Volume 199 - Issue 9

The dilemmas of prostate cancer screening

Authors:  Nathan Lawrentschuk, Declan G Murphy and Anthony J Costello

Med J Aust 2013; 199 (9): 583. || doi: 10.5694/mja13.10779
Published online: 4 November 2013
To the Editor: We read with interest Del Mar and colleagues’ “re-examination” of the evidence for prostate cancer screening.1 Rather than presenting a balanced view, they have pursued a lopsided and flawed review of the data. First, they have given equal weighting to the results of the screening trials from Europe (ERSPC [European Randomized Study of Screening for Prostate Cancer]) and North America (PLCO [Prostate, Lung, ...

To the Editor: We read with interest Del Mar and colleagues’ “re-examination” of the evidence for prostate cancer screening.1 Rather than presenting a balanced view, they have pursued a lopsided and flawed review of the data.

First, they have given equal weighting to the results of the screening trials from Europe (ERSPC [European Randomized Study of Screening for Prostate Cancer]) and North America (PLCO [Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial]), when clearly the contamination of the “non-screened” arm of the PLCO (about 50% of men in the non-screening arm were actually screened) is, by any statistical analysis, a failure of study design. The authors’ comment that “those on either side of the debate read the same information but interpret it differently, declaring that it supports their unchanged positions”,1 is disingenuous. What they should point out is that opposers of screening point to a flawed study (PLCO), and supporters of selective screening use a superior trial (ERSPC). As Hugosson and Carlsson’s article highlights, they also fail to include the latest update from the ERSPC.2

Second, Del Mar et al misrepresent the positive effect that prostate-specific antigen testing has had on prostate cancer mortality. Between 1991 and 2010, the age-standardised mortality rate for prostate cancer fell from 44/100 000 to 31/100 000, a 30% reduction.3

Australia has embraced surveillance,4 further minimising the impact of overdiagnosis, the very problem that even the ERSPC trial raises. But over time, the number of men needed to treat will continue to fall, resulting in harm reduction, and appropriately selected men will have radical treatment, saving lives. This perspective is missed by Del Mar et al.


Authors


Competing interests


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