› Forums › Cutaneous Melanoma Community › Skin Cancer/ Melanoma to Tumors in Lungs
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Eileensulliv.
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- December 5, 2015 at 10:25 am
I'm not too sure how this works or if anyone will even see my post. I have never been on one of these health websites where nice people support one another and perhaps answer some questions. I hope this gets to someone because I am at the very early stages of researching my Father's condition. I am 24 years old and my amazing Dad is over 60 years old. He has had skin cancer and cases of melanoma for as long as I can remember. Taking trips to the lake or beach he would begin to develope these bright pink sores all over his skin. In his late thirties, to fifties, to now mid sixties he has had these sores. Only a few at a time. Some little scabs and some were so bad huge holes were cut out of his cheek, calves, and back. Never fun to see your dad get cut up and get these sores even with how careful he was with sun protection and constant check ups with docs.
Well today December 5th my Dad called my mom after the doctors office and explained he has tumors in in lungs. My mom asked how many?…… All my dad could say was ………Honey a lot, the Dr. Said "multiple". My Dad came home and we tri d to stay optimistic but multiple tumors is not a good sign and they might be spreading. We find out in a few days (next week) more details. If they can be removed, how early in the stages are the tumors, exactly how many, and what the chances are of us winning this fight. Like I mentioned before I am 24 years old, a senior at the University of Utah and already getting impressions to switch to a medical path. Meaning if any of you have insight, experiences, knowledge, or cold hard blunt information about a situation like my Father's please feel free to give feedback. Good or bad don't be shy, because the more information the better and I know this is a part of life. Please please respond if you have anything to share.
Thank you, thank you.
Trey, A son who loves his father.
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- December 5, 2015 at 1:38 pm
Hi Trey,
There are many folks on this board who will be there to support your family and help answer your questions. If your father has tumors in his lungs he has Stage IV cancer. If all the repeated skin lesions you remember were melanoma (not basal or squamous cell) he may well have melanoma to his lungs, but usually a biopsy is needed to be certain of the type of lung tumor he is dealing with. Regardless of type of lung cancer, scans of the rest of his body and an MRI of his brain would probably be wise to make sure there is nothing else going on.
If your father does have Stage IV melanoma, it is very important that he is followed by an oncologist/facility who works with melanoma patients…not just a general oncologist. I know Huntsman does good work. If lung tumors are large they are sometimes removed surgically. They can also be treated with specially directed radiation (SRS – stereotactic radiation). If there are many small tumors..or they are simply inoperable due to location…and even if you have one of the procedures I described…systemic therapy would be needed. On that front…things are very much improved in melanoma….with three types of systemic treatments FDA approved today that were not available in 2010: BRAF inhibitors that melanoma patients can take orally if their tumors have a certain mutation, anti-PD1 (2 products: Keytruda and Opdivo), as well as anti-CTLA4 (often referred to as ipi or Yervoy)….with those last two given in an IV. So if your dad has melanoma…he does have treatment options. I have been dealing with melanoma since 2003…had brain and lung mets in 2010…was treated much as described above…and am disease free.
As you have more questions, folks on this board will help you find answers. Your dad has reason to hope. I wish you and your family well. Celeste
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- December 5, 2015 at 1:38 pm
Hi Trey,
There are many folks on this board who will be there to support your family and help answer your questions. If your father has tumors in his lungs he has Stage IV cancer. If all the repeated skin lesions you remember were melanoma (not basal or squamous cell) he may well have melanoma to his lungs, but usually a biopsy is needed to be certain of the type of lung tumor he is dealing with. Regardless of type of lung cancer, scans of the rest of his body and an MRI of his brain would probably be wise to make sure there is nothing else going on.
If your father does have Stage IV melanoma, it is very important that he is followed by an oncologist/facility who works with melanoma patients…not just a general oncologist. I know Huntsman does good work. If lung tumors are large they are sometimes removed surgically. They can also be treated with specially directed radiation (SRS – stereotactic radiation). If there are many small tumors..or they are simply inoperable due to location…and even if you have one of the procedures I described…systemic therapy would be needed. On that front…things are very much improved in melanoma….with three types of systemic treatments FDA approved today that were not available in 2010: BRAF inhibitors that melanoma patients can take orally if their tumors have a certain mutation, anti-PD1 (2 products: Keytruda and Opdivo), as well as anti-CTLA4 (often referred to as ipi or Yervoy)….with those last two given in an IV. So if your dad has melanoma…he does have treatment options. I have been dealing with melanoma since 2003…had brain and lung mets in 2010…was treated much as described above…and am disease free.
