New paper below.
My first reaction was Why? With oligo-mets (i.e. only a few), the idea is to treat as one would the primary cancer; by surgery &/or radiation. Why use a systemic approach for very limited mets?
& then there is the STAMPEDE trial that found benefit primarily in high volume cases - which oligometastatic disease clearly isn't. The paper does mention this. However:
"Oligometastatic patients may not all share the same biology. Advanced imaging techniques may help to more accurately identify truly oligometastatic patients. Molecular markers will be necessary to distinguish oligometastatic patients who fare well enough with androgen deprivation therapy alone as opposed to those for whom upfront chemotherapy may be beneficial. Emerging molecular markers of docetaxel sensitivity, such as loss of lysine-specific demethylase 5d, warrant prospective validation with one goal of identifying oligometastatic patients with greatest likelihood of benefit from this strategy."
I had a solitary met at L5 zapped in 2015. I can't imagine my doctor suggesting Taxotere, even if he was an oligo-doubter, which many are.
-Patrick
ncbi.nlm.nih.gov/pubmed/288...
Curr Opin Urol. 2017 Aug 16. doi: 10.1097/MOU.0000000000000446. [Epub ahead of print]
Chemotherapy for oligometastatic prostate cancer.
Dorff TB1, Sweeney CJ.
Author information
Abstract
PURPOSE OF REVIEW:
To analyze recent trials of upfront chemotherapy to determine how this paradigm can be applied to oligometastatic prostate cancer patients.
RECENT FINDINGS:
Upfront chemotherapy prolongs survival in metastatic prostate cancer, according to the ChemoHormonal Therapy versus Androgen Ablation Randomized Trial for Extensive Disease in Prostate Cancer and STAMPEDE docetaxel trials. However, the benefit is driven by the high volume subset and may not apply to low-volume/oligometastatic patients.
SUMMARY:
Oligometastatic patients may not all share the same biology. Advanced imaging techniques may help to more accurately identify truly oligometastatic patients. Molecular markers will be necessary to distinguish oligometastatic patients who fare well enough with androgen deprivation therapy alone as opposed to those for whom upfront chemotherapy may be beneficial. Emerging molecular markers of docetaxel sensitivity, such as loss of lysine-specific demethylase 5d, warrant prospective validation with one goal of identifying oligometastatic patients with greatest likelihood of benefit from this strategy.
PMID: 28817399 DOI: 10.1097/MOU.0000000000000446