ImmunoAdvocates Adrienne Other Cancer La historia de Adrienne En 2005, Adrienne se enteró de que tenía el síndrome de Lynch, una mutación genética heredada que aumentaba significativamente el riesgo de desarrollar varios tipos de cáncer. Ocho años después le diagnosticaron cáncer ampular metastásico. Se sometió a quimioterapia durante 13 meses, que no funcionó. Cuando las pruebas genéticas del tumor indicaron inestabilidad microsatelital alta (IMS), su oncólogo le recomendó que se inscribiera en un ensayo clínico de pembrolizumab (Keytruda®). Poco más de dos meses después, el cáncer había desaparecido. Siguió con el tratamiento durante dos años, y viajaba desde su casa en Nueva York hasta el Johns Hopkins, en Baltimore. A más de dos años desde su último tratamiento, sigue sin cáncer y ha vuelto a su ajetreada vida: trabaja, pasa tiempo con sus cuatro hijas, practica yoga, juega al tenis y viaja con su familia y amigos. PUESTA AL DÍA a diciembre de 2019: Adrienne sigue sin cáncer y habló en la Conferencia del CRI para pacientes de inmunoterapia llevada a cabo en Baltimore el 16 de noviembre de 2019. Questions and Answers How and when did you first learn you had cancer? I had just had a short haircut and was sitting on the steps in my house under a skylight playing with my one-and-a-half-year-old daughter when my wife looked down and noticed a spot on my scalp. So I went to a dermatologist who conducted a biopsy. Two days later I had the results and was immediately referred to the John Wayne Cancer Institute for treatment. How did you learn about immunotherapy and why did you decide to do it? My first clinical trial was for a vaccine and each arm of the study included an immunotherapy booster. When I started trial three, biochemotherapy, it included two immunotherapies, IL2 and Interferon. My sixth and pivotal trial was with ipilimumab, which became Yervoy once approved by the FDA. In each case, there were limited options available to me and I chose to keep pursuing treatments to stay alive. Whether it was immunotherapy or chemotherapy or surgery, I wanted whatever gave me the best chance of preventing recurrence or later surviving. What was treatment like? Did you have any side effects? Treatment on Yervoy was not bad at all. I would drive about three hours to San Diego from Los Angeles post-treatment and get into bed as I would get achy by then and really be ready for sleep. Next day I would head to the gym. I had some of the main, initial side effects which I was told were positively correlated with a response to the drug, so I was happy to get them. I developed severe diarrhea which was treated with steroids. I developed a horrible itch which is not easily treated. But the alternative was death so I’m OK with that. My advice is listen to your nurses and doctors and report all side effects as instructed. There is never anything to be embarrassed about and they are there to help. How did immunotherapy compare to other treatments you may have received, if any? Immunotherapy saved my life. In my humble opinion, nothing else compared. The side effects were tolerable and treatable, and the disruption to my life was minimal. Other than the one day I was required in Los Angeles, I never skipped a beat. Are there things that surprise you about the cancer experience? Probably the most significant surprise is how people react. There are some whom you expect to be there every step of the way for you who are incapable of dealing with cancer and treatments. And there are others who show up out of virtually nowhere who really get it and are there for you. What would you want another patient to know about immunotherapy or about participating in a clinical trial? Given that I enrolled in six clinical trials in my journey, I am obviously a believer in participating in clinical trials. The first kept cancer away for at least five years, while the last saved my life. Along the way, the other trials mostly kept me alive while waiting for the ultimate trial that succeeded. Immunotherapy simple fits in that realm and is absolutely worth trying if your doctors believe it is the best option for you.
