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OH CRAP!  Part NUMBER 2 - Can I Have Dueling Cancers?

5/20/2017

6 Comments

 
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Part two of my kidney saga. To view part one CLICK HERE.

​I had my visit with Dr. Thiel of Mayo Jacksonville the head of the Urology Department, and in his words "The Kidney Tumor Must Come Out!"  OH CRAP!  The malignancy risk of Bosniak III cystic lesions is thought to be approximately 50%, however the reported malignancy rates range from 31% to 100%. The good news is that he feels the location of the tumor will allow its removal without much if any effect on my overall kidney function. More good news the National Cancer Institute lists the average life expectancy of kidney cancer at 14 to 15 years, well above the 5.5 years for myeloma.    

Dr. Thiel  said in the old days kidney cancer was seldom if ever found before it had spread to other parts of the body, but with new imaging like CT and MRI, it is often found earlier with a much better prognosis.  They usually find it early by happenstance, without any observable symptoms. How kidney cancer was discovered in the past is because of pain in the  back or side, and/or blood in the urine.  I did not have any of these symptoms, but now have noticed a low grade feeling in my lower left side.  This may just be my mind playing tricks on me, and all myeloma patients can relate to these feelings during their myeloma journey.   

So at this point the plan is to have Robotic Surgery(partial resection of my left kidney) on June 2nd  with a machine called the Da Vinci Robot. To me it looks more like a spider or octopus. Apparently this method provides for a quicker recovery and from what I understand Dr. Thiel is the best there is in the Southeastern USA.  If practice makes perfect Dr. David(Scissorhands) Thiel has performed thousands of surgeries and over 300 with the Da Vinci Robot.  In addition, I asked him about outcomes, and with a hint of humor asked if his patients dropped like flies after Robotic surgery? He said he has not lost anyone. Not a bad batting average!   

I asked if I would have radiation or chemo after the surgery.  It was a surprise to me but he indicated radiation will kill the kidney and there are no drugs which have shown efficacy in the treatment of kidney cancer.  The standard of care is to remove the kidney, a far simpler procedure than a resection, and with most people the remaining kidney will do the work required all by itself. However with people like me who have kidney insufficient from my myeloma, I would be back on dialysis, and that would not be fun. 

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Cancer can be so inconvenient!  We had planned on being in Wisconsin for the summer starting in May, however this has temporarily derailed those plans.  We could have had this done at Mayo Rochester, but the Mayo system seems to operate like three separate hospitals.  I have had all the testing at Mayo and it is on their system, but because I am not a Mayo Rochester patient I can not get an opinion if I can go to Rochester for treatment without a visit first.  Dr. Thiel had said I should use his name when I called his counterpart in Rochester and I assumed it would make this a seamless transition.  It hasn't yet.  I guess I was surprised because of the close interactions of the tightly knit  myeloma specialist community at Mayo, or maybe that is just my misconception.  

​Good luck and may God Bless your cancer journey.   For more information on multiple myeloma survival rates and treatments CLICK HERE and you can follow me on twitter at: https://twitter.com/grpetersen1
6 Comments
Sheri Baker
5/20/2017 05:46:52 pm

Wow Gary! So sorry to hear you are going through this. My thoughts and prayers are with you.

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Gary Petersen link
5/21/2017 05:49:10 am

Sheri, thank you for the thoughts and prayers. I knew myeloma patients had a higher risk of secondary cancers, but wishful thinking made me think NOT ME! Well it was ME, and as my friend Pat Killingsworth had provided a great blog post explaining his thoughts on secondary cancers and you can read it if you go the the link: http://multiplemyelomablog.com/2015/06/my-opinion-many-secondary-cancers-go-unreported.html

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Kathleen Farrell
5/21/2017 08:03:43 am

I have kidney cancer. I was diagnosed in 2008 at Hospital of the Iniversity of Pennsylvania. It was a huge one sitting on my left kidney and pushing up into my spleen. Had radical nephrectomy and did well. It is metastatic at this point and I am on treatment. Times have changed and there is a myriad of treatment options that was not available 10 years ago. Please check out smartpatients.com, there are so many of us dealing with multiple problems. I was diagnosed with MGUS 4 years ago and have to be monitored. If you have any questions please feel free to ask. Good luck.

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Gary Petersen link
5/21/2017 02:48:28 pm

Kathleen, thank you so much for the heads up about new treatment options. I visit smartpatients for myeloma, but will be visiting for kidney cancer as well. Good luck and God Bless your metastatic cancer journey/Gary Petersen

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Mark
6/11/2017 11:40:30 am

Sorry to read about this. Prayers being sent that this will be taken care of and you can spend the summer enjoying "brats and beer" in Wisconsin.

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Gary Petersen link
6/12/2017 09:41:06 am

Mark, Prayers are always welcome and appreciated. I have now talked with Mayo Jacksonville, Mayo Rochester, and Mt. Sinai in New York, and have decided to delay the surgery until the beginning of August. Two of them said it would be best to getting it done in a few months, the other said based on my myeloma it might be wise to watch and wait. I have a bias for action, so watch and wait is out, and I also have a bias for "Practice makes perfect" and I have chosen the doctor who has performed over 3000 of these procedures. Best Regards Mark/Gary

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    Gary R. Petersen
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