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Myeloma today: Disease definitions and treatment advances
Rajkumar, S. Vincent

Mayo Clinic

American Journal of Hematology | November 13, 2015 | Volume: 91 | Issue: 1 | Pages: 90-100

10.1002/ajh.24236 | PMID 26565896 Get It

There have been major advances in the diagnosis, staging, risk‐stratification, and management of multiple myeloma (MM). In addition to established CRAB (hypercalcemia, renal failure, anemia, and lytic bone lesions) features, new diagnostic criteria include three new biomarkers to diagnose the disease: bone marrow clonal plasmacytosis ≥60%, serum involved/uninvolved free light chain ratio ≥100, and >1 focal lesion on magnetic resonance imaging. MM can be classified into several subtypes based on baseline cytogenetics, and prognosis varies according to underlying cytogenetic abnormalities. A Revised International Staging System has been developed which combines markers of tumor burden (albumin, beta‐2 microglobulin) with markers of aggressive disease biology (high‐risk cytogenetics and elevated serum lactate dehydrogenase). Although the approach to therapy remains largely the same, the treatment options at every stage of the disease have changed. Carfilzomib, pomalidomide, panobinostat, daratumumab, elotuzumab, and ixazomib have been approved for the treatment of the disease. These drugs combined with older agents such as cyclophosphamide, dexamethasone, thalidomide, bortezomib, and lenalidomide dramatically increase the repertoire of regimens available for the treatment of MM. This review provides a concise overview of recent advances in MM, including updates to diagnostic criteria, staging, risk‐stratification, and management. Am. J. Hematol. 91:90–100, 2016. © 2015 Wiley Periodicals, Inc.
AASLD guidelines for treatment of chronic hepatitis B
Bzowej, Natalie, Chang, Kyong‐Mi , Hwang, Jessica , Jonas, Maureen M. , Murad, M. Hassan , Terrault, Norah A. , Murad, M Hassan , Chang, Kyong-Mi

Mayo Clinic

Hepatology | November 13, 2015 | Volume: 63 | Issue: 1 | Pages: 261-283

10.1002/hep.28156 | PMID 26566064 Get It

Antiviral therapy for chronic hepatitis B viral infection in adults: A systematic review and meta‐analysis
McMahon, Brian J. , Brown, Robert S., Wong, John B. , Ahmed, Ahmed T. , Farah, Wigdan , Almasri, Jehad , Alahdab, Fares , Benkhadra, Khalid, Mouchli, Mohamed A., Singh, Siddharth , Mohamed, Essa A. , Dabrh, Abd Moain Abu , Murad, M. Hassan , Mohammed, Khaled , Abu Dabrh, Abd Moain, Murad, Mohammad Hassan, Lok, Anna S. , Prokop, Larry J. , Wang, Zhen , Murad, M Hassan , Abu Dabrh, Abd Moain , Farah, Wigdan , Alahdab, Fares

Mayo Clinic

Hepatology | November 13, 2015 | Volume: 63 | Issue: 1 | Pages: 284-306

10.1002/hep.28280 | PMID 26566246 Get It

Chronic hepatitis B viral (HBV) infection remains a significant global health problem. Evidence‐based guidelines are needed to help providers determine when treatment should be initiated, which medication is most appropriate, and when treatment can safely be stopped. The American Association for the Study of Liver Diseases HBV guideline methodology and writing committees developed a protocol a priori for this systematic review. We searched multiple databases for randomized controlled trials and controlled observational studies that enrolled adults ≥18 years old diagnosed with chronic HBV infection who received antiviral therapy. Data extraction was done by pairs of independent reviewers. We included 73 studies, of which 59 (15 randomized controlled trials and 44 observational studies) reported clinical outcomes. Moderate‐quality evidence supported the effectiveness of antiviral therapy in patients with immune active chronic HBV infection in reducing the risk of cirrhosis, decompensated liver disease, and hepatocellular carcinoma. In immune tolerant patients, moderate‐quality evidence supports improved intermediate outcomes with antiviral therapy. Only very low‐quality evidence informed the questions about discontinuing versus continuing antiviral therapy in hepatitis B e antigen‐positive patients who seroconverted from hepatitis B e antigen to hepatitis B e antibody and about the safety of entecavir versus tenofovir. Noncomparative and indirect evidence was available for questions about stopping versus continuing antiviral therapy in hepatitis B e antigen‐negative patients, monotherapy versus adding a second agent in patients with persistent viremia during treatment, and the effectiveness of antivirals in compensated cirrhosis with low‐level viremia. Conclusion: Most of the current literature focuses on the immune active phases of chronic HBV infection; decision‐making in other commonly encountered and challenging clinical settings depends on indirect evidence. (H epatology 2016;63:284–306)
Critical Appraisal and Review of Management Strategies for Severe Fibrosis During Penile Implant Surgery
Trost, Landon , Patil, Mukul, Kramer, Andrew

Mayo Clinic

The Journal of Sexual Medicine | November 13, 2015 | Volume: 12 | Issue: Supplement_7 | Pages: 439-447

