Hydroxyurea & Skin Cancers?: Hi I’ve had two... - MPN Voice

MPN Voice

10,874 members15,189 posts

Hydroxyurea & Skin Cancers?

katiewalsh profile image
18 Replies

Hi

I’ve had two squamous cell skin cancers in the past 6 months. I know Hydroxyurea is supposed to increase our risk of skin cancers. Does anyone know if having 2 in 6 months means I need to switch meds? I’ll ask my MPN doctor soon but just wanted to find out what you folks may have been told. Thanks. Katie

Written by
katiewalsh profile image
katiewalsh
To view profiles and participate in discussions please or .
Read more about...
18 Replies
hunter5582 profile image
hunter5582

I would certainly switch off HU fs I had two skin cancers in 6 months. There are other options that do not carry this risk.

katiewalsh profile image
katiewalsh in reply tohunter5582

thanks, Hunter

EPguy profile image
EPguy

I see your prior post about increasingly severe dry eyes. Is that still troubling you? Are you any meds or medical history that could cause it?

katiewalsh profile image
katiewalsh

not sure the cause but I had it treated with lipiflow (sp?) which helped a lot. I also use prescription eye drops daily.

ainslie profile image
ainslie

its not unheard of on Hydroxy, maybe time to try Peg or Bes or Rux

katiewalsh profile image
katiewalsh in reply toainslie

Thanks for replying. I’m worried about the potential problems so many experience on those other drugs but I don’t think I have a choice given the skin cancers so close in time. Katie

Strumin210 profile image
Strumin210

I have been taking 1000mg. Of hydroxurea for awhile then two weeks ago I quit taking it due to various reasons one of them being skin cancer ( higher risk) taking this medicine. My visual migraines came back so I started back on it yesterday. Don't know whether that answer helps. I have been starting and stopping this a couple of months now and it's got my wife kind of upset over they way I start it back then when it makes me feel horrible I quit it again. Maybe you or someone on the forum can help me also. It's not made much difference in my platelets but they did come down from a million to 786,000. Any help would be appreciated. Hope all goes well with you and you stop getting these. Sending prayers and hope from LA ( LOWER Alabama )

katiewalsh profile image
katiewalsh in reply toStrumin210

thanks for writing. I’ve been on HU for 10 years & only had skin cancers these last 6 months. Your experience with migraines is scary as I’ve had one for 2 days & im still on HU. Thanks also for your prayers & hope. Katie

lakeview65 profile image
lakeview65

I have ET, on Hydroxyurea for the past 3 years. I had many A&K ‘s before my diagnosis but I am wondering if Hydroxyurea is just turning them all into Basel Cell now. I had Moh’s 2 months ago on the side of my nose, they could not get it all so Dr. froze the edges and I am now on a 6 week treatment of Imiquimod covering the whole nose and a bit into the cheeks. This is not fun at all, feel like I should be in hiding.

But, 3 months ago I got bit by a bug on my forehead and it never went away, it turned into Basel Cell right away, now doing SRT for this spot.

MPN Dr is in Tampa, I stayed away due to hurricanes. I need a long discussion with him.

Hydroxy is wonderful for me, virtually no side effects until now….

Posted on here was a very informative you tube talk about this very scenario. I will try and find it again.

Best of luck, I am in hiding and driving for SRT 3 times a week, 7 weeks.

katiewalsh profile image
katiewalsh in reply tolakeview65

hi thanks for your reply. Your note really motivates me to find a replacement for HU. What you’re going through sounds very difficult. Like you. HU has been ideal for me with no problems for 10 years until now. Was the you tube thing a discussion by patients or medical people? My doctor is also in Tampa. at Moffitt, and I’ve written to him and am waiting for a reply. So many folks have problems with the other drugs that I dread switching. Good luck with your skin cancer problems. Katie

lakeview65 profile image
lakeview65

I am not home but if you google MPN skin cancer you tube you will see a link to a talk from a Dr in the UK, i believe it was just from a month ago.

katiewalsh profile image
katiewalsh in reply tolakeview65

thanks, will do.

Mazcd profile image
MazcdPartnerMPNVoice in reply tokatiewalsh

Hi Katie, this is the video about skin cancers healthunlocked.com/mpnvoice...

katiewalsh profile image
katiewalsh in reply toMazcd

Thanks very much for sending MAZ. Katie

givingITMybest profile image
givingITMybest

I blossomed in skin cancers while on Hydroxiaurea. That and developing extremes fatigue caused me to switch. I tried an experimental med, but ultimately am now on Besremi. The skin cancers are slowing down, it's been 2-3 years since I've taken HU, but for awhile I had things zapped or removed every 6 months.

katiewalsh profile image
katiewalsh in reply togivingITMybest

Thanks for writing. Are you saying you continued to have skin cancers for a few years after stopping HU? Katie

PVPVPV profile image
PVPVPV

Hi there

I was on hydroxy for about ten years and then had a skin cancer on myy forehead, duly removed. I was aware of the link with hydroxy and therefore assumed it was the cause. But my dermatologist said there was just as much chance that the cancer could have been due to exposure to sun as a child. I am fair-skinned and did get a lot of exposure to sun back in the 50s and 60s. I didn't like the look of the side-effects of the alternatives to hydroxy so I stuck with hydroxy. I had various skin problems - Bowen's disease, actinic keratosis - but no more cancer.

Regards

katiewalsh profile image
katiewalsh in reply toPVPVPV

Thanks so much for letting me know. Katie

Not what you're looking for?

You may also like...

Ruxolitinib and skin cancers

Hi. I’ve just seen that ruxolitinib has now been approved for PV, which is great, BUT do take care...
Gipsy123 profile image

Hydroxyurea and skin cancer

I was diagnosed with JAK2 ET last September and have been on Hydroxyurea since then, with good...
Minify profile image

Ruxolitinib and Skin Cancer

Contacting on behalf of my 78 year old husband . He was diagnosed with Polycythemia Vera MPN and...
waddles22 profile image

Ruxalitinib and Peg interferon

AS previously mentioned my husband {He has PV and MPN} has for the past 6 years been on Ruxolitinib...
waddles22 profile image

Skin burning and tearing feeling when stretching skin

For the last few months my skin is becoming increasingly sensitive. When I crouch down, for...
Anag profile image

Moderation team

Debinha profile image
DebinhaAdministrator
Mazcd profile image
MazcdPartner

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.