Stereotactic Radiation for brain mets

sgodshall

Does anyone have any info on SRS? We have completed WBR and MAY be a candidate for SRS. I have read some info and the long term side effects look awful. Any info would be appreciated.

Lung cancer (large cell) with mets to brain
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As long as there is Life, there is Hope.

Husband (44) with LC, mets to brain, lymph nodes and bones. Received Carbo/Taxol, currently in a clinical trail. Had WBR, stereotactic radiation to brain

brainman

I do. In fact, I have had it but not for brain mets... for primary brain cancer. With me, they first made a mask for me from this plastic mesh so that my head was in the exact same position every time. Then they did a high resolution MRI to map out the exact area they wanted to target. The technical process might be hard to understand but for me as the patient, it was very easy once I got accustomed to having my head bolted down to the table. The radiation source moved around my head sending out lower than Whole Brain Radiation dosages from several different directions so that only where the radiation beams crossed received the full dosage. It really is not that hard. I did experience some temporary, localized hair loss. I would think that there would be much less long term damage than with WBR... at least that is what its intention is.
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Jim
Site Administrator and long-term cancer survivor
1992 Astrocytoma grade 2, left motor strip
2005 Recurrence this time said to be an Oligodendroglioma grade 3, same location.
http://cancerforums.net/viewtopic.php?t=2405My Story Part 1: http://cancerforums.net/viewtopic.php?t=2528
My Story Part 2: http://cancerforums.net/viewtopic.php?p=7350
My Story Part 3: http://cancerforums.net/viewtopic.php?t=8029
Blog http://jimhawkinsport.blogspot.com/

koikkeril · Super Moderator Joined: 29 Jul 2007 Posts: 334

Hi,
Just pooped in to say hello and got stuck in to reading about Jim's bolted head... Rolling Eyes

Cant say I know anything about this line of treatment. Daniels is different and now of course everything has stopped. But! I will pray for you and keep you in my thoughts. Hoping you are a good candidate and gets through this battle nicely.... God Bless Koik
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Husband diagnosed with stage 1V NSCLC Febuary 2007.....Lost his battle August 27th 2008 but lives on in my heart.

sgodshall

We will be starting treatment next week, with 5 "doses". I really have confidence with our newest addition to the team. He spent 1 1/2 hours with us, and explained in detail. It felt good to received some good news, its been awhile. Thanks to everyone who post, it is wonderful to have such a great network.
_________________
As long as there is Life, there is Hope.

Husband (44) with LC, mets to brain, lymph nodes and bones. Received Carbo/Taxol, currently in a clinical trail. Had WBR, stereotactic radiation to brain

koikkeril · Super Moderator Joined: 29 Jul 2007 Posts: 334

[quote="god shall"]We will be starting treatment next week, with 5 "doses". I really have confidence with our newest addition to the team. He spent 1 1/2 hours with us, and explained in detail.

Hi godshall
Glad to hear treatment is starting...it makes all the difference in the knowledge that something good can come from it.. For your sake I am hoping so and I will be praying and thinking of you whilst I am away..
Stay tuned and positive like you are now and I am sure all will go well.
Hugs and best wishes...God Bless..Koik
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Husband diagnosed with stage 1V NSCLC Febuary 2007.....Lost his battle August 27th 2008 but lives on in my heart.

dano

Hello sgodshall;
I had the whole brain radiation, which was a scary though at the the time, but in two months time I went 5 to 10 mets in my brain. The blessing is that the mets were small and the treatments should be very effective against them, I was afraid of missing any unseen mets with the selective radiation method, which at first they said I could have with the 5 mets. Having the whole brain method done has risks but it seems that brain cancer is riskier to my health. So no doubt I'll have some troubles, it has effected my hearing already and likely permanently. It is a bother but a small price to pay for extended life. I hope you can report back soon so we can continue to share along with you.
God Bless
Dan
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54 year old male in Hawaii
Diagnosed Nov. 9,2007 with NSCLC IV
with Mets to the lymphs and brain
Had full brain radiation treatment in Jan 08
Currently on chemo treatments every 3 weeks
with Alimta
and taking Lovenox for blood clots
Now back to work full time
http://cancerforums.net/viewtopic.php?t=9993

sgodshall

Dano
My husband received WBR first, now we move on to stereotactic. The tumors (5) improved "marginally". One is 2.9cm x 2.4cm. It showed the least change. Currently receiving Carbo/Taxol, for lung. New scan showed no growth, no shrinkage. It seems we go from one battle to another. I have read your post and know you understand that. Hope you had a great "get away". Very Happy

Husband in is 40's.
_________________
As long as there is Life, there is Hope.

Husband (44) with LC, mets to brain, lymph nodes and bones. Received Carbo/Taxol, currently in a clinical trail. Had WBR, stereotactic radiation to brain

dano

sgodshall
This must be very upsetting to go through with that large of a brain met and little gain on controlling it. My mets are much smaller. I hope you can keep the faith that God can do a work on this. I will be praying for you and your husband. I wish I had other answers to give.
God Bless
Dan
_________________
54 year old male in Hawaii
Diagnosed Nov. 9,2007 with NSCLC IV
with Mets to the lymphs and brain
Had full brain radiation treatment in Jan 08
Currently on chemo treatments every 3 weeks
with Alimta
and taking Lovenox for blood clots
Now back to work full time
http://cancerforums.net/viewtopic.php?t=9993

sgodshall · Posted: Fri Aug 15, 2008 9:44 pm Post subject: Update

2 down and 3 to go. Hubby doing great, has perked up alot this week.
_________________
As long as there is Life, there is Hope.

Husband (44) with LC, mets to brain, lymph nodes and bones. Received Carbo/Taxol, currently in a clinical trail. Had WBR, stereotactic radiation to brain

koikkeril · Super Moderator Joined: 29 Jul 2007 Posts: 334

Hi There,
Its good to hear some better news...Just hearing that your husband has perked up makes the forum shine a little..I pray that it continues and I am thinking of you...

God Bless.....Koik
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Husband diagnosed with stage 1V NSCLC Febuary 2007.....Lost his battle August 27th 2008 but lives on in my heart.

LizNDale

Hello sgodshell, how are things going for you and for your husband?

Liz
_________________
My Mother - Stage IV NSCLC - Adenocarcinoma
Mets to Adrenal Glands and Brain
Diagnosed Thursday June 12th 2008
Died Sunday September 7th 2008

Her Story:
http://cancerforums.net/about9639.html
Her Statement of Faith Memorial:
http://cancerforums.net/viewtopic.php?t=10528

sgodshall

Let's stand up and say HURRAY! Last stereotactic treatment is tomorrow, he is doing GREAT! He has been able to work this week except for treatment days. He was off his Dexadron and lost 22 lbs. in 8 days, luckily Dr. put him back on and his is eating again. I feel very blessed this week - all the prayers are working.
_________________
As long as there is Life, there is Hope.

Husband (44) with LC, mets to brain, lymph nodes and bones. Received Carbo/Taxol, currently in a clinical trail. Had WBR, stereotactic radiation to brain

sgodshall

YEA!! Hubby has finished with his last treatment and doing great! Chemo is Friday, but it feels like we get a break from driving and doctors for the week. He feels "normal" this week and energy has increases, appetite back and he's eating everything in site. I realize that our "Normal" has changed, but this week feels like before LC. We won't know results from tx for 6 weeks, but for TODAY we are hopeful.
_________________
As long as there is Life, there is Hope.

Husband (44) with LC, mets to brain, lymph nodes and bones. Received Carbo/Taxol, currently in a clinical trail. Had WBR, stereotactic radiation to brain

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