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| ILLINOIS MEDICAL ONCOLOGY SOCIETY www.imos-illinois.com |
IMOS Upcoming Events Monthly Teleconference: Wednesday, August 24, 2011 2011 IMOS Board of Directors President IMOS Corporate Members (as of 6/30/11)
Gold Thank you for the value you add to IMOS! New Logo, New Look! We hope you enjoy our newly redesigned IMOS NewsLine. Please email us if you have any questions, comments, or news you'd like to see appear in the next NewsLine.
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— Summer 2011 — |
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President's Message: 2011: An Outstanding Year for IMOS!
Dear Colleague, This year has been an outstanding year for oncology in Illinois. Membership in the Illinois Medical Oncology Society (IMOS) is now open to include practice managers, oncology pharmacists, nurse practitioners, specialists in oncology contracts, billers, coders, and other oncology business staff. The practice administrators merged into IMOS, bringing their skills and knowledge to our organization. Here are some of the highlights of the last year:
As my presidency comes to a close, I want to thank you for your interest in our state society and wish my colleague, Dr. Tim Kuzel, best wishes for his presidency in 2011–2013. New Resource Now Available to IMOS Members IMOS members recently received an email about a new resource available to them as a benefit of being an IMOS member. This new tool, Patient Assistance: Educating and Empowering Cancer Patients and Their Families, developed by the State Society Education Series, is designed to help members provide their patients with the information they need when resources are limited. Targeted to patients who would benefit from financial assistance, this guide provides an overview of patient assistance programs, including eligibility requirements. It serves as a starting point for patients to begin the application process. The brochure may be downloaded and printed either professionally or in house. It may also be used in conjunction with ACCC's Patient Assistance and Reimbursement Programs: A Guide for Community Cancer Centers, which provides quick and easy access to the forms patients may need to apply for assistance. To access this resource, go to the IMOS website. IMOS is one of seven states that sponsors the State Society Education Series for their members. The series includes educational programs, webinars, and resource materials to assist in providing quality care for cancer patients. State societies in Arizona, Hawaii, Indiana, Iowa, South Carolina, and Virginia also participate in the Series. Monthly Teleconferences for Practice Managers, Administrators, and Billing Personnel Every month IMOS sponsors teleconferences for practice managers, administrators, and billing personnel. These teleconferences provide the business staff of oncology practices with opportunities to network, compare strategies, and address issues of interest. Teleconferences take place the fourth Wednesday of every month at 12:00 pm CT, and the topics vary from month to month. Please mark your calendars for the following dates: August 24, September 21, and October 26. Contact satterbury@accc-cancer.org for the call–in information. Drugs in the News from IMOS Corporate Members AMGEN INC. (www.amgen.com) announced that the Food and Drug Administration (FDA) has approved Xgeva™ (denosumab) to help prevent skeletal-related events (SREs) in patients with cancer that has metastasized and damaged the bone. Skeletal-related events include bone fractures from cancer and bone pain requiring radiation. Xgeva is a monoclonal antibody that targets a protein involved in cancer-related bone destruction called human RANKL. Xgeva is not approved for patients with multiple myeloma or other cancers of the blood. Xgeva’s safety and effectiveness were confirmed in three randomized, double-blind clinical studies in 5,723 patients comparing Xgeva with Zometa. The head-to-head trials evaluated Xgeva delivered every four weeks as a 120 mg subcutaneous injection vs. Zometa® (zoledronic acid) delivered every 4 weeks via a 15-minute intravenous infusion, adjusted for kidney function per the labeled instructions. (Oncology Issues, January/February 2011) NOVARTIS PHARMACEUTICALS CORPORATION (www.novartis.com) announced that the FDA has approved Afinitor® (everolimus) tablets for patients with subependymal giant cell astrocytoma (SEGA), a benign brain tumor associated with tuberous sclerosis (TS), who require therapeutic intervention but are not candidates for curative surgical resection. (Oncology Issues, January/February 2011) GENENTECH, a member of the Roche Group, and Biogen Idec (www.gene.com) announced that the Food and Drug Administration (FDA) has approved Rituxan© (rituximab) as a maintenance treatment for patients with advanced follicular lymphoma who responded to initial treatment with Rituxan plus chemotherapy (induction treatment). This approval was based on data from the Phase III PRIMA study, which showed continuing Rituxan administration every two months for two years in patients who responded to initial treatment with Rituxan plus chemotherapy, nearly doubled the likelihood of them living without the disease worsening (progression-free survival) compared to those who stopped treatment. (Oncology Issues, March/April 2011) The FDA approved SCHERING CORPORATION’S (www.merck.com) Sylatron™ (peginterferonalfa-2b) for the treatment of patients with melanoma with microscopic or gross nodal involvement within 84 days of definitive surgical resection, including complete lymphadenectomy. The approval was based on a single trial, EORTC18991, an open label, multi-center trial enrolling 1,256 patients. The recommended dose and schedule for Sylatron is 6 mcg/kg/week, subcutaneously for 8 doses, followed by 3 mcg/kg/week subcutaneously. The maximum treatment period is 5 years (260 weeks). Sylatron is contraindicated in patients with a history of anaphylaxis to peginterferon alfa-2b or interferon alfa-2b, in patients with autoimmune hepatitis, and in patients with hepatic decompensation (Child-Pugh score >6 [class B and C]). (Oncology Issues, May/June 2011) CELGENE CORPORATION (www.celgene.com) announced that the FDA has granted accelerated approval for its supplemental new drug application (sNDA) for an additional indication for Istodax (romidepsin) for injection for the treatment of peripheral T-cell lymphoma (PTCL) in patients who have received at least one prior therapy. Istodax is also approved for the treatment of cutaneous T-cell lymphoma (CTCL) in patients who have received at least one prior systemic therapy. (Celgene Corporation, Press Release, June 16, 2011) The FDA approved Afinitor® (everolimus) Tablets (NOVARTIS PHARMACEUTICALS CORPORATION, www.novartis.com) for the treatment of progressive neuroendocrine tumors of pancreatic origin (PNET) in patients with unresectable, locally advanced or metastatic disease. (Oncology Issues, July/August 2011) Welcome New IMOS Members!
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For more information about Illinois Medical Oncology Society (IMOS) You are receiving this message because you are affiliated with IMOS and we believe you will benefit from this information. |
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