F. Schoder et B. Tribukait, CLINICAL UTILITY OF CELLULAR DNA MEASUREMENTS IN PROSTATE CARCINOMA, Scandinavian journal of urology and nephrology, 1994, pp. 51-63
At a WHO consensus conference on Early Diagnosis and Prognostic Parame
ters in Localized Prostate Cancer, a working group discussed the clini
cal utility of DNA measurements in stages T2 and T3 prostate carcinoma
. Incidentally discovered prostate cancer of stage T1 was excluded. Th
e members of the working group, representing various clinical and labo
ratory disciplines, discussed technical considerations of DNA measurem
ents by flow and image analysis, pretreatment prediction of prognosis,
and posttreatment clinical relevance. The group agreed to subdivide t
umors into diploid, tetraploid and non-tetraploid aneuploid, expressin
g various degrees of aggressiveness and gave guidance for the definiti
on of limits of these groups. The panel agreed that knowledge on DNA p
loidy prior to treatment is of value in treatment decisions, particula
rly when surveillance is a treatment option. Aneuploid tumors can be e
xpected to respond very poorly to either irradiation oi endocrine ther
apy, and the presence of aneuploid tumor, either on pretreatment biops
ies or in radical prostatectomy specimens, is an ominous sign. The ide
ntification of a group of patients with a uniformly poor prognosis sho
uld encourage medical oncologists and basic scientists to develop adeq
uate treatment options for this particular group. The panel expressed
a strong opinion that DNA ploidy should be uniformly studied in clinic
al trials, particularly in patients with localized prostate cancer.