Temodar advice/info

cdavis07
cdavis07 Member Posts: 11
edited March 2014 in Brain Cancer #1
My husband who is 28 is about to start taking Temodar for his oligodendroglioma III. We are still waiting on a deletion report to determine if radiation is needed but the Temodar is a definate. This is our first course of treatment so we have no idea what to expect except what the doctors have told us. Any info we should know or be prepared for? Anything that helped with the side effects? Any info is much appreciated.
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Comments

  • mpatelpharm
    mpatelpharm Member Posts: 6
    My husband took Temodar for
    My husband took Temodar for 8 months and tolerated it pretty well. You take it 5 days every month. They should give your husband a anti-nausea med (kytril, zofran), and you take this 1 hour prior to the temodar. The kytril causes alot of constipation so you have to give something for that as well.(miralax or dulcolax). Otherwise its a fairly ok drug.

    Im sorry to hear that you are going through this. I also have a young husband (35 y/o) who was diagnosed 1 year ago with a brainstem glioma. We also have two little kids so it makes it even harder.
    Wish you the best in this long emotional journey...
  • Carrie King
    Carrie King Member Posts: 48
    Temodar
    My husband who is 36 yrs old started to take Temodar for his oligodendroglioma II. He has the deletions. He got fatigued and a little nauseous around day 4. However, once he decided to take the anti nausea pills, it was a lot better.

    He only took 1 months worth because we then found a Neurosurgeon who said he COULD do a resection and believed it could be done safely (we were originally told no). His 4.8 cm tumor went to 5mm. No neuro deficits. We are know awaiting a MRI Oct 4th since it has been three months. Depending on that, they will decide on Temodar (since this tumor is chemo sensitive), or stereotatic radiation.
  • cdavis07
    cdavis07 Member Posts: 11

    Temodar
    My husband who is 36 yrs old started to take Temodar for his oligodendroglioma II. He has the deletions. He got fatigued and a little nauseous around day 4. However, once he decided to take the anti nausea pills, it was a lot better.

    He only took 1 months worth because we then found a Neurosurgeon who said he COULD do a resection and believed it could be done safely (we were originally told no). His 4.8 cm tumor went to 5mm. No neuro deficits. We are know awaiting a MRI Oct 4th since it has been three months. Depending on that, they will decide on Temodar (since this tumor is chemo sensitive), or stereotatic radiation.

    Thank you
    We are still waiting on the deletion report. At first the surgeon felt my husband would not need radiation but now it depends on the deletions. We had our follow up with the nuero-oncologist and he would have started him this week on Temodar but he wants to see what the report says. I hope your husband is doing well. How does he deal with it? How do you?
  • mpatelpharm
    mpatelpharm Member Posts: 6
    cdavis07 said:

    Thank you
    We are still waiting on the deletion report. At first the surgeon felt my husband would not need radiation but now it depends on the deletions. We had our follow up with the nuero-oncologist and he would have started him this week on Temodar but he wants to see what the report says. I hope your husband is doing well. How does he deal with it? How do you?

    My husband is not doing
    My husband is not doing well. He was doing well up to about 1 month ago. He had been on temodar for 8 months and was in great remission. It was like he was back to normal.

    Today, he has lost 50% of his leg function and his speech is gone. We started him on physical therapy and speech therapy.

    Im sure as you all know that being a caretaker to a cancer spouse is harder than the actual patient. Not only do i have him to take care of, i also have two little girls aged 2 and 4. We have both set of grandparents close by to help with food, kids, etc... but still the emotional toll this takes on us... no one can help with.

    At the moment.. we take day by day. We are hoping that the new IV Chemo they have put him on will help him.

    Please pray for me!
  • cdavis07
    cdavis07 Member Posts: 11

    My husband is not doing
    My husband is not doing well. He was doing well up to about 1 month ago. He had been on temodar for 8 months and was in great remission. It was like he was back to normal.

    Today, he has lost 50% of his leg function and his speech is gone. We started him on physical therapy and speech therapy.

    Im sure as you all know that being a caretaker to a cancer spouse is harder than the actual patient. Not only do i have him to take care of, i also have two little girls aged 2 and 4. We have both set of grandparents close by to help with food, kids, etc... but still the emotional toll this takes on us... no one can help with.

    At the moment.. we take day by day. We are hoping that the new IV Chemo they have put him on will help him.

    Please pray for me!

