Experiences with

Cabazitaxel

Unfortunately my brother(55 years) failed his treatment with Cabazitaxel and now we are looking for clinical trials. He has done triplet therapy with Nubequa and Docetaxel, Zytiga and prednisone and radiotherapy for his hip and now Cabazitaxel.

Anyone have positive experience with Cabazitaxel/Jetvana?

I plan to be treated with cabazitaxel which has less side effects. I know all individuals have different situations, Appreciate Cabazitaxel users to respond as to edema, hair loss, etc. Thanks.

If you did Cabazitaxel before docetaxel, then let me know what your experience was like. I know Cabazitaxel comes after Docetaxel.

For people that Docetaxel worked, why do they typically switch you to Cabazitaxel for the 2nd time of chemo instead of repeating the Docetaxel? Thanks.

Psa 101.68 Doc stopping my treatment of Cabazitaxel and starting Pluvicto. Does anyone have feedback? PSMA scan shows more activity in the bones and lymph nodes.

MO suggested cabazitaxel (1st choice) or enzalutamide (discouraged because cancer is aggressive). Any data/experience that combined enzalutamide and cabazitaxel would be better?

This discovery has placed him out of contention for both Pluvicto and cabazitaxel.

More in lengthy bio, Hi, Will Cabazitaxel And Carboplatin treatment for pca Adenocarcinoma kill growing tumour mass on prostate bed and liver metastasis?

Here I am, wondering where to go next and contemplating if chemo with cabazitaxel is the way to go. Does anyone have any experience with this drug? with thanks, Luylu

I have had 7 cycles of docetaxel and 3 of cabazitaxel. The oncologist wants to continue with another 7 cycles of cabazitaxel. My question is how much of this poison can the body handle. Does this chemo destroy things permanently in the body. I know that the fatigue is taking over.

That same day he did the cabazitaxel, a low dose, and has been feeling great since. Minimal side affects except fatigue. His coloring is back to normal and he has no pain at all. He had bloodwork done this week and his PSA went from 395 to 466. We are so grateful he is feeling good but confused.

I’m not sure what other options I have but until I get further advice I'm continuing with cabazitaxel. It's not a great choice as I’m sure it’s given me treatment induced macrocytosis and the reduced oxygen has seriously impacted my stamina.

He underwent chemotherapy (10 rounds of Cabazitaxel) and today was his last one! I would like to know what the next steps,according to your personal experience! He will have scans and everything to see the results of the chemotherapy!

I'm pretty sure he'll have to go through Cabazitaxel after that and it'll be much harder on him. He tolerates Pluvicto very well outside of some fatigue the first week. Thank you. I hope this treatment works as well for everyone as it did for my father. Please don't give up hope!

Switched to Cabazitaxel and currently on the 5th cycle. Since starting the Cabazitaxil my PSA has been raising and lowering. I am currently having some scans done to confirm if there is progression. What is going on? What causes the PSA to react like this.

Cabazitaxel 2. Docetaxel 3. Enzalutamide 4. Apalutamide 5. Abiraterone 6. Bicalutamide 7. Niraparib 8. Olaparib 9. Degarelix 10. Lupron 11. Castration 12. Pluvicto 13. Keytruda 14.

I have switched from Docetaxel to Cabazitaxel. Should I still take the Grastofil injections?

She mentioned another chemo treatment - cabazitaxel. Has anyone in the group had similar treatments and how did the chemo help after previous fails. His history, diagnosed in 2022 with stage 4b with mets to the bones - 6 spots.

Since 2020 he has completed chemo (got almost a yr of good results), zytiga (about 7 months good results), xtandi (about 8 months good results), Lymparza (never worked), lutecien (stopped after 2 infusions), Cabazitaxel, and this past July was the 1 st participant in new car t trial at Penn.