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381 citation(s) found for "Weiss, A".

Improvement in Functioning and Psychological Distress in Adolescents With Postural Orthostatic Tachycardia Syndrome Following Interdisciplinary Treatment
Bruce, Barbara K. , Harrison, Tracy E. , Bee, Susan, Luedtke, Connie A. , Porter, Co-burn J., Hayes, Sarah , Allman, Daniel A., Ale, Chelsea M. , Weiss, Karen E. , Bee, Susan M, Fischer, Philip R. , Hayes, Sarah E

Mayo Clinic

Clinical Pediatrics | March 16, 2016 | Volume: 55 | Issue: 14 | Pages: 1300-1304

10.1177/0009922816638663 | PMID 26983448 Get It

Significant functional impairment and psychological distress have been observed in adolescent patients with postural orthostatic tachycardia syndrome (POTS). Interdisciplinary rehabilitation programs have been shown to be beneficial in the treatment of chronic pain in adults and adolescents. Only preliminary data have examined interdisciplinary rehabilitation efforts in patients with POTS. This study evaluated the impact of an interdisciplinary rehabilitation program on the functional impairment and psychological distress in 33 adolescents diagnosed with POTS. Patients included in the study were adolescents ages 11 to 18 diagnosed with POTS. Measures completed at admission and discharge from the program included the Functional Disability Index, Center for Epidemiological Studies–Depression–Child scale, and the Pain Catastrophizing Scale for Children. After participation in the 3-week program, adolescents with POTS demonstrated a significant increase in overall functional ability and significant reductions in depression and catastrophizing.
Rituximab extended schedule or retreatment trial for low tumour burden non‐follicular indolent B‐cell non‐Hodgkin lymphomas: Eastern Cooperative Oncology Group Protocol E4402
Williams, Michael E. , Gascoyne, Randy D. , Krauss, John C. , Swinnen, Lode J., Peterson, Christopher G., Sborov, Mark D., Martín, Sabrina , Weiss, Matthias , Ehmann, W. Christopher, Horning, Sandra J., Hong, Fangxin , Wagner, Lynne I. , Habermann, Thomas M. , Schuster, Stephen J. , Kahl, Brad S.

Mayo Clinic

British Journal of Haematology | March 12, 2016 | Volume: 173 | Issue: 6 | Pages: 867-875

10.1111/bjh.14007 | PMID 26970533 Get It

SummaryThe rituximab extended schedule or retreatment trial (RESORT; E4402) was a phase 3 randomized prospective trial comparing maintenance rituximab (MR) versus a retreatment (RR) dosing strategy in asymptomatic, low tumour burden indolent lymphoma. A planned exploratory sub‐study compared the two strategies for small lymphocytic (SLL) and marginal zone lymphomas (MZL). Patients responding to rituximab weekly × 4 were randomized to MR (single dose rituximab every 3 months until treatment failure) or RR (rituximab weekly × 4) at the time of each progression until treatment failure. The primary endpoint was time to treatment failure (TTTF). Patients with SLL (n = 57), MZL (n = 71) and unclassifiable small B‐cell lymphoma (n = 3) received induction rituximab. The overall response rate (ORR) was 40% [95% confidence interval (CI) 31–49%; SLL ORR 22·8%; MZL ORR 52·1%]; all 52 responders were randomized. At a median of 4·3 years from randomization, treatment failure occurred in 18/23 RR and 15/29 MR. The median TTTF was 1·4 years for RR and 4·8 years for MR (P = 0·012); median time to first cytotoxic therapy was 6·3 years for RR and not reached for MR (P = 0·0002). Survival did not differ (P = 0·72). In low tumour burden SLL and MZL patients responding to rituximab induction, MR significantly improved TTTF as compared with RR.
Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages
Emile, Jean‐François , Abla, Oussama , Fraitag, Sylvie , Horne, AnnaCarin , Haroche, Julien , Requena‐Caballero, Luis, Jordan, Michael B. , Allen, Carl E. , Charlotte, Frédéric , Egeler, R. Maarten , Herrera, Juana Gil, Henter, Jan‐Inge , Jankú, Filip , Mérad, Miriam , Rollins, Barret J., Tazi, Abdellatif , Vassallo, Robert , Weiss, Lawrence M. , Astigarraga, Itziar , Donadieu, Jean , Abdel‐Wahab, Omar , Diamond, Eli L. , Fischer, Alain , Picarsic, Jennifer , Rodríguez‐Galindo, Carlos , Vassallo, Robert , Emile, Jean-François , Allen, Carl E