    Mphatelpharm, I'm sorry to
    Mphatelpharm, I'm sorry to hear your husband isn't doing well. I hope you keep strong for him and your 2 little girls. I'm sure we are close in age and dealing with this at any age is difficult but when young it seems much harder. I feel like I should be senior citizen not turning 30. I believe in positive engergy and I am sending some your way. It makes me happy that you have some family close to help out. Even little things help. I hope the iv chemo works for your hubby and he gets better very fast. I'm sure he has great doctors and hopsitals working to make him better. I am praying for you and your family.
  • Carrie King
    Carrie King Member Posts: 48

    My husband is not doing
    My husband is not doing well. He was doing well up to about 1 month ago. He had been on temodar for 8 months and was in great remission. It was like he was back to normal.

    Today, he has lost 50% of his leg function and his speech is gone. We started him on physical therapy and speech therapy.

    Im sure as you all know that being a caretaker to a cancer spouse is harder than the actual patient. Not only do i have him to take care of, i also have two little girls aged 2 and 4. We have both set of grandparents close by to help with food, kids, etc... but still the emotional toll this takes on us... no one can help with.

    At the moment.. we take day by day. We are hoping that the new IV Chemo they have put him on will help him.

    Please pray for me!

    Praying for you, your
    Praying for you, your husband and your babies.
  • Carrie King
    Carrie King Member Posts: 48
    cdavis07 said:

    Thank you
    We are still waiting on the deletion report. At first the surgeon felt my husband would not need radiation but now it depends on the deletions. We had our follow up with the nuero-oncologist and he would have started him this week on Temodar but he wants to see what the report says. I hope your husband is doing well. How does he deal with it? How do you?

    Catherine--
    My husband is doing amazing -- he for the most part hasn't let this affect him at all. He is the most positive person I know.

    Me - I am supportive and fight for him. I "watch out" for him as he is still missing his bone flap (due to infection). I do this "too much" as I "am not his Mother". So you get the idea. . . .

    I try to keep busy and pray all the time. I work in the ER which probably isn't good as I imagine everything in the world that can happen to him.

    I think a support group would be great.
  • aranda
    aranda Member Posts: 11

    Catherine--
    My husband is doing amazing -- he for the most part hasn't let this affect him at all. He is the most positive person I know.

    Me - I am supportive and fight for him. I "watch out" for him as he is still missing his bone flap (due to infection). I do this "too much" as I "am not his Mother". So you get the idea. . . .

    I try to keep busy and pray all the time. I work in the ER which probably isn't good as I imagine everything in the world that can happen to him.

    I think a support group would be great.

    My thoughts and prayers are with you ladies
    My husband was diagnosed with astrocytoma grade3 in June of 09. It has been a long, hard fight. He has gone through 2 crainiotomies, insertion of chemo wafers, wound care, had a drain inserted to relieve pressure and fluid, radiation, and still taking temodar. He has more bad days then good, and we enjoy those good days. This morning he had his first seizure. He had fallen out of bed during his seizure, it was one of the scariest moments I had seen. You ladies are the same or close to us in age, sorry I am just going on and on but I hadn't found people who are really in the same situation as us. My thoughts and prayers are with you ladies and your families.
  • Fusionera
    Fusionera Member Posts: 10
    Temodar Advice/Info
    Hi C Davis,

    I am the Queen of Temozolomide...no joke. I took it in clinical trial from 1996-97, and of course it was approved by the FDA as a standard treatment in 2000. I can tell you that many people do tolerate it well and it works for them but everyone is different. The two side effects that I experienced were fatigue and lowered platelet counts. I almost missed the last dose of the trial because my platelets got too low. After three weeks of waiting and weekly blood tests, my counts became normal again and I finished the trial. Your husband's doctor may recommend iron pills or extra iron in his diet - you'd have to check with him/her.

    I did not get sick on Temozolomide, but I will advise to make sure that he has a GREAT antinausea med like Kytril or Zofran. Kytrial worked well for me on my last bout with this 5 years ago but I was also taking a heavier chemo. Zofran was fine in the 90s when I was on Temozolomide alone and it may be for your husband - talk to his doctor about the best choice for him.

    I still worked my full time job the whole time I was in the Temozolomide trial. I was tired and did not do too much in the way of activities outside of work but the quality of my life did not suffer too much either. I was not "flattened" by the Temozolomide, thank God.

    Feel free to e-mail me privately if I can help. Will keep you and your husband in my prayers.

    Johanna
  • cdavis07
    cdavis07 Member Posts: 11
    Fusionera said:

    Temodar Advice/Info
    Hi C Davis,

    I am the Queen of Temozolomide...no joke. I took it in clinical trial from 1996-97, and of course it was approved by the FDA as a standard treatment in 2000. I can tell you that many people do tolerate it well and it works for them but everyone is different. The two side effects that I experienced were fatigue and lowered platelet counts. I almost missed the last dose of the trial because my platelets got too low. After three weeks of waiting and weekly blood tests, my counts became normal again and I finished the trial. Your husband's doctor may recommend iron pills or extra iron in his diet - you'd have to check with him/her.

