Cisplatin/Vinorelbine and diabetes - The Roy Castle Lu...

The Roy Castle Lung Cancer Foundation

5,952 members3,549 posts

Cisplatin/Vinorelbine and diabetes

Bramwater profile image
8 Replies

My brother has been diagnosed with nonsmall cell adenocarcinoma (he had a lobe of his lung removed and one lymph node was positive). He is to be started on Cisplatin and Vinorelbine very soon. He also has had diabetes for some time. I am assuming he will be at increased risk of peripheral neuropathy because of his diabetes. Does anyone have any advice on how to reduce the risk of this side effect or how to deal with it once you have it? Thanks on behalf on my brother (we live in Canada).

Written by
Bramwater profile image
Bramwater
To view profiles and participate in discussions please or .
Read more about...
8 Replies
dancerjane58 profile image
dancerjane58

I also was diagnosed with non-small adenocarcinoma with lymph node involvement. My chemo regimen was cisplatin and navelbene. Unfortunately, I did have nerve damage in my feet and have deal with that going forward. It has been almost 5 years and I am cancer free. It is a small price to pay. I do get Vitamin B12 injections 2x per month and it does help. Also, keeping my feet warm relieves some discomfort. Good luck to you

Bramwater profile image
Bramwater in reply todancerjane58

Thanks so much for taking the time to reply. I will relay this information to my brother. He is very scared to start treatment and I think knowing that you survived and are coping will be very helpful for him.

Hi I also had cystplatin and vinerabaline ,mop up chemo after surgery .I had my last dose in July this year and do have numb feet and the occasional numb finger.I think this of neuropathy is slightly different to the usual neuropathy .My feet get cold but my circulation doesn't appear to be impaired and pain not an issue for me just slightly annoying .I did have numb toes on my right foot before any treatment caused by the cancer so that was already causing a problem .I too adenocarcinoma non small cell and found in two lymph nodes .After my third session of chemo I found the fingers in my right hand going numb ,which alarmed me so they changed my chemo regime slightly from cystplatin to carboplatin which seemed to do the trick ,they are not a problem now .I wish your brother well ,the chemo is horrid but I was convinced that my cancer was coming back about 3weeks after surgery as some of the original symptoms were recurring and have now gone again .So I think it is worth the discomfort.Wishing your brother well .Diane .

Bramwater profile image
Bramwater in reply to

Thanks Diane....sounds like the chemo was awful but that it worked for you. Thanks for this information. I will pass it along to my brother who is nervously waiting for his first treatment.

jillygirl profile image
jillygirl

I have peripheral neuropathy, It might be worth asking your oncologist for vitamin B6 if he feels any numbness starting. I have only just finished my treatment , but the numbness is not as bad as it was at the beginning of the treatment.

Take care, xx

Bramwater profile image
Bramwater in reply tojillygirl

Thanks Jillygirl, I called my brother who has just finished his first day of chemo and read him your reply. His first day went without a hitch and he was able to eat supper so hopefully this bodes well for him.

I don't have diabetes but there is a good section on Cancer uk about chemo and diabetes, obviously your brother may need to do his tests more often as chemo can cause loss of appetite, sickness etc and this would upset his sugar levels. Although the anti sickness tablets i have have always worked for me as long as you take them befor the nausea starts.

4 years ago on my first run in with L C I had Cisplatin and Vinorelbine but the Cistplatin gave me a Tinnitus so I switched to the sister drug Carboplatin which is a bit less harsh and although I still have a bit of Tinnitus it is not too debilitating.

I have also neuropathy to my hands whic can really tingle especially in the mornings and sometimes even as if they are not mine, however a few stretches slaps etc seems too settle down and I really do not then have much more problem during the day.

The fact your brother has had surgery is good and his team are working towards curing him so it's a big positive for him to go along with this thought.

We all react differently to treatment but hopefully he will get through his without too many difficulties.

Just remember the old Hollies classic.

Good Luck rab

Bramwater profile image
Bramwater in reply to

Thanks Rabbie,

I have forwarded your message onto my brother.

Not what you're looking for?

You may also like...

Chemo Starts Next Tuesday - Cisplatin and Vinorelbine

Saw the Consultant two weeks ago and introductory meeting today where all the gorey and not so...

Cisplatin versus Carboplatin

This is my first post. Having had a lower right lobectomy in late December 2016, I am now 6 days...
Davthomp profile image

Cisplatin & Gemcitabine what to expect? Any advice?

We have been for a 2nd opinion at a private hospital in london & have found an amazing dr who was...
Kennawade profile image

My brother

Hi everyone - we're just starting out on this journey & trying to stay calm. My brother is 61 -...

Palliative chemo - pemotrexid and cisplatin

Hi, I've been reading posts on here for a week or two, since my mum was diagnosed with terminal...
Esme85 profile image

Moderation team

See all

Top community tags

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.