As you have more questions, folks on this board will help you find answers. Your dad has reason to hope. I wish you and your family well. Celeste
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- December 5, 2015 at 1:38 pm
Hi Trey,
There are many folks on this board who will be there to support your family and help answer your questions. If your father has tumors in his lungs he has Stage IV cancer. If all the repeated skin lesions you remember were melanoma (not basal or squamous cell) he may well have melanoma to his lungs, but usually a biopsy is needed to be certain of the type of lung tumor he is dealing with. Regardless of type of lung cancer, scans of the rest of his body and an MRI of his brain would probably be wise to make sure there is nothing else going on.
If your father does have Stage IV melanoma, it is very important that he is followed by an oncologist/facility who works with melanoma patients…not just a general oncologist. I know Huntsman does good work. If lung tumors are large they are sometimes removed surgically. They can also be treated with specially directed radiation (SRS – stereotactic radiation). If there are many small tumors..or they are simply inoperable due to location…and even if you have one of the procedures I described…systemic therapy would be needed. On that front…things are very much improved in melanoma….with three types of systemic treatments FDA approved today that were not available in 2010: BRAF inhibitors that melanoma patients can take orally if their tumors have a certain mutation, anti-PD1 (2 products: Keytruda and Opdivo), as well as anti-CTLA4 (often referred to as ipi or Yervoy)….with those last two given in an IV. So if your dad has melanoma…he does have treatment options. I have been dealing with melanoma since 2003…had brain and lung mets in 2010…was treated much as described above…and am disease free.
As you have more questions, folks on this board will help you find answers. Your dad has reason to hope. I wish you and your family well. Celeste
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- December 5, 2015 at 3:37 pm
Hey Trey,
Celeste is one of the best folks on this board – I echo everything she told you! I especially agree with finding a specialist.
I have less medical advice and simply know this disease as a patient. My biggest piece of advice is to stay positive. The people I've seen who do well remain positive. Also, now is the time to have melanoma (I know, no one wants this, but results are much better now than 5+ years ago.)
I had tumors in my liver (basically throughout ALL my liver) and throughout my body. Later they found some in my lungs. I am at this moment cancer free because of new treatment options and a great specialist.
There is hope – stay positive!
Ashley
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- December 5, 2015 at 3:37 pm
Hey Trey,
Celeste is one of the best folks on this board – I echo everything she told you! I especially agree with finding a specialist.
I have less medical advice and simply know this disease as a patient. My biggest piece of advice is to stay positive. The people I've seen who do well remain positive. Also, now is the time to have melanoma (I know, no one wants this, but results are much better now than 5+ years ago.)
I had tumors in my liver (basically throughout ALL my liver) and throughout my body. Later they found some in my lungs. I am at this moment cancer free because of new treatment options and a great specialist.
There is hope – stay positive!
Ashley
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- December 5, 2015 at 3:37 pm
Hey Trey,
Celeste is one of the best folks on this board – I echo everything she told you! I especially agree with finding a specialist.
I have less medical advice and simply know this disease as a patient. My biggest piece of advice is to stay positive. The people I've seen who do well remain positive. Also, now is the time to have melanoma (I know, no one wants this, but results are much better now than 5+ years ago.)
I had tumors in my liver (basically throughout ALL my liver) and throughout my body. Later they found some in my lungs. I am at this moment cancer free because of new treatment options and a great specialist.
There is hope – stay positive!
Ashley
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- December 5, 2015 at 5:52 pm
Hi Trey,
In 2009 they found 8 tumors spread across both my lungs. Because there were that many they felt surgery was not an option, they felt more disease was probably present if there were that many.
In 2010 after a biopsy to confirm they were melanoma, they were put into remission by a very low percentage of success systemic treatment, called high dose IL2. So far those haven't recurred. Some disease escaped elsewhere, via lymph nodes or lungs probably. Treatments have kept those from running too far amok so far.
Systemic tratments have come a long way since 2010. Your Dad probably stands a good chance of getting imto a combo (multi drug) clinical trial if he wants. That's what I've been doing foe the last 21 months.