    I did not get sick on Temozolomide, but I will advise to make sure that he has a GREAT antinausea med like Kytril or Zofran. Kytrial worked well for me on my last bout with this 5 years ago but I was also taking a heavier chemo. Zofran was fine in the 90s when I was on Temozolomide alone and it may be for your husband - talk to his doctor about the best choice for him.

    I still worked my full time job the whole time I was in the Temozolomide trial. I was tired and did not do too much in the way of activities outside of work but the quality of my life did not suffer too much either. I was not "flattened" by the Temozolomide, thank God.

    Feel free to e-mail me privately if I can help. Will keep you and your husband in my prayers.

    Johanna

    Thank you.
    Paul is actually starting his second round of Temodar tonight. Kinda worried because he has been having some bad headaches. Just spoke to the doctor today and we are going in next week for a check up. His MRI on Oct 25th looked great but for some reason he is having some issues. The first round of Temodar went well. He felt a little sick but he is taking Zofran which seems to help. I just hope his body works the kinks out. It kills me to see him in pain or suffering. Hopefully the doctor will be able help him with the headaches and other pains.

    Did you do the Gliadel Chemo wafers? Paul did and I worry that they may be causing his issues. The benefit of them is great so if these are the side effects and temporary then that is ok. Just need it to stop soon.

    Thanks for checking in and helping me out.

    Catherine
  • j_waffles
    j_waffles Member Posts: 22
    I'm 27 and on round 5 of
    I'm 27 and on round 5 of Temodar. I've been doing pretty well (apart from the past couple of weeks, but I think it's something other than the Temodar). I think what we have going for us is that we're young and our bodies can withstand more than the old folks. Also, I recommend that your husband uses a anti-nausea med (I use Zofran) 30 mins prior to taking Temodar. It works for me... and the one time I was late to take the Temodar after the Zofran because I fell asleep, I had a rolling stomach. Not fun.
  • Blanca831
    Blanca831 Member Posts: 8
    Temodar treatment
    Hello! I am 28 years old and I just finished up my 4th round of temodar and I am glad to say I have not had any side effects whatsoever. I take an anti nasuea pill 20 min before the Temodar. I am proud to say that I havent even felt tired, or any nasuea which are the most common effects. Every person is different but thank goodness I am going through this treatment free of any side effects! Hope your husbands treatment goes as well as mine.
  • KMPonder
    KMPonder Member Posts: 102
    My husband just finished 10
    My husband just finished 10 straight months of Temodar, after initially taking 44 days with his radiation of a lower dosage of Temodar. He consistantly took the Zofran, anti-nausea pill, one hour before taking the chemo. He never felt nauseous from it. The biggest side effect he had was fatigue. Because he went back to work full-time teaching after the radiation/44 days of chemo, I am sure that added to his fatigue. He'd come home and nap or head to bed early and rest most weekends. He rebounded in the summer, because he wasn't teaching, even on the chemo. I can tell you since he's been off, his energy level is so significantly better, but he's also been given Ritalin to help with the fatigue.

    It's important to remember no two people are alike, but my prayer is he'll tolerate it as well as my husband and be able to work and/or do many of the things he enjoys. Rest is essential, though.

    If possible, try to keep up a level of exercise he may be comfortable with. We tried to just walk as much as we could. There were days he didn't feel like it, but he typically felt better if he pushed through and took at least a short walk. (He wasn't big into exercise before.)

    All the very best through this, and make sure to take care of yourself, too!
  • KMPonder
    KMPonder Member Posts: 102

    My husband is not doing
    My husband is not doing well. He was doing well up to about 1 month ago. He had been on temodar for 8 months and was in great remission. It was like he was back to normal.

    Today, he has lost 50% of his leg function and his speech is gone. We started him on physical therapy and speech therapy.

    Im sure as you all know that being a caretaker to a cancer spouse is harder than the actual patient. Not only do i have him to take care of, i also have two little girls aged 2 and 4. We have both set of grandparents close by to help with food, kids, etc... but still the emotional toll this takes on us... no one can help with.

    At the moment.. we take day by day. We are hoping that the new IV Chemo they have put him on will help him.

    Please pray for me!

