Nervous about switching from Letrazole to Exemestane
Hi - I have been on Letrazole for 2 years (invasive ductal carcinoma, node positive, did chemo and radiation, double mastectomy and oophorectomy...was diagnosed right after my 46th bday). Recently I've had neuropathy for the first time (it moves around/switches which limbs it affects...strangest thing). Ruled out metastasis with spine and brain MRI plus chest CT and bone scan (insurance wouldn't cover PET). Anyway, my oncologist said to try a "drug holiday" to see if the letrazole could be causing it. The numbness is noticeably better after a week off the letrazole (but not gone). He suggested I could switch to Exemestane to see if it solves the problem but I am nervous to make the change -- sort of feels like the devil you know is better than the devil you don't? My question is -- has anyone had a bad experience with Exemestane (beyond the obvious hot flashes/joint pain as I'm used to those?). I'm specifically nervous about the "mild androgenic effects" that it can have. I have lost my breasts and just finally grew my hair back out -- I don't want anything to make me feel any less feminine than I already do at times. Thanks for anything you can share!
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I have the same problem which is why I’m hesitant to stop medications. Did chemo because oncotype positive. Tumor marker dropped about 20 points (needed to drop 50 to hit high normal), then after 3 months started back up again almost to start level. At that point, he ordered brain MRI and pet scan. Neither of which showed new tumor growth. Then it dropped back to where it was before, then another 10 points and that’s where I sit. He said it can happen and as long as stays stable, monitor but not considered a problem. Easy to say but sits in your mind that maybe there’s a reason. And yes, I’ve read multiple articles about tumor marker specificity and that some feel they’re worthless but my doctor still uses them for monitoring and I have to feel he knows what he’s doing. I’ll look into the Pectasol (haven’t heard about that before), already researching other naturals like mushrooms.
I’m on Anastrozole and it’s the best so far. Takes 6 weeks to 2 mos for side effects to lessen. And some physical therapy
have you tried magnesium supplements? f not, it's worth a try. Take them before you go to bed.
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1 ReactionThank you! I started it two nights ago and have not experienced the awful cramps so far 🙏
I was on Letrazole since my mastectomy about a year ago. I could barely move with the joint pain and I had edema really bad in both legs--but especially my right leg along with constipation at 79 and weight gain. I mistook side effects for old age which is true 🙂 - but after reading about the side effects and moving became increasingly difficult- I stopped to see if a change off it would make a difference. It wasn't even 2 days that my joint pain, edema cleared up dramatically... Losing weight and constipation are still a work in progress but much better. Walking 4-5000 steps, and 10-12 glasses of water daily didn't touch the side effects! I was hesitant to stop. but so glad I did. 4 more years of pain, swelling. My Dr wants me to try exemestane- I hesitate with looking at side effects.. but will give it a try.
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5 ReactionsNatural estrogen's blocker is suggested by NutritionFacts.org Dr Greger who is a Vegan but will you follow him using plant base food, he shows you research papers but not sure if they do trials like the pharma do when they develop drugs. Really not sure, the world is pro pharma who at the end produce drugs that save lives and makes tons of money but you have to spend more money on side effects, rather producing drugs with natural ingredients which has no side effects so we don't need to spend more money to buy drugs to treat side effects!
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5 ReactionsI hope you are able to get some answers that are helpful. It is truly a roller coaster ride, dealing with cancer and the treatment for cancer!
Thank you for responding- we do live in a pro pharma world that desperately needs to blend with our natural health Drs hoping one day there will be drugs that help without horrible side effects -a milestone for all. a hopeful thought.
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3 ReactionsI think it’s time that people were more honest - it’s often put across as ‘ take these you are ok’ far from the reality .
I certainly feel I was not given enough information and feel it’s expected of me to ‘feel ok’.
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1 ReactionI agree with all you say and I have found more sense and support from this forum than from my supposed ‘support’ agencies .
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