Mayo Clinic

Blood | March 10, 2016 | Volume: 127 | Issue: 22 | Pages: 2672-2681

10.1182/blood-2016-01-690636 | PMID 26966089 Get It

Abstract The histiocytoses are rare disorders characterized by the accumulation of macrophage, dendritic cell, or monocyte-derived cells in various tissues and organs of children and adults. More than 100 different subtypes have been described, with a wide range of clinical manifestations, presentations, and histologies. Since the first classification in 1987, a number of new findings regarding the cellular origins, molecular pathology, and clinical features of histiocytic disorders have been identified. We propose herein a revision of the classification of histiocytoses based on histology, phenotype, molecular alterations, and clinical and imaging characteristics. This revised classification system consists of 5 groups of diseases: (1) Langerhans-related, (2) cutaneous and mucocutaneous, and (3) malignant histiocytoses as well as (4) Rosai-Dorfman disease and (5) hemophagocytic lymphohistiocytosis and macrophage activation syndrome. Herein, we provide guidelines and recommendations for diagnoses of these disorders.
First-in-Human Phase I/II Study of NEOD001 in Patients With Light Chain Amyloidosis and Persistent Organ Dysfunction
Landau, Heather , Comenzo, Raymond L. , Seldin, David C. , Weiss, Brendan M. , Zonder, Jeffrey A. , Merlini, Giampaolo , Schönland, Stefan , Walling, Jackie , Kinney, Gene G. , Koller, Martin, Schenk, Dale B., Guthrie, Spencer , Liedtke, Michaela , Seldin, David, Weiss, Brendan, Zonder, Jeffrey, Guthrie, Spencer D, Gertz, Morie A. , Merlini, Giampaolo , Schönland, Stefan

Mayo Clinic

Journal of Clinical Oncology | February 8, 2016 | Volume: 34 | Issue: 10 | Pages: 1097-1103

10.1200/jco.2015.63.6530 | PMID 26858336 Get It

Purpose Light chain (AL) amyloidosis is caused by the accumulation of misfolded proteins, which induces the dysfunction of vital organs. NEOD001 is a monoclonal antibody targeting these misfolded proteins. We report interim data from a phase I/II dose-escalation/expansion study of NEOD001 in patients with AL amyloidosis and persistent organ dysfunction (NCT01707264). Patients and Methods Patients who had completed at least one previous anti–plasma cell-directed therapy, had partial hematologic response or better, and had persistent organ dysfunction received NEOD001 intravenously every 28 days. Dose levels of 0.5, 1, 2, 4, 8, 16, and 24 mg/kg were evaluated (3 + 3 study design). Primary objectives were to determine the maximum tolerated dose and the recommended dose for future studies and to evaluate safety/tolerability. Secondary and exploratory objectives included pharmacokinetics, immunogenicity, and organ responses on the basis of published consensus criteria. Results Twenty-seven patients were enrolled in seven cohorts (dose-escalation component). No drug-related serious adverse events (AEs), discontinuations because of drug-related AEs, dose-limiting toxicities, or antidrug antibodies were reported. The most frequent AEs were fatigue, upper respiratory tract infection, cough, and dyspnea. Recommended dosing was 24 mg/kg. Pharmacokinetics support intravenous dosing every 28 days. Of 14 cardiac-evaluable patients, eight (57%) met the criteria for cardiac response and six (43%) had stable disease. Of 15 renal-evaluable patients, nine (60%) met the criteria for renal response and six (40%) had stable disease. Conclusion Monthly infusions of NEOD001 were safe and well tolerated. Recommended future dosing was 24 mg/kg. Organ response rates compared favorably with those reported previously for chemotherapy. A phase II expansion is ongoing. A global phase III study (NCT02312206) has been initiated. Antibody therapy targeting misfolded proteins is a potential new therapy for the management of AL amyloidosis.
Phase I Study of PSMA-Targeted Docetaxel-Containing Nanoparticle BIND-014 in Patients with Advanced Solid Tumors
Hoff, Daniel D. Von , Mita, Monica , Ramanathan, Ramesh K., Mita, Alain C. , LoRusso, Patricia , Burris, Howard A. , Hart, Lowell L., Low, Susan C. , Parsons, Donald M., Zale, Stephen E., Summa, Jason M., Youssoufian, Hagop , Sachdev, Jasgit C. , Weiss, Glen J.

