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Myeloma, Party Of Two: What’s Behind Door #4?
By: Tabitha Tow Burns; Published: June 27, 2018 @ 7:25 pm | Comments Disabled
Lately, I’ve been thinking about how myeloma treatment is like being a contestant on a game show. You never know what’s lurking behind the screens once you get called up from the audience. It could be a new car, or it could be a “wah-wah-wah.”
Today, my husband Daniel completed his 3rd cycle of Kyprolis (carfilzomib), Revlimid (lenalidomide), and dexamethasone (Decadron) for his multiple myeloma. In a week, he will have his next round of myeloma labs, and then we’ll meet with his myeloma specialist to discuss his progress. That’s when we’ll find out what’s behind “Door #4.”
Last month, we learned that Daniel had “only” achieved a partial response to therapy after completing two cycles of his treatment. This month, after the completion of his third cycle, we will find out whether he has achieved a complete response.
Did you catch that? Only a partial response. When discussing his results with others, Daniel called it “mixed news.” He was concerned that this might indicate that the treatment wasn’t working as well for him as we need.
The good news is that Daniel has already reached a partial response, which is the required minimum for him to be a candidate for the autologous stem cell transplant that his care team is planning for him in August. Also, as his stem cell specialist explained, while a deeper response is desired, less than 15 percent of his patients achieve a stringent complete response. So why are complete responses and stringent complete responses the goal? According to our specialist, some studies have shown that patients who achieve a complete response to therapy are more likely to have longer progression-free survival after stem cell transplant.
We’re into the sixth year with Daniel’s myeloma specialist, and we’ve learned to read her pretty well. Today, she is as calm and measured as always, but we sense her concern and we’re grateful for it. She has already come up with a plan for the fourth cycle of Daniel’s treatment, in case he needs it. To encourage a deeper response prior to transplant, she has requested pre-approval for Darzalex (daratumumab) from our insurance company. It would be added to his current treatment cocktail if his myeloma labs do not show a deep enough response after his third cycle. The thinking is that between the Kyprolis (a proteasome inhibitor), and Revlimid (an immunomodulatory agent), dexamethasone (a corticosteroid), and Darzalex (a monoclonal antibody), that this multi-pronged approach might drive better results in combination.
If he has not achieved a complete response and he is approved for the addition of Darzalex to his treatment cocktail, our infusion time for his therapy increases another seven hours for the first infusion and about five hours for future infusions. This is on top of the 2.5-hour infusion of his current treatment that he receives twice a week.
Most days we find ourselves at the hospital for most of the day when he receives treatment because it takes so much time for his blood to be drawn and then analyzed prior to his infusion. Two- to four-hour waits are not uncommon for us, so by the time we get back to the treatment area for his infusion, it’s a long day. With Darzalex, it sounds like it will be even longer. I may need to invest in some noise canceling headphones and strategies to combat restlessness for my good “patient,” but all of that is a great bargain if we’re getting a complete response in exchange.
I understand that these end-of-cycle markers are just one of several milestones to come. As many readers have already experienced, the final measure of response depth will be made after Daniel’s stem cell transplant. However, it hasn’t escaped our notice that these end-of-cycle markers measuring his response to treatment are guiding his treatment decisions, and they definitely have us thinking about the implications.
We hope that a stringent complete response is awaiting him at the end of all this and that we will have at least five years of progression-free survival before he has to do this again. By that time, who knows, the entire treatment landscape may have changed. Hopefully we’ll have found an easier way to treat this disease, if not cure it.
So, here we are waiting for next week. It never gets boring on this myeloma game show. We’re spinning the wheel, awaiting what’s behind “Door #4,” and hoping that it’s a complete response. I’m just glad that we get to play the game where we do, and that his specialist keeps the game plans coming.
Tabitha Tow Burns writes a monthly column for The Myeloma Beacon. Her husband Daniel was diagnosed with smoldering myeloma in 2012 after initially being told he had MGUS. You can view a list of her previously published columns here [1].
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