Remembering Gianni Bonadonna by KURT SAMSON
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NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Myeloid Growth Factors
NCCN Guidelines Index MGF Table of Contents Discussion NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines® ) Myeloid Growth Factors Version 2.2013 NCCN.org Continue Version 2.2013, 08/02/13 © National Comprehensive Cancer Network, Inc. 2013, All rights reserved. The NCCN Guidelines® and this illustration may not be reproduced in any form without the express written permission of NCCN®. NCCN Guidelines Version 2.2013 Panel Members NCCN Guidelines Index MGF Table of Contents Myeloid Growth Factors Discussion * Jeffrey Crawford, MD/Chair †‡ Susan Hudock, PharmD å Lee S. Schwartzberg, MD † ‡ Þ Duke Cancer Institute The Sidney Kimmel Comprehensive St. Jude Children's Research Hospital/ Cancer Center at Johns Hopkins The University of Tennessee Health Science James Armitage, MD † x Center- The West Clinic UNMC Eppley Cancer Center at Dwight D. Kloth, PharmD å å The Nebraska Medical Center Fox Chase Cancer Center Sepideh Shayani, PharmD City of Hope Comprehensive Cancer Center Lodovico Balducci, MD † ‡ David J. Kuter, MD, DPhil † ‡ Moffitt Cancer Center Massachusetts General David P. Steensma, MD†‡Þ Hospital Cancer Center Dana-Farber/Brigham and Women’s Pamela Sue Becker, MD, PhD ‡ Þ x Cancer Center Fred Hutchinson Cancer Research Center/ Gary H. Lyman, MD, MPH † ‡ å Seattle Cancer Care Alliance Duke Cancer Institute Mahsa Talbott, PharmD Vanderbilt-Ingram Cancer Center Douglas W. Blayney, MD † Brandon McMahon, MD ‡ Stanford Cancer Institute Robert H. Lurie Comprehensive Cancer Saroj Vadhan-Raj, MD † Þ Center of Northwestern University The University of Texas Spero R. Cataland, MD ‡ MD Anderson Cancer Center The Ohio State University Comprehensive Hope S. Rugo, MD † ‡ x Cancer Center - James Cancer Hospital UCSF Helen Diller Family Peter Westervelt, MD, PhD † Siteman Cancer Center at Barnes- and Solove Research Institute Comprehensive Cancer Center Jewish Hospital and Washington University School of Medicine Mark L. -
Breast Pathology
28A ANNUAL MEETING ABSTRACTS Breast Pathology Clincopathologic parameters n=68(%) Predominant MC 101 Overexpression of FoxO3a Is Associated with Lymph Node Squamous 31(45.5) Metastasis and Poor Disease-Free Survival in Triple-Negative Breast Spindle 15(22) Cancers Chondroid 9(13) Rehman Abdul, Yumin Chung, Hyein Ahn, Jongmin Sim, Min Sung Chung, Kiseok Jang. Osseous 4(6) Hanyang University College of Medicine, Seoul, Republic of Korea. Background: Triple negative breast cancer (TNBC) is the most aggressive type of breast Pseudoangiomatous 6(9) cancer, whichis a heterogeneous group and has no proven molecular target. FoxO3a, Mixed 2(3) a transcription factor, is involved in wide spectrum of biological processes, including HG sarcomatoid 1(1.5) cell cycle progression, proliferation, DNA damage repair, and apoptosis.Recently, DCIS with metaplastic features 14(52) accumulating evidences suggests that FoxO3a act as a tumor suppressorin variety Squamous 11(78.5) of human cancers. However,the previous studies usingTNBC cell lines have shown controversial results. The aim of this study was to investigate the clinicopathological Chondroid 2(14) significance and role of FoxO3a in the progression of TNBC. Rhabdoid 1(7.5) Design: Tissue microarrays consisting of 124 cases of TNBC were studied for FoxO3a None 13(48) expression by immunohistochemistry and interpreted by semi-quantitative scoring Grade system. The FoxO3a expression correlated with various clinicopathological parameters, 1 1(1.5) including patient’s survival. Furthermore, cultured TNBC cell lines (MDA-MB-231, MDA-MB-468, BT20) were assessed for FoxO3a expression by western blot. MDA- 2 3(4.5) MB-468 breast cancer cell line was transiently transfected with exogenous siRNA, 3 64(94) which wasspecific for FoxO3a. -
PATTERNS of FATIGUE and FACTORS INFLUENCING FATIGUE DURING ADJUVANT BREAST CANCER CHEMOTHERAPY by Ann Malone Berger a DISSERTATI
PATTERNS OF FATIGUE AND FACTORS INFLUENCING FATIGUE DURING ADJUVANT BREAST CANCER CHEMOTHERAPY By Ann Malone Berger A DISSERTATION Presented to the Faculty of The Graduate College in the University of Nebraska In Partial Fulfillment of Requirements For the Degree of Doctor of Philosophy Nursing Under the Supervision of Professor Susan Noble Walker Medical Center Omaha, Nebraska December, 1996 Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. TITLE Patterns of Fatigue and Factors Influencing Fatigue During Adjuvant Breast Cancer Chemotherapy BY Ann Malone Berger APPROVED DATE 11/25/96 Susan Noble Walker Lynne Farr________________________________ 11/25/96 Anne Kessinger 11/25/96 11/25/96 Ada Lindsey _______________________________________ _______ T . 