1st Recurrence
Well, I had 10 great healthy months and now my first recurrence. Ironically, a year to the day that I was declared NED, I had my port put back in on Friday. Start chemo again tomorrow.
My question is has anybody had Carbo/Doxil for recurrence after Cisplatin/Taxol the first time around? Was it easier? Did you lose your hair?
Just wondering what I might expect. Thanks in advance.
Comments
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3750lsd, I am sorry I cannot
3750lsd, I am sorry I cannot help you with an answer Carbo/Doxil, but I think if you "Search" for Doxil there is one if not more discussions on it. I know I have seen it, and if you don't see it here you might want to "Search" in the Uterine board. I can't remember where I saw it (must be that darn chemo-brain)
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Thank you for getting back toNoTimeForCancer said:3750lsd, I am sorry I cannot
3750lsd, I am sorry I cannot help you with an answer Carbo/Doxil, but I think if you "Search" for Doxil there is one if not more discussions on it. I know I have seen it, and if you don't see it here you might want to "Search" in the Uterine board. I can't remember where I saw it (must be that darn chemo-brain)
Thank you for getting back to me.
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My story
My story isn't exactly like yours...I have been in constant treatment for nearly 3 years. I had the typical first-line treatment and debulking, followed by IV/IP chemo, then a year of monthly taxol. Then gemzar, a dose or two of avastin, followed by doxil and now topetecan.
My hair had a hard time growing with the taxol, but after that, the other drugs didin't seem to bother my hair.
The only drug that gave me problems was doxil. I had a horrible, horrible reaction after the second dose. Extremely painful blisters over hands, feet, mouth and throat, any where skin touches skin (Yes, EVERYWHERE skin touches skin!) I was in very bad shape and in a wheelchair for three weeks. I don't mean to scare you because I know my reaction was extreme and not the typical at all. I would suggest you take seriously all the warnings about avoiding heat and especially avoiding anything that causes friction on the skin. Like holding the handles of a bicycle. Or, carrying a suitcase. Really, just be very, very careful...pamper yourself...don't do anything! Really, just tell people, you know, I have to really not risk my hands or my skin.
I am so sorry you have the disappointment of a recurrence, but you smacked it down before and I am sure you will do it again! Sending you all my best wishes.
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Hiwholfmeister said:My story
My story isn't exactly like yours...I have been in constant treatment for nearly 3 years. I had the typical first-line treatment and debulking, followed by IV/IP chemo, then a year of monthly taxol. Then gemzar, a dose or two of avastin, followed by doxil and now topetecan.
My hair had a hard time growing with the taxol, but after that, the other drugs didin't seem to bother my hair.
The only drug that gave me problems was doxil. I had a horrible, horrible reaction after the second dose. Extremely painful blisters over hands, feet, mouth and throat, any where skin touches skin (Yes, EVERYWHERE skin touches skin!) I was in very bad shape and in a wheelchair for three weeks. I don't mean to scare you because I know my reaction was extreme and not the typical at all. I would suggest you take seriously all the warnings about avoiding heat and especially avoiding anything that causes friction on the skin. Like holding the handles of a bicycle. Or, carrying a suitcase. Really, just be very, very careful...pamper yourself...don't do anything! Really, just tell people, you know, I have to really not risk my hands or my skin.
I am so sorry you have the disappointment of a recurrence, but you smacked it down before and I am sure you will do it again! Sending you all my best wishes.
I don't have any experience with this chemo cocktail but I wanted you to know that I am sending lots of prayers and good wishes your way! May this chemo combo kick your cancer's butt to the curb!
Warmly,
Kelly
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I can't really comment on your particular cocktail; I was diagnosed stage IV ovar in Feb. 2006. Besides the surgery , debulking, etc. I had 6 mo. of carbo & cispl, then 6 mo. cispl. & gemzar. I didnt experience much problem with the gemzar. Recurrence, which was expected "at some time" wasn't until May of 2014.....I had weekly cocktails of cispl. & taxol for 5 months and am now NED The taxol was pretty hard on me, had a couple of tranfusions and iron treatments, and neuropathy at the end. I am happy to say the neuropathy is S L O W L Y getting better.........I am just now FINALLY having some really good days.....guess I am just impatient since everyone was getting excited about the last chemo (0CTOBER 20!), so I thought I should feel better sooner. What has gotten me thru this, besides having a supportive hubby (except when he is overwhelmed, which is expected) is that I made my OWN schedule: if I knew it was going to be a really crappy day, I would announce I was spending the day on the couch being useless and probably sleeping. I didn't try to act like I was having a wonderful time. That was so much easier on me, as the patient, and also hubby, the caregiver, knew it was a day for him hang out with buddies or roam around Home Depot. Take care of yourself........I wish you the least problem free chemo possible...........
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