Besremi - 6 month update: Hi, I thought you might... - MPN Voice

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Besremi - 6 month update

JohnSC profile image
25 Replies

Hi,

I thought you might be interested in an update of my experience to date with Besremi.

I started on Besremi 6 months ago as I was proving to be HU resistant and Pegasys and Ruxolitnib were both considered inappropriate due to my medical history.

For the first 3 months I transitioned off HU by reducing my tablets by 1/week while gradually increasing my fortnightly injection of Besremi. I started the transition by reducing HU to 15 tablets/week supplemented by a small injection of 50 mcg of Besremi. The effect of Besremi was immediate and dramatic as I no longer require venesections and since this initial dose I have achieved complete haematological response.

I have since increased the Besremi gradually to 250 mcg every 2 weeks with no side effects and my consultant has described the result so far as excellent and transformative.

I am discussing with my consultant whether to increase the period between injections from 2 weeks to initially 3 weeks and eventually every 4 weeks.

I am very happy to be on Besremi as it seems to be having a positive impact on my PV while allowing me to live a normal life.

Please bear in mind that this is my experience of Besremi and should you start on a course of treatment your experience may differ for better or worse.

John

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25 Replies
HFrank profile image
HFrank

Hi JohnSCVery happy to heard your positive result.

Best wish.

ggrana profile image
ggrana

Hello JohnC ! Omg I’m so happy to hear this good news!!! You are very fortunate to be able to get this medicine as I am in the United States, New Jersey waiting desperately. I pray you continue to do well. I have been very frustrated since my numbers are at 1.2 million with four capsules of hydroxyurea a day I hope to be able to get this medication soon and hope it will be my help to reducing that number. God bless you!

Paul123456 profile image
Paul123456

Thanks John, great news

Any idea how dosage levels compare with Pegasys? ie if on Pegasys at say 100 mcg weekly would you move to 100 mcg Ropeg every other week or 200 mcg? Or is a Ropeg dosage more potent so need less?

Ropeg appears to be very expensive and comes in 250 mcg syringes which allow two shots but must be used within 4 weeks?

Best Paul

JohnSC profile image
JohnSC in reply to Paul123456

Hi Paul,

Sorry I can’t advise on Pegasys to Besremi transition as I was on HU before starting Besremi. I know my consultant discussed in detail how to best transition with the experts running the Besremi trials and it would probably be best if your consultant also contacted them should you decide to move onto it.

John

Whitehair51 profile image
Whitehair51

Maybe these responses mean your immune system kicked in better this time?

hunter5582 profile image
hunter5582

Glad to hear you have had a positive experience with Besremi. I am currently having great success with Pegasys, but will likely switch when it becomes available in the USA. That will hopefully be in November.

Wishing you continued success going forward.

Artemide profile image
Artemide

Thanks for sharing so happy for you I’m in Canada and on Pegasys since 10 years once a month now but a low dose not totally controlled platelets around 500K want to switch to Besremi when available

MPNBlog profile image
MPNBlog

Thank you for taking the time to update us John. It's great that you have responded so well! It's good for us all to have such a positive posting. Many thanks and stay well.

FG251 profile image
FG251

Lovely to read positive news first thing! As someone with ET who is about to come off HU (after 10 months) by request and not because of intolerance or resistance, may I ask why Pegysus was considered inappropriate? I thought that Besremi was ‘just’ a longer-lasting formulation.

JohnSC profile image
JohnSC in reply to FG251

Hi,

I had a bad reaction to Pegasys when the dose was increased so I was taken off it.

Besremi is a cleaner more longer lasting interferon and I am tolerating it well.

FG251 profile image
FG251 in reply to JohnSC

Gotcha! Well, it’s good news for you - and hopefully I’ll have a good response on Pegysus…

EPguy profile image
EPguy in reply to JohnSC

This is a real life example of the improvement Besremi offers. The mfr claims this is supposed to happen, I've not seen a real example before.

In the US if a drug is approved for example for PV, the Dr can prescribe "off label" for ET. But getting insurance to cover can be harder, although if PEG is being covered Ropeg should be at least as easy.

Before that can happen we need the Ropeg FDA approval in US.

Miriammusic profile image
Miriammusic

That is wonderful John! It is so encouraging that there seem to be new drugs on the horizon.

Wyebird profile image
Wyebird

Absolutely thrilled for you🥳🤩. Enjoy life as much as possible you never know what’s around the corner.

Meatloaf9 profile image
Meatloaf9

Thank you for posting your experience. Great news. Hoping it works for you forever. Please keep us all posted as time goes by, best to you always.

Solyesh profile image
Solyesh

Great news! I recently switched from HU to Peg. I discussed Besremi with my MPN specialist but it is not approved (yet) locally for ET (only PV) - so far Peg has been great so hoping that continues!

Bluetop profile image
Bluetop

Sounds really positive. Thanks for posting and very pleased for you!

Aldebaran25 profile image
Aldebaran25

It is so encouraging to read this, thanks John! and I know that we are all different, but still great to know. 😊

Bobadog profile image
Bobadog

Hi John,Do you live in the UK?

I’m being treated in Guildford and London,and I’m very interested to discover where Besremi is presently available/being used,

Many thanks,

Bobby

(Jak 2 PV :phlebotomy and aspirin..commencing Peg Interferon next week)

JohnSC profile image
JohnSC in reply to Bobadog

Hi Bobby,

Sorry for the slow reply. Besremi is not yet available via the NHS so I have had to go private to obtain it. Hopefully it will be approved soon so the it will become more widely available.

John

Elizka profile image
Elizka

Hi there,

Did you have any ongoing PV complications? I really don't at all. I keep my HCT controlled with phlebotomies, take aspirin and I'm good. So while I was waiting for this exciting drug, I'm concerned about all the possible risks.

JohnSC profile image
JohnSC in reply to Elizka

Hi,

So far so good when it comes to complications. I haven’t yet got to my final dose age as it takes time to find the ideal long term dose but I am feeling positive. With regard to all the risks, Besremi is no different to other drugs. They all have comprehensive lists of possible complications, but in my opinion the potential that Besremi’s has to positively change the course of the cancer outways the small risk of adverse events.

John

IrishSarah profile image
IrishSarah

Late to the party but thrilled to see your update John! Great to hear you’re responding so well to Besremi

Buggerbear profile image
Buggerbear

Thanks John for sharing your wonderful news!!! Wishing you the best with Besremi and please keep us informed of your progress!!

katiewalsh profile image
katiewalsh

Hi. That’s such great news! I’m very happy for you. I’m thinking of asking to get on it when I see my doc soon & wonder if you could explain in more detail what your hematological response was. Thanks Katie

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