stereotactic radiotherapy for supraclavicular lymph node mets

upsofloating
upsofloating Member Posts: 466 Member
edited June 2011 in Uterine/Endometrial Cancer #1
Had consult today with radiation oncologist to evaluate targeted treatment of upsc recurrence in supraclavicular lymph nodes. Treatment is basically palliative in that we are not going for cure.

After lengthy discussion and extensive review of detailed disease history, followed by review of possible radiotherapy options, we agreed that best route is stereotactic radiotherapy, a technique that delivers high dose radiation to very precise targets that allows for fewer treatments, with less collateral damage and side effects. I will be scheduled for a planning session shortly and current expectation is that it can be done in 6 sessions, 3 per week over 2 weeks - I believe this is referred to as fractionated stereotactic radiotherapy. Goal is to limit side effects as much as possible while delivering effective treatment. Sounds quite doable after which I will revisit chemo options with gyn-onc. I'm really glad to have this option available since location of nodes is quite close to esophagus and trachea and this state-of-the-art Varian Trilogy RapidArc therapy is an image-guided radiation therapy and is delivered faster and with extreme accuracy, more so than cyberknife technology, reducing side effects/problems usually associated with radiotherapy.

Has anyone else had this done?

Always nice to have a treatment plan in the works.
Annie

Comments

  • california_artist
    california_artist Member Posts: 816 Member
    #2
    Dear Annie
    The second sentence in the opening paragraph stopped my heart short. How easily we have learned to talk about and use words like pallative care and other heartbreaking terms. I ache for how you may feel now. But, maybe it isn't so. In my heart of heart of hearts, I will always believe there is a cure in all our futures.

    Anything I can do let me know.

    Love to you and yours,

    Claudia
  • paris11
    paris11 Member Posts: 159
    #3
    SBRT
    Annie,

    I discussed SBRT with my Radiation Oncologist at Northwestern. I was not eligible because of the proximity of the lymph node to the bowel. NORTHWESTERN has had much success with this treatment.

    All the best to you,

    Connie
  • Rewriter
    Rewriter Member Posts: 493 Member
    #4
    california_artist said:

    Dear Annie
    The second sentence in the opening paragraph stopped my heart short. How easily we have learned to talk about and use words like pallative care and other heartbreaking terms. I ache for how you may feel now. But, maybe it isn't so. In my heart of heart of hearts, I will always believe there is a cure in all our futures.

    Anything I can do let me know.

    Love to you and yours,

    Claudia

    Annie
    I'm glad that you have a treatment plan that you consider doable and that I hope will give you many more years of quality living.

    I, too, was stopped by the word "palliative." Isn't it true that many cancers that can't be cured can still be managed as chronic diseases, with the person still being able to have quality of life? You, and many other women here, have proven that to be true.

    I wish you peace, the strength to continue your integrative practices, and the expectation of a cure down the road. Treatments seem to be getting better all of the time.

    My heart is with you.

    Jill
  • upsofloating
    upsofloating Member Posts: 466 Member
    #5
    Thanks Claudia, Jill, and
    Thanks Claudia, Jill, and Connie for your good thoughts. I guess i've gotten into the 'doc-speak' way of referring to such things. Palliative to me always sounded like on your way to hospice, but i'm not there yet. My gyn-onc is not terribly encouraging about further systemic treatment but i'll revisit that after radiation. Meanwhile, this past week, I've played 2 games of golf (one long, one short course), enjoyed an 8-mile bike ride, and doing my 2-3 mile neighborhood walks. Tomorrow it's off to my local Relay for Life to try (and that's a really big try!) to make my 18 mile goal. I did 17 miles last year - it's one mile for every year I have lived with cancer (breast 18, and heading for 4 for UPSC). My husband decided that we best start with one lap for each year, they try for 2 laps per, then 3, and if we can make it by the 24-hr deadline and the body holds out, we'll do the 4 laps per, to make the 18 miles. One foot in front of the other ;-)
    Annie
  • fuzzytrouble
    fuzzytrouble Member Posts: 212
    #6
    upsofloating said:

    Thanks Claudia, Jill, and
    Thanks Claudia, Jill, and Connie for your good thoughts. I guess i've gotten into the 'doc-speak' way of referring to such things. Palliative to me always sounded like on your way to hospice, but i'm not there yet. My gyn-onc is not terribly encouraging about further systemic treatment but i'll revisit that after radiation. Meanwhile, this past week, I've played 2 games of golf (one long, one short course), enjoyed an 8-mile bike ride, and doing my 2-3 mile neighborhood walks. Tomorrow it's off to my local Relay for Life to try (and that's a really big try!) to make my 18 mile goal. I did 17 miles last year - it's one mile for every year I have lived with cancer (breast 18, and heading for 4 for UPSC). My husband decided that we best start with one lap for each year, they try for 2 laps per, then 3, and if we can make it by the 24-hr deadline and the body holds out, we'll do the 4 laps per, to make the 18 miles. One foot in front of the other ;-)
    Annie

