The Cancer Survivors Network (CSN) is a peer support community for cancer patients, survivors, caregivers, families, and friends! CSN is a safe place to connect with others who share your interests and experiences.

Thank you for being a part of the Cancer Survivor Network community. Survivors and caregivers like you have played a unique role in fostering an online environment that encourages connection among those needing support, community, and education. On May 28, the Network will be discontinued. More details are available here . If you have any questions, contact CSNSupportTeam@cancer.org. Thanks again for the support you’ve provided each other over the years. We remain committed to supporting you in other ways throughout your cancer journey.

1st Recurrence

3750lsd
3750lsd CSN Member Posts: 7

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

  • NoTimeForCancer
    NoTimeForCancer CSN Member Posts: 3,629 Member
    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)

  • 3750lsd
    3750lsd CSN Member Posts: 7

    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

    Thank you for getting back to me.

  • wholfmeister
    wholfmeister CSN Member Posts: 315
    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.

  • lovesanimals
    lovesanimals CSN Member Posts: 1,366 Member

    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.

    Hi

    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

  • pandagypsy
    pandagypsy CSN Member Posts: 113 Member

    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 Money Mouth 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...........Sealed