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3473 citation(s) found for "Dana, SE".

Follow-Up Care, Surveillance Protocol, and Secondary Prevention Measures for Survivors of Colorectal Cancer: American Society of Clinical Oncology Clinical Practice Guideline Endorsement
Meyerhardt, Jeffrey A. , Mangu, Pamela B., Flynn, Patrick J. , Korde, Larissa A. , Loprinzi, Charles L. , Minsky, Bruce D. , Petrelli, Nicholas J. , Ryan, Kim, Schrag, Deborah H., Wong, Sandra L. , Benson, Al B. , Schrag, Deborah , Meyerhardt, Jeffrey A , Wong, Sandra

Journal of Clinical Oncology | November 12, 2013 | Volume: 31 | Issue: 35 | Pages: 4465-4470

10.1200/jco.2013.50.7442 | PMID 24220554 Get It

Purpose The American Society of Clinical Oncology (ASCO) has a policy and set of procedures for endorsing recent clinical practice guidelines that have been developed by other professional organizations. Methods The Cancer Care Ontario (CCO) Guideline on Follow-up Care, Surveillance Protocol, and Secondary Prevention Measures for Survivors of Colorectal Cancer was reviewed by ASCO for methodologic rigor and considered for endorsement. Results The ASCO Panel concurred with the CCO recommendations and recommended endorsement, with the addition of several qualifying statements. Conclusion Surveillance should be guided by presumed risk of recurrence and functional status of the patient (important within the first 2 to 4 years). Medical history, physical examination, and carcinoembryonic antigen testing should be performed every 3 to 6 months for 5 years. Patients at higher risk of recurrence should be considered for testing in the more frequent end of the range. A computed tomography scan (abdominal and chest) is recommended annually for 3 years, in most cases. Positron emission tomography scans should not be used for surveillance outside of a clinical trial. A surveillance colonoscopy should be performed 1 year after the initial surgery and then every 5 years, dictated by the findings of the previous one. If a colonoscopy was not preformed before diagnosis, it should be done after completion of adjuvant therapy (before 1 year). Secondary prevention (maintaining a healthy body weight and active lifestyle) is recommended. If a patient is not a candidate for surgery or systemic therapy because of severe comorbid conditions, surveillance tests should not be performed. A treatment plan from the specialist should have clear directions on appropriate follow-up by a nonspecialist.
Health-related quality of life in children and young adults with post-thrombotic syndrome: Results from a cross-sectional study
Kumar, Riten , Rodriguez, Vilmarie , Matsumoto, Jane M., Khan, Shakila P. , Weaver, Amy L. , McBane, Robert D. , Beebe, Timothy J. , Heit, John A. , McBane, Robert , Kumar, Riten

Pediatric Blood & Cancer | November 6, 2013 | Volume: 61 | Issue: 3 | Pages: 546-551

10.1002/pbc.24840 | PMID 24347376 Get It

Spectral characteristics of breast vibro-acoustography images
Whaley, Dana H. , Urban, Matthew W. , Kinnick, Randall R., Greenleaf, James F. , Alizad, Azra , Fatemi, Mostafa , Urban, Matthew W

The Journal of the Acoustical Society of America | October 31, 2013 | Volume: 120 | Issue: 5_Supplement | Pages: 3269-3269