    Annie
    When I was told that it was not curable, I thought I was a goner. I am thankful for every day that my feet hit the floor, and that I can function pretty well. I think keeping busy helps us forget and we feel good which helps a lot. When I found out that my ct scan looked good and could go off chemo, I felt wonderful and wanted to do tons of stuff. I wish you all the best with your next round and have a good time at the Relay for Life and your golfing. Like you said "one foot in front of the other".
    Hugs from Oregon,
    Sharon
  • Kaleena
    Kaleena Member Posts: 2,088 Member
    #7
    upsofloating said:

    Thanks Claudia, Jill, and
    Thanks Claudia, Jill, and Connie for your good thoughts. I guess i've gotten into the 'doc-speak' way of referring to such things. Palliative to me always sounded like on your way to hospice, but i'm not there yet. My gyn-onc is not terribly encouraging about further systemic treatment but i'll revisit that after radiation. Meanwhile, this past week, I've played 2 games of golf (one long, one short course), enjoyed an 8-mile bike ride, and doing my 2-3 mile neighborhood walks. Tomorrow it's off to my local Relay for Life to try (and that's a really big try!) to make my 18 mile goal. I did 17 miles last year - it's one mile for every year I have lived with cancer (breast 18, and heading for 4 for UPSC). My husband decided that we best start with one lap for each year, they try for 2 laps per, then 3, and if we can make it by the 24-hr deadline and the body holds out, we'll do the 4 laps per, to make the 18 miles. One foot in front of the other ;-)
    Annie

    Annie:
    Thinking of you. But
    Annie:

    Thinking of you. But you go girl! Way to go, biking, golf and walks. I bet you will make that 18 mile goal! I am sending you cyber energy to keep you going.

    My best to you, Annie. Sending you hugs (((Annie)))

    Kathy
  • Rewriter
    Rewriter Member Posts: 493 Member
    #8
    upsofloating said:

    Thanks Claudia, Jill, and
    Thanks Claudia, Jill, and Connie for your good thoughts. I guess i've gotten into the 'doc-speak' way of referring to such things. Palliative to me always sounded like on your way to hospice, but i'm not there yet. My gyn-onc is not terribly encouraging about further systemic treatment but i'll revisit that after radiation. Meanwhile, this past week, I've played 2 games of golf (one long, one short course), enjoyed an 8-mile bike ride, and doing my 2-3 mile neighborhood walks. Tomorrow it's off to my local Relay for Life to try (and that's a really big try!) to make my 18 mile goal. I did 17 miles last year - it's one mile for every year I have lived with cancer (breast 18, and heading for 4 for UPSC). My husband decided that we best start with one lap for each year, they try for 2 laps per, then 3, and if we can make it by the 24-hr deadline and the body holds out, we'll do the 4 laps per, to make the 18 miles. One foot in front of the other ;-)
    Annie

    You may surprise your gyn-onc
    by responding really well to the radiation and being an excellent candidate for further systemic treatment. In the meantime, I'm amazed by your level of activity, and I'm so impressed by your 18-mile goal. Keep those endorphins flowing, and continue to really enjoy your life. You are an inspiration!


    Jill
  • daisy366
    daisy366 Member Posts: 1,458 Member
    #9
    Rewriter said:

    You may surprise your gyn-onc
    by responding really well to the radiation and being an excellent candidate for further systemic treatment. In the meantime, I'm amazed by your level of activity, and I'm so impressed by your 18-mile goal. Keep those endorphins flowing, and continue to really enjoy your life. You are an inspiration!


    Jill

    Annie and palliative
    Thanks for the info. I also had tx for supraclavicular lymph node mets close to windpipe but this option was not presented to me - not sure why. I had 7 weeks of Tomo radiation along with fractionated carboplatin chemo. docs called this synergistic - use of both chemo and RT. RT doc said tomo is low dose and accurate and I indeed did have painful effect on esophagus and throat. But it did the trick - no evidence disease on follow-up PET.

    Your treatment sounds very state of art - I hope it effectively does the trick.

    Re: term "palliative". I consulted my hubbie who is hospice social worker -he said this refers to tx that is not curative. I guess my treatments would also be considered palliative because at beginning I was told my upsc would be chronic, rather than curable.

    Annie, God speed. Sending my best wishes and lots of love to you. Mary Ann
  • RoseyR
    RoseyR Member Posts: 471 Member
    #10
    All Our Support!

    Dear Annie,

    You are one of the most inspiring members on our boards, I've always thought, so know we are all WITH you.

    And always remember that the term "palliative," while not signalling a cure, implies an "easing" that can often be sustained for years at a time.

    Am so glad you have access to this state-of-the-art option. Given what you've already overcome, you may be able to surmount this episode with your usual spunk and spirit.

