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Dive into the research topics where Nancy P. Mendenhall is active.

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Featured researches published by Nancy P. Mendenhall.


International Journal of Radiation Oncology Biology Physics | 1999

Consensus statement on postmastectomy radiation therapy

Jay R. Harris; Pat Halpin-Murphy; Marsha D. McNeese; Nancy P. Mendenhall; Monica Morrow; Nicholas J. Robert

1. Reduction in the recurrence rate of clinically detectable local-regional disease by PMRT is evident. 2. The most recent randomized controlled trials, including two well-designed trials using modern radiation techniques, have shown a moderate and statistically significant improvement in survival. 3. Consultation with a radiation oncologist should occur in postmastectomy node-positive patients. Patients with 4 or more positive lymph nodes should receive radiation therapy to improve local control and perhaps survival as well. Greater benefit was seen in patients with 1-3 positive nodes and in patients with smaller tumor burdens. 4. In all patients, the chest wall should be treated. 5. The treatment of internal mammary nodes remains controversial. 6. A supraclavicular field can be used to encompass the axillary apex and supraclavicular area in selected node-positive patients (particularly those with 4 or more positive nodes). A posterior axillary radiation field may be considered in patients with incomplete axillary dissection. 7. Effort should be made to minimize the dose to heart and lung. 8. The optimal sequencing of chemotherapy and PMRT remains uncertain.


Head and Neck-journal for The Sciences and Specialties of The Head and Neck | 1989

Carcinoma of the skin of the head and neck with perineural invasion.

William M. Mendenhall; Robert J. Amdur; Lorna Sohn Williams; Anthony Mancuso; Scott P. Stringer; Nancy P. Mendenhall

Perineural invasion is observed in a small subset of patients with carcinomas of the skin of the head and neck.


Cancer | 2003

Angiosarcoma after breast-conserving therapy

Alan T. Monroe; S.J. Feigenberg; Nancy P. Mendenhall

Angiosarcoma arising in the irradiated breast after breast‐conserving therapy is being reported with increasing frequency. As more women undergo breast‐conserving therapy, the incidence can be expected to increase. Surgeons, medical oncologists, and radiation oncologists will be faced with difficult management decisions for this aggressive disease.


American Journal of Clinical Oncology | 2005

Head and Neck Mucosal Melanoma

William M. Mendenhall; Robert J. Amdur; Russell W. Hinerman; John W. Werning; Douglas B. Villaret; Nancy P. Mendenhall

Purpose:The purpose of this article is to discuss the optimal treatment and outcomes for head and neck mucosal melanoma. Methods:Review the pertinent literature. Results:Head and neck mucosal melanoma is a rare entity comprising less than 1% for all Western melanomas. It usually arises in the nasal cavity, paranasal sinuses, and oral cavity. The optimal treatment is surgery. The likelihood of local recurrence after resection is approximately 50%. Radiotherapy (RT) reduces the likelihood of local failure but probably does not enhance survival, which is primarily impacted by advanced T stage and the presence of regional metastases. The 5-year survival rates vary from approximately 20 to 50%. Although the median time to relapse is roughly 1 year or less, late failures are common and cause-specific survival continues to decline after 5 years. Conclusion:The optimal treatment is surgery. Postoperative RT improves local-regional control but may not impact survival. Definitive RT may occasionally cure patients with unresectable local-regional disease or at least provide long-term palliation.


American Journal of Clinical Oncology | 2006

Giant cell tumor of bone.

William M. Mendenhall; Robert A. Zlotecki; Mark T. Scarborough; C. Parker Gibbs; Nancy P. Mendenhall

Objective:To discuss the treatment and outcomes for giant cell tumor (GCT) of bone. Materials and Methods:Review of the pertinent literature. Results:GCT is a rare benign bone lesion most often found in the extremities of women in the third and fourth decades of life. Surgery is the mainstay of treatment and usually consists of intralesional curettage; local control rates range from 80% to 90% after this procedure. Patients with extensive, recurrent, and/or biologically more aggressive tumors may require wide excision. A small subset of patients with incompletely resectable GCTs or with lesions that are surgically inaccessible may be treated with moderate-dose radiotherapy (45–50 Gy) and have a 65% to 80% likelihood of being locally controlled. Conclusion:The majority of patients with GCTs are effectively treated with intralesional curettage. Wide excision or radiotherapy is necessary to cure a relatively limited subset of patients with extensive, aggressive, and/or incompletely resectable GCTs.


