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Dive into the research topics where Linda S. Elting is active.

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Featured researches published by Linda S. Elting.


Cancer | 2004

Clinical practice guidelines for the prevention and treatment of cancer therapy-induced oral and gastrointestinal mucositis.

Edward B. Rubenstein; Douglas E. Peterson; Mark M. Schubert; Dorothy Keefe; Deborah B. McGuire; Joel B. Epstein; Linda S. Elting; Philip C. Fox; Catherine D. Cooksley; Stephen T. Sonis

Oral and gastrointestinal (GI) mucositis can affect up to 100% of patients undergoing high‐dose chemotherapy and hematopoietic stem cell transplantation, 80% of patients with malignancies of the head and neck receiving radiotherapy, and a wide range of patients receiving chemotherapy. Alimentary track mucositis increases mortality and morbidity and contributes to rising health care costs. Consequently, the Multinational Association of Supportive Care in Cancer and the International Society for Oral Oncology assembled an expert panel to evaluate the literature and to create evidence‐based guidelines for preventing, evaluating, and treating mucositis.


Cancer | 2007

Updated clinical practice guidelines for the prevention and treatment of mucositis

Dorothy Keefe; Mark M. Schubert; Linda S. Elting; Stephen T. Sonis; Joel B. Epstein; Judith E. Raber-Durlacher; Cesar A. Migliorati; Deborah B. McGuire; Ronald D. Hutchins; Douglas E. Peterson

Considerable progress in research and clinical application has been made since the original guidelines for managing mucositis in cancer patients were published in 2004, and the first active drug for the prevention and treatment of this condition has been approved by the United States Food and Drug Administration and other regulatory agencies in Europe and Australia. These changes necessitate an updated review of the literature and guidelines. Panel members reviewed the biomedical literature on mucositis published in English between January 2002 and May 2005 and reached a consensus based on the criteria of the American Society of Clinical Oncology. Changes in the guidelines included recommendations for the use of palifermin for oral mucositis associated with stem cell transplantation, amifostine for radiation proctitis, and cryotherapy for mucositis associated with high‐dose melphalan. Recommendations against specific practices were introduced: Systemic glutamine was not recommended for the prevention of gastrointestinal mucositis, and sucralfate and antimicrobial lozenges were not recommended for radiation‐induced oral mucositis. Furthermore, new guidelines suggested that granulocyte–macrophage‐colony stimulating factor mouthwashes not be used for oral mucositis prevention in the transplantation population. Advances in mucositis treatment and research have been complemented by an increased rate of publication on mucosal injury in cancer. However, additional and sustained efforts will be required to gain a fuller understanding of the pathobiology, impact on overall patient status, optimal therapeutic strategies, and improved educational programs for health professionals, patients, and caregivers. These efforts are likely to have significant clinical and economic impact on the treatment of cancer patients. Cancer 2007;109:820–31.


Journal of Clinical Oncology | 2001

Platelet Transfusion for Patients With Cancer: Clinical Practice Guidelines of the American Society of Clinical Oncology*

Charles A. Schiffer; Kenneth C. Anderson; Charles L. Bennett; Steven L. Bernstein; Linda S. Elting; Miriam Goldsmith; Michael Goldstein; Heather Hume; Jeffery J. McCullough; Rosemary McIntyre; Bayard L. Powell; John M. Rainey; Scott D. Rowley; Paolo Rebulla; Michael B. Troner; Alton H. Wagnon