    You are awesome, amazing, beautiful. A model for us all.


    Love,
    Rosey
  • RoseyR
    RoseyR Member Posts: 471 Member
    #11
    All Our Support!

    Dear Annie,

    You are one of the most inspiring members on our boards, I've always thought, so know we are all WITH you.

    And always remember that the term "palliative," while not signalling a cure, implies an "easing" that can often be sustained for years at a time.

    Am so glad you have access to this state-of-the-art option. Given what you've already overcome, you may be able to surmount this episode with your usual spunk and spirit.

    You are awesome, amazing, beautiful. A model for us all.


    Love,
    Rosey
  • kkstef
    kkstef Member Posts: 688 Member
    #12
    upsofloating said:

    Thanks Claudia, Jill, and
    Thanks Claudia, Jill, and Connie for your good thoughts. I guess i've gotten into the 'doc-speak' way of referring to such things. Palliative to me always sounded like on your way to hospice, but i'm not there yet. My gyn-onc is not terribly encouraging about further systemic treatment but i'll revisit that after radiation. Meanwhile, this past week, I've played 2 games of golf (one long, one short course), enjoyed an 8-mile bike ride, and doing my 2-3 mile neighborhood walks. Tomorrow it's off to my local Relay for Life to try (and that's a really big try!) to make my 18 mile goal. I did 17 miles last year - it's one mile for every year I have lived with cancer (breast 18, and heading for 4 for UPSC). My husband decided that we best start with one lap for each year, they try for 2 laps per, then 3, and if we can make it by the 24-hr deadline and the body holds out, we'll do the 4 laps per, to make the 18 miles. One foot in front of the other ;-)
    Annie

    Thinking of you!
    Annie,

    I was so sorry to hear your latest news, but it sounds like you have a very good plan of attack and it certainly does sound like cutting edge technology. I am awed by your level of energy....and am anxious to hear how the Relay for Life went.

    Know that all of us are cheering you on!! You are always so calm, knowledgeable, and strong.....a true inspiration to others!!

    Big Hugs,

    Karen
  • upsofloating
    upsofloating Member Posts: 466 Member
    #13
    upsofloating said:

    Thanks Claudia, Jill, and
    Thanks Claudia, Jill, and Connie for your good thoughts. I guess i've gotten into the 'doc-speak' way of referring to such things. Palliative to me always sounded like on your way to hospice, but i'm not there yet. My gyn-onc is not terribly encouraging about further systemic treatment but i'll revisit that after radiation. Meanwhile, this past week, I've played 2 games of golf (one long, one short course), enjoyed an 8-mile bike ride, and doing my 2-3 mile neighborhood walks. Tomorrow it's off to my local Relay for Life to try (and that's a really big try!) to make my 18 mile goal. I did 17 miles last year - it's one mile for every year I have lived with cancer (breast 18, and heading for 4 for UPSC). My husband decided that we best start with one lap for each year, they try for 2 laps per, then 3, and if we can make it by the 24-hr deadline and the body holds out, we'll do the 4 laps per, to make the 18 miles. One foot in front of the other ;-)
    Annie

    Thanks so much for all the
    Thanks so much for all the positive thoughts and well wishes. You were there giving me strength to go the distance to reach my goal of 18 miles. Meeting the challenge is symbolic in giving me hope that I can continue to meet, face, and overcome life's ongoing vicissitudes. And the space between those vicissitudes makes the fight so worthwhile.
    My best wishes to all of you to meet and overcome your challenges as well.
    Annie
  • upsofloating
    upsofloating Member Posts: 466 Member
    #14
    RoseyR said:

    All Our Support!

    Dear Annie,

    You are one of the most inspiring members on our boards, I've always thought, so know we are all WITH you.

    And always remember that the term "palliative," while not signalling a cure, implies an "easing" that can often be sustained for years at a time.

    Am so glad you have access to this state-of-the-art option. Given what you've already overcome, you may be able to surmount this episode with your usual spunk and spirit.

    You are awesome, amazing, beautiful. A model for us all.


    Love,
    Rosey

    Above comment included you
    Above comment included you too, Rosey! I never get the right hierarchy of comment location :P
    Annie
  • HellieC
    HellieC Member Posts: 524 Member
    #15
    RoseyR said:

    All Our Support!

    Dear Annie,

    You are one of the most inspiring members on our boards, I've always thought, so know we are all WITH you.

    And always remember that the term "palliative," while not signalling a cure, implies an "easing" that can often be sustained for years at a time.

    Am so glad you have access to this state-of-the-art option. Given what you've already overcome, you may be able to surmount this episode with your usual spunk and spirit.

    You are awesome, amazing, beautiful. A model for us all.


    Love,
    Rosey

    Hear, hear
    You are an inspiration to us all - long may it continue, Annie
    Love
    Helen

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