International Journal of Radiation Oncology Biology Physics | 1996

Radiotherapy in the management of orbital lymphoma

Timothy W. Bolek; H.Michael Moyses; Robert B. Marcus; Lemuel Gorden; Russell L. Maiese; Nidal M. Almasri; Nancy P. Mendenhall

PURPOSE This retrospective study reviews the treatment technique, disease outcome, and complications of radiotherapy used in the management of lymphoma involving the orbits. PATIENTS & METHODS Thirty-eight patients were treated between May 1969 and January 1995, with a median follow-up of 8.3 years. All patients had biopsy-proven orbital lymphoma. Twenty patients who had limited disease were treated with curative intent, and 18 patients who had known systemic disease were treated with palliative intent. Of the 20 patients treated with curative intent, 14 had low-grade and 6 had intermediate- or high-grade disease. None received chemotherapy. Most patients received treatment with 250 kVP or 60Co radiation, using either an en face anterior field or wedged anterior and lateral fields. Median treatment dose was 25 Gy. Lens shielding was performed if possible. For patients treated for cure, cause-specific survival and freedom from distant relapse were calculated using the Kaplan-Meier method. RESULTS Control of disease in the orbit was achieved in all but 1 patient, who developed an out-of-field recurrence after irradiation of a lacrimal tumor and was salvaged with further radiotherapy. In the patients treated curatively, the 5-year rate of actuarial freedom from distant relapse was 61% for those with low-grade and 33% for those with intermediate/high-grade disease (p = 0.08). Cause-specific survival at 5 years was 89% for patients with low-grade and 33% for those with intermediate/high-grade disease (p = 0.005). Two patients with low-grade disease had contralateral orbital failures; both were salvaged with further irradiation. Acute toxicity was minimal. Cataracts developed in 7 of 21 patients treated without lens shielding and 0 of 17 patients treated with lens shielding. No patient developed significant late lacrimal toxicity. CONCLUSION Radiotherapy is a safe and effective local treatment in the management of orbital lymphoma.


Journal of Clinical Oncology | 2005

Phase II Trial of Individualized Rituximab Dosing for Patients With CD20-Positive Lymphoproliferative Disorders

Lucio N. Gordan; William B. Grow; Annette Pusateri; Vonda Douglas; Nancy P. Mendenhall; James W. Lynch

PURPOSE To determine the feasibility and efficacy of pharmacokinetic (PK) -based maintenance dosing of rituximab and possibly design a more rational maintenance schedule. PATIENTS AND METHODS Patients with CD20-positive lymphoproliferative disorders were treated with four weekly infusions of rituximab 375 mg/m(2). All patients without progressive disease were then monitored for 1 year and received a single infusion of 375 mg/m(2) when the level decreased below 25 microg/mL. RESULTS Twenty-nine of 31 patients were assessable with a variety of histologic subtypes. The overall response rate (ORR) for the entire group was 59% with 27% complete responses (CRs) and 32% partial responses. The median PFS for all patients was 19 months, with a median follow-up of 25 months. In 22 patients with low-grade non-Hodgkins lymphoma (LGNHL), the ORR was 63% with 36% CR and median progression-free survival (PFS) has not been reached. Of 29 assessable patients, 22 were available for PK-based maintenance. The median time to repeat bolus was 5 months (range, 1 to 9 months) for the first, 3.5 months (range, 2 to 5 months) for the second, and 3 months (range, 2 to 4 months) for the third infusion. Ninety-five percent of patients required three or fewer infusions to be maintained in the therapeutic range. CONCLUSION Individualized PK dosing for rituximab produced efficacy comparable to other published maintenance strategies. PK data from this trial suggest that a rational maintenance strategy in patients with LGNHL would be a single dose of 375 mg/m(2) of rituximab every 3 to 4 months.


