I was prescribed oral Xeloda together with infusions of oxiliplatin, but had to discontinue the Xeloda. My body smply could not tolerate the drug and while taking Xeloda I lost more than one pound per day, snd had relentless nausea and terrible pain in my hands and feet. After one three-week cycle my doctor discontinued the Xeloda. I was able to complete treatment with the oxiliplatin. This was in 2004 and I am cancer free today. Ask your mother's doctor for something else.
will xeloda given alone treat both tumours in chest wall with mestases in liver.
ya...but it seems mom has two different cells one is in breast and other in liver (some he3+, i guess) ,for oncolet the breast cells are being controlled but not the liver cells ,thats why disease has reoccured in liver ,is what the reply the doctor gave me,so in order to control both,mom needs to take oncolet and xeloda together....
5KGS AT 5FT HEIGHT, WE ARE TREATING THE METS WHICH HAS GONE TO HER LUNGS AND BONES AND LIVER WITH XELODA 1GRAM TWICE A DAY FOR 14 DAYS, AND THEY SCARED US WITH THE SIDE EFFECTS,BUT WE ARE ALSO GIVING HER HOMEOPATHY. WE ARE GIVING A GOOD NUTRITIONAL DIET ALONG WITH A PROTINEX SUPPLEMENT. ON 5TH OF FEB IS HER APPOINTMENT WITH THE ONCO. I HOPE XELODA HAS ARRESTED THE GROWTH OF CANCER CELLS. IF IT HAS CAN YOU TELL ME HOW MANY CYCLES CAN SHE TAKE WITHOUT IT DOING MUCH HARM.
My husband was diagnosed with colon Cancer in Feb 2007. He took chemo drug Xeloda and had standard radiation. During a check up in January 2008, tumors were found in his lungs- one in each lung, sizes: 7mm and 13mm. He took chemo: Folfox, Avastin, Oxaliplatin, and Xeloda until April 2008. The April CT scan revealed that the tumors had grown slightly and that there were four more small nodules visable.
My mom took Xeloda also as a maintenance drug for colorectal cancer. Typically diet and exercise do not affect CEA levels; however, inflammation can affect it. Sometimes CEA levels will rise if there is any type of inflammation. I know this is a scary time. Feel free to send me a message if you need to talk.
I am taking Xeloda and hoping that will help shrink this huge tumor. I cannot take infusion chemotheraphy for this as my side effects were so extreme the first time that Xeloda seems to be my only choice. However, I mostly would like to know what sort of bandages I could use if it breaks through and what can be done to diminish the rancid odor.
This discussion is related to <a href='/posts/show/260889'>ulcerating tumor</a>.
Within a month, the breast cancer started in her skin around the site of the node. She now has a red rash (skin mets) in approx half of her chest wall and is getting Chemo (Xeloda) and Herceptin. My question is, the skin is beginning to "harden" around the node removal surgery site. What does this mean? Any other comments on Skin mets would be greatly appreciated.
My Husband has Stage 4 Esophageal Cancer he is on treatments for a clinical trial Avastin, Xeloda, Oxaliplatin He has been on the Trial since early March 2010 he was diagnosed the end of February 2010 He is 35 years old and other then the Cancer has been in perfect health the treatments started off well but he developed stage 3-4 Neuropathy in August in his hands and feet. They have continued with the trial with just the Avastin and Xeloda which he is still taking.
My onco tried me on taxol, and avastin, then xeloda. Neither of these worked. He suggests that I try Jemzar. I have stage IV mestatic breast cancer that has spread to my spine. I was dx in Feb 2002. I have previously been on different chemo.surgery, hormonal.. arimidex, aromosin, fasoldex . and several radiation treatments. I am undecided on doing any more chemo. My cancer , of course , is er/pr positive. Is there any advice on this chemo. or is there another hormonal I could try.
When I enterered the trial in 2006, it was just for suboptimally debulked patients, but I think it has expanded to optimally debulked patients now. It is with avastin and has 3 arms, so I had 2 chances to get avastin and will never know whether or not I did. I am now in the monitoring stage and get CT scans every 3 months for 2 years (I have one more year). For the 2 year monitoring, there's, of course no possible individual benefit for me.
Dr. put her on Xeloda and Tykerb. She is on a 2 week on, 1 week off cycle. Her side effects have been severe. (i.e dehydration, throwing up, no appetite, mouth sores, nausea, you name it, she has it)
Her last visit to the Dr. (she goes about twice a week) just yesterday, he told her (in her words) that "everything is shrinking, and you'll have to be on this for the rest of your life.
I was prescribed Zofran for severe nausea I experienced during radiation and chemotherapy (5-FU, oxiliplatin and Xeloda.) It was not particularly helpful for me. The prescription was for 30 pills and cost $1200 USD. I do not recall the dose.
Because the Zofran did not help, I took it only for a short time, maybe 10-14 days. I did not experience any side effects specifically from the Zofran, or any benefits either.
Hope this info is helpful.
Hi Judi,
This sounds like the "red hand and foot syndrome" you get with Xeloda (another chemo treatment). Does it get hot and itch?
I found that using cold packs from the freezer when it was itching/burning helped to relieve the symptoms.
As for the skin peeling I used Shea Butter. Just the shea butter without any additives (like perfume). It is expensive but I shopped on ebay (wonderful place!
Hello again,
Apologies for not getting back to you before. I go to The Christie for my chemo on Tuesdays and it wipes me out for a couple of days.
I have lobular breast cancer which is hormone receptive but I am not sure of the status. I know that it feeds off oestrogen which is why I was given Arimidex (wonderful stuff) but it was stopped when they discovered I had osteoporosis.
This refers to a Sentinel node biopsy I had 6 years ago. The surgeon suggested it and I blindly trusted him to have it done. First, no family was allowed in with me. (If they had, they would have realized the trauma that I was going through). With the first injection, I bolted upright, fully screaming. It was the WORST pain I have ever been through. He had his assistants push me back down on the table and kept going with me screaming nonstop. I was so frightened. I was in a daze.
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