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12583 citation(s) found for "Vu, John A".

Meta-Analysis of Phase II Cooperative Group Trials in Metastatic Stage IV Melanoma to Determine Progression-Free and Overall Survival Benchmarks for Future Phase II Trials
Liu, Ping-Yu, Chapman, J. W. , Niedzwiecki, Donna , Sondak, Vernon K. , Eisenhauer, Elizabeth A. , Parulekar, Wendy R. , Saxman, Scott, Korn, Edward L. , Lee, Sandra J. , Chapman, Judith‐Anne W. , Suman, Vera J. , Moon, James , Atkins, Michael B. , Markovic, Svetomir N. , Kirkwood, John M. , Niedzwiecki, Donna

Journal of Clinical Oncology | January 30, 2008 | Volume: 26 | Issue: 4 | Pages: 527-534

10.1200/jco.2007.12.7837 | PMID 18235113 Get It

Purpose Objective tumor response rates observed in phase II trials for metastatic melanoma have historically not provided a reliable indicator of meaningful survival benefits. To facilitate using overall survival (OS) or progression-free survival (PFS) as an endpoint for future phase II trials, we evaluated historical data from cooperative group phase II trials to attempt to develop benchmarks for OS and PFS as reference points for future phase II trials. Patients and Methods Individual-level and trial-level data were obtained for patients enrolled onto 42 phase II trials (70 trial arms) that completed accrual in the years 1975 through 2005 and conducted by Southwest Oncology Group, Eastern Cooperative Oncology Group, Cancer and Leukemia Group B, North Central Cancer Treatment Group, and the Clinical Trials Group of the National Cancer Institute of Canada. Univariate and multivariate analyses were performed to identify prognostic variables, and between-trial(-arm) variability in 1-year OS rates and 6-month PFS rates were examined. Results Statistically significant individual-level and trial-level prognostic factors found in a multivariate survival analysis for OS were performance status, presence of visceral disease, sex, and whether the trial excluded patients with brain metastases. Performance status, sex, and age were statistically significant prognostic factors for PFS. Controlling for these prognostic variables essentially eliminated between-trial variability in 1-year OS rates but not in 6-month PFS rates. Conclusion Benchmarks are provided for 1-year OS or OS curves that make use of the distribution of prognostic factors of the patients in the phase II trial. A similar benchmark for 6-month PFS is provided, but its use is more problematic because of residual between-trial variation in this endpoint.
Response to Letter Regarding Article, “Serial Biomarker Measurements in Ambulatory Patients With Chronic Heart Failure: The Importance of Change Over Time”
Hartman, Karen, Grill, Diane E. , Burritt, Mary F., Rodeheffer, Richard J. , Burnett, John C. , Jaffe, Allan S. , Miller, Wayne L. , Jaffe, Allan S.

Circulation | January 28, 2008 | Volume: 117 | Issue: 4 | Pages: No page available

10.1161/circulationaha.107.740936 Get It

To Be or Not TB
Tom, Andrea, Dean, Diana S., Wilson, John

Thyroid | January 28, 2008 | Volume: 18 | Issue: 1 | Pages: 77-80

10.1089/thy.2007.0146 | PMID 18302521 Get It

Analysis of Repeat Nephron Sparing Surgery as a Treatment Option in Patients With a Solid Mass in a Renal Remnant
Magera, James S., Frank, Igor, Lohse, Christine M. , Leibovich, Bradley C. , Cheville, John C. , Blute, Michael L.