Mayo Clinic

Clinical Cancer Research | February 4, 2016 | Volume: 22 | Issue: 13 | Pages: 3157-3163

10.1158/1078-0432.ccr-15-2548 | PMID 26847057 Get It

Abstract Purpose: First-in-human phase I trial to determine the safety, pharmacokinetics, and antitumor activity of BIND-014, a novel, tumor prostate-specific membrane antigen (PSMA)–targeted nanoparticle, containing docetaxel. Experimental Design: Patients with advanced solid tumors received BIND-014 every three weeks (n = 28) or weekly (n = 27), with dose levels ranging from 3.5 to 75 mg/m2 and 15 to 45 mg/m2, respectively. Results: BIND-014 was generally well tolerated, with no unexpected toxicities. The most common drug-related toxicities (>20% of patients) on either schedule included neutropenia, fatigue, anemia, alopecia, and diarrhea. BIND-014 demonstrated a dose-linear pharmacokinetic profile, distinct from docetaxel, with prolonged persistence of docetaxel-encapsulated circulating nanoparticles. Of the 52 patients evaluable for response, one had a complete response (cervical cancer on the every three week schedule) and five had partial responses (ampullary adenocarcinoma, non–small cell lung, and prostate cancers on the every-three-week schedule, and breast and gastroesophageal cancers on the weekly schedule). Responses were noted in both PSMA-detectable and -undetectable tumors. Conclusions: BIND-014 was generally well tolerated, with predictable and manageable toxicity and a unique pharmacokinetic profile compared with conventional docetaxel. Clinical activity was noted in multiple tumor types. The recommended phase II dose of BIND-014 is 60 mg/m2 every three weeks or 40 mg/m2 weekly. Clin Cancer Res; 22(13); 3157–63. ©2016 AACR.
Critically re-evaluating a common technique
Geisbush, Thomas , Jones, Lyell K. , Weiss, Michael , Mozaffar, Tahseen , Gronseth, Gary , Rutkove, Seward B. , Narayanaswami, Pushpa , Jones, Lyell K

Mayo Clinic

Neurology | December 24, 2015 | Volume: 86 | Issue: 3 | Pages: 218-223

10.1212/wnl.0000000000002292 | PMID 26701380 Get It

Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine
Burns, Ted M., Smith, Gordon, Allen, Jeffrey A. , Amato, Anthony A. , Arnold, W. David , Barohn, Richard J., Benatar, Michael , Bird, Shawn J. , Bromberg, Mark B. , Chahin, Nizar, Ciafaloni, Emma , Corse, Andrea M. , David, William S., Dimberg, Elliot L., Sousa, De , Donofrio, Peter D., Dyck, P. James B. , Engel, Andrew G. , Ensrud, Erik , Ferrante, Mark A., Freimer, Miriam , Gable, Karissa , Gibson, Summer, Gilchrist, James M. , Goldstein, Jonathan , Gooch, Clifton L. , Goodman, Brent P., Gorelov, Dmitri, Gospe, Sídney M. , Goyal, Namita , Guidon, Amanda C. , Guptill, Jeffrey T. , Gutmann, Laurie , Gutmann, Ludwig , Gwathmey, Kelly , Harati, Yadollah, Harper, C. Michel , Hehir, Michael K. , Hobson‐Webb, Lisa D., Howard, James F. , Jackson, Carlayne E. , Jones, Sarah , Juel, Vern C. , Kaminski, Henry J. , Kennelly, Kathleen D., Khella, Sami, Khoury, Julie, Kincaid, John C., Kissel, John T., Kolb, Noah , Lacomis, David , Larriviere, Daniel G., Lewis, Richard A. , Litchy, William J. , Logigian, Eric L. , Lou, Jau-Shin, MacGowen, Daniel J.L., Maselli, Ricardo A. , Massey, Janice M., Mauermann, Michelle L. , Mathews, Katherine D. , Meriggioli, Matthew N. , Moon, Joon-Shik, Mozaffar, Tahseen , Nations, Sharon , Ostrow, Lyle W. , Pascuzzi, Robert M. , Peltier, Amanda , Ruzhansky, Katherine , Ross, Mark A., Rubin, Devon I., Russell, James A., Sachs, George, Salajegheh, Mohammad, Saperstein, David , Scelsa, Stephen N. , Selcen, Duygu , Shaibani, Aziz , Silvestri, Nicholas J. , Singleton, J. Rob, Smith, Benn E., So, Yuen T., Solórzano, Guillermo, Sorenson, Eric J. , Srinivasen, Jayashri, Tavee, Jinny , Tawil, Rabi , Thaisetthawatkul, Pariwat , Thornton, Charles A. , Trivedi, Jaya , Vernino, Steven , Wang, Annabel K., Webb, Tyler A., Weiss, Michael D. , Windebank, Anthony J. , Wolfe, Gil I. , Crum, Brian A. , Dimberg, Elliot, Chahin, Nizar, Cohen, Jeffrey Allen , Johnson, Nicholas E , Karam, Chafic , Ladha, Shafeeq , Li, Yuebing , Miller, Robert G. , Nowak, Richard J. , Richman, David P. , Shieh, Perry B. , Kolb, Noah A , Mauermann, Michelle L , Gutmann, Laurie , Allen, Jeffrey A , Arnold, W David , Vernino, Steven , Kaminski, Henry

