Guest guest Posted December 20, 2001 Report Share Posted December 20, 2001 Hi , The following is a reply I made yesterday to someone else's question regarding Radiation treatment(s). The exact same answer applies concerning med. levels. Just substitute the word meds. where you read RAI in my note to Gwynne. Essentially what I've said is that treatment for ThyCa (Radiation tx or med. prescribing) is done differently from place to place. Your doctors' knowledges are not in keeping with today's standard of care with regard to thyroid cancer treatment. (also see Dr. Ain below) this is the type of information from Dr. Ain that it was that I was suggesting that you forward to your doctor in my previous E-Mail to you concerning matters of treatment. The figures for tsh level that your doctors are suggesting are numbers that apply to people _with_ thyroids. Two things must be considered after undergoing a tt. 1.) tsh levels _must_ be kept <0.10 for purpose of suppression of any cancer that may remain. 2.) The numbers for t4 _will_ be high due to # 1 and t3 will be lower than what is considered normal for those of whom have normally functioning thyroids. Nick _________________________________________________________________________ Date: Wed, 19 Dec 2001 14:49:48 -0500 Subject: Re: RAI " causing damage " --> Gwynne In-reply-to: <9vqieh+mq4peGroups> Hi Gwynne, Your question is quite complex regarding " then why is there a need to individually calculate doses -- why not give everyone the same dose? " Most " first-doses " of RAI for ThyCa that are given for cases " seen and thought to be " the 'least' troublesome in every observable regard from the medical-technical point of view _are_ for the most part, handled as " giving the same dose to all " BUT.. the DIFFERENCE is " PLACE " . No, not " place " as in where the cancer is ( as it really should be..) but in " place " as to " What doctor, which hospital; which state; what region.. who the doctor(s) studied with.. what country etc.etc. Since the tools necessary for assessing just where, how much and what kind/type/degree of thyca that an individual may have.. are not yet available (those such as Dr. Ain & his research are trying to solve these issues of detection, identification and treatment thereof) . So then. there is no " exact science " as to treatment protocol for thyroid cancer. Don't lose heart.. because, except for a very small percentage of persistent cases.. we seem to somehow, manage to survive. Unless other tools for detection and assessment are found.. RAI will continue to be the weapon of choice. The " ammunition " (RAI initial dosing standard) will probably be increasing world wide. Dr. Ain, and others are have already moved in this direction. Some doctors come from schools-of-thought that adhere to a " 30 mCi first dose " philosophy. Others pick another number. Unless there are other observed complications that a well-schooled ThyCa-Doctor would most usually find during the course of his diagnostic work-up...initial treatment is mostly by-guess & by-golly because " that's the way we do it around here " . " As long as each single I-131 dose is within the safety margins of 200 REM marrow exposure and less than 80 mCi I-131 retained in the lung at 48 hrs (this may permit single doses up to 650 mCi in some patients), there should be no permanent ill consequences from necessary thyroid cancer treatment. " (Dr. Ain) _____________________________________________________________________________ Gwynne, the following is what would be the necessary process and procedure to determine the _maximum_ individual dose that may be administered before causing harm outside of the intended cancerous thyca cells. In _most_ cases (and in none that I know of: my experience being, obviously, very limited) I doubt that Dosemitry testing is performed pre-ablation-RAI with most " common/usual " " simple " cases of thyroid cancer involvement. If all thyca-treating doctors were schooled by the same instructions from the same schools...then _most_ would apply RAI dosages, as instructed. However.. doctors that choose to think " out-side-the-box " (the Dr. Ain's) and challenge " conventional-wisdom " (local institutional thinking) then set about " building a better mouse-trap " . Dr. Ain pushes (cautiously) the limits of knowledge and applies his wisdom to thinking about the results of his research and how the information applies to better protocol of treatment and care for thyroid cancer. Skin cancer is the most usual and thyroid, the least common of cancers. Our disease is referred to as an " orphan " disease and receives the least amount of support in terms of research money. This is not to say that great effort isn't being deployed. But what it does mean..is that there isn't a concerted, focused number working the task. When the U.S. came to a resolve to land on the moon.. it was done. This is called " throwing money at it " . Ain't a lot of money being devoted to thyroid cancer research. So we're stuck with " by gosh & by golly " for the most part. Until such time that a critical-mass of research effort is deployed in the interest of solving ThyCa. We have no clear choice(s) unless we come upon those and a few others.. such as Dr. Ain. _____________________________________________________________________________ And no.. I do not agree that " ..the RAI that we don't " uptake " in thyroid tissue must then settle elsewhere in our body until we pass it? " This isn't what happens because _oly thyroid-cells_ up-take IODINE to which the radiation is attached. Relatively speaking.. RAI exists (stays) in the body for a very short period of time. Given within known, prescribed limits.. RAI is not _known_ to cause other damage or damage to other tissue except for salivary glands. For your doctors to believe or have led you to believe that " damage in/to the neck " can occur leads me to understand that they may know a lot but they don't know enough to be treating ThyCa. Copy Dr. Ain's e-mails and bring them