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75 citation(s) found for "Ryder, J R".

A multidisciplinary approach to toxicity management of modern immune checkpoint inhibitors in cancer therapy
Kottschade, Lisa A. , Brys, Adam K. , Peikert, Tobias, Ryder, Mabel , Raffals, Laura E., Brewer, Jerry D., Markovic, Svetomir, Kottschade, Lisa, Raffals, Laura E. , Mosca, Paul J. , Markovic, Svetomir N. , Ryder, Mabel

Melanoma Research | June 16, 2016 | Volume: 26 | Issue: 5 | Pages: 469-480

10.1097/cmr.0000000000000273 | PMID 27306502 Get It

Immune-related Adverse Events (irAEs) are the most significant toxicities associated with the use of checkpoint inhibitors, and result from disinhibition of the host’s immune homeostasis. The adverse effects experienced from immunotherapy are significantly different from those of chemotherapy and, to a lesser extent, targeted therapy. Early recognition and diagnosis of these toxicities is often challenging, but is critically important because of the potentially life-threatening nature and associated morbidity. Gastrointestinal, dermatologic, endocrine, and liver toxicities are the most commonly observed. Less commonly, the eyes, pancreas, kidneys, lungs, bone marrow, or nervous system may be affected. Although most irAEs may resolve with supportive care or discontinuation of drug, in severe cases, they may require hospitalization and immune suppressants, such as steroids, and/or may even cause death. The management of immune-related side effects requires a multidisciplinary approach.
Promises and Perils of Molecularly Targeted Therapeutics in Anaplastic Thyroid Cancer
Bible, Keith C. , Chintakuntlawar, Ashish V. , Ryder, Mabel , Chintakuntlawar, Ashish V , Ryder, Mabel

Journal of Oncology Practice | June 11, 2016 | Volume: 12 | Issue: 6 | Pages: 521-522

10.1200/jop.2016.013144 | PMID 27288466 Get It

Most patients with a small papillary thyroid carcinoma enjoy an excellent prognosis and may be managed with minimally invasive therapy or active surveillance
Castro, M. Regina , Ryder, Mabel , Brito, Juan P. , Hay, Ian D. , Morris, John C., Ryder, Mabel , Brito, Juan P

Cancer | June 16, 2015 | Volume: 121 | Issue: 18 | Pages: 3364-3365

10.1002/cncr.29468 | PMID 26079806 Get It

Lateralization of mesial temporal lobe epilepsy with chronic ambulatory electrocorticography
King‐Stephens, David , Mirro, Emily A. , Weber, Peter, Laxer, Kenneth D. , Ness, Paul C. Van, Salanova, Vicenta , Spencer, David , Heck, Christianne, Jobst, Barbara C. , Shields, Donald C. , Bergey, Gregory K. , Eisenschenk, Stephan, Rossi, Marvin A. , Sperling, Michael R. , Nair, Dileep , Gwinn, Ryder P. , Park, Yong D., Rutecki, Paul , Fountain, Nathan B. , Wharen, Robert E. , Miller, Ian , Barkley, Gregory L., Geller, Eric B., Berg, Michel J., Sadler, Toni, Sun, Felice T., Morrell, Martha J. , Cole, Andrew J , Goldman, Alica M. , Worrell, Gregory A. , Gross, Robert E. , Cole, Andrew J. , Hirsch, Lawrence J. , Edwards, Jonathan C. W. , Sperling, Michael R , Fountain, Nathan , Jobst, Barbara , Nair, Dileep R , Morrell, Martha J

