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Showing results for tags 'pneumonectomy'.
Hi guys, My dad was diagnosed with NSCLC(Squamous cell) on October.In my state where we live (Kosovo), is really difficult to find a PET scan machine.So in this way, we didn't want to lose time.Doctors said that our best option is to do an MRI to check if there the cancer has spread to other parts.Thank God, the result showed that the cancer is only in left lung and the size of tumor is 33mm.The tumor is near big blood vessels and is difficult to do a pneumonectomy.In this case the doctor suggested my father to start a neoadjuvant chemotherapy with 3 cycle (Carboplatin + Paclitaxel) and after that we have to do a PET scan outside Kosovo to check if the tumor to check how many lymph nodes are affected and how much the tumor shrinked.Now he is in second week of third cycle of chemotherapy. During the chemotherapy, he gained 10 pounds.I know this might sound weired, but yes, he gained 10 ! During chemotherapy, he didn't feel any of chemotherapy effects, expect hair loss.Even his half lung is blocked, he never had problems with breath.He told me that he can breath better now.We have run a lot of times on mountain and the didn't have any problem. His blood test are just amazing ! He even has better test blood than me ! His heart result are also perfect.He Now I have a questions for you. What is the impact of this chemotherapy combination on mediastinal lymph nodes ? After all these good signs, is his body trying to "tell" us, that the chemotherapy is helping him ? Best regards from me !
Good morning Members, For some of you that have followed my last post or not, here is the background info. My mom was diagnosed Stage 3A NSCLC. Her tumor is 6cm, 4.1x 3.8 x 5.8, located in the central upper left lobe and beginning to invade left main pulmonary artery. I was told that resection is possible following neoadjuvant therapy. I was given a choice of standard chemotherapy for three months OR 2 infusions of nivolumab as a trial for 4 weeks. I contemplated which first line therapy choice I would use for the last five days. However, I received a call and now was told that upon further review of the case, the team wants to move forward straight to surgery and do adjuvant chemotherapy afterwards due to fear of disease progression leaving my mom unresectable. I was not informed of what kind of resection is planned just yet. I’d like to know the risks/recovery expected with a resection of this size and location. How quickly must chemotherapy be initiated after a surgery? Is there a strong chance of hidden disease spreading as a result of surgery without having systemic chemo first? If members can weigh in with their thoughts and experiences, that would be great!