Guest guest Posted September 19, 2011 Report Share Posted September 19, 2011 Hello folks, I would appreciate input on the " ABT-263 plus High-Dose Retuximab or High-Dose Retux only " clinical trial as a first line of treatment. I've been on W & W since 2004 with Dr. Kipps and feel very fortunate to have gone that long (Unmutated, 65% Zap 70+, but with 13q14). I'm definitely feeling a much lower energy level these days. In view of the promising treatments coming along, I'd like to avoid using chemo agents this first time around to preserve as much health as possible. I would greatly appreciate people's thoughts on this and to hear if anyone is has participated in this trial. Thanks very much. Sharon The numbers: WBC=84, 90% lymphocytes, 10% neuts, 14.2% hemoglobin, 161 platelets, 2.5 B2M, Low IG's, 4.92 RBC. Growing nodes; spleen @ 6 cm, liver @ 14 cm. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 20, 2011 Report Share Posted September 20, 2011 ABT-263 is a very interesting molecule that will hopefully become an important part of CLL treatment in the future, along with PCI-32765 and CAL-101. ABT-263 was tested first, but due to " issues " with the company, its development has been really slow. The only toxicity that is routinely seen is thrombocytopenia, which is due to shortened platelet survival. As a result, the body does " adapt " to it. It is important to remember that while the drug is discontinued abruptly at the end of the trial, there should not be any rebound, as the vast majority of the cells will have been eliminated by then. The " flares " that we are seeing are really in those who have not achieved near complete resolution of the disease. Rick Furman, MD Ron wrote: /message/16045 Sharon wrote: /message/16043 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2011 Report Share Posted September 22, 2011 I have been on ABT-263 over two years now. I did Rituxan once a week for 4 weeks two years ago. I just recently had a bmb which showed 20% CLL, this was down from 30% a year ago. So, the ABT has continued to work for me. I have no side effects since it changed to pill form. How long will it work? Your guess is as good as mine. They are letting me continue on the drug for as long as it works. Lori Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2011 Report Share Posted September 22, 2011 Lori, I assume you are in a study. Could you share the NCT number so that we can look at it on clinicaltrials.gov ? And where are you getting treatment? All the best, Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2011 Report Share Posted September 23, 2011 Lori: Thanks for sharing your information; it's quite encouraging. I agree with Lynn that we'd like to know more about your treatment situation. If it is a trial, which one? I think the trial I'm considering is ABT4710n. Also, can you share any of your beginning and current stats, beyond the BMB? Ron: Can you tell us why you feel these options aren't right for you? Thanks, again. Sharon Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2011 Report Share Posted September 23, 2011 Thank you for the clarification, Dr. Furman. How does the body adapt to thrombocytopenia? Very interesting. I'm wondering because I'm noticing that I am definitely bruising more easily and my platelets are currently at 236 (they were 160 in July). Thanks, again. Sharon Dr. Furman wrote: /message/16046 Quote Link to comment Share on other sites More sharing options...
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