Do any of you have experience of joint pains while on Avastin only (and so not caused by chemo drugs)?
I read posts from 3/4 years ago on this subject and you'd think that by now oncologists would have accepted that joint pains can be a side-effect of Avastin. Mine does not think so and has said that the only way we could be sure is by stopping the Avastin to see if it improves. My last CT scan showed the metastases were "significantly regressed" so Avastin is working and I don't want to stop it. I could accept the pain if I knew it was a side-effect (and would just concentrate on pain management) but if it's not a side-effect, what is it? I'm waiting for an appointment with a rheumatologist.
I'd love to know what others are experiencing on Avastin. I also have digestive problems not caused by my ovarian cancer, or the debulking, or other chemo drugs (apparently) as I'm not on any and my Onc does not believe in 'late effects'.
Thank you,
Iris
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Irisisme
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I am on avastin only, and a couple of months ago I told my onc. I was having muscle pain (not joint pain) and he told me to try Hidroxil vitimin B1 B6 B12 this has improved my muscle pain greatly. You could ask your onc if this would help you. hope you get sorted. xx
Hi Iris, I too on avastin only after my chemo in March. Apparently it is one of the side effects of avastin plus the chemo effect which can last up to a year. Chemo is accumulative so we can still have the side effects even after treatment. The sole of my feet is really painful sometimes and mentioned it to my consultant oncologist. She said it's because of the chemo. I hope you feel better soon. I normally take paracetamol when it's really bad. I can not walk far because of the pain sometimes. Take care. Xxx
Thanks, I am sure what I am experiencing are side effects but both my oncologist and specialist nurse don't believe in what the rest of us know! Weird.
My last chemo was January and I am on 3 weekly avastin . Joint and muscle pain and stiffness are definitely a side effect and are listed as so . Suggest you print out the Macmillan cancer support sheet and give it to your oncologist with relevant section highlighted !
Things that help me , regular walking - sometimes don't feel like it but have noticed it really helps ( think it helps to reduce the inflammation) , paracetamol, baths in Epsom salts .
I did miss a cycle of my avastin due to eye problems which they wanted to check out and I was defiantly less stiff and achy .
Hope this helps . Hang on in there . Glad it is working for you but sorry you are having this discomfort .
I love Purple Irises! Yes, I may just print it out and present it to them. I take paracetamol and have oramorph now too. I've got an exercise regime from a physiotherapist but haven't tried Epsom salts, I've just got a sleeve to go over my PICC line suitable for baths (it's been showers only up to now) so I'll give the Epsom salts a go.
Iris is my mums name and my middle name , purple my favourite colour , ( was a primary school teacher and taught purple class ) and love purple amethysts wear them all the time , have links with healing and positivity. ( and have certainly needed both on this journey !)
Meant to say also agree with Luchie , the affects of chemo can last much longer and avastin delays healing so can compound any joint or numbness left by chemo . I had terrible knee problems when first started ( was a weakness before) . Physio , and reflexology are also good . Love Kim x
It sounds ridiculous but I found the more I exercised during Avastin the easier the joint pain was. It was always worse after sitting for any length of time. A walk or a run and then eventually I would go to the gym really really improved my joint pain.
More exercise? Yes, I am very stiff in the mornings before I get moving and after I've been sitting so what you say makes sense. I always do a series of stretches to get moving. I get so tired so quickly, though. I am seeing the physio tomorrow and will discuss a regime.
Totally agree although I have never been up to running even before diagnosis . But who knows could be part of the new me !
Aches definitely got better when I was doing more walking when we got our rescue dog and I had to walk at a quicker pace . And yes so stiff when first get up or if sitting too long . But do get tired and have to pace myself 😀Kim x
Hi Iris I finished Avastin in March and my calves, ankles and shoulders continually ached. I noticed after about 6 weeks after treatment all my aches went. I'd recommend bathing in Epsom Salts for 20 mins.. worked for me. Keep going it's all worth it. Love Michelle xx
It's so good to hear I'm not alone in having these problems - and that they go away after treatment. I've already increased my walking; but increasing it slowly. A big pot of Epsom salts is on the shopping list! XX
Hi Iris and all the ladies. Yes my joint and muscle pain has been incredible and I also take the vitamin B complete. My Onc also says this is not a side affect of the Avastin even when I told her I had been lots of things that indicated it was. My last Avastin infusion was May 25th and not going to continue, I am still after four full weeks experiencing extrem muscle and joint pain. I read a blog from someone and he said it took him a full two months before he found relief from the pain after he stopped the Avastin.