    God bless you. I just can't
    God bless you. I just can't imagine you going through this with such small children. I hope you'll post again and let us know how things are going. It's so hard on our loved ones battling the cancer, but it's tough on us caregivers. I know we'd do anything to take all the pain away for them. So glad you do have family who can help. Not sure I could have made it through some days without both sets of parents.
  • TomK
    TomK Member Posts: 9
    cdavis07 said:

    Thank you
    We are still waiting on the deletion report. At first the surgeon felt my husband would not need radiation but now it depends on the deletions. We had our follow up with the nuero-oncologist and he would have started him this week on Temodar but he wants to see what the report says. I hope your husband is doing well. How does he deal with it? How do you?

    Deletion Report?
    I see a few entries for that related to Temodar-what is that right now I am taking Temodar amd radiation 5 days per week.
  • curly123
    curly123 Member Posts: 4
    temodar reactions
    I have brain surgery on Arril fools' day of this year after whish I waited a good 6 weeks for my body to recover after which I had 40 treatments of radiation at the same time ingesting Temodar pills. One pill a day 250 mg. I was fortunate in that I was given anti nausea pills and in general just like the taste of food. I found that memory,taste and eating place a great role... example if you h ave a cold snd go to your favorite restaurant and order your favorite meal when you taste it ,it would'nt taste right,why because your taste buds are messed up from from your cold...well that is like chemoX10!
    I was given a wonderful piece of advice to share... eat foods had you so not have result memories of....it worked for me!
  • curly123
    curly123 Member Posts: 4

    My husband is not doing
    My husband is not doing well. He was doing well up to about 1 month ago. He had been on temodar for 8 months and was in great remission. It was like he was back to normal.

    Today, he has lost 50% of his leg function and his speech is gone. We started him on physical therapy and speech therapy.

    Im sure as you all know that being a caretaker to a cancer spouse is harder than the actual patient. Not only do i have him to take care of, i also have two little girls aged 2 and 4. We have both set of grandparents close by to help with food, kids, etc... but still the emotional toll this takes on us... no one can help with.

    At the moment.. we take day by day. We are hoping that the new IV Chemo they have put him on will help him.

    Please pray for me!

    alternatives?
    I am sorry to hear about your husband...I was on chemo...now on Avastin...I feel very good... my ongoloist wants to see how I am going with Avastin before bringing in Themora again.
    I am being cared for at Jeff in Philly.My fr is both a Oncologist and Neurolist.He is looking at my symptoms as well as my mri. I had 80% of the tumor by surgery. Hope this helps
  • curly123
    curly123 Member Posts: 4
    cdavis07 said:

    Thank you.
    Paul is actually starting his second round of Temodar tonight. Kinda worried because he has been having some bad headaches. Just spoke to the doctor today and we are going in next week for a check up. His MRI on Oct 25th looked great but for some reason he is having some issues. The first round of Temodar went well. He felt a little sick but he is taking Zofran which seems to help. I just hope his body works the kinks out. It kills me to see him in pain or suffering. Hopefully the doctor will be able help him with the headaches and other pains.

    Did you do the Gliadel Chemo wafers? Paul did and I worry that they may be causing his issues. The benefit of them is great so if these are the side effects and temporary then that is ok. Just need it to stop soon.

    Thanks for checking in and helping me out.

    Catherine

    temodar...zofran to be sure!
    The wholetime that i was on temodar I was on zofran to be sure!I missed a dose and I felt like I was at sea.
    However, if Paul is having issues with swelling in his brain he should be getting other medicine.
  • RLR
    RLR Member Posts: 36
    Temodar
    Hello:

    I am 56 and have had glio blastoma grade4 since Dec 08 and had surgery in Jan,09. I have been on Temadar ever since that time. The biggest thing I can tell you to help is to drink a LOT OF WATER and I mean a LOT. Before I was drinking a lot of water when taking the pill I would get sick and vomit every night. When I say a lot I always drink about 2 to 3 -20 ounce glasses of water after taking the chemo. I always take it at about 6:00 to 7:00 pm along with the anti-nausea pill and drink the water before 9:00 or 10:00 pm. I have never gotten sick after doing this.
    As you can see I have been on chemo for 1 1/2 years now and my Doctor says will be on it the rest of my life.But it has been working very very good for me!
    Good luck
  • alohajimmy
    alohajimmy Member Posts: 7
    temodore
    My daughter was on it for 18 months. Other than some tiredness, this drug did not inhibit her lifestyle much. She was on both a 5/28 and a 45/60 schedule. - One concern is that in time the tumor develops a means of creating an enzyme which blocks the temodore. One trial is combine the temodore with another drug which aims to prevent the enzyme from interfering with the temodore.