Journal of Urology | January 28, 2008 | Volume: 179 | Issue: 3 | Pages: 853-856

10.1016/j.juro.2007.10.049 | PMID 18221957 Get It

Dynamic phases of peroneal and tibial intraneural ganglia formation: a new dimension added to the unifying articular theory
Spinner, Robert J. , Amrami, Kimberly K. , Wolanskyj, Alexandra P. , Desy, Nicholas M. , Wang, Huan , Benarroch, Eduardo E. , Skinner, John A. , Rock, Michael G., Scheithauer, Bernd W., Wolanskyj-Spinner, Alexandra P

Journal of Neurosurgery | January 24, 2008 | Volume: 107 | Issue: 2 | Pages: 296-307

10.3171/jns-07/08/0296 | PMID 17695383 Get It

Object The pathogenesis of intraneural ganglia has been a controversial issue for longer than a century. Recently the authors identified a stereotypical pattern of occurrence of peroneal and tibial intraneural ganglia, and based on an understanding of their pathogenesis provided a unifying articular explanation. Atypical features, which occasionally are observed, have offered an opportunity to verify further and expand on the authors' proposed theory. Methods Three unusual cases are presented to exemplify the dynamic features of peroneal and tibial intraneural ganglia formation. Results Two patients with a predominant deep peroneal nerve deficit shared essential anatomical findings common to peroneal intraneural ganglia: namely, 1) joint connections to the anterior portion of the superior tibiofibular joint, and 2) dissection of the cyst along the articular branch of the peroneal nerve and proximally. Magnetic resonance (MR) images obtained in these patients demonstrated some unusual findings, including the presence of a cyst within the tibial and sural nerves in the popliteal fossa region, and spontaneous regression of the cysts, which was observed on serial images obtained weeks apart. The authors identified a clinical outlier, a case that could not be understood within the context of their previously reported theory of intraneural ganglion cyst formation. Described 32 years ago, this patient had a tibial neuropathy and was found at surgery to have tibial, peroneal, and sciatic intraneural cysts without a joint connection. The authors' hypothesis about this case, based on their unified theory, was twofold: 1) the lesion was a primary tibial intraneural ganglion with proximal extension followed by sciatic cross-over and distal descent; and 2) a joint connection to the posterior aspect of the superior tibiofibular joint with a remnant cyst within the articular branch would be present, a finding that would help explain the formation of different cysts by a single mechanism. The authors proved their hypothesis by careful inspection of a recently obtained postoperative MR image. Conclusions These three cases together with data obtained from a retrospective review of the authors' clinical material and findings reported in the literature provide firm evidence for mechanisms underlying intraneural ganglia formation. Thus, expansion of the authors' unified articular theory permits understanding and elucidation of unusual presentations of intraneural cysts. Whereas an articular connection and fluid following the path of least resistance was pivotal, the authors now incorporate dynamic aspects of cyst formation due to pressure fluxes. These basic principles explain patterns of ascent, cross-over, and descent down terminal nerve branches based on articular connections, paths of diminished resistance to fluid flow within recognized anatomical compartments, and the effects of fluctuating pressure gradients.
Unilateral deep brain stimulation of the subthalamic nucleus for Parkinson disease
Putzke, John D., Uitti, Ryan J. , Lucas, John A. , Turk, Margaret F., Kall, Bruce A., Wharen, Robert E. , Slowinski, Jerzy L.

Journal of Neurosurgery | January 24, 2008 | Volume: 106 | Issue: 4 | Pages: 626-632