10.1111/jsm.12985 | PMID 26565574 Get It

Abstract Introduction Penile corporal fibrosis represents a challenging clinical scenario for surgeons placing penile prostheses (PP). Because of its rarity, a small number of series with limited follow-up have reported outcomes in this cohort. Aim The aim of this study was to perform a critical appraisal of the corporal excavation technique, discuss its relevance to contemporary practice, and review alternative surgical methods and outcomes. Methods A critical review was performed of the 2006 article by Montague and Angermeier, “Corporeal excavation: new technique for penile prosthesis implantation in men with severe corporeal fibrosis.” Notable inclusions and omissions were described, with emphasis placed on methodology and outcomes. A PubMed search from 1990 to June 2015 was then performed to review and summarize the literature on managing corporal fibrosis during PP surgery. Main Outcome Measures The main outcome measures used were the major contributions and limitations of the 2006 article describing outcomes of the corporal excavation technique. Results Corporal excavation is a relevant surgical technique for managing severe corporal fibrosis. Compared with alternatives, excavation achieves successful placement of PP without need for grafting and with few complications. The article was limited by several notable omissions including relevant patient demographic and disease characteristics, patient selection, and minimal descriptions of complications and outcomes. Alternative techniques include use of specialized dilators, counter incisions, reconstruction with graft placement, minimal scar tissue excision, and endoscopic resection. Because of limited data, no specific algorithm for managing corporal fibrosis can be prescribed. Conclusions Corporal fibrosis is a challenging clinical scenario and requires surgical experience and specialized techniques to manage appropriately. Corporal excavation represents one of several viable techniques, which may be chosen based on surgeon’s preference and clinical factors.
Sex Steroids Influence Brain-Derived Neurotropic Factor Secretion From Human Airway Smooth Muscle Cells
Wang, Sheng-Yu, Freeman, Michelle, Sathish, Venkatachalem , Prakash, Y. S. , Freeman, Michelle R, Wang, Sheng-Yu, Thompson, Michael A. , Pabelick, Christina M. , Prakash, Y S , Sathish, Venkatachalem

Mayo Clinic

Journal of Cellular Physiology | November 13, 2015 | Volume: 231 | Issue: 7 | Pages: 1586-1592

10.1002/jcp.25254 | PMID 26566264 Get It

Impact of access to NCI‐ and NCCN‐designated cancer centers on outcomes for multiple myeloma patients: A SEER registry analysis
Advani, Pooja , Yang, Dongyun , Ghosh, Radhika , Swaika, Abhisek, Foran, James M. , Colón‐Otero, Gerardo , Chanan‐Khan, Asher , Chanan-Khan, Asher, Ailawadhi, Sikander , Roy, Vivek

Mayo Clinic

Cancer | November 13, 2015 | Volume: 122 | Issue: 4 | Pages: 618-625

10.1002/cncr.29771 | PMID 26565660 Get It

BACKGROUNDNational Cancer Institute (NCI)/National Comprehensive Cancer Network (NCCN)–designated cancer centers (CCs) offer patients state‐of‐the‐art treatment, but their impact on multiple myeloma (MM) patient outcomes has not been evaluated.METHODSAdult MM patients diagnosed between 1973 and 2011 were identified from the Surveillance, Epidemiology, and End Results database and were stratified by the county of residence at the time of diagnosis and the year of CC designation. The influence of NCI/NCCN CC access, race, and the year of diagnosis on overall survival (OS) was evaluated with a Cox regression model.RESULTSA statistically significant OS improvement was noted in patients diagnosed after 1995 with access to 2 or more NCI CCs overall (P = .002 for 1996‐2002; P < .001 for 2003‐2011) and by race for whites (hazard ratio [HR] for 1996‐2002, 0.85; 95% confidence interval [CI], 0.78‐0.91; HR for 2003‐2011, 0.85; 95% CI, 0.79‐0.91) but not for nonwhites. For NCCN access, improvement was seen in 1996‐2002 (P = .003), in 2003‐2011 (P < .001), and by race for whites (HR, 0.917; 95% CI, 0.88‐0.95) and nonwhites (0.94; 95% CI, 0.89‐0.99), but within nonwhites, this was true only for African Americans (AAs; HR, 0.88; 95% CI, 0.81‐0.97) and not for Asians, Hispanics, or Native Americans.CONCLUSIONSImprovement in OS was seen in MM patients diagnosed after 1995 with access to 1 NCCN CC or 2 or more NCI CCs. NCI access benefited only whites, whereas NCCN access benefited only white and AA patients. No OS benefit was seen for any subgroup with access to only 1 NCI center. Eliminating racial disparities in health care access and utilization is needed to improve outcomes. Cancer 2016;122:618–625. © 2015 American Cancer Society.
It's not too late: a proposal to standardize the terminology of “late‐onset” cytomegalovirus infection and disease in solid organ transplant recipients
Razonable, Raymund R. , Blumberg, Emily A.