10.1121/1.4776997 Get It

Vibro-acoustography image is a function of the dynamic characteristics of the object at the vibration (difference) frequency (df). The dynamic characteristic of tissue is closely related to pathology. Therefore, it is important to evaluate image features versus df. Here, the influence of df on breast vibro-acoustography images is studied by scanning human breast at various df values ranging from 20 to 90 kHz. The subjects were chosen from a group of volunteers with different breast abnormalities. Images were compared subjectively to study image features and the appearances of breast lesions versus df. It is demonstrated that having a collection of images of the same tissue at different df values generally provides a better perception of the tissue structure and improves lesion identification. In most cases, higher df resulted in a higher signal-to-noise ratio and thus a higher image quality. Finally, a frequency-compounded images was obtained by calculating the weighted sum of images at different df values. It is demonstrated that image compounding normally improves visualization of breast tissue and abnormalities. [Work supported by NIH Grant EB-00535 and Grant BCTR0504550 from the Susan G. Komen Breast Cancer Foundation. Disclosure: Parts of the techniques used here are patented by MF and JFG.]
Long‐term results of the phase II trial of the oral mTOR inhibitor everolimus (RAD001) in relapsed or refractory Waldenstrom Macroglobulinemia
Ghobrial, Irene M. , LaPlant, Betsy, Hayman, Suzanne R. , Camoriano, John , Lacy, Martha Q. , Bergsagel, P. Leif , Chuma, Stacey, Bergsagel, P. Leif , Witzig, Thomas E. , Gertz, Morie A. , DeAngelo, Daniel J. , Treon, Steven P. , Ghobrial, Irene M

American Journal of Hematology | October 29, 2013 | Volume: 89 | Issue: 3 | Pages: 237-242

10.1002/ajh.23620 | PMID 24716234 Get It

Everolimus is an oral raptor mTOR inhibitor and has shown activity in patients with Waldenstrom's macroglobulinemia (WM). This study examines a large cohort of patients with relapsed/refractory WM with long‐term follow up for survival. Patients were eligible if they had measurable disease, a platelet count >75,000 × 106/L, an absolute neutrophil count >1,000 × 106/L. Patients received everolimus 10 mg PO daily and were evaluated monthly. A success was defined as a complete or partial response (PR); minor responses (MR) were recorded and considered to be of clinical benefit. Sixty patients were enrolled and treated. The overall response rate (ORR) was 50% (all PR); the clinical benefit rate including MR or better was 73% (95% CI: 60–84%) with 23% MR. The median time to response for patients who achieved PR was 2 months (range, 1–26). The median duration of response has not been reached and median progression‐free survival (PFS) was 21 months. Grade 3 or higher toxicities (at least possibly related to everolimus) were observed in 67% of patients. The most common grade 3 or 4 toxicities were anemia (27%), leukopenia (22%), and thrombocytopenia (20%). Other nonhematological toxicities were diarrhea (5%), fatigue (8%), stomatitis (8%) and pulmonary toxicity (5%). Everolimus has a high single‐agent activity of 73% including MR, with a progression free survival of 21 months, indicating that this agent is active in relapsed/refractory WM. Am. J. Hematol. 89:237–242, 2014. © 2013 Wiley Periodicals, Inc
Progress in breast vibro-acoustography: Imaging breast lesions
Whaley, Dana H. , Greenleaf, James F. , Alizad, Azra , Fatemi, Mostafa

The Journal of the Acoustical Society of America | October 25, 2013 | Volume: 121 | Issue: 5_Supplement | Pages: 3110-3110

10.1121/1.4782045 Get It

Vibro-acoustography is an imaging method based on the sound emitted due to the harmonic motion of tissue induced by the radiation force of focused ultrasound. This paper presents recent progress in vibro-acoustography of human breast. Matching vibro-acoustography and mammography images are acquired using a combined mammography/vibro-acoustography machine. Images of various types of breast masses are investigated and their characteristics features are compared. The study includes malignant masses, benign masses such as fibroadenomas, cysts, calcified lesions, and surgical scars. Image features, such as lesion borders, interior texture, and speculation pattern, are studied. Vibro-acoustography images demonstrate that calcified masses normally show sharp borders, benign noncalcified masses have smooth texture, and, in some cases, malignant masses are characterized with spiculation. These results, which are based on the data collected from an ongoing study, indicate that the above-mentioned image features may be used for differentiation of breast masses. It is noted that more data from a larger population are needed to establish the results in a statistical sense. [Work supported by NIH Grant EB-00535 and Grant BCTR0504550 from the Susan G. Komen Breast Cancer Foundation. Disclosure: Parts of the techniques used here are patented by MF and JFG.]
In vivo breast vibro-acoustography
Whaley, Dana H. , Greenleaf, James F. , Fatemi, Mostafa , Alizad, Azra

