Citations

Mayo Clinic

Clear

6593 citation(s) found for "Ha, Richard".

Human Granulocyte Colony-Stimulating Factor in Children With High-Risk Acute Lymphoblastic Leukemia: A Children’s Cancer Group Study
Heath, John A. , Steinherz, Peter G. , Altman, Arnold J., Sather, Harland N., Jhanwar, Suresh C., Halpern, Steven, Pieters, Richard S., Shah, Narayan R., Steinherz, Laurel J., Tannous, Raymond, Terry, William W. , Trigg, Michael E.

Journal of Clinical Oncology | April 15, 2003 | Volume: 21 | Issue: 8 | Pages: 1612-1617

10.1200/jco.2003.07.129 | PMID 12697887 Get It

Purpose: To investigate the effect of granulocyte colony-stimulating factor (G-CSF) on hematopoietic toxicities, supportive care requirements, time to complete intensive therapy, and event-free survival (EFS) and overall survival (OS) in children with high-risk acute lymphoblastic leukemia (HR-ALL). Patients and Methods: A total of 287 children with HR-ALL were randomly assigned to intensive chemotherapy regimens (New York I [NY I] or NY II) as part of the Children’s Cancer Group (CCG)-1901 protocol. The induction phases consisted of five drugs (vincristine, prednisone, l-asparaginase, daunorubicin, and cyclophosphamide). Initial consolidation comprised six-agent chemotherapy combined with 18 Gy of total-brain irradiation. Patients were randomly assigned to receive G-CSF (5 μg/kg/day) during either induction or initial consolidation. A crossover study analysis was done on the 259 patients who completed both phases of therapy. Results: The mean time to neutrophil recovery (≥ 0.5 × 109/L) was reduced with G-CSF (16.7 v 19.1 days, P = .0003); however, patients who received G-CSF did not have significantly reduced episodes of febrile neutropenia (149 v 164, P = .41), positive blood cultures (57 v 61, P = .66), or serious infections (75 v 79, P = .62). Hospitalization (14.0 v 13.9 days, P = .87) and induction therapy completion times (NY I, 30.3 v 31.3 days, P = .11; NY II, 33.4 v 32.3 days, P = .40) were not significantly altered. There were no differences in 6-year EFS (P = .24) or OS (P = .54) between patients receiving or not receiving G-CSF on CCG-1901, NY I and NY II. Conclusion: Children with high-risk ALL do not appear to benefit from prophylactic G-CSF.
Gap Between Clinical Trials and Clinical Practice
Frye, Robert L. , Brooks, Maria M. , Nesto, Richard W.

Circulation | April 14, 2003 | Volume: 107 | Issue: 14 | Pages: 1837-1839

10.1161/01.cir.0000066419.24566.28 | PMID 12695282 Get It

Modeling and Risk Prediction in the Current Era of Interventional Cardiology
Holmes, David R. , Selzer, Faith , Kelsey, Sheryl F., Holubkov, Richard , Cohen, Howard, Williams, David O., Detre, Katherine M., Johnston, Janet M. , Holubkov, Richard

Circulation | April 14, 2003 | Volume: 107 | Issue: 14 | Pages: 1871-1876

10.1161/01.cir.0000065229.72905.78 | PMID 12668511 Get It

Background— Validation of in-hospital mortality models after percutaneous coronary interventions using multicenter data remains limited. Methods and Results— This study evaluated whether multivariable mortality models developed during the pre-stent era by New York State, American College of Cardiology (ACC)–National Cardiovascular Data Registry, Northern New England Cooperative Group, Cleveland Clinic Foundation, and the University of Michigan are relevant in patients undergoing percutaneous coronary intervention in the 1997 to 1999 National Heart, Lung, and Blood Institute Dynamic Registry. Of 4448 Dynamic Registry patients, 73% received ≥1 stent and 28% received a IIB/IIIA receptor inhibitor. In-hospital mortality occurred in 64 patients (1.4%). The New York state model predicted mortality in 69 patients (1.5%; 95% confidence bounds [CI], 0.89% to 1.70%); Northern New England predicted mortality in 60 patients (1.3%; 95% CI, 1.0% to 1.7%); and Cleveland Clinic predicted mortality in 76 patients (1.7%; 95% CI, 1.3% to 2.1%). Among high-risk subgroups, with these 3 models, observed and predicted in-hospital mortality rates in general were not different. The other 2 models yielded different results. The University of Michigan predicted fewer deaths (n=47; 1.1%; 95% CI, 0.7% to 1.3%), and the ACC Registry model predicted 603 deaths (13.5%; 95% CI, 12.6% to 14.4%). Using the ACC Registry model, predicted mortality was higher than observed in each subgroup. Conclusions— Application of 5 mortality risk models developed from different data sets to patients undergoing percutaneous coronary intervention in the Dynamic Registry predicted, in 3 models, mortality rates that were not significantly different than those observed. In both high and low risk subgroups, the University of Michigan slightly underpredicted mortality, and the ACC Registry predicted significantly higher mortality than that observed.
Phase III Study of Interferon Alfa-NL as Adjuvant Treatment for Resectable Renal Cell Carcinoma: An Eastern Cooperative Oncology Group/Intergroup Trial
Messing, Edward M. , Manola, Judith , Wilding, George, Propert, Kathleen J., Fleischmann, Jonathan, Crawford, E. David , Pontes, J. Edson, Hahn, Richard G., Trump, Donald L.