Epilepsia | May 19, 2015 | Volume: 56 | Issue: 6 | Pages: 959-967

10.1111/epi.13010 | PMID 25988840 Get It

Summary Objective Patients with suspected mesial temporal lobe ( MTL ) epilepsy typically undergo inpatient video–electroencephalography ( EEG ) monitoring with scalp and/or intracranial electrodes for 1 to 2 weeks to localize and lateralize the seizure focus or foci. Chronic ambulatory electrocorticography ( EC oG) in patients with MTL epilepsy may provide additional information about seizure lateralization. This analysis describes data obtained from chronic ambulatory EC oG in patients with suspected bilateral MTL epilepsy in order to assess the time required to determine the seizure lateralization and whether this information could influence treatment decisions. Methods Ambulatory EC oG was reviewed in patients with suspected bilateral MTL epilepsy who were among a larger cohort with intractable epilepsy participating in a randomized controlled trial of responsive neurostimulation. Subjects were implanted with bilateral MTL leads and a cranially implanted neurostimulator programmed to detect abnormal interictal and ictal EC oG activity. EC oG data stored by the neurostimulator were reviewed to determine the lateralization of electrographic seizures and the interval of time until independent bilateral MTL electrographic seizures were recorded. Results Eighty‐two subjects were implanted with bilateral MTL leads and followed for 4.7 years on average (median 4.9 years). Independent bilateral MTL electrographic seizures were recorded in 84%. The average time to record bilateral electrographic seizures in the ambulatory setting was 41.6 days (median 13 days, range 0–376 days). Sixteen percent had only unilateral electrographic seizures after an average of 4.6 years of recording. Significance About one third of the subjects implanted with bilateral MTL electrodes required >1 month of chronic ambulatory EC oG before the first contralateral MTL electrographic seizure was recorded. Some patients with suspected bilateral MTL seizures had only unilateral electrographic seizures. Chronic ambulatory EC oG in patients with suspected bilateral MTL seizures provides data in a naturalistic setting, may complement data from inpatient video‐ EEG monitoring, and can contribute to treatment decisions.
Two‐year seizure reduction in adults with medically intractable partial onset epilepsy treated with responsive neurostimulation: Final results of the RNS System Pivotal trial
Heck, Christianne, King‐Stephens, David , Nair, Dileep , Jobst, Barbara C. , Barkley, Gregory L., Salanova, Vicenta , Gwinn, Ryder P. , Skidmore, Christopher , Ness, Paul C. Van, Bergey, Gregory K. , Park, Yong D., Miller, Ian , Geller, Eric B., Rutecki, Paul , Zimmerman, Richard S. , Spencer, David , Leiphart, James W., Wharen, Robert E. , Fessler, James, Fountain, Nathan B. , Eisenschenk, Stephan, Duckrow, Robert B., Hirsch, Lawrence J. , Bazil, Carl W., O’Donovan, Cormac A. , Sun, Felice T., Courtney, Tracy A., Seale, Cairn G. , Morrell, Martha J. , Massey, Andrew D. , Cole, Andrew J. , Smith, Michael C. F. , Goldman, Alica M. , Edwards, Jonathan , Worrell, Gregory A. , Gross, Robert E. , Fountain, Nathan , Hirsch, Lawrence J , Jobst, Barbara , Nair, Dileep R , Skidmore, Christopher , Morrell, Martha J

Epilepsia | February 24, 2014 | Volume: 55 | Issue: 3 | Pages: 432-441

10.1111/epi.12534 | PMID 24621228 Get It

Summary Objective To demonstrate the safety and effectiveness of responsive stimulation at the seizure focus as an adjunctive therapy to reduce the frequency of seizures in adults with medically intractable partial onset seizures arising from one or two seizure foci. Methods Randomized multicenter double‐blinded controlled trial of responsive focal cortical stimulation (RNS System). Subjects with medically intractable partial onset seizures from one or two foci were implanted, and 1 month postimplant were randomized 1:1 to active or sham stimulation. After the fifth postimplant month, all subjects received responsive stimulation in an open label period ( OLP ) to complete 2 years of postimplant follow‐up. Results All 191 subjects were randomized. The percent change in seizures at the end of the blinded period was −37.9% in the active and −17.3% in the sham stimulation group (p = 0.012, Generalized Estimating Equations). The median percent reduction in seizures in the OLP was 44% at 1 year and 53% at 2 years, which represents a progressive and significant improvement with time (p < 0.0001). The serious adverse event rate was not different between subjects receiving active and sham stimulation. Adverse events were consistent with the known risks of an implanted medical device, seizures, and of other epilepsy treatments. There were no adverse effects on neuropsychological function or mood. Significance Responsive stimulation to the seizure focus reduced the frequency of partial‐onset seizures acutely, showed improving seizure reduction over time, was well tolerated, and was acceptably safe. The RNS System provides an additional treatment option for patients with medically intractable partial‐onset seizures.