The Journal of the Acoustical Society of America | October 23, 2013 | Volume: 117 | Issue: 4_Supplement | Pages: 2586-2586

10.1121/1.4809451 Get It

Vibro-acoustography is based on audio-frequency harmonic vibrations induced in the object by the radiation force of focused ultrasound. The resulting object vibration produces a hydrophone detectable acoustic emission that is a function of regional dynamic properties of the object at the vibration frequency. The amplitude of the hydrophone signal is mapped into an image that represents the object’s vibro-acoustic response to the radiation force by scanning the focused ultrasound across the object. Contrast in Vibro-acoustography images represent several properties of the object, including the dynamic characteristics at the audio frequency and scattering and absorption properties at the ultrasound frequency. A Vibro-acoustography system has been combined with a stereo-tactic x-ray mammography system for in vivo breast imaging and has been tested on a number of volunteers. Resulting images show soft tissue structures and microcalcifications within breast with high contrast, high resolution, and no speckles. The results have been verified using x-ray mammograms of the breast. The encouraging results from in vitro and in vivo experiments suggest further development of vibro-acoustography may lead to a new clinical breast imaging modality. [Work supported in part by a grant from the Susan G. Komen Breast Cancer Foundation. Vibro-acoustography is patented by MF and JFG.]
Lipid droplet breakdown requires Dynamin 2 for vesiculation of autolysosomal tubules in hepatocytes
Schulze, Ryan J. , Weller, Shaun G. , Schroeder, Barbara, Krueger, Eugene W. , Chi, Susan , McNiven, Mark A. , Casey, Carol A.

Journal of Cell Biology | October 21, 2013 | Volume: 203 | Issue: 2 | Pages: 315-326

10.1083/jcb.201306140 | PMID 24145164 Get It

Lipid droplets (LDs) are lipid storage organelles that in hepatocytes may be catabolized by autophagy for use as an energy source, but the membrane-trafficking machinery regulating such a process is poorly characterized. We hypothesized that the large GTPase Dynamin 2 (Dyn2), well known for its involvement in membrane deformation and cellular protein trafficking, could orchestrate autophagy-mediated LD breakdown. Accordingly, depletion or pharmacologic inhibition of Dyn2 led to a substantial accumulation of LDs in hepatocytes. Strikingly, the targeted disruption of Dyn2 induced a dramatic four- to fivefold increase in the size of autolysosomes. Chronic or acute Dyn2 inhibition combined with nutrient deprivation stimulated the excessive tubulation of these autolysosomal compartments. Importantly, Dyn2 associated with these tubules along their length, and the tubules vesiculated and fragmented in the presence of functional Dyn2. These findings provide new evidence for the participation of the autolysosome in LD metabolism and demonstrate a novel role for dynamin in the function and maturation of an autophagic compartment.
The symptom burden of cancer: Evidence for a core set of cancer‐related and treatment‐related symptoms from the Eastern Cooperative Oncology Group Symptom Outcomes and Practice Patterns study
Cleeland, Charles S. , Chang, Victor T. , Sloan, Jeff A. , O’Mara, Ann M., Weiss, Matthias , Mendoza, Tito R. , Lee, Ju‐Whei, Zhao, Fengmin , Gilman, Paul , Lee, Ju‐Whei , Fisch, Michael , Mendoza, Tito , Chang, Victor T-S