Journal of Clinical Oncology | March 27, 2003 | Volume: 21 | Issue: 7 | Pages: 1214-1222

10.1200/jco.2003.02.005 | PMID 12663707 Get It

Purpose: To evaluate the role of adjuvant interferon alfa after complete resection of locally extensive renal cell carcinoma. Patients and Methods: A total of 283 eligible patients with pT3–4a and/or node-positive disease were randomly assigned after radical nephrectomy and lymphadenectomy to observation or to interferon alfa-NL (Wellferon, Burroughs-Wellcome, Research Park, NC) given daily for 5 days every 3 weeks for up to 12 cycles. Patients were stratified on the basis of pathologic stage. Patients remained on treatment until documented recurrence, excessive toxicity, or patient/physician preference deemed removal appropriate. Results: At median follow-up of 10.4 years, median survival was 7.4 years in the observation arm and 5.1 year in the treatment arm (log-rank P = .09). Median recurrence-free survival was 3.0 years in the observation arm and 2.2 years in the interferon arm (P = .33). Performance status (P = .003), nodal status (N2 v N0, P < .0001), and tumor stage (P = .0002) were significant prognostic factors in multivariate analysis. A proportional hazards model examining the effects of treatment arm and time to recurrence on survival after recurrence among patients who recurred found that random assignment to interferon treatment (P = .009) and shorter time to recurrence (P < .0001) were independent predictors of shorter survival after recurrence. Although no lethal toxicities were observed, severe (grade 4) toxicities including neutropenia, myalgia, fatigue, depression, and other neurologic toxicities occurred in 11.4% of those randomly assigned to interferon treatment. Conclusion: Adjuvant treatment with interferon did not contribute to survival or relapse-free survival in this group of patients.
Surgical treatment of adult primary hepatic sarcoma
Poggio, Juan Lucas , Nagorney, David M. , Rowland, C, Kay, Paul , Young, Richard M. , Donohue, J H, Nascimento, Antonio G.

Journal of British Surgery | March 11, 2003 | Volume: 87 | Issue: 11 | Pages: 1500-1505

10.1046/j.1365-2168.2000.01564.x | PMID 11091236 Get It

Abstract Background Primary sarcomas of the liver are extremely rare in adults. Optimal therapeutic approaches remain unclear. Methods Twenty consecutive adult patients who had surgical treatment for primary hepatic sarcomas were reviewed. Patient age ranged from 23 to 80 years. Other than one patient with primary hepatic angiosarcoma who had a history of thorium dioxide colloid (Thorotrast) exposure 23 years before diagnosis, no predisposing causes were apparent. Nineteen patients had hepatic resection and one patient had an orthotopic liver transplant. No patient received neoadjuvant chemotherapy or radiotherapy but radiotherapy was delivered intraoperatively in one patient. Results Leiomyosarcoma was the most common histological type of sarcoma diagnosed (five of 20 patients), followed by malignant solitary fibrous tumour (four) and epithelioid haemangioendothelioma (three). Fourteen tumours were high-grade sarcomas and six were low grade malignancies. Thirteen patients developed a recurrence. Distant metastases (ten patients) and intrahepatic recurrence (six) were the predominant sites of initial treatment failure. Six patients received salvage chemotherapy. Histological grade was the only factor significantly associated with overall patient survival (P = 0·03). With complete resection, patients with high-grade tumours had a 5-year survival rate of 18 (95 per cent confidence interval 5–62) per cent compared with 80 (52–100) per cent for patients with low-grade tumours. The 5-year survival rate for all 20 patients was 37 (20–60) per cent. Conclusion Surgical resection is the only effective therapy for primary hepatic sarcomas at present. Better adjuvant therapy is necessary, especially for high-grade malignancies, owing to the high failure rate with operation alone.
RELIABILITY OF A SIMPLE SHOULDER ENDURANCE TEST
Johnson, Marjorie E., Skow, Anne, An, Kai‐Nan , Hughes, Richard E. , O’Driscoll, Shawn W.

Journal of Musculoskeletal Research | March 7, 2003 | Volume: 03 | Issue: 03 | Pages: 195-200

10.1142/s0218957799000208 Get It

Reduced shoulder endurance in rotator cuff tear patients has been observed clinically. A simple and inexpensive shoulder endurance test protocol was developed. This study reports the test-retest reliability of the protocol. Twenty healthy volunteers without a history of shoulder pathology participated in the study. Each subject was tested twice, each on a separate day. Test-retest correlation coefficients of the arm endurance times were 0.59 and 0.60 for the dominant and nondominant sides, respectively. The protocol appears promising for assessing shoulder function.
Radiation Dose in Computed Tomography of the Heart
Morin, Richard L. , Gerber, Thomas C., McCollough, Cynthia H.