Mayo Clinic

Muscle & Nerve | December 13, 2015 | Volume: 53 | Issue: 2 | Pages: 165-168

10.1002/mus.25009 | PMID 26662952 Get It

Psychosocial Dimensions and Functioning in Youth With Postural Orthostatic Tachycardia Syndrome
McTate, Emily , Weiss, Karen E. , McTate, Emily

Mayo Clinic

Clinical Pediatrics | November 18, 2015 | Volume: 55 | Issue: 10 | Pages: 979-982

10.1177/0009922815616890 | PMID 26581359 Get It

Interdomain B in ZAP-70 Regulates but Is Not Required for ZAP-70 Signaling Function in Lymphocytes
Zhao, Qihong , Williams, Brandi L., Abraham, Robert T. , Weiss, Arthur

Mayo Clinic

Molecular and Cellular Biology | October 26, 2015 | Volume: 19 | Issue: 1 | Pages: 948-956

10.1128/mcb.19.1.948 | PMID 9858619 Get It

Improved Outcomes After Autologous Hematopoietic Cell Transplantation for Light Chain Amyloidosis: A Center for International Blood and Marrow Transplant Research Study
D’Souza, Anita , Dispenzieri, Angela , Wirk, Baldeep , Zhang, Mei-Jie , Kyle, Robert A. , Kumar, Shaji , Comenzo, Raymond L. , Cornell, Robert F. , Weiss, Brendan M. , Freytes, César O. , Scott, Emma C. , Landau, Heather , Moreb, Jan S. , Costa, Luciano J. , Ramanathan, Muthalagu , Kamble, Rammurti T., Olsson, Richard F. , Ganguly, Siddhartha , Kindwall‐Keller, Tamila L. , Hari, Parameswaran , Huang, Jiaxing, Peter Gale, Robert, Savani, Bipin N. , Vogl, Dan T. , Landau, Heather J., Callander, Natalie S. , Nishihori, Taiga , Kindwall-Keller, Tamila L, Mark, Tomer M, Zhang, Mei‐Jie , Huang, Jiaxing , Gertz, Morie A. , Gale, Robert Peter , Lazarus, Hillard M. , Wood, William A. , Mark, Tomer M , D'Souza, Anita , Dispenzieri, Angela , Olsson, Richard F , Costa, Luciano J , Hari, Parameswaran

Mayo Clinic

Journal of Clinical Oncology | September 14, 2015 | Volume: 33 | Issue: 32 | Pages: 3741-3749

10.1200/jco.2015.62.4015 | PMID 26371138 Get It

Purpose Autologous hematopoietic cell transplantation, or autotransplantation, is effective in light-chain amyloidosis (AL), but it is associated with a high risk of early mortality (EM). In a multicenter randomized comparison against oral chemotherapy, autotransplantation was associated with 24% EM. We analyzed trends in outcomes after autologous hematopoietic cell transplantation for AL in North America. Patients and Methods Between 1995 and 2012, 1,536 patients with AL who underwent autotransplantation at 134 centers were identified in the Center for International Blood and Marrow Transplant Research database. EM and overall survival (OS) were analyzed in three time cohorts: 1995 to 2000 (n = 140), 2001 to 2006 (n = 596), and 2007 to 2012 (n = 800). Hematologic and renal responses and factors associated with EM, relapse and/or progression, progression-free survival and OS were analyzed in more recent subgroups from 2001 to 2006 (n = 197) and from 2007 to 2012 (n = 157). Results Mortality at 30 and 100 days progressively declined over successive time periods from 11% and 20%, respectively, in 1995 to 2000 to 5% and 11%, respectively, in 2001 to 2006, and to 3% and 5%, respectively, in 2007 to 2012. Correspondingly, 5-year OS improved from 55% in 1995 to 2000 to 61% in 2001 to 2006 and to 77% in 2007 to 2012. Hematologic response to transplantation improved in the latest cohort. Renal response rate was 32%. Centers performing more than four AL transplantations per year had superior survival outcomes. In the multivariable analysis, cardiac AL was associated with high EM and inferior progression-free survival and OS. Autotransplantation in 2007 to 2012 and use of higher dosages of melphalan were associated with a lowered relapse risk. A Karnofsky score less than 80 and creatinine levels 2 mg/m2 or greater were associated with worsened OS. Conclusion Post-transplantation survival in AL has improved, with a dramatic reduction in early post-transplantation mortality and excellent 5-year survival. The risk-benefit ratio for autotransplantation has changed, and randomized comparison with nontransplantation approaches is again warranted.