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Re[3]: Urgent Request for Medical Isotope Production Support
>From: dr_fisher@ccmail.pnl.gov
>Date: Mon, 25 Nov 1996 17:28 -0800 (PST)
>Subject: Re[3]: Urgent Request for Medical Isotope Production Support
>To: ratcher@uab.edu, garthy@owt.com, dose-net@ORAU.GOV
>Cc: kkrohn@u.washington.edu, re_schenter@ccmail.pnl.gov
>MIME-version: 1.0
>
> Response to Bob Atcher:
>
> 1. Many among the current operations staff at FFTF agree with you and
> believe FFTF can be run the most economically as a privatized
> facility. That is their proposal. The rapid retrieval system has
> been designed and is part of that proposal.
>
> 2. Advanced Nuclear & Medical Systems, Richland, has submitted a
> proposal to DOE to privatize the FFTF. There are several other larger
> companies that would like the same opportunity. You are right that
> the medical isotope mission will depend on the tritium mission. The
> current debate is not on FFTF as a medical isotope production
> facility, but rather whether FFTF can produce sufficient
> tritium to meet an interim national need. That is being studied
> by the JASONS. It is also under intense study and scrutiny by
> the Department of Energy and the Department of Defense.
>
> 3. The primary purpose of FFTF was never isotope production. FFTF
> was built to test components for the nation's breeder program, which
> was canceled by President Carter. It did demonstrate isotope
> production capabilities during its operations during some of the
> tests.
>
> 4. The IOM report did not consider alternative missions for FFTF,
> because there were not any at that time. We all agree that isotope
> production was not sufficient to justify the $60-80 million/year
> cost of FFTF operations. That argument is past history. The people
> who will benefit are those who currently work at FFTF. These are
> scientists, engineers, craftsmen, and support staff who made the FFTF
> successful in the first place. Bob, it takes initiative on the part
> of dedicated people like this to make good things happen.
>
> 4. The FFTF will produce those isotopes for which there is a
> commercial market. If privatized, FFTF will compete in the private
> sector, just like any business in a capitalistic society. The other
> option is to let the taxpayer pick up the current costs of FFTF in
> stand-by mode ($50 million/year) where nothing is produced. There are
> more than 60 isotopes under consideration for FFTF production. Many
> of these are indeed in short supply, such as precursors to
> bismuth-213. Gadolinium-153 is still in demand, in fact, I have
> purchased more than $25,000 worth this year alone from the Russians
> for essential purposes! Our Lab also purchased something like $75,000
> worth of cobalt-60 this year from the Canadians. The I-131 market
> (also from Canada) will also greatly increase as radiolabeled
> antibodies using I-131 receive FDA approval. The FFTF team believes
> in domestic isotope supply rather than dependence on foreign sources.
>
>
>
>
>
>
>
>
>
>______________________________ Reply Separator
>_________________________________
>Subject: Re[2]: Urgent Request for Medical Isotope Production Support
>Author: ratcher@uab.edu at -SMTPlink
>Date: 11/25/96 3:19 PM
>
>
>At 12:50 11/25/96, dr_fisher@ccmail.pnl.gov wrote:
>> In response to Bob Atcher's comments, below, I believe the medical
>> community and dose-netters need to understand a few more points:
>>
>> 1) The Institute of Medicine report on reactor-produced radionuclides
>> has been widely criticized because it discounted or completely
>> overlooked the possibilities of producing medical isotopes at DOE
>> reactor facilities (HFIR, ATR, FFTF, and ACRR), it failed in a major
>> way to account for the need for therapeutic radionuclides, and it
>> assumed that the Univ. of Missouri Research Reactor could meet
>> essentially all the needs for medical isotopes in the U.S.
>
>It was widely criticized by DOE-types who didn't believe that the reactors
>within the DOE system, regardless of their abilities to produce isotopes
>economically and in a timely fashion, were given fair hearing. When the
>economics of the reactors were included, as they were in the IOM report, the
>DOE reactors fell far short. In fact, the FFTF has no capability for short
>term irradiations and would require about $10 million (in FY92 funds) in
>modifications for installation of a pneumatic system for fast insertion and
>removal of targets.
