.affiliationother | Memorial Sloan Kettering Cancer Center, New York, New York, USA | |
dc.contributor.affiliationother | Weill Cornell Medical College, New York, New York, USA | |
dc.description.bitstreamurl | https://deepblue.lib.umich.edu/bitstream/2027.42/140047/1/onco1230.pdf | |
dc.identifier.doi | 10.1634/theoncologist.2016-0055 | |
dc.identifier.source | The Oncologist | |
dc.identifier.citedreference | RJ Motzer, BI Rini, DF McDermott. Nivolumab for metastatic renal cell carcinoma: Results of a randomized phase II trial. J Clin Oncol. 2015; 33: 1430 – 1437. | |
dc.identifier.citedreference | FS Hodi, SJ O’Day, DF McDermott. Improved survival with ipilimumab in patients with metastatic melanoma. N Engl J Med. 2010; 363: 711 – 723. | |
dc.identifier.citedreference | C Robert, GV Long, B Brady. Nivolumab in previously untreated melanoma without BRAF mutation. N Engl J Med. 2015; 372: 320 – 330. | |
dc.identifier.citedreference | JS Weber, SP D’Angelo, D Minor. Nivolumab versus chemotherapy in patients with advanced melanoma who progressed after anti‐CTLA‐4 treatment (CheckMate 037): A randomised, controlled, open‐label, phase 3 trial. Lancet Oncol. 2015; 16: 375 – 384. | |
dc.identifier.citedreference | C Robert, J Schachter, GV Long. Pembrolizumab versus ipilimumab in advanced melanoma. N Engl J Med. 2015; 372: 2521 – 2532. | |
dc.identifier.citedreference | MA Postow, J Chesney, AC Pavlick. Nivolumab and ipilimumab versus ipilimumab in untreated melanoma. N Engl J Med. 2015; 372: 2006 – 2017. | |
dc.identifier.citedreference | J Larkin, V Chiarion‐Sileni, R Gonzalez. Combined nivolumab and ipilimumab or monotherapy in untreated melanoma. N Engl J Med. 2015; 373: 23 – 34. | |
dc.identifier.citedreference | Yervoy (ipilimumab) [package insert]. Princeton, NJ: Bristol‐Myers Squibb Co. 2013. | |
dc.identifier.citedreference | Opdivo (nivolumab) [prescribing information]. Princeton, NJ: Bristol‐Myers Squibb Co. 2014. | |
dc.identifier.citedreference | Keytruda (pembrolizumab) [prescribing information]. Kenilworth, NJ: Merck & Co., Inc. 2015. | |
dc.identifier.citedreference | J Brahmer, KL Reckamp, P Baas. Nivolumab versus docetaxel in advanced squamous‐cell non‐small‐cell lung cancer. N Engl J Med. 2015; 373: 123 – 135. | |
dc.identifier.citedreference | Paz‐Ares L, Horn L, Borghaei H et al. Phase III, randomized trial (CheckMate 057) of nivolumab versus docetaxel in advanced non‐squamous (non‐SQ) cell non‐small cell lung cancer (NSCLC). Poster presented at: American Society of Clinical Oncology 2015 Annual Meeting; May 29‐June 2, 2015; Chicago, IL. | |
dc.identifier.citedreference | Bauer TM, McCleod M, Chandler JC et al. A phase IIIb/IV safety trial of nivolumab (NIVO) in patients (pts) with advanced or metastatic non‐small cell lung cancer (NSCLC) who have progressed during or after receiving at least one prior systemic regimen. Poster presented at American Society of Clinical Oncology 2015 Annual Meeting; May 29–June 2, 2015; Chicago, IL. | |
dc.identifier.citedreference | Hodi FS, Postow MA, Chesney J et al. Clinical response, PFS and safety in patients with advanced melanoma receiving nivolumab combined with ipilmumuab versus ipilimumab monotherapy in CheckMate 069 study. Poster presented at: American Society of Clinical Oncology 2015 Annual Meeting; May 29‐June 2, 2015; Chicago, IL. | |
dc.identifier.citedreference | U.S. Department of Health and Human Services, National Institutes of Health, National Cancer Institute. Common Terminology Criteria for Adverse Events (CTCAE). Version 4.03. Available at http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010‐06‐14_QuickReference_5x7.pdf. Accessed February 8, 2016. | |
dc.identifier.citedreference | R Sundar, BC Cho, JR Brahmer. Nivolumab in NSCLC: Latest evidence and clinical potential. Ther Adv Med Oncol. 2015; 7: 85 – 96. | |
dc.identifier.citedreference | SL Topalian, FS Hodi, JR Brahmer. Safety, activity, and immune correlates of anti‐PD‐1 antibody in cancer. N Engl J Med. 2012; 366: 2443 – 2454. | |
dc.identifier.citedreference | J Naidoo, DB Page, BT Li. Toxicities of the anti‐PD‐1 and anti‐PD‐L1 immune checkpoint antibodies. Ann Oncol. 2015; 26: 2375 – 2391. | |
dc.identifier.citedreference | C Robert, A Ribas, JD Wolchok. Anti‐programmed‐death‐receptor‐1 treatment with pembrolizumab in ipilimumab‐refractory advanced melanoma: A randomised dose‐comparison cohort of a phase 1 trial. Lancet. 2014; 384: 1109 – 1117. | |
dc.identifier.citedreference | JS Weber, SJ Antonia, SL Topalian, et al. Safety profile of nivolumab (NIVO) in patients (pts) with advanced melanoma (MEL): A pooled analysis. J Clin Oncol. 2015; 33 9018a, suppl. | |
dc.identifier.citedreference | Bristol‐Myers Squibb Company. Risk Evaluation and Mitigation Strategy (REMS). Initial REMS approval: 03/2011; most recent modification: 02/2012. Available at http://www.fda.gov/downloads/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/UCM249435.pdf. Accessed February 8, 2016. | |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.