New to treatment: Does anyone take Acalbrutinib... - CLL Support

CLL Support

23,339 members40,047 posts

New to treatment

Notreall profile image
10 Replies

Does anyone take Acalbrutinib and Co-Trimoxazole?

Written by
Notreall profile image
Notreall
To view profiles and participate in discussions please or .
Read more about...
10 Replies
Eucalyptus22 profile image
Eucalyptus22

Hi,

Yes I take Acalabrutinib. Started last October. Was on Co-Trimoxazole to begin with but got quite a nasty allergic reaction to it. Was covered in a severe rash head to toe, with swollen lips and tongue. They changed me to Atovaquone and thats been ok.

I have been on Acalabrutinib for 8 months and after 4 months my bloods were all in the normal range. I had been stage 3 aggressive.

I am sure you will do very well on this drug. There aren't many side effects and what there is seem to be well tolerated by most people.

In my case the only downside seems to be the effect it has had on producing any antibodies to the covid vaccine i.e. none! I suspect that will also apply to the flu vaccine this winter.

Having said that, I am a much healthier person than 8 months ago.

I hope you do well on this drug.

Notreall profile image
Notreall in reply toEucalyptus22

Many thanks for the input , I am just about to start acalabrutinib and am trying to gather as much information as possible about that and associated drugs as i did not realise there was a need to take additional medication!

Jillinill profile image
Jillinill

Yes, for the past month, I've been taking both acalabrutinib and Bactrim (aka Co-Trimoxazole, Trimethoprim / Sulfamethoxazole, Brands: Bactrim DS, Sulfatrim, Bactrim). I'm taking a 400/80mg prophylactic dose, 3 days per week MWF. It's not at full dose for treatment of infections, but it's a good prophylactic dose to prevent pneumonia, a potential side effect of treatment. I had some ground glass spots in my lungs which disappeared with full dose Bactrim. It also seems to also prevent my previously pesky UTIs, which used to required full dose Bactrim and Keflex.

As an azole antibacterial, it can increase gut uptake of acalabrutinib by slight inhibition of enzyme CYP3A4. If taken simultaneously with acalabrutinib or ibrutinib it can cause increased GI or other side effects. I always take Bactrim along with prophylactic acyclovir to prevent shingles. Both can impact CYP3A4, so I take them at least 4 hours after acalabrutinib to prevent bowel issues that I had experienced for over a year when taking it simultaneously with my previous treatment ibrutinib.

I don't seem to have any side effects from these prophylactics, and happy that they keep my safe from infections, especially as I'm neutropenic with only 0.2 neutrophils right now. Hope the combo works as well for you as it has for me.

Zeus52 profile image
Zeus52

Yes I’ve been on that combination for 2 months now with excellent results and very little by way of side effects. I did take the advice to drink between 2 and 3 litres of water a day. Had telephone consultation on Monday and WBC down to 6.9 from 147, haemaglobin back up to 119 and neutrophils of 3.0. I was amazed how fast my swollen lymph nodes disappeared- good luck with your treatment Notreall !

Hi

Co-Trimoxazole is used to help people from developing pneumonia when bloods/immunity is low. I developed a rash after a few days. However, this was stopped and I then used a nebuliser, at home, once a month with pentamidine.

SERVrider profile image
SERVrider

Yes, I was on the compassionate early access scheme with Acalabrutinib and Co- Trimoxazole. Now Acalabrutinib is licensed in the UK it comes in proper "Calquence" boxes and blister packs. I have had no reaction that I can put down to the Co-Trimoxazole.

greenfliss profile image
greenfliss

I've been taking Acalabrutinib for 4 months (compassionate use), together with Co-Trimoxazole and Aciclovir and was a bit surprised I had to take all 3 (was also on Allopurinol for the first month). As SERVrider says it now comes as Calquence in helpful blister packs with pix of a sun and a moon so you can monitor whether you've remembered to take them morning and evening! You will need to be quite organised about the regime as Co-Trimoxazole is only 3 per week, Acal is 2 per day and Acicolvir is 3 per day!

lankisterguy profile image
lankisterguyVolunteer

Hi Notreall,-

The other drugs are added as prophylactics (a medicine or course of action used to prevent disease) to compensate for your weakened immune system.

-

We CLL patients are more likely to get Shingles - so Acyclovir ( Valtrex/Valacyclovir, Famivir, etc.) is used to reduce that risk.

-

During clinical trials the research showed that some targeted drugs or just the increased CLL activity increased the risk of a fungal pneumonia called pneumocystis uptodate.com/contents/treat....

The Bactrim / Co-Trimoxazole or Atovaquone can lower the risk of both fungal and bacterial pneumonias.

-

Len

PaulaS profile image
PaulaSVolunteer

I took Co-Trimoxazole along with Ibrutinib (similar to Acalabrutinib).

Like Eucalyptus22 the Co-Trimoxazole gave me nasty rashes so I had to stop it (the Co-Tri not the Ibrutinib). I wasn't given an alternative antibiotic. I seem to be OK without the Co-Tri, but I do have good neutrophil levels, unlike some folk.

We're all different and people react differently to drugs.

Wishing you all the best as you start your treatment.

Paula

Graham64 profile image
Graham64

Hi. I started on that combination 3 year ago, but was allergic to co-trimoxazole - got an all over body rash. That got changed to Azithromycin, and no problems since than.

Not what you're looking for?

You may also like...

New to treatment

Began treatment of calquence one month ago with no bad side effects but my doctor wants to add...
buglin profile image

New Treatment!

Hi Everybody, My blood counts have gone haywire. I finished a round of...
john133 profile image

My new CLL Treatment

My oncologist is recommending a drip of Rituxan and Bendamustine for my CLL treatment to replace...
umpireman profile image

Feedback on my new treatment options, what to do?

Hi everyone. So here goes: in short, after a long period of watch and wait, I have been told I...
Davdow profile image

Time to start treatment?

In W&W for about 18 months. My WBC has risen to about 115 but I have no significant symptoms....
Elam profile image

Moderation team

See all
AussieNeil profile image
AussieNeilAdministrator
Newdawn profile image
NewdawnAdministrator
CLLerinOz profile image
CLLerinOzAdministrator

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.