Accelerated Radiation Therapy - Good Idea or Bad?
Hi,
I will begin radiation treatment in two weeks. My oncologist told me that I am a good candidate for Accelerated Radiation treatment in which they will give me higher doses for three weeks instead of the usual six week plan. Does anyone have any experience with this? I've been told that the side effects and effectiveness of the treatment are the same with the accelerated treatment as with the non-accelerated treatment. Is that true?
Thanks so much.
Comments
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From what I've read, hyperfractionated radiation works well.Itis primarily for women who live in rural areas who can'tesily get to a treatment facility for radiation. If you live near a hospital, I would probably stick to a traditional radiation treatment schedule. If you live far away, you should use the hyperfractionated radiation schedule.
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Hmmm. I live in New York City and so going to the radiation place is an easy commute. My oncologist was recommending the accelerated treatment because it is less disruptive to my daily life to go for three weeks than to go for six. So, that is why I am asking what is the down side to doing the accelerated treatment?
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Hi,
I just finished accelerated treatment, twice a day for 5 days. I can't compare to longer treatment but it is nice to be finished. I am very tired and sore. I worked through the first three days but took the last two off due to tiredness and migraine headache. I am wondering how long the tiredness might last?
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I did the accelerated partial breast external beam 5 days twice a day. I did not have fatigue. I did have a very sore breast for a couple of months. I still get pains in the breast sometimes, and it still feels a little warmer even though rads was 1.5 years ago.
Cheryl
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Well now they have decided that I should not have the accelarated treatment and stick to the usual 6 week schedule. Thanks everyone for your input.
amy
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I'm signing up for the accerlarated rads and hope to get it. I'm impatient and don't want to have to go for the 33 treatments then boosts. So I really want this. I'm getting tattood today and I'm alot more nervous than I thought I would be I've been up since 4:00am and wish I could have slept normally today. I hear the tatooing takes awhile and I have a very bad back so I'm worried that I'm going to screw up and then they won't want for the rapid study up here. Guess I'll just do the best I can.
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Amysharp, I just finished radation tx which I recieved double the dose, 21 tx and 4 boost. I had a an allergic reaction to the rads toward the end. My skin did not tolerated it very well, my left breast was burned, swollen and blistered open. I used lots of cream 3 x day and finally went to doing dombrax soaks to help with the burning. My experience with radation was not that good and the staff was not clued in to my emotional status. I hope your experience is better than mine and the staff is kind toward needs. Let me know how it goes. Blackjack
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dlroux I am Glad to hear that you are finished - How are you doing since you have finished this type of radiation? I am suppose to start mine on Monday and am scared to death. Reading others stories is helping me stay sane. I am 38 with 1cm DCIS, ER+
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I have also been undergoing accelerated radiation....the rad onc told me that he has only used this version for inflammtory breast cancer. Since I received all of my chemo in CA, and have moved to OR, I was a bit freaked out in general when I started the treatments. I have since learned that the fractionization reduces the total amount of rads that I will receive (a bit) and my treatment will last a total of 22 days, of which I have completed 1/2. Some pinkness, which is increasing as treatment continues, and a bit of difficulty swallowing, which i did not expect. I am using aloe vera for the skin, and monitoring the "lump in the throat" this weekend.
I am wondering if there are other Inflammatory BC patients who have been undergoing this treatment form., and how you're doing/did with it.
Jeanlin
63 years old, diagnosed 3/31/07, TAC chemo started 5/9/07, bilateral mastectomy 8/16/07, Taxol infused 9/8/07, fractionated radiation (2x per day) started 11/ 14/07.
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I haven't had my radiation yet but I understand that this is common practice for IBC at MD Anderson in Texas, one of the leading centers in the world for IBC. My own radiologist didn't recommend it for me. I have to question her again about this after my surgery.
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I asked my radiation oncologist if I could have the accelerated treatment because I was leaving the country for a month and a half, and I barely had time to finish six weeks of rads. He told me that because of my breast size (I'm fairly large breasted) I wasn't a good candidate for it. He was so funny. He's a little Chinese man (from China), and he was trying to find a way to explain it to me. Here's the best he could come up with: It's like the difference between cooking a large roast and cooking a small one. LOL Apparently, the higher levels of radiation required to get through all my breast tissue in the accelerated treatment would be much harder on me. He didn't recommend it. I'm doing the six weeks.
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Thats funny Jukief, my rad onc hoped my boobs were large enough and said keep eating, and I just made it into the trial. I have my last treatment tomorrow and I'm really getting red, the techs also asked me today if I wanted to go to the nursing station for a script for cream, but the creams offered have steroid in them and I just don't want another steroid in my body. So for now I'm sticking with Aloe Vera gel only, if it gets to the point where I can't stand it. I might change my mind but I really hope the aloe will do the job. Lots of redness and it really sort of popped up fast. Over the weekend all of a sudden I had redness on my chest, so no more v-necks for awhile. Does the discolouration go away? I hope so. Pearl
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Hi Amyshap, My radiation oncologist presented the option of the 15 day high dose external radiation. I did some research & this is nicknamed the "Canadian" protocol. It is widely used in Canada where there is a very long waiting list for radiation. From what I read, the fatigue & burning is more pronounced in this shorter version. I opted for the internal high dose radiation - brachytherapy & I am glad I went that route.
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Hi,
Thanks again all for your advice. My radiologist turned me down for the accelerated treatment because the areas to be treated were angled in a way that made it impossible. I'm halfway through regular treatment and I sure wish it was over now.
amy -
Ohhh, I just found this thread, after posting two weeks ago about the 3 week accelerated treatment. This was offered to me but I decided I wanted to go more traditional. Yes, it was first conceived in Canada and Memorial Sloan Kettering is an advocate of this treatment.
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Snowyday, I had the same experience with breast size...my cavity could not be more than 30% of my breast in order to qualify for the study. I'm doing the external 2x daily for 5 days. Today was day three. I'm seeing some burning now, and my incision is more sensitive than it was a week ago.
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I need to make a decision on this ASAP and this post is 5 years old....any thoughts/experiences? (I had left side DCIS and lumpectomy revealed a 1 mm microinvasion so I had a re-excision with clear margins)
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LeeLeeLynn, are you looking at the internal or external kind? I had the internal 5 day 3 years ago.
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Kira, It would we external over 3 weeks or 6 depending on the "coin flip"
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I went through the excellerated treatment during Dec 2012. I had 2 treatments on one day so that I could finish on Dec 31, and get all of the treatments covered in the 2012 insurance. I really had no side effects. I qualified due to my small breast size and early stage. I was very happy that my RO routinely evaluates this patients for this option. No one outside my immediate family knew I had surgery or radiation. I was able to do all the things that I would normally do during the holidays. I watch my diet now and keep my BMI at a healthy level and take arimidex. I suppose I am one of the lucky ones to not suffer from too many side effects.
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