So that's my story with lung mets.
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- December 5, 2015 at 5:52 pm
Hi Trey,
In 2009 they found 8 tumors spread across both my lungs. Because there were that many they felt surgery was not an option, they felt more disease was probably present if there were that many.
In 2010 after a biopsy to confirm they were melanoma, they were put into remission by a very low percentage of success systemic treatment, called high dose IL2. So far those haven't recurred. Some disease escaped elsewhere, via lymph nodes or lungs probably. Treatments have kept those from running too far amok so far.
Systemic tratments have come a long way since 2010. Your Dad probably stands a good chance of getting imto a combo (multi drug) clinical trial if he wants. That's what I've been doing foe the last 21 months.
So that's my story with lung mets.
-
- December 5, 2015 at 5:52 pm
Hi Trey,
In 2009 they found 8 tumors spread across both my lungs. Because there were that many they felt surgery was not an option, they felt more disease was probably present if there were that many.
In 2010 after a biopsy to confirm they were melanoma, they were put into remission by a very low percentage of success systemic treatment, called high dose IL2. So far those haven't recurred. Some disease escaped elsewhere, via lymph nodes or lungs probably. Treatments have kept those from running too far amok so far.
Systemic tratments have come a long way since 2010. Your Dad probably stands a good chance of getting imto a combo (multi drug) clinical trial if he wants. That's what I've been doing foe the last 21 months.
So that's my story with lung mets.
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- December 5, 2015 at 7:59 pm
Hi Trey! I know this is a scary time for your family, and I am sorry you are going through this. You have received great information from the posts above, and again, it's extremely important to seek out a melanoma specialist. I was first diagnosed in 2006… Had surgery and was cancer free until my latest diagnosis in January 2015. I had an in-transit met in my back (close to my original site) and multiple mets in my lungs and small intestine and mesenteric lymph nodes. I had the tumor in my back surgically removed, and started on the yervoy and Opdivo combination trial in late February. After one dose of the two meds, all of my tumors shrunk, and some disappeared altogether! I only had the one dose of the two meds combined due to side effects, but continued with doses of just Opdivo every two weeks. So far, my scans show stable disease since June, and my next scan is on Thursday! I have continued to work 40 hour work weeks with only a few minor bumps in the road… My quality of life during treatments has been outstanding! I am hoping your family receives some good news this week… Best of luck!
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- December 5, 2015 at 7:59 pm
Hi Trey! I know this is a scary time for your family, and I am sorry you are going through this. You have received great information from the posts above, and again, it's extremely important to seek out a melanoma specialist. I was first diagnosed in 2006… Had surgery and was cancer free until my latest diagnosis in January 2015. I had an in-transit met in my back (close to my original site) and multiple mets in my lungs and small intestine and mesenteric lymph nodes. I had the tumor in my back surgically removed, and started on the yervoy and Opdivo combination trial in late February. After one dose of the two meds, all of my tumors shrunk, and some disappeared altogether! I only had the one dose of the two meds combined due to side effects, but continued with doses of just Opdivo every two weeks. So far, my scans show stable disease since June, and my next scan is on Thursday! I have continued to work 40 hour work weeks with only a few minor bumps in the road… My quality of life during treatments has been outstanding! I am hoping your family receives some good news this week… Best of luck!
-
- December 5, 2015 at 7:59 pm
Hi Trey! I know this is a scary time for your family, and I am sorry you are going through this. You have received great information from the posts above, and again, it's extremely important to seek out a melanoma specialist. I was first diagnosed in 2006… Had surgery and was cancer free until my latest diagnosis in January 2015. I had an in-transit met in my back (close to my original site) and multiple mets in my lungs and small intestine and mesenteric lymph nodes. I had the tumor in my back surgically removed, and started on the yervoy and Opdivo combination trial in late February. After one dose of the two meds, all of my tumors shrunk, and some disappeared altogether! I only had the one dose of the two meds combined due to side effects, but continued with doses of just Opdivo every two weeks. So far, my scans show stable disease since June, and my next scan is on Thursday! I have continued to work 40 hour work weeks with only a few minor bumps in the road… My quality of life during treatments has been outstanding! I am hoping your family receives some good news this week… Best of luck!
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Tagged: cutaneous melanoma
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