Thanks, Sonshine, I will be prepared to wait. What did your Onc advise for the joint pains? Was there ever a diagnosis if she didn't believe it was a side effect? It's so frustrating- and the pains are continuing (although advice from this blog not had a chance to take effect yet, so maybe things will improve) xx
Hi Iris......my Onc totally dismissed my words about my side affects and said she would set me up to see an Internest so I just said I would see one of my own and let it be, I knew from everything I had read that she was wrdong. It is very frustrating. Thats why I decided to stop. The side affects from my last one in May have been far worse than the previous ones. I have a friend who is a Pharmacist from the States and he did some research and said the approx. time for the side affects to completely go away would be from 2 dto 5 months, depending on ones metabolism.
I am on the ICON8b trial and was supposed to have a total of 18 avastin injections - the first 6 with carbo/taxol I ended up only having 16 and had to stop due to peripheral neuropathy. That was back in December. With nerve pain or numbness there is no guarantee it will ever get better. Vitamin B6, cymbalta, lyrica, Chinese herbal medicine and acupuncture have all helped and about a month ago the pain really started to improve.
If your oncologist will not pay attention to the Macmillan info, look up avastin on the Mayo Clinic site. Muscle and joint pain feature as side effects.
Sorry to hear you had to stop Avastin due to the neuropathy . I hope you're doing ok. I haven't got the numbness so it's not obviously neuropathy that I have - just the joint pains. I'm seeing a rheumatologist on 13/7 so maybe he'll shed some light on it - and maybe will agree it's a side effect! Thank you.
Thank you for the input.......because I´m in Ecuador and my Onc does not speak English, I always have and interpreter with me, I decided just to let it go. My GYN who does speak english and was trained in the US does agree with the side affects. So now on the road to detting over all this and start my life again. I of course always pray I won´t have this battle again.
You need to badger your Oncologist to get you better pain management - or go elsewhere. I was on Avastin and started getting painful joints. My Oncologist was useless so I went to my GP and got a referral to a rheumatologist. It would have been a long wait on NHS so I went private-£300 later and I was told I had early onset osteoarthritis in hands, knees and hips, and impingement in both shoulders. He injected a steroid into both shoulder joints (which I barely felt) and I was almost pain free for the next 3-4 months! If you have health insurance so much the better, if not make sure you get your GP to arrange the blood tests the rheumatologist will need; they are expensive! £300 is a lot if your on a tight budget but I still think it was worth it for me.
Otherwise get your GP to refer you to a Pain Clinic, and if you are under a Hospice they will do it.
I still think it was/is probably the Avastin but both my Oncologist and the Rheumatologist said it was unlikely and the only way to know is to stop the Avastin and see if the pain improves- but then you would be allowing the cancer a blood supply again- not a good idea.
I 'm doing Avastin every 2 weeks to reduce a swelling of the brain due to radio and proton in the same area of a brain tumor. It is working but I suffer from Rheumatoid arthritis and I'm taking hydroxychloroquine to get right of the pain.
Now it is 4 years that I am taking this medication and all of a sudden stopped working. I have pain all over the joints and heels, stiff muscles, neck and shoulder. Today I had my 5 of 6 treatment and as usually the nurse asked me if I had any pain. I thought it was not related but I told her any way. She said it was the Avastin cause me the pain and when I wont do it anymore the pain will go away. In the mid time if the pain persist, I can take Advil or Tylenol. I tried both and don't work for me so I decided to take Glucosamine and UC-II, it helped a little but I get confort in the thing I am done with this treatment in 2 weeks and this pain will disappear. I will keep you updated
I am in Avastin now.... my left shoulder s killing me. I tried Ibuprofen 800 mg a lot of pain killers nothing help! I am thinking to quit to the treatment!
I was wondering about the joint muscle and bone pain myself. I am on Avastin and have knee, ankle, Achilles tendon pain and shoulder pain. It is most prominent the first week after my 3 week cycle. I believe it is the avastin. Walking and hiking helps. The pain resolves with activity.
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