FDA Letter Supports CMS Decision On Medicare Coverage Of Anemia Drugs
Main Category: Medicare / Medicaid / SCHIPAlso Included In: Regulatory Affairs / Drug Approvals; Blood / Hematology
Article Date: 18 Oct 2007 - 8:00 PDT
FDA officials in a letter dated Oct. 12 said that the agency supports a recent decision by CMS that will limit Medicare coverage for use of anemia medications -- Aranesp, manufactured by Amgen, and Procrit, manufactured by Johnson & Johnson -- in cancer patients, CQ HealthBeat reports (Reichard, CQ HealthBeat, 10/16). According to a 61-page "national coverage determination" announced in July, Medicare will cover the medications, synthetic forms of the protein erythropoietin, to treat anemia caused by chemotherapy but not anemia caused by cancer.
Under the decision, Medicare will cover the medications to treat anemia in cancer patients whose hemoglobin levels decrease to less than 10 grams per deciliter of blood. The decision will allow local Medicare contractors to determine whether to cover the medications to treat patients with myelodysplastic syndrome, a condition that can lead to leukemia (Kaiser Daily Health Policy Report, 10/2). The letter, released on Tuesday by Reps. Pete Stark (D-Calif.) and Henry Waxman (D-Calif.), said that the decision is "generally consistent" with information on recommended use of the medications in cancer patients (Bloomberg/Los Angeles Times, 10/17).
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In a statement, Stark said, "The FDA letter confirms ... Medicare's new national coverage determination is consistent with the FDA's recommendations and scientific research," adding, "Excessive use" of such drugs "increases the risk of tumor progression in cancer patients. Medicare's action will prevent excessive use and protect patients' lives." Waxman said, "Clearly, the FDA letter confirms that the Medicare coverage decision is appropriately based on science."
Amgen and J&J have lobbied Congress to reverse the decision and have collected signatures from majorities in the House and Senate in support of the move. In a statement, Amgen said, "Amgen continues to urge CMS to quickly respond to the oncology community's collective concerns by allowing patients access to the medicines their doctors believe are a critical part of their cancer care" (CQ HealthBeat, 10/16).
Reprinted with kind permission from http://www.kaisernetwork.org. You can view the entire Kaiser Daily Health Policy Report, search the archives, or sign up for email delivery at http://www.kaisernetwork.org/dailyreports/healthpolicy. The Kaiser Daily Health Policy Report is published for kaisernetwork.org, a free service of The Henry J. Kaiser Family Foundation© 2005 Advisory Board Company and Kaiser Family Foundation. All rights reserved.
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FDA Sides With CMS In Anemia Drug Battle
posted by Gregory D. Pawelski on 19 Oct 2007 at 5:47 pmThe FDA backed CMS' National Coverage Decision (NCD), which limited use of the drugs because they have been shown to spur tumor growth.
The FDA has stated that the health risks associated with the use of pharmaceutical EPO (ESAs) for cancer patients include: Promotion of tumor growth in patients with advanced breast, head and neck, lymphoid, and non-small cell lung malignancies in studies adminstered EPO to target a hemoglobin of >12 g/dL, and have not been excluded with lower target hemoglobin levels.
The FDA believes that the approved labeling and CMS's National Coverage Decision are generally consistent in their recommendations regarding the use of pharmaceutical EPO in patients with cancer undergoing chemotherapy.
FDA's approved labeling recommends use of the lowest dose necessary to avoid the need for blood transfusions and transfusions are not normally given to patients whose hemoglobin is 10 g/dL or higher. The recommendation in the approved labeling that the hemoglobin not exceed 12 g/dL in cancer patients "is intended as an upper safety limit, not a target for therapy."
A “growth factor” is about twenty small proteins that attach to specific receptors on the surface of stem cells in bone marrow and promote differentiation and maturation of these cells into morphotic constituents of blood. And blood is a circulating tissue composed of fluid plasma and cells (red blood cells, white blood cells, platelets).
Problems with blood composition or circulation can lead to downstream tissue (which is made up of cells) dysfunction. If pharmaceutical EPO stimulates the bone marrow to make red blood cells, it could feed the growth of tumors in cancer patients.
Again, if ASCO has a complaint about CMS payment policy, it should provide evidence to the physicians at that agency who made the decision. There is no evidence that pharmaceutical EPO results in improved survival, "TUMOR CONTROL," health-related quality of life at any hemoglobin level in cancer patient undergoing chemotherapy.
Federal laws bar drug companies from paying doctors to prescribe medicines that are given in pill form and purchased by patients from pharmacies. But companies can rebate part of the price that doctors pay for drugs, like the anemia medicines, which they dispense in their offices as part of treatment.
The anemia drugs are injected or given intravenously in physicians’ offices or dialysis centers. Doctors receive the rebates after they buy the drugs from the companies. But they also receive reimbursement from Medicare or private insurers for the drugs, often at a markup over the doctors’ purchase price.
It's still your mother's chemotherapy concession. Although the new Medicare bill tried to curtail the drug concession, private insurers still go along with it. What needs to be done is to remove the profit incentive from the choice of drug treatments. Let's take physicians out of the retail pharmacy business and force them to be doctors again!!!
http://www.house.gov/stark/news/110th/letters/20071012-esa.pdf
http://www.fda.gov/bbs/topics/NEWS/2007/NEW01582.html
http://www.nytimes.com/2007/05/09/business/09anemia.html?_r=3&hp=&oref=slogin&pagewanted=print&oref=slogin&oref=slogin
http://www.healthyskepticism.org/news/2007/Jun.php
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