tali wrote:Hi,
I am 36 and a poor responder and have had 4 failed cycles:
IVF #1 – BCP, Lupron, FSH and Menopur – Produced one mature follicle, converted to IUI - BFN
IVF #2 – Antagonist protocol, BCP, FSH, Menopur and Ganerelix – Produced 1 mature follicle, which was lost before retrieval??, explanation was that I may have ovulated on my own and I was converted to IUI – BFN
IVF #3 – Antagonist protocol, same as #2 – RE’s recommendation was to keep trying – produced 1 mature follicle, made it to retrieval, embryo did not survive
IVF #4 – Changed REs, EPP protocol, Estrogen patch, Ganerelix, Gonal F and Menopur – Produced 4 mature follicles, transferred 2 embryos (8 cell and 4 cell) on day 3 – BFN
I have always been on very high doses 400 - 600 ius. I have recently heard about low or no stim cycles and have heard that I may respond the same as I have with high doses. Although I realize that this may not increase my chances, it would be cheaper and get us more chances. My last cycle was almost 10k of my insurance money just for the meds.
We have thought about DE as a possible next option, but for now, just can't justify the cost of DE when we still have insurance money left.
Not sure if all REs do this and how the process works, I have a f/u with my RE next week and wanted to have some info on this before I talk to him. I would appreciate your thoughts.
Tali
Sorry to hear of this.
I don't see how a no stim cycle could get the same response as 600 IU of FSH. FSH is no placebo. No stim and low stim cycles are associated with poor response and high cancellation rates.
At 36, the response is usually better than that.
But you are facing a double whammy. The more they stimulate you to finally get some embryos, the worse they make your endometrium. That's why the chance of success, even per transfer, is lower with these poor responders.
Normally this is the point where donor cycle IVF gets recommended, as a donor cycle would have maybe 5x the chance of success. But you have more insurance coverage, so that changes the economics because it changes who pays for it.
There are some interesting, if not convincing, reports of increased ovarian response in low responders after androgen priming. This means that some doctors think testosterone makes the ovaries more sensitive to FSH stimulation. There are two studies of testosterone patches (take a look at Balasch et al 2006, they studied patients with 2 prior canceled stims, and got decent responses from most of them) and of DHEA. The testosterone studies included only 5 days of priming, while the DHEA is often used for months. There are side effects of androgens, some you might or might not like.
Another idea is the flare cycle.
Of course, both could be used.
None of these are miracle cures, but some believe they help. Maybe they do. We've tried flare cycles and gotten some surprisingly high responses, but not reliably so. Never tried the androgens.