#72593 04-07-2008 01:20 PM | Joined: Apr 2008 Posts: 7 Member | | Member Joined: Apr 2008 Posts: 7 | Hi everyone- Even though this is my first time posting I have been coming to this site since January when my mother was diagnosed with oral cancer. She had a white patch on her gums which she thought may be thrush, it turned into a growth she went to the dentist which told her that she needed to have a deep cleaning. She had that done and nothing improved the growth continued to get larger, she finally was referred to a periodontist who immediately told her to go to the oral surgeon to get a biopsy. The biopsy result show she had squamous Cell Carcinoma and was advised to contact her medical insurance company for referral to head and neck oncology.
She has Kaiser for her insurance so her options were limited were she could go for her treatment. She first meet with the head and neck surgeon who said they would present her case to their tumor board on Monday and would call to let us know their recommendations. They ended up recommending surgery that would include removing the jaw because the tumor had invaded the bone, and then removing a bone,muscle and tissue from her leg and resculpting a new jaw. They also did a neck disection.
She had the surgery on feb 19. The surgery went well and the intial lab results were clear margins. But the next day she had a heart attack while in ICU. She spent two weeks in the hospital to make sure her heart was ok. It test on her heart didn't show any damages and the doctors said it was probably from the stress of her surgery.
She also has a wound on her neck that the stitches came apart due to some radiation she had 40 years ago for Hodgkins. The wound still has not healed all the way.
Anyway the reason I feel we now are so confused is that we met with the radiologist on friday regarding radiation, and they are telling us that are leaving it up to her regarding receiving radiation.
They said she was T4N0MO, grade 1 and they told the chance of reoccurance is about 50% maybe a little less if she opted for no Radiation. If she Received Radiation it would be IMRT 5 days a week for 6 weeks, but she would have to deal with the side effects plus because she has had previous rads to her neck the side effects could be worse, but would cut down the chance of reoccurance in half. Even her surgeon said he didn't know if it was him what he would do.
My mom is terrible about making desisions and keeps asking me what she should do?
Anyone with any advice would be appreciated.
Sorry I wrote so much I thought it would help to know the background.
Sherri
CG to mom, T4N0M0, Surgery to remove jaw and reconstruct with bone from leg
| | | | | Joined: Sep 2006 Posts: 8,311 Senior Patient Advocate Patient Advocate (old timer, 2000 posts) | | Senior Patient Advocate Patient Advocate (old timer, 2000 posts) Joined: Sep 2006 Posts: 8,311 | Sherri,
Was/is she a tobacco user? How old is she? How about alcohol consumption? What is her general health condition? How much radiation did she receive before? Did they mention any concurrent chemo with the radiation?
David
Age 58 at Dx, HPV16+ SCC, Stage IV BOT+2 nodes, non smoker, casual drinker, exercise nut, Cisplatin x 3 & concurrent IMRT x 35,(70 Gy), no surgery, no Peg, Tx at Moffitt over Aug 06. Jun 07, back to riding my bike 100 miles a wk. Now doing 12 Spin classes and 60 outdoor miles per wk. Nov 13 completed Hilly Century ride for Cancer, 104 miles, 1st Place in my age group. Apr 2014 & 15, Spun for 9 straight hrs to raise $$ for YMCA's Livestrong Program. Certified Spin Instructor Jun 2014.
| | | | | Joined: Apr 2008 Posts: 7 Member | | Member Joined: Apr 2008 Posts: 7 | David- I thought I covered everything but I guess I left out some important info.
She is 66 years old, a non-smoker, non-drinker. I don't know exactly how much radiation she had previously I just know that it was 43 years ago when technology wasn't as good. I think it was cobalt. It burned her entire neck. Generally her health is ok. She takes blood pressure meds,thyroid med and cholesterol med.
Hope this helps.
Sherri
CG to mom, T4N0M0, Surgery to remove jaw and reconstruct with bone from leg
| | | | | Joined: Jun 2007 Posts: 10,507 Likes: 8 Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) | | Administrator, Director of Patient Support Services Patient Advocate (old timer, 2000 posts) Joined: Jun 2007 Posts: 10,507 Likes: 8 |
Sherri:
Welcome to OCF. You will find lots of support here. Sorry that I cant give you advice, Im sure there is someone here who would be able to help you.
After reading your post, I just wanted to say I hope your mother feels better soon. She has gone thru so much with the surgery and then the heart attack on top of it. Your mom is lucky to have you as her caregiver.
ChristineSCC 6/15/07 L chk & by L molar both Stag I, age44 2x cispltn-35 IMRT end 9/27/07 -65 lbs in 2 mo, no caregvr Clear PET 1/08 4/4/08 recur L chk Stag I surg 4/16/08 clr marg 215 HBO dives 3/09 teeth out, trismus 7/2/09 recur, Stg IV 8/24/09 trach, ND, mandiblctmy 3wks medicly inducd coma 2 mo xtended hospital stay, ICU & burn unit PICC line IV antibx 8 mo 10/4/10, 2/14/11 reconst surg OC 3x in 3 years very happy to be alive | | | | | Joined: Mar 2008 Posts: 46 Contributing Member (25+ posts) | | Contributing Member (25+ posts) Joined: Mar 2008 Posts: 46 | I think you should do what I did. I wieghed all the options and made my choices based on the pros and cons. The Choice has to be hers though. talk to the R/O carefully and say, Mom, here is the deal if you do and here is the deal if you do not. What do ya want to do? Heck, you can get a second opinion as well if that helps.
