This is a submission to a minor journal, of a complicated material, attempting to do something that is clinically very difficult.
I'm not trying to dismiss this research, but please don't expect this to ever be clinically available.
This is a submission to a minor journal, of a complicated material, attempting to do something that is clinically very difficult.
I'm not trying to dismiss this research, but please don't expect this to ever be clinically available.
Submitters: "Please use the original title, unless it is misleading or linkbait; don't editorialize." https://news.ycombinator.com/newsguidelines.html
If the original title won't fit HN's 80 char limit, it can usually be shortened, as we did here.
> In the same manner, the trained deep learning for pancreatic cancer urine dataset (Figs. S13a–c) clearly showed superior classification performance with a sensitivity of 98.6% and a specificity of 100% (99.3% accuracy, 0.9892 AUC, 59 epochs).
1) All the authors have South Korean institutional affiliations
2) "Detection of human biofluids such as blood, tears, saliva, sweat, and urine is important for clinical analysis of various physiological patterns" (First sentence, seems to be missing a word)
3) "differentiate patients from the normal group with high sensitivity and specificity" (abstract, patients and normal group is an odd way of phrasing this)
That being said...it had never occurred to me that nueral networks might be a useful way of interpreting spectroscopy data, that is a really cool insight
I think we are at the technology level to really make medicine significantly more affordable and available, at the cost of many high paying doctor’s jobs. Same can be said for lawyers. These are powerful groups that will not take being automated lightly.
> The dataset was randomly divided into 70% training subset (1420 for prostate and 692 for pancreatic), 15% validation subset (304 and 148), and 15% test subset (304 and 148).
> The developed platform successfully classified the human prostate and pancreatic cancer urines in a label-free method supported by two types of deep learning networks, with high clinical sensitivity and specificity.
I don't have access to the full article so I can't see the numbers. It's not on the hub of science yet either.
Suppose that the percentage of people with prostate cancer at any one time is 1 in 1000 (i.e., then "base rate" is 1 in 1000). (Turns out this is actually on the same order of magnitude as real number [2].). And suppose this test has 99% sensitivity and 99% specificity.
And suppose you test 1,000,000 people.
Of those 1,000,000 people, 1,000 will actually have prostate cancer, and 999,000 will not.
Of those 1000 that actually have it, 990 will have a positive test (true positive), and 10 will have a negative test (false negative).
Of the 999,000 people who don't actually have it, 989,010 will have a negative test (true negative), and 9,990 will have a positive test (false positive).
So even with a test of 99% accuracy, if you get a positive result, your chances of actually having prostate cancer are still only 990 / 10980, or about 9%; 91% of the positives will be false positives.
And of course, the more rare