7. 11/25/96 L a m Zimmerman ______ ___ ______________________ SUPERVISORY COMMITTEE GRADUATE COLLEGE UNIVERSITY OF NEBRASKA Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. PATTERNS OF FATIGUE AND FACTORS INFLUENCING FATIGUE DURING ADJUVANT BREAST CANCER CHEMOTHERAPY Ann Malone Berger, Ph.D. University of Nebraska, 1996 Advisor: Susan Noble Walker, Ed.D. Women beginning adjuvant chemotherapy for breast cancer seek information from health professionals regarding fatigue, but knowledge regarding this distressing symptom is currently limited. The purposes of this study were to describe the patterns of fatigue and of factors influencing fatigue across the first three cycles of chemotherapy and to determine the extent to which health and functional status, chemotherapy protocol, physical activity behaviors, activity/rest cycles, nutrition behaviors and status, stress management behaviors, interpersonal relations behaviors, symptom distress and reaction to the diagnosis of cancer explain fatigue at each treatment and predict fatigue at the mid-point of the first three chemotherapy cycles. -
Protein Expression, Survival and Docetaxel Benefit in Node-Positive Breast Cancer Treated with Adjuvant Chemotherapy in the FNCL
Jacquemier et al. Breast Cancer Research 2011, 13:R109 http://breast-cancer-research.com/content/13/6/R109 RESEARCHARTICLE Open Access Protein expression, survival and docetaxel benefit in node-positive breast cancer treated with adjuvant chemotherapy in the FNCLCC - PACS 01 randomized trial Jocelyne Jacquemier1,2, Jean-Marie Boher3, Henri Roche4, Benjamin Esterni3, Daniel Serin5, Pierre Kerbrat6, Fabrice Andre7, Pascal Finetti2, Emmanuelle Charafe-Jauffret1,2,8, Anne-Laure Martin9, Mario Campone10, Patrice Viens8,11, Daniel Birnbaum2, Frédérique Penault-Llorca12 and François Bertucci2,8,11* Abstract Introduction: The PACS01 trial has demonstrated that a docetaxel addition to adjuvant anthracycline-based chemotherapy improves disease-free survival (DFS) and overall survival of node-positive early breast cancer (EBC). We searched for prognostic and predictive markers for docetaxel’s benefit. Methods: Tumor samples from 1,099 recruited women were analyzed for the expression of 34 selected proteins using immunohistochemistry. The prognostic and predictive values of each marker and four molecular subtypes (luminal A, luminal B, HER2-overexpressing, and triple-negative) were tested. Results: Progesterone receptor-negativity (HR = 0.66; 95% CI 0.47 to 0.92, P = 0.013), and Ki67-positivity (HR = 1.53; 95% CI 1.12 to 2.08, P = 0.007) were independent adverse prognostic factors. Out of the 34 proteins, only Ki67- positivity was associated with DFS improvement with docetaxel addition (adjusted HR = 0.51, 95% CI 0.33 to 0.79 for Ki67-positive versus HR = 1.10, 95% CI 0.75 to 1.61 for Ki67-negative tumors, P for interaction = 0.012). Molecular subtyping predicted the docetaxel benefit, but without providing additional information to Ki67 status. -
Original Article Efficacy of Metronomic Chemotherapy with Oral Cyclophosphamide and Methotrexate in Patients with Non-Hodgkin
Int J Clin Exp Med 2016;9(2):3893-3900 www.ijcem.com /ISSN:1940-5901/IJCEM0015875 Original Article Efficacy of metronomic chemotherapy with oral cyclophosphamide and methotrexate in patients with non-Hodgkin lymphoma: a retrospective analysis at a single institution Joo Young Jung, Geundoo Jang, Hunho Song, Hyeong Su Kim, Dae Ro Choi, Jung Hye Kwon, Ho Young Kim, Boram Han, Jung Han Kim, Hyo Jung Kim, Dae Young Zang Department of Internal Medicine, Hallym University Sacred Heart Hospital, Hallym University Medical Center, Anyang-si, Korea Received September 8, 2015; Accepted January 12, 2016; Epub February 15, 2016; Published February 29, 2016 Abstract: Metronomic chemotherapy is an emerging strategy offering a potentially less toxic yet effective treatment modality. We evaluated the efficacy and safety of low-dose metronomic (LDM) chemotherapy in relapsed or refracto- ry non-Hodgkin lymphoma (NHL) by retrospectively reviewing the data of 16 NHL patients who were treated with oral cyclophosphamide plus methotrexate (CM) as LDM chemotherapy. The patients received oral cyclophosphamide (50 mg per day) and oral methotrexate (2.5 mg twice weekly) until disease progression or unacceptable toxicity was noted. Fifteen NHL patients were evaluable in the study. The overall best response rate was 53.3% (2 complete responses and 5 partial responses), with 6.7% of patients achieving stable disease. The median treatment duration was 4.8 months (range, 1.45-25.3 months); the median overall and progression-free survival times were 12.1 and 6.6 months, respectively; and the median response duration was 8.7 months. Only 4 patients were managed with further salvage chemotherapy.