with you to the meetings. Gently.. ask them to read this information concerning ThyCa. Sincerely, Nick _____________________________________________________________________________ +++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++ Date: Sat, 01 Apr 2000 23:58:02 -0500 Subject: Re: Dosemitry testing Patty-- When I had dosimetry a couple of years ago, I had the scan dose (2 mCi I-131) , then every day for a (5-day) week I did a 24-hour urine collection and took it in to the hospital and they took a blood sample and checked me with the geiger counter. They checked the urine samples and blood samples for retention of RAI. They then calculated the maximum allowed dose to deliver 200 RADS to the blood. They came up with two figures, one based on whole body clearance data and the other based on urine clearance data. I think there are two methods of doing dosimetry. This one was called whole body dosimetry (using the method of Memorial Sloan-Kettering Medical Center).. Interestingly enough, the actual dose I ended up receiving was much less than either of these figures because it was limited by the rating of the hospital's room. Dorothy On Sat, 1 Apr 2000 09:10:56 -0800 " Patty Byrne " writes: I believe the dosemitry involves testing to see > how much > RAI an individual can consume before it will affect the bone > marrow...???? > Am I correct in this assessment ? Has anyone done this testing > before, can > you enlighten me ? Is it a once and done test or ongoing ? > +++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++ At 12/19/01 05:23 PM, you wrote: >Nick: > >I don't have a follow up with my new endo until Feb, so I will >address with her then. Also, I don't have a follow up with nuc med >doc until April, so I will address with them later too! > >What puzzles me about your response is that if there's no risk of >other damage (as you said), then why is there a need to individually >calculate doses -- why not give everyone the same dose? Do you agree >that the RAI that we don't " uptake " in thyroid tissue must then >settle elsewhere in our body until we pass it? This is the basis for >the nuc med docs telling me that they didn't want to dose me to high >and risk causing damage to other tissues in my neck. > >Again, I will ask more questions next time and try to gain proof if I >can. > >Gwynne Bambach - Michigan > > > > >, > > > > > > (STUFF DELETED) > > > > > > >Too much RAI can cause damage to healthy tissues in the neck area, >so > > >the RAI calculation is very critical in trying dose high enough; >but > > >not too high that it causes damage. > > > > > >To minimize damage from RAI, my dose was cut back to 101.5 mCi >(and a > > >plan for a second ablation 12 months later was discussed). > > > > (STUFF DELETED) > > > > > > > > >Gwynne Bambach - Michigan > > >Pap w fol var, tumor 1.7cm, lymph node mets > > >DX 12/21/00 (age 36) > > >TT 1/5/01 > > >RAI 4/11/01 101.5 mCi > > > (delayed 3 months due to iodine from previous CT scan) > > >2nd RAI upcoming 4/2002 ___________________________________________________________________________ ********************************************************************************\ ************************** (Dr. Ain) Date: Tue, 08 Jun 1999 09:11:49 -0400 Subject: Correction (TSH < 0.10): Re: TSH Level Debate In-reply-to: <v04003a00b382c117b8d1@[128.163.70.31]> Sender: thyca-approval@... To: thyca@... Reply-to: thyca@... Message-id: <v04003a02b382c6c00d41@[128.163.70.31]> MIME-version: 1.0 Content-type: text/enriched; charset=us-ascii Content-transfer-encoding: 7BIT Precedence: bulk References: >Regarding the TSH isssue: > It is my practice and teaching to maintain TSH values in my thyroid cancer patients to less than 0.10 mU/L. TSH is clearly a growth factor for thyroid cancer cells, although extremely aggressive varieties grow well independently of TSH. The most recent, well done study supports this practice [Pujol P, Daures J-P, Nsakala N, Baldet L, Bringer J, Jaffiol C. 1996 Degree of thyrotropin suppression as a prognostic determinant in differentiated thyroid cancer. J Clin Endocrinol Metab. 81:4318-4323]. The reason for this is consequent to known features of the cell biology of thyroid cancer cells as well as clinical epidemiological evidence as above. It is easily done with careful titration of the levothyroxine dose, good compliance by the patient, and careful follow-up. In less than 10% of patients, a small dose of a beta-blocker, to counteract an increased heart rate, may be useful. Recent studies have shown that a careful TSH suppression, as described, does not significantly increase bone loss [Marcocci C, Golia F, Bruno-Bossio G, Vignali E, Pinchera A. 1994 Carefully monitored levothyroxine suppressive therapy is not associated with bone loss in premenopausal women. J Clin Endocrinol Metab. 78:818-823]. There is no significant side effect when done carefully in most patients. > This is to be considered " standard of care. " Unfortunately, the " art of medicine " is sometimes too artful and subjective. >**************PLEASE BE ADVISED********************** >THE INFORMATION CONTAINED IN THIS COMMUNICATION IS INTENDED >FOR EDUCATIONAL PURPOSES ONLY. IT IS NOT INTENDED, NOR SHOULD >IT BE CONSTRUED, AS SPECIFIC MEDICAL ADVICE OR DIRECTIONS. ANY >PERSON VIEWING THIS INFORMATION IS ADVISED TO CONSULT THEIR OWN >PHYSICIAN(S) ABOUT ANY MATTER REGARDING THEIR MEDICAL CARE. >************************************************* > B. Ain, M.D. >Associate Professor of Internal Medicine >Director, Thyroid Nodule & Oncology Clinical Service >Director, Thyroid Cancer Research Laboratory >Division of Endocrinology and Molecular Medicine >Department of Internal Medicine, Room MN520 >University of Kentucky Medical Center >800 Rose Street, Lexington, Kentucky 40536-0084 ********************************************************************************\ ************************** Quote Link to comment Share on other sites More sharing options...
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