Prayers to you and your mother.
john
Stage 4A SSC Left Tonsil, back of tongue and Lymph nodes on left side. Tonsil removed, Chemo and Radiation treatments completed on June 26, 2008.
| | | | | Joined: Sep 2006 Posts: 8,311 Senior Patient Advocate Patient Advocate (old timer, 2000 posts) | | Senior Patient Advocate Patient Advocate (old timer, 2000 posts) Joined: Sep 2006 Posts: 8,311 | Sherri, If she is in doubt then she needs to get another opinion. I went to 5 different cancer doctors before I thought I could make an informed decision. Has any of her docs mention the possible cause of the SCC? Have her slides been tested for HPV?
David
Age 58 at Dx, HPV16+ SCC, Stage IV BOT+2 nodes, non smoker, casual drinker, exercise nut, Cisplatin x 3 & concurrent IMRT x 35,(70 Gy), no surgery, no Peg, Tx at Moffitt over Aug 06. Jun 07, back to riding my bike 100 miles a wk. Now doing 12 Spin classes and 60 outdoor miles per wk. Nov 13 completed Hilly Century ride for Cancer, 104 miles, 1st Place in my age group. Apr 2014 & 15, Spun for 9 straight hrs to raise $$ for YMCA's Livestrong Program. Certified Spin Instructor Jun 2014.
| | | | | Joined: Nov 2002 Posts: 3,552 Patient Advocate (old timer, 2000 posts) | | Patient Advocate (old timer, 2000 posts) Joined: Nov 2002 Posts: 3,552 | Kaiser won't pay for 5 separate opinions. You may get them to pay for one however and I would ask for a consult with City of Hope CCC since you are in LA. (I assumed you were in LA)
Clinical trials have conducted on re-irradiating previously radiated patients and have found the side effects to be tolerable. The cobalt does add a twist to it since the recent clinicals involved ionizing radiation.
Hodgkins is typically treated by a light dose of whole body radiation. The down side of it was as the source weakened they had to increase the exposure time which could cause skin damage due to the "dark radiation" aspect of it. Only third world countries still use cobalt today.
The decision has to be about risk & benefit. The RO (and/or even the MO) is the best qualified to help you with the decision.
Last edited by Gary; 04-08-2008 02:26 AM.
Gary Allsebrook *********************************** Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2 Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy) ________________________________________________________ "You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
| | | | | Joined: Apr 2008 Posts: 7 Member | | Member Joined: Apr 2008 Posts: 7 | Thank you everyone for your advise. We are going to try and get a second opinion. The Kaiser RO & MO both said the pro's and Con's are about 50/50. Does anyone any recommendations in the Los Angeles area? I will also call City of Hope.
Sherri
CG to mom, T4N0M0, Surgery to remove jaw and reconstruct with bone from leg
| | | | | Joined: Aug 2005 Posts: 307 Platinum Member (300+ posts) | | Platinum Member (300+ posts) Joined: Aug 2005 Posts: 307 | Hi Sherri,
We live in Southern California and when my husband was diagnosed with oral cancer we had Kaiser Insurance. I have to say I was impressed with the treatment they gave him. His ENT was in Woodland Hills, but he went for his radiation treatments in L.A.
Now we have Blue Cross and he goes for his follow up check ups through UCLA Medical Center, Head/Neck Dept. They are excellent. You might want to check with them too.
Best of luck,
Shelley
Caregiver to husband Ron. Throat Cancer. Finished 35 radiation treatments on 11/21/04. 8/2/11 small lesion on lower gum, laser Procedure to remove. 3/6/12 Doc. removed another lesion on outside of his neck. Did a skin graft from his chest to replace the skin on his neck. Went to Heaven on 6/24/12.
| | | | | Joined: Nov 2002 Posts: 3,552 Patient Advocate (old timer, 2000 posts) | | Patient Advocate (old timer, 2000 posts) Joined: Nov 2002 Posts: 3,552 | Sherri, I have to agree with Shelley, I too have Kaiser and have had excellent care from them, always in compliance with NCCN Oncology Practice Guidelines. They paid for me to go the UCSFCCC for my RT. Things are changing at Kaiser. They are building dedicated cancer centers and are stopping outsourcing RT and bringing it in house. No doubt in anticipation of the 36 million baby boomers. FYI, most of us had 50/50 odds, or worse, (mine was technically 38.2% chance of 5 year survival). Keep focused on risk/benefit and not statistics. City of Hope is a CCC in the LA area. http://www.cityofhope.org/home.htm
Gary Allsebrook *********************************** Dx 11/22/02, SCC, 6 x 3 cm Polypoid tumor, rt tonsil, Stage III/IVA, T3N0M0 G1/2 Tx 1/28/03 - 3/19/03, Cisplatin ct x2, IMRT, bilateral, with boost, x35(69.96Gy) ________________________________________________________ "You are a mist that appears for a little while and then vanishes" (James 4:14 NIV)
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