>>
>> 2) A lot has changed since the IOM report was prepared in 1994.
>> The current proposal to operate the Fast Flux Test Facility near
>> Richland, Washington, identifies tritium production and excess
>> weapons plutonium burn-up as its primary missions (see Science,
>> October 25, 1996, Letters). The current proposal is to privatize
>> the operation and not support it with federal taxpayer money. Any
>> medical isotope production would come as a bonus, taking advantage
>> of target positions in the reflector area and a new rapid retrieval
>> target assembly. This means that the economic picture has
>> substantially changed. No one expects isotope production to pay for
>> reactor operations, and under the current proposal, operation of the
>> reactor is covered by its new primary missions.
>
>2. What private entity is going to support tritium production and waste
>burnup? This simply puts isotope production into the same parasitic mode
>that it is at nearly every other facility within the DOE system. IF
>funding for the primary mission goes away, there is NO WAY that isotope
>production can support this activity. Then the users are left without any
>source of isotopes.
>
>>
>> 3) The local community (Tri-Cities of Eastern Washington) is outraged
>> that DOE has been planning to spend $500 million to tear down the
>> FFTF. The FFTF is the newest and most modern of the DOE reactors.
>> It is one of the most important engineering accomplishments of the
>> century. It represents a taxpayer investment of about $2 Billion.
>> It has a stellar performance record for meeting mission objectives,
>> radiation safety, essentially zero environmental emissions, and
>> reactor safety. It has a unique design that provides a large
>> target volume, high neutron flux, and broad energy spectrum for
>> maximum isotope productivity. During its 12 years of operations, it
>> produced a number of medical isotopes that were not otherwise
>> available, and it can do a lot more for the medical community in the
>> future.
>
>There is no question that this reactor had substantial advantages for
>isotope production. After all, that was its primary mission. The fact is,
>however, that this mission is no longer feasible and the economics don't
>justify its restart.
>
>>
>> 4) The privatization proposal includes a commitment to fund medical
>> applications research for radioisotopes ($5 million/year).
>>
>What privatization proposal? There is nothing in the letter about this.
>Why not put this up so it can be examined closely.
>
>> Given this new perspective, I find no justification for hanging onto
>> the IOM report as rationale to not restart the FFTF. I urge each of
>> you who read this to carefully consider the petition you received
>> earlier.
>>
>The fact is that the IOM report was done by experts who had no financial
>interest in its conclusions other than to have the isotopes available.
>This FFTF proposal is being pushed by people who will benefit materially if
>it comes to pass. That alone should alert people about its veracity and
>reliability.
>
>> Darrell R. Fisher
>> Pacific Northwest National Laboratory
>> Richland, Washington 99352
>> 509-376-3736
>> dr_fisher@pnl.gov
>>
>
>None of the isotopes listed in the letter are in short supply now. At last
>count, the supply of Mo-99, as a percentage of world demand, will approach
>300 % in three years when the MapleX reactors come on line. Gd-153 is no
>longer used for bone density studies; Co-60 is not used for external beam
>therapy except in the most backwards countries nor is it used for
>brachytherapy; and Ac-227 hasn't even been reviewed by any panel of experts
>for its utility. In short, the list of isotopes that are in "short supply"
>don't have any basis in reality. For example, clinical trials of alpha
>emitters have already begun at Sloan Kettering.
>
>There are three isotopes currently in clinical practice or undergoing
>clinical trials for bone pain therapy - Sr-89 (already FDA approved),
>Sm-153 and Sn-117m. The availability of Re-186 is hardly an issue. There
>is not a single study of AIDS showing therapeutic potential of radiolabeled
>antibodies. There is no shortage now or predicted for I-131.
>
>In summary, the letter is filled with a laundry list of justifications that
>are not backed by reality.
>
>
>Robert W. Atcher, Ph.D.
>ratcher@uab.edu
>Cardiovascular Disease Div., Dept. of Medicine,
>Univ of Alabama at Birmingham
>Office 205 975 5702
>Office FAX 205 975 8740
>