Mayo Clinic

Transplant Infectious Disease | November 13, 2015 | Volume: 17 | Issue: 6 | Pages: 779-784

10.1111/tid.12447 | PMID 26771688 Get It

Salvage autologous fascial sling after failed synthetic midurethral sling: Greater than 3‐year outcomes
Petrou, Steven P. , Davidiuk, Andrew, Rawal, Bhupendra, Thiel, David D. , Davidiuk, Andrew J, Arnold, Michelle, Arnold, Michelle L.

Mayo Clinic

International Journal of Urology | November 13, 2015 | Volume: 23 | Issue: 2 | Pages: 178-181

10.1111/iju.13003 | PMID 26563492 Get It

ObjectiveTo determine long‐term surgical outcomes of salvage autologous fascial sling placement after a failed synthetic midurethral sling.MethodsWomen who had undergone autologous fascial sling placement without concomitant pelvic surgery for a failed synthetic midurethral sling utilizing mesh with a minimum follow up of 36 months were identified. Charts were reviewed, and patients were contacted by telephone. Success was determined by the Patient Global Impression of Improvement. Secondary measures included the Incontinence Severity Index questionnaire, patient recommendation of the autologous fascial sling and need for further incontinence surgery.ResultsA total of 35 patients met the criteria, and 21 were successfully contacted. Of those contacted, the median age at surgery was 67 years (range 53–81 years) and at the time of the survey was 75 years (range 63–84 years) with median follow up of 74 months (range 36–127 years). Preoperatively, 12 patients (57.1%) had urethral hypermobility and 13 patients (61.9%) had mixed urinary incontinence. Eight patients (38.1%) had concomitant sling excision with five of those combined with urethrolysis at the time of the salvage operation. Patient Global Impression of Improvement success was noted in 16 patients (76.2%). A total of 11 patients (52.4%) were dry or had slight incontinence by the Incontinence Severity Index. One patient required additional anti‐incontinence surgery (4.8%). A total of 18 patients (85.7%) recommended the autologous fascial sling. No statistical impact was noted with sling excision (P = 0.62), mixed urinary incontinence (P = 0.61), age at surgery (P = 0.23), age at follow up (P = 0.15), length of follow up (P = 0.71) or first surgery type (transobturator tape vs retropubic; P = 1.00).ConclusionsAutologous fascial sling provides reasonable long‐term success as a salvage operation for failed midurethral slings.
Vasculitic neuropathy following exposure to minocycline
Baratta, John M. , Dyck, P. James B. , Brand, Patricio , Thaisetthawatkul, Pariwat , Engelstad, JaNean , Goodman, Brent P., Goodman, Brent, Karam, Chafic , Baratta, John M

Mayo Clinic

Neurology Neuroimmunology & Neuroinflammation | November 13, 2015 | Volume: 3 | Issue: 1 | Pages: No page available

10.1212/nxi.0000000000000180 | PMID 26601119 Get It

Hormonal and Reproductive Factors and Risk of Myeloproliferative Neoplasms in Postmenopausal Women
Leal, Alexis D. , Thompson, Carrie A. , Wang, Alice H., Vierkant, Robert A. , Ross, Julie A. , Virnig, Beth A , Habermann, Thomas M. , Mesa, Ruben A. , Cerhan, James R. , Vierkant, Robert A

Mayo Clinic

Cancer Epidemiology, Biomarkers & Prevention | November 13, 2015 | Volume: 25 | Issue: 1 | Pages: 151-157

10.1158/1055-9965.epi-15-0613 | PMID 26564251 Get It

AbstractBackground: Hormonal and reproductive history has been associated with risk of some hematologic malignancies, but their role in myeloproliferative neoplasms (MPN) is largely unknown.Methods: Using a population-based cohort study, we evaluated the association of these factors with risk of MPN overall, and for essential thrombocythemia (ET) and polycythemia vera (PV) specifically. Incident MPN cases from 1993 to 2004 were identified via linkage to Medicare. RR and 95% confidence intervals (CI) were estimated utilizing Cox proportional hazard regression.Results: After &gt;250,000 person-years of follow-up, 257 cases of MPN were identified (172 ET, 64 PV). Ever use of hormone therapy (HT) was associated with an increased risk of ET (RR = 1.63; 95% CI, 1.19–2.23) but a decreased risk of PV (RR = 0.58; 95% CI, 0.34–0.98). There were no statistically significant associations of oral contraceptives or reproductive factors with MPN risk overall, or by MPN subtype. Bilateral oophorectomy was associated with increased risk of ET (RR = 1.58; 95% CI, 1.11–2.25) and decreased risk of PV (RR = 0.32; 95% CI, 0.12–0.88). There was no association of ovulatory years with ET risk; however, there was increased risk of PV (RR = 1.68 for &gt;36.8 compared with ≤27.6 years; P trend = 0.045). Adjustment for potential confounding factors did not alter these associations.Conclusions: HT use and bilateral oophorectomy had opposite associations for ET and PV. Except for ovulatory years and PV risk, reproductive history did not appear to play a role in the etiology of MPN.Impact: This study suggests different mechanistic impacts of estrogen, and perhaps distinct etiologies, for the two major MPN subtypes. Cancer Epidemiol Biomarkers Prev; 25(1); 151–7. ©2015 AACR.