OBJECTIVE To determine the most effective, evidence-based approach to the use of platelet transfusions in patients with cancer. OUTCOMES Outcomes of interest included prevention of morbidity and mortality from hemorrhage, effects on survival, quality of life, toxicity reduction, and cost-effectiveness. EVIDENCE A complete MedLine search was performed of the past 20 years of the medical literature. Keywords included platelet transfusion, alloimmunization, hemorrhage, threshold and thrombocytopenia. The search was broadened by articles from the bibliographies of selected articles. VALUES Levels of evidence and guideline grades were rated by a standard process. More weight was given to studies that tested a hypothesis directly related to one of the primary outcomes in a randomized design. BENEFITS/HARMS/COST: The possible consequences of different approaches to the use of platelet transfusion were considered in evaluating a preference for one or another technique producing similar outcomes. Cost alone was not a determining factor. RECOMMENDATIONS Appendix A summarizes the recommendations concerning the choice of particular platelet preparations, the use of prophylactic platelet transfusions, indications for transfusion in selected clinical situations, and the diagnosis, prevention, and management of refractoriness to platelet transfusion. VALIDATION Five outside reviewers, the ASCO Health Services Research Committee, and the ASCO Board reviewed this document. SPONSOR American Society of Clinical Oncology


Cancer | 2003

The burdens of cancer therapy: Clinical and economic outcomes of chemotherapy-induced mucositis

Linda S. Elting; Catherine D. Cooksley; Mark S. Chambers; Scott B. Cantor; Ellen Manzullo; Edward B. Rubenstein

Mucositis is a common but poorly studied problem among patients with solid tumors. The authors examined the clinical and economic outcomes of oral and gastrointestinal (GI) mucositis among patients receiving myelosuppressive chemotherapy.


Clinical Infectious Diseases | 1997

Outcomes of Bacteremia in Patients with Cancer and Neutropenia: Observations from Two Decades of Epidemiological and Clinical Trials

Linda S. Elting; Edward B. Rubenstein; Kenneth V. I. Rolston; Gerald P. Bodey

The prognostic significance of major organ and tissue infection was examined in 909 episodes of bacteremia that were selected from 10 consecutive, randomized clinical trials of antibiotic therapy for infection in patients with cancer and neutropenia. Extensive tissue infection significantly compromised response to initial therapy (38% vs. 74%; P < .0001), ultimate outcome of infection (73% vs. 94%; P < .0001), median time to normalization of temperature (5.3 days vs. 2.5 days; P < .0001), and survival (P < .0001). Other poor prognostic factors revealed by logistic regression included shock (P < .0001) and bacteremia caused by Pseudomonas species (P = .03), Clostridium species (P = .006), or a pathogen resistant to antibiotics used for initial therapy (P < .0001). Recovery of the granulocyte count predicted a superior response (P < .0001). Although the overall mortality rate was not significantly increased when patients with bacteremia due to gram-negative organisms initially received monotherapy or when patients with bacteremia due to gram-positive organisms received delayed vancomycin therapy, these strategies increased the duration of therapy by 25%. Patients with bacteremia due to alpha-hemolytic streptococcus died more often when vancomycin was not included in the initial empirical regimen (P = .004). Because of the prognostic significance of extensive tissue or major organ infection, this factor should be considered in decisions concerning modification of therapy and use of colony-stimulating factors. The cost-effectiveness of initial monotherapy and delayed vancomycin therapy remains to be demonstrated.


Cancer | 2014

MASCC/ISOO clinical practice guidelines for the management of mucositis secondary to cancer therapy

Rajesh V. Lalla; Joanne M. Bowen; Andrei Barasch; Linda S. Elting; Joel B. Epstein; Dorothy Keefe; Deborah B. McGuire; Cesar A. Migliorati; Ourania Nicolatou-Galitis; Douglas E. Peterson; Judith E. Raber-Durlacher; Stephen T. Sonis; Sharon Elad

Mucositis is a highly significant, and sometimes dose‐limiting, toxicity of cancer therapy. The goal of this systematic review was to update the Multinational Association of Supportive Care in Cancer and International Society of Oral Oncology (MASCC/ISOO) Clinical Practice Guidelines for mucositis.