10.3171/jns.2007.106.4.626 | PMID 17432714 Get It

Object The object of this study was to assess the results of unilateral deep brain stimulation (DBS) of the subthalamic nucleus (STN) for management of advanced Parkinson disease (PD). Methods A clinical series of 24 patients (mean age 71 years, range 56–80 years) with medically intractable PD, who were undergoing unilateral magnetic resonance imaging–targeted, electrophysiologically guided STN DBS, completed a battery of qualitative and quantitative outcome measures preoperatively (baseline) and postoperatively, using a modified Core Assessment Program for Intracerebral Transplantations protocol. The mean follow-up period was 9 months. Statistically significant improvement was observed in the Unified Parkinson's Disease Rating Scale (UPDRS) Part II score (18%), the total UPDRS PART III score (31%), the contralateral UPDRS Part III score (63%), and scores for axial motor features (19%), contralateral tremor (88%), rigidity (60%), bradykinesia (54%), and dyskinesia (69%), as well as the Parkinson's Disease Quality of Life questionnaire score (15%) in the on-stimulation state compared with baseline. Ipsilateral symptoms improved by approximately 15% or less. Performance on the Purdue pegboard test improved in the contralateral hand in the on-stimulation state compared with the off-stimulation state (38%, p < 0.05). The daily levodopa-equivalent dose was reduced by 21% (p = 0.018). Neuropsychological tests revealed an improvement in mental flexibility and a trend toward reduced letter fluency. There were no permanent surgical complications. Of the 16 participants with symmetrical disease, five required implantation of the DBS unit on the second side. Conclusions Unilateral STN DBS is an effective and safe treatment for selected patients with advanced PD. Unilateral STN DBS provides improvement of contralateral motor symptoms of PD as well as quality of life, reduces requirements for medication, and possibly enhances mental flexibility. This method of surgical treatment may be associated with a reduced risk and may provide an alternative to bilateral STN DBS for PD, especially in older patients or patients with asymmetry of parkinsonism.
Dynamic phases of peroneal and tibial intraneural ganglia formation: a new dimension added to the unifying articular theory
Spinner, Robert J. , Amrami, Kimberly K. , Wolanskyj, Alexandra P., Desy, Nicholas M. , Wang, Huan , Benarroch, Eduardo E. , Rock, Michael G., Scheithauer, Bernd W., Skinner, John A.

Neurosurgical Focus | January 24, 2008 | Volume: 22 | Issue: 6 | Pages: 1-12

10.3171/foc.2007.22.6.1 Get It

Object The pathogenesis of intraneural ganglia has been a controversial issue for longer than a century. Recently the authors identified a stereotypical pattern of occurrence of peroneal and tibial intraneural ganglia, and based on an understanding of their pathogenesis provided a unifying articular explanation. Atypical features, which occasionally are observed, have offered an opportunity to verify further and expand on the authors' proposed theory. Methods Three unusual cases are presented to exemplify the dynamic features of peroneal and tibial intraneural ganglia formation. Results Two patients with a predominant deep peroneal nerve deficit shared essential anatomical findings common to peroneal intraneural ganglia: namely, 1) joint connections to the anterior portion of the superior tibiofibular joint, and 2) dissection of the cyst along the articular branch of the peroneal nerve and proximally. Magnetic resonance (MR) images obtained in these patients demonstrated some unusual findings, including the presence of a cyst within the tibial and sural nerves in the popliteal fossa region, and spontaneous regression of the cysts, which was observed on serial images obtained weeks apart. The authors identified a clinical outlier, a case that could not be understood within the context of their previously reported theory of intraneural ganglion cyst formation. Described 32 years ago, this patient had a tibial neuropathy and was found at surgery to have tibial, peroneal, and sciatic intraneural cysts without a joint connection. The authors' hypothesis about this case, based on their unified theory, was twofold: 1) the lesion was a primary tibial intraneural ganglion with proximal extension followed by sciatic cross-over and distal descent; and 2) a joint connection to the posterior aspect of the superior tibiofibular joint with a remnant cyst within the articular branch would be present, a finding that would help explain the formation of different cysts by a single mechanism. The authors proved their hypothesis by careful inspection of a recently obtained postoperative MR image. Conclusions These three cases together with data obtained from a retrospective review of the authors' clinical material and findings reported in the literature provide firm evidence for mechanisms underlying intraneural ganglia formation. Thus, expansion of the authors' unified articular theory permits understanding and elucidation of unusual presentations of intraneural cysts. Whereas an articular connection and fluid following the path of least resistance was pivotal, the authors now incorporate dynamic aspects of cyst formation due to pressure fluxes. These basic principles explain patterns of ascent, cross-over, and descent down terminal nerve branches based on articular connections, paths of diminished resistance to fluid flow within recognized anatomical compartments, and the effects of fluctuating pressure gradients.
Safety of Laparoscopic Adrenalectomy in Patients with Large Pheochromocytomas: A Single Institution Review
Porterfield, John R. , Farley, David R.