Circulation | February 18, 2003 | Volume: 107 | Issue: 6 | Pages: 917-922

10.1161/01.cir.0000048965.56529.c2 | PMID 12591765 Get It

Single-cell nonphotochemical hole burning of ovarian surface epithelial carcinoma and normal cells
Walsh, Richard J. , Matsuzaki, Satoshi , Reinot, T. , Hayes, John M. , Kalli, Kimberly R., Hartmann, Lynn C., Small, Gerald J.

Proceedings of the National Academy of Sciences | February 18, 2003 | Volume: 100 | Issue: 4 | Pages: 1685-1689

10.1073/pnas.0437668100 | PMID 12574511 Get It

Persistent spectral nonphotochemical hole-burning (NPHB) spectroscopy has recently been applied to dye molecules in cells. The sensitivity of NPHB to the nanoenvironment of the probe is well established. It has been shown that NPHB applied to bulk suspensions of cultured human cells can distinguish between normal and cancer cells. Thus, NPHB has potential as a diagnostic cancer tool. For this reason, the methodology is referred to as hole-burning imaging, by analogy with MRI. The optical dephasing time ( T 2 ) of the dye in hole-burning image replaces the proton T 1 relaxation time in MRI. In addition to the T 2 mode of operation, there are four other modes including measurement of the spectral hole growth kinetics (HGK). Reported here is that the selectivity and sensitivity of NPHB operating in the HGK mode allow for distinction between normal and carcinoma cells at the single-cell level. The ovarian cell lines are ovarian surface epithelial cells with temperature-sensitive large T antigens (analogously normal) and ovarian surface epithelial carcinoma (OV167) cells. The mitochondrial specific dye used was rhodamine 800 (Molecular Probes). This carbocationic dye is highly specific for the outer and inner membranes of mitochondria. In line with the results for bulk suspensions of the two cell lines, the hole-burning efficiency for OV167 cells was found to be significantly higher than that for normal cells. Theoretical analysis of the HGK data leads to the conclusion that the degree of structural heterogeneity for the probe–host configurations in OV167 cells is lower than in the normal cells. Possible reasons for this are given.
Both B and T lymphocytes may be clonally involved in myelofibrosis with myeloid metaplasia
Reeder, Terra L. , Bailey, Richard J., Dewald, Gordon W., Tefferi, Ayalew

Blood | February 12, 2003 | Volume: 101 | Issue: 5 | Pages: 1981-1983

10.1182/blood-2002-07-2341 | PMID 12406879 Get It

A combination of magnetic cell sorting (MACS) and fluorescent in situ hybridization (FISH) techniques was used to detect clonal cytogenetic markers in different myeloid and lymphoid cell types of the peripheral blood from 4 patients with myelofibrosis with myeloid metaplasia (MMM) that was associated with either a 13q− or a 20q− karyotypic abnormality. Interphase cytogenetics studies demonstrated abnormal clonal FISH signal patterns in neutrophil, myeloid, erythroid, megakaryocyte, and B- and T-cell preparations in 3 of the 4 patients. In one patient, FISH results were within normal limits in T cells and slightly abnormal in B cells. In general, the percentage of abnormal nuclei was variable in both lymphocyte populations but always higher in B lymphocytes compared with T lymphocytes. The current study provides direct evidence for the clonal involvement of both B and T lymphocytes in MMM. A larger study is needed to clarify the relevance of the observed interpatient heterogeneity in clonal constitution.
The Workforce in Otolaryngology‐Head and Neck Surgery: Moving into the Next Millennium
Pillsbury, Harold C., Cannon, C. Ron, Holzer, Susan E. Sedory, Jacoby, Itzhak, Benninger, Michael S. , Denneny, James C. , Cheng, Eme Y., Hagner, Alison P., Meyer, Gregg S. , Nielsen, David R. , Smith, Richard V.

Otolaryngology–Head and Neck Surgery | February 4, 2003 | Volume: 123 | Issue: 3 | Pages: 341-356

10.1067/mhn.2000.109761 | PMID 10964321 Get It

OBJECTIVEThe goal was to examine the current scope of otolaryngologists’ practices, their geographic distribution, and the roles otolaryngologists and other specialists play in caring for patients with otolaryngic and related conditions of the head and neck.STUDY DESIGNA large national survey and administrative claims databases were examined to develop practice profiles and compile a physician supply for otolaryngology. A focus group of otolaryngologists provided information to model future scenarios.RESULTSThe current and predicted workforce supply and demographics are at a satisfactory level and are decreasing as a proportion of the increasing population. Empiric data analysis supports the diverse nature of an otolaryngologist's practice and the unique role for otolaryngologists that is not shared by many other providers. Together with the focus group results, the study points to areas for which more background and training are warranted.CONCLUSIONSThis study represents a first step in a process to form coherent workforce recommendations for the field of otolaryngology.