Lancet Oncology | 2006

Bisphosphonate-associated osteonecrosis: a long-term complication of bisphosphonate treatment

Cesar A. Migliorati; Michael A. Siegel; Linda S. Elting

We present current knowledge of bisphosphonate-associated osteonecrosis, a new oral complication in oncology. It was first described in 2003, and hundreds of cases have been reported worldwide. The disorder affects patients with cancer on bisphosphonate treatment for multiple myeloma or bone metastasis from breast, prostate, or lung cancer. Bisphosphonate-associated osteonecrosis is characterised by the unexpected appearance of necrotic bone in the oral cavity. Osteonecrosis can develop spontaneously or after an invasive surgical procedure such as dental extraction. Patients might have severe pain or be asymptomatic. Symptoms can mimic routine dental problems such as decay or periodontal disease. Intravenous use of pamidronate and zoledronic acid is associated with most cases. Other risk factors include duration of bisphosphonate treatment (ie, 36 months and longer), old age in patients with multiple myeloma, and a history of recent dental extraction. We also discuss pathobiology, clinical features, management, and future directions for the disorder.


Cancer | 1993

Outpatient Treatment of Febrile Episodes in Low-Risk Neutropenic Patients with Cancer

Edward B. Rubenstein; Kenneth V. I. Rolston; Carmen P. Escalante; Ellen Manzullo; Pamela Hughes; Andrew Fender; Linda S. Elting; Gerald P. Bodey; Frankie A. Holmes; John W. Loewy; Betty Moreland; Kathryn Kennedy; Robert S. Benjamin

Background. Hospitalization and intravenous (IV) broad‐spectrum antibiotics are the standard of care for all febrile neutropenic patients with cancer. Recent work suggests that a low‐risk population exists who might benefit from an alternate approach.


Journal of Clinical Oncology | 2009

Incidence, Treatment Costs, and Complications of Lymphedema After Breast Cancer Among Women of Working Age: A 2-Year Follow-Up Study

Ya Chen Tina Shih; Ying Xu; Janice N. Cormier; Sharon H. Giordano; Sheila H. Ridner; Thomas A. Buchholz; George H. Perkins; Linda S. Elting

PURPOSE This study estimated the economic burden of breast cancer-related lymphedema (BCRL) among working-age women, the incidence of lymphedema, and associated risk factors. METHODS We used claims data to study an incident cohort of breast cancer patients for the 2 years after the initiation of cancer treatment. A logistic regression model was used to ascertain factors associated with lymphedema. We compared the medical costs and rate of infections likely associated with lymphedema between a woman with BCRL and a matched control. We performed nonparametric bootstrapping to compare the unadjusted cost differences and estimated the adjusted cost differences in regression analysis. RESULTS Approximately 10% of the 1,877 patients had claims indicating treatment of lymphedema. Predictors included treatment with full axillary node dissection (odds ratio [OR] = 6.3, P < .001) and chemotherapy (OR = 1.6, P = .01). A geographic variation was observed; women who resided in the West were more likely to have lymphedema claims than those in the Northeast (OR = 2.05, P = .01). The matched cohort analysis demonstrated that the BCRL group had significantly higher medical costs (


Clinical Infectious Diseases | 2001

Adenovirus infections in adult recipients of blood and marrow transplants

Alberto M. La Rosa; Richard E. Champlin; Nadeem Q. Mirza; James Gajewski; Sergio Giralt; Kenneth V. I. Rolston; I. Raad; Kalen L. Jacobson; Dimitrios P. Kontoyiannis; Linda S. Elting; Estella Whimbey

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Gerald P. Bodey

University of Texas MD Anderson Cancer Center

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Kenneth V. I. Rolston

University of Texas MD Anderson Cancer Center

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Catherine D. Cooksley

University of Texas MD Anderson Cancer Center

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Edward B. Rubenstein

University of Texas MD Anderson Cancer Center

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Victor Fainstein

University of Texas at Austin

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Scott B. Cantor

University of Texas MD Anderson Cancer Center

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Sharon H. Giordano

University of Texas MD Anderson Cancer Center

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Thomas A. Buchholz

University of Texas MD Anderson Cancer Center

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Elenir B C Avritscher

University of Texas MD Anderson Cancer Center

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