World Journal of Surgery | January 22, 2008 | Volume: 32 | Issue: 5 | Pages: 845-846

10.1007/s00268-007-9395-6 Get It

Surgery for Cushing’s Syndrome: An Historical Review and Recent Ten‐year Experience
Porterfield, John R. , Thompson, Geoffrey B. , Chow, John T., Fryrear, Raymond, Heerden, Jon A. van, Farley, David R. , Atkinson, John L. D., Meyer, Fredric B. , Abboud, Charles F., Nippoldt, Todd B., Natt, Neena, Erickson, Dana , Carpenter, Paul C., Richards, Melanie L. , Carney, J. Aidan, Larson, Dirk, Schleck, Cathy D. , Churchward, Marilyn, Grant, Clive S., Young, William F. , Vella, Adrian

World Journal of Surgery | January 14, 2008 | Volume: 32 | Issue: 5 | Pages: 659-677

10.1007/s00268-007-9387-6 | PMID 18196319 Get It

AbstractBackgroundCushing’s syndrome (CS), due to multiple etiologies, is a disorder associated with the ravages of cortisol excess. The purpose of this review article is to provide a historical synopsis of surgery for CS, review a recent 10‐year period of operative management at a tertiary care facility, and to outline a practical approach to diagnosis and management.Materials and MethodsFrom 1996 to 2005, 298 patients underwent 322 operative procedures for CS at Mayo Clinic, Rochester, Minnesota. A retrospective chart review was carried out. Data was gathered regarding demographics, preoperative assessment, procedures performed, and outcomes. Data are presented as counts and percentages. Five‐year survival rates were calculated where applicable by the Kaplan‐Meier method. Statistical analysis was carried out with SAS, version 9 (SAS Institute, Inc., Cary, NC).ResultsTwo‐hundred thirty‐one patients (78%) had ACTH‐dependent CS and 67 patients (22%) had ACTH‐independent CS. One‐hundred ninety‐six patients (66%) had pituitary‐dependent CS and 35 patients (12%) had ectopic ACTH syndrome. Fifty‐four patients (18%) had cortisol‐secreting adenomas, 10 patients (3%) had cortisol‐producing adrenocortical carcinomas, and 1% had other causes. Cure rates for first time pituitary operations (transsphenoidal, sublabial, and endonasal) were 80% and 55% for reoperations. Most benign adrenal processes could be managed laparoscopically. Five‐year survival rates (all causes) were 90%, 51%, and 23% for adrenocortical adenomas, ectopic ACTH syndrome, and adrenocortical carcinomas, respectively.ConclusionsSurgery for CS is highly successful for pituitary‐dependent CS and most ACTH‐independent adrenal causes. Bilateral total adrenalectomy can also provide effective palliation from the ravages of hypercortisolism in patients with ectopic ACTH syndrome and for those who have failed transsphenoidal surgery. Unfortunately, to date, adrenocortical carcinomas are rarely cured. Future successes with this disease will likely depend on a better understanding of tumor biology, more effective adjuvant therapies and earlier detection. Clearly, IPSS, advances in cross‐sectional imaging, along with developments in transsphenoidal and laparoscopic surgery, have had the greatest impact on today’s management of the complex patient with CS.
Radical Nephrectomy for pT1a Renal Masses May be Associated With Decreased Overall Survival Compared With Partial Nephrectomy
Thompson, R. Houston, Boorjian, Stephen A. , Lohse, Christine M. , Leibovich, Bradley C. , Kwon, Eugene D., Cheville, John C. , Blute, Michael L.

Journal of Urology | January 9, 2008 | Volume: 179 | Issue: 2 | Pages: 468-473

10.1016/j.juro.2007.09.077 | PMID 18076931 Get It