Cancer | 1983

Primary lymphoma of the central nervous system. Computerized tomography scan characteristics and treatment results for 12 cases

Nancy P. Mendenhall; Timothy L. Thar; O. Frank; Barbara Harty-Golder; William E. Ballinger; Rodney R. Million

A retrospective analysis of 12 patients with primary central nervous system non‐Hodgkins lymphoma seen from 1958 to 1980 was carried out with emphasis on diagnostic evaluation and treatment results. Computerized tomography (CT) scans were found to be the most valuable diagnostic tool both for initial evaluation as well as follow‐up. Characteristic CT scan features were identified and are discussed. Three patients had a history of previous immunosuppression; two had preceding and concurrent uveitis. Nine of the 12 patients were treated primarily with radiation therapy. Three patients were diagnosed at autopsy and had not received definitive therapy. Size of lesion proved to be the most important prognostic factor and appeared to be related to location. Gross total excision of tumor did not appear to improve survival. Two patients were alive with no evidence of disease at 38 and 48 months, respectively. Recurrences were noted from 1 to 33 months after diagnosis (median, 14 months), suggesting the advisability of long‐term follow‐up prior to presumption of cure. From these results and a review of the literature, possible treatment approaches are presented. Cancer 52:1993‐2000, 1983.


Laryngoscope | 2009

Radiotherapy for cutaneous squamous and basal cell carcinomas of the head and neck

William M. Mendenhall; Robert J. Amdur; Russell W. Hinerman; Armand B. Cognetta; Nancy P. Mendenhall

To discuss the role of radiotherapy (RT) in the treatment of cutaneous squamous and basal cell carcinomas of the head and neck.


European Urology | 2015

Defining a standard set of patient-centered outcomes for men with localized prostate cancer.

Neil E. Martin; Laura Massey; Caleb Stowell; Chris H. Bangma; Alberto Briganti; Anna Bill-Axelson; Michael L. Blute; James Catto; Ronald C. Chen; Anthony V. D'Amico; Günter Feick; John M. Fitzpatrick; Steven J. Frank; Michael Froehner; Mark Frydenberg; Adam Glaser; Markus Graefen; Daniel A. Hamstra; Adam S. Kibel; Nancy P. Mendenhall; Kim Moretti; Jacob Ramon; Ian Roos; Howard M. Sandler; Francis J. Sullivan; David A. Swanson; Ashutosh Tewari; Andrew J. Vickers; Thomas Wiegel; Hartwig Huland

BACKGROUND Value-based health care has been proposed as a unifying force to drive improved outcomes and cost containment. OBJECTIVE To develop a standard set of multidimensional patient-centered health outcomes for tracking, comparing, and improving localized prostate cancer (PCa) treatment value. DESIGN, SETTING, AND PARTICIPANTS We convened an international working group of patients, registry experts, urologists, and radiation oncologists to review existing data and practices. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS The group defined a recommended standard set representing who should be tracked, what should be measured and at what time points, and what data are necessary to make meaningful comparisons. Using a modified Delphi method over a series of teleconferences, the group reached consensus for the Standard Set. RESULTS AND LIMITATIONS We recommend that the Standard Set apply to men with newly diagnosed localized PCa treated with active surveillance, surgery, radiation, or other methods. The Standard Set includes acute toxicities occurring within 6 mo of treatment as well as patient-reported outcomes tracked regularly out to 10 yr. Patient-reported domains of urinary incontinence and irritation, bowel symptoms, sexual symptoms, and hormonal symptoms are included, and the recommended measurement tool is the Expanded Prostate Cancer Index Composite Short Form. Disease control outcomes include overall, cause-specific, metastasis-free, and biochemical relapse-free survival. Baseline clinical, pathologic, and comorbidity information is included to improve the interpretability of comparisons. CONCLUSIONS We have defined a simple, easily implemented set of outcomes that we believe should be measured in all men with localized PCa as a crucial first step in improving the value of care. PATIENT SUMMARY Measuring, reporting, and comparing identical outcomes across treatments and treatment centers will provide patients and providers with information to make informed treatment decisions. We defined a set of outcomes that we recommend being tracked for every man being treated for localized prostate cancer.

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Z. Li

University of Florida

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Z. Su

University of Florida

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