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08/01/2010 02:53 PM
Bettyg
 
Posts: 27227
VIP Member
I'm an Advocate

CMS to Consider Evidence on Bone Growth Agent

By Emily P. Walker, Washington Correspondent, MedPage Today

Published: July 30, 2010

WASHINGTON --

The Medicare Evidence Development and Coverage Advisory Committee (MEDCAC) will meet in September to consider available evidence for using bone morphogenetic protein (BMP) for a number of on-label and off-label uses.

BMP is an increasingly popular bone growth agent used as a substitute for iliac crest bone graft during spinal fusion.

The use of BMP has been increasing rapidly, and most surgeons are using it off-label, according to Kevin Ong, PhD, managing engineer at Exponent, an engineering and scientific consulting firm based in Menlo Park, Calif.

Ong presented research at this year's American Academy of Orthopaedic Surgeons, held in New Orleans in March, that found from 2003 to 2007, the use of BMP more than quadrupled from 23,900 to 103,194 procedures.

Although the FDA has approved BMP only for anterior lumbar interbody fusion, only 16.6% of the procedures in the study involved the approved use, researchers said.

Currently, two recombinant BMPs -- rhBMP-2 and rhBMP-7 -- have some form of FDA approval and are commercially available in the U.S.

Although it is believed that BMP is safe and effective for a variety of these off-label uses, there are concerns about the agent, including both its cost and medical issues such as potential heterotopic bone formation, transient bone resorption, soft tissue swelling, seroma formation, and radiculitis.

In particular, medical questions focus on BMP's use in the anterior cervical spine.

Just this week, the FDA's Orthopaedic and Rehabilitation Devices Advisory Panel split over whether to recommend approval for the investigational Medtronic spine stabilization device called Amplify, which uses rhBMP-2 -- citing lack of data to prove that the benefits outweigh the risks for degenerative disc disease patients.

The panel voted 6-5 (with three abstentions) that the benefits of the Amplify device outweighed its harms.

While Medtronic's other spine device, Infuse, also uses rhBMP-2, Amplify is the first combination product utilizing rhBMP-2 for posterolateral fusion treatment of degenerative disc disease.

The FDA panel was concerned about a possible slightly increased risk for cancer in patients who received Amplify in Medtronic's clinical trials compared with patients who underwent standard spinal fusion.

An FDA analysis of Medtronic's clinical trials showed that after two years, 1.7% of patients exposed to rhBMP-2 had cancer, compared with 1.3% of patients not exposed to the protein, although the difference was not statistically significant (P=0.291).

There were 15 cancer cases among the Amplify group, which was almost triple the number in the control group; three-quarters of the cancer deaths during the study occurred among the Amplify group, according to an FDA presentation.

The FDA is not required to follow the advice of its advisory panels, but it often does.

The MEDCAC members will discuss the clinical benefits and harms of on- and off-label use of BMPs at their meeting in Baltimore on Sept. 22.

Panelists will vote on how confident they are that BMPs improve at least one clinically meaningful health outcome for a number of on- and off-label uses.

Ultimately, the panel's decisions could influence whether and how CMS pays for procedures involving BMPs.

Primary source:

Centers for Medicare and Medicaid Services

Source reference:

"MEDCAC Meetings" Centers for Medicare and Medicaid Services

http://tinyurl.com/2adh8bd

© 2004-2010 MedPage Today, LLC. All Rights Reserved.

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.
Reply

10/02/2010 10:49 PM  Top
Bettyg
 
Posts: 27227
VIP Member
I'm an Advocate

Not Enough Evidence to Use BMP Off-Label, Panel Says

By Emily P. Walker, Washington Correspondent, MedPage Today

Published: September 22, 2010

BALTIMORE --

A Medicare advisory committee has voted that there is not enough evidence to warrant off-label use of recombinant human bone morphogenetic protein, or BMP, for bone surgery.

The bone growth agent is increasingly being used as a substitute for iliac crest bone graft during spinal fusion and tibial fractures.

Currently, two recombinant BMPs -- BMP-2 and BMP-7 -- have some form of FDA approval and are commercially available in the U.S.

There are only six uses explicitly approved by the FDA.

But, in an analysis presented at Wednesday's meeting of the Medicare Evidence Development and Coverage Advisory Committee (MEDCAC), a Blue Cross Blue Shield Association researcher estimated that up to 73% of all procedures using BMP are for off-label uses.

Other estimates place that figure closer to 85%.

Although many off-label uses are considered safe, notable concerns have surfaced recently, including formation of bone in unwanted locations and the potential for the protein to fuel the growth of cancer cells or spark adverse immune system reactions.

The MEDCAC panel voted that there is adequate evidence to support using BMP for FDA-approved uses for lumbar spine fusion and open tibial fractures.

But the panel was not at all confident about endorsing the use of the proteins for another lumbar spine indication for which the FDA granted special humanitarian device exemption.

Such exemptions are granted for drugs or devices to treat conditions that affect fewer than 4,000 people, but does not require the company to demonstrate effectiveness.

The panel also expressed extremely low confidence that using BMPs off-label in the cervical spine would produce any clinically meaningful health outcomes, echoing a study published in the Journal of the American Medical Association last year that found that BMP increased complications.

(See Spinal Fusion Agent Raises Costs, Complication Rates).

"There is some evidence to support [BMPs] if you confine your use to FDA-approved indications," said panel vice-chairman Saty Satya-Murti, a neurologist in Wichita, Kan. "There is not enough evidence to support off-label use."

Panelists at Thursday's meeting did not address whether or when Medicare should pay for BMPs -- that meeting is likely still a few years off.

Rather, Thursday's meeting was more of a message to industry on what questions still must be answered about the protein, Satya-Murti told MedPage Today.

Chief among them: What are the long-term effects of using BMPs?

About 90% of all studies on BMPs are funded by industry -- an issue that has raised eyebrows in the past.

When a group of FDA advisers met in January 2002 to consider whether to recommend marketing approval for BMP-2, one of them raised a question about the research findings that Medtronic, the maker of Infuse, filed with the agency as part of its application process.

The advisory panel member pointed out that nine of the doctors who authored the BMP-2 research submitted to the FDA had a financial stake in the product.

Moreover, the studies by those nine all had findings that were twice as good as studies from researchers who did not have a financial interest in the product.

Several MEDCAC panelists expressed concern about the dearth of nonindustry funded BMP studies.

However, getting those studies would mean the federal government would need to put up some funding for research grants, said Satya-Murti.

The FDA is expected to make a decision soon on whether to grant marketing approval for Medtronic's investigational spine stabilization device Amplify, which uses rhBMP-2.

In July an FDA advisory panel split over whether to recommend approval for Amplify, citing lack of data to prove that the benefits outweigh the risks for degenerative disc disease patients.

Although Medtronic's other spine device, Infuse, also uses rhBMP-2, Amplify is the first combination product utilizing rhBMP-2 for posterolateral fusion treatment of degenerative disc disease.

http://tinyurl.com/2g4o8oj

© 2004-2010 MedPage Today, LLC. All Rights Reserved.

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.
Reply

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