Here's what the CHAARTED study reported after extended follow-up on early chemohormonal therapy in men with metastatic hormone-sensitive PC:
"For those with low-volume disease, no OS benefit was observed"ascopubs.org/doi/10.1200/JCO.2017.75.3657People throw around the term "aggressive" a lot --I know I have! But as we learn more about
the natural history of prostate cancer, we learn that there are windows of opportunity in the disease's progression when different therapies become more or less effective. Chemo has never demonstrated any effectiveness in several studies of its use before RP, and its effect on radiosensitization was very small. The cancer in its less advanced state is just not susceptible to an antimitotic effect of the microtubule binding that taxanes do. It is only when metastases are more developed that the microtubule binding becomes fatal. Similarly, trials of Provenge before the cancer has become metastatic and castration-resistant have proven it to be completely ineffectual. Zytiga did not yet demonstrate any efficacy before there were metastases in hormone-sensitive men. It has recently shown efficacy in non-metastatic men who were already castration resistance. This demonstrates that these very toxic medicines each has its own place and time to be used - its Goldilocks moment. Using it too soon, only provides toxicity. Using it to late diminishes any survival benefit.