Cancer | October 11, 2013 | Volume: 119 | Issue: 24 | Pages: 4333-4340

10.1002/cncr.28376 | PMID 24114037 Get It

BACKGROUND A set of common cancer‐related and treatment‐related symptoms has been proposed for quality of care assessment and clinical research. Using data from a large, multicenter, prospective study, the authors assessed the effects of disease site and stage on the percentages of patients rating these proposed symptoms as moderate to severe. METHODS The severity of 13 symptoms proposed to represent “core” oncology symptoms was rated by 3106 ambulatory patients with cancer of the breast, prostate, colon/rectum, or lung, regardless of disease stage or phase of care; 2801 patients (90%) repeated the assessment 4 to 5 weeks later. RESULTS At the time of the initial assessment, approximately 33% of the patients reported ≥ 3 symptoms in the moderate‐to‐severe range; 11 of the 13 symptoms were rated as moderate to severe by at least 10% of all patients and 6 were rated as moderate to severe by at least 20% of those receiving active treatment. Fatigue/tiredness was the most severe symptom, followed by disturbed sleep, pain, dry mouth, and numbness/tingling. More patients with lung cancer and patients receiving active treatment reported moderate to severe symptoms. Percentages of symptomatic patients increased by disease stage, less adequate response to therapy, and declining Eastern Cooperative Oncology Group performance status. The percentages of patients reporting moderate to severe symptoms were stable across both assessments. CONCLUSIONS The results of the current study support a core set of moderate to severe symptoms that are common across outpatients with solid tumors, that can guide consideration of progression‐free survival as a trial outcome, and that should be considered in clinical care and in assessments of quality of care and treatment benefit. Cancer 2013;119:4333–4340 . © 2013 American Cancer Society .
Pediatric melanoma: Analysis of an international registry
Averbook, Bruce J., Delman, Keith A. , Gow, Kenneth W. , Sondak, Vernon K. , Messina, Jane L. , Pittelkow, Mark R. , Ecker, Phillip M., Testori, Alessandro , Curiel‐Lewandrowski, Clara , Jukic, D.M., Lee, Sandra J. , Zager, Jonathan S. , Sabel, Michael S. , Markovic, Svetomir N. , Swetter, Susan M. , Leachman, Sancy A. , Go, Ronald S. , Kirkwood, John M.

Cancer | September 11, 2013 | Volume: 119 | Issue: 22 | Pages: 4012-4019

10.1002/cncr.28289 | PMID 24022819 Get It

BACKGROUNDThe management of pediatric melanoma (PM) has largely been extrapolated from adult data. However, the behavior of PM appears to differ from its adult counterparts. Therefore, an international PM registry was created and analyzed.METHODSTwelve institutions contributed deidentified clinicopathologic and outcome data for patients diagnosed with PM from 1953 through 2008.RESULTSOverall survival (OS) data were reported for 365 patients with invasive PM who had adequate follow‐up data. The mean age of the patients was 16 years (range 1 year‐21 years). The 10‐year OS rate, 80.6%, tended to vary by patient age: 100% for those aged birth to 10 years, 69.7% for those aged > 10 years to 15 years, and 79.5% for those aged > 15 years to 20 years (P = .147). Patients with melanomas measuring ≤ 1 mm had a favorable prognosis (10‐year OS rate of 97%), whereas survival was lower but similar for patients with melanomas measuring > 1 mm to 2 mm, > 2 mm to 4 mm, and > 4 mm (70%, 78%, and 80%, respectively; P = .0077). Ulceration and lymph node metastasis were found to be correlated with worse survival (P = .022 and P = .017, respectively). The 10‐year OS rate was 94.1% for patients with American Joint Committee on Cancer stage I disease, 79.6% for those with stage II disease, and 77.1% for patients with stage III disease (P < .001).CONCLUSIONSTumor thickness, ulceration, lymph node status, and stage were found to be significant predictors of survival in patients with PM, similar to adult melanoma. There is a trend toward increased survival in children aged ≤ 10 years versus adolescents aged > 10 years. Further analyses are needed to probe for potential biological and behavioral differences in pediatric versus adult melanoma. Cancer 2013;119:4012–4019. © 2013 American Cancer Society.