I took teclistamab cqyv for one year. Took my numbers down to zero in a couple of months. Then I elected to go off tecvali to see how long I stay without multiple myeloma
It has been 6 months and still at zero. Blood tests every 3 months. Hope it holds forever. It was not approved by fda until now

Thanks for sharing. I am on Empliciti and pomalyst. I get the empliciti every 4 weeks and pomalyst 21 days and off 7 days. I have been on this regimen for almost 2 years. I just had labs done October 22, and numbers are still high, and the M-Spike is 1.4. Most times I feel alright. I started doing my own research because my doctors don't mention new treatments, and we have had so many changes in our Cancer Centers. At first, I did research on Car-T cell that appears to have a lot of side effects (cytokines). Then I read about BiTE and there is a better success rate. After reading these posts and seeing how you all have good results, I will have discussions with my oncologist and hematologist. Overall, I have more good days than bad days. But I want to experience remission and a better quality of life. God, I am so grateful to You, and I know you own the plan for my life. You said You will not withhold no "good thing" from me. Everyone, if it's God's will, I will continue to live and do it according to His way. You know... I am truly blessed. We know who has the FINAL say.

Hello Lena, haven’t heard from you in a while. I wish I knew more about the treatment you’re inquiring about. Wish you all the best!❤️

Yes I'm on a clinical trial and have monthly injections with Talquetamb along with Daratumumab. I started 1-2-23 and last testing I am MRD Negative (no cancer found). Brain fog is gone and I feel pretty much normal again. Hope I never have to do chemo again.!!