Search the Community
Showing results for tags 'squamous cell carcinoma'.
Hello all, I am new to the forum and pretty new to the cancer world. I have experienced very little with cancer as my loved ones that have been diagnosed in the past were older and chose not to be treated. My boyfriend (45 years old) started having "allergies" in Feb 20. By April 20 he had signs of sinusitis but refused to go to the doctor. May 20 he started wheezing etc when he coughed. Mid May he felt so bad he stayed in bed all day and finally agreed to go to an urgent care that evening. They diagnosed him with pneumonia/suspect COVID (he ended up being negative). He quit smoking that day (partly because he didn't even have energy to get out of the bed). 9 days later, he wasn't any better so he went back and they treated him again for pneumonia. June 10 he went back again because he still felt horrible (after I begged him to go) and they sent him to the ER because they "saw something they didn't like." Due to COVID, I was not allowed to go in with him but they started working him up right away. They did a CAT scan while he was in the ER and immediately decided to admit him to do a bronchoscopy with biopsy, which was done June 12. They discharged him that day with orders to get a PET scan. The biopsy came back as squamous cell carcinoma of the lung and the PET scan came back showing the tumor being 5.4 x 5.6 in the upper left lobe. We had issues getting him in with the Dr he was supposed to see so we contacted University of Md Baltimore Greenebaum Cancer Center. They immediately put us in contact with a thoracic surgeon, who we met with 6/24. He told us that my boyfriend needed to have surgery right away to remove the whole left lung. He also said he was passing the case off to a higher up in the hospital, who we met with virtually the next day. After that virtual appointment, they had my boyfriend scheduled for all types of tests pre-surgery. On 6/26, that doctor presented the case to the tumor board and another Dr spoke up about a trial that **MAY** be able to save his lower lobe of the lung. The main symptom that my boyfriend has had is severe coughing (no blood, just occasional sputum). He declines that he is SOB but he can't walk around the house one circle without stopping to catch his breath (which he also declines). We haven't spoke with the Dr that suggested the trial yet, that comes in two days, but we already have concerns. His Dr said it would be 2-3 months of treatment and then surgery to remove the upper lobe. This doesn't solve the problem of the cough. He has been bed ridden for a week now, as it is the only way to keep the cough halfway calm. We have tried cough drops, sugar free candies, warm tea with lemon/honey, gingerale, cepacol drops, throat spray, etc. My boyfriends inclination is to move forward with the surgery ASAP so that the cough is gone, and then go through treatment. Can anyone give any advise? For those that have faced the same decisions, what did you do and would you make the same decision again?
I have a question to pose and hopefully I can get some solid answers to help me to make some decisions. Caution-long post as much to relate that goes with my questions! In May 2014 I was diagnosed with stage IV squamous cell carcinoma lung cancer with mets to my liver. There was no primary tumor and it was diagnosed via a liver biopsy. The cancerous lesions are "mostly" small and are widely spread in both lungs, lymph nodes in lung area and liver. I did a six month chemo combo of Carboplaten/Abraxane. I had a small amount of shrinkage of the lesions and the majority of the lesions just remained stable. Three months after the end of chemo I was "technically" stable but due to having some progression I was able to get into a clinical trial of Nivolumab (Opdivo). Two months into that treatment my CT scan showed me completely stable, which was a surprise for my doctor as his other patients mostly responded with good results after four months or so on the drug. Once Opdivo was released by the FDA for use on squamous lung cancer I moved out of the trial and began to use as a regular patient. My recent scan showed some growth and initially my doctor wanted to take me off of the drug and switch to Gemzar. He thought on it some more and decided to let me go for about six and a half weeks in the Opdivo and then scan again to see if the progression had stopped so that I was stable or better yet-shrinkage. But I was told to continue to think of possibly using the Gemzar. I think he may have opted for the additional period of time on the Opdivo as I was more inclined at that point to just stop all treatment rather than going back on chemo. I found zero quality of life in the first treatment in that six months and for an additional two months as I finally revived. I have looked at many posts at another lung cancer support group I belong to and they reported that Gemzar had much milder side effects (but still had some hair loss, nausea/vomiting that could be controlled by medication and most reported it causing issues with the blood cells, making the need for those dreadful Neupogen injections the norm through most of treatment and a very few had to have blood transfusions. But I also noted that the majority of the patients on Gemzar had adenocarcinoma and not squamous. So my questions: 1) Is there a noted difference for potential different outcomes in the effectiveness of Gemzar based on having adenocarcinoma vs squamous? 2) What were the major side effects you experienced on Gemzar. Did you lose your hair or if it thinned, was it a marked amount. Did you find that you needed treatment to get your WBCs back in line often on this drug? 3) If I did not have remarkable results on the first line choice of the two chemo drugs in the beginning, can I honestly expect the Gemzar to make a difference? (My question is based on the fact that they did not chose this drug first-so if the first treatment was more effective to give me a chance-can I really expect a drug not shown for helping I the beginning to now stabilize or shrink my lesions and if so---why? Does having had a previous doublet treatment make your body respond better at a later date to this drug.) I am trying to understand the reasoning. 4) Last but not least, has anyone with squamous lung cancer been on the Opdivo and gone back and forth on progression and stability or shrinkage? I ask this as I am so tentative to going the chemo route again that I am thinking of just stopping all treatment and just going the palliative care route. Knowing this, a friend asked why not just stay on the the Opdivo rather that go without any treatment since the side effects are minimal and it "might" even do some good? I am digging deep so that I can make the right choice. I have been given this six and a half weeks of Opdivo to see if the progression continues and that will be toward the end of this month. I had Hashimoto's thyroiditis hypothyroidism lurking in the background but not yet diagnosed when I began the Opdivo treatment and I began that with the full knowledge that if mine was Hashimoto's that it would have a major flare. Mine did flare and the endocrinologist I am now seeing said that my values were so high that he feels sure that my thyroid is totally burned out forever. I felt good on the Opdivo until this flared and I crashed quickly and had horrible fatigue and slept nearly around the clock. As they get my thyroid in line I feel a bit better as I go along. My lab values look fabulous and nothing is out of range and except for some issues with my joints that is not linked to cancer-I feel good and do not appear I'll most of the time. Based on my increased feeling of good health as they thyroid regulates I keep looking at the possibility of living as much time as I can on the Opdivo with the knowledge that it might do no good vs zero treatment if I cannot find some truly solid data to make me open to going the Gemzar chemo route. I will welcome anyone's feedback of personal experience, links to articles which address any of this as related to squamous lung cancer as the response to various drugs with squamous and adenocarcinoma appear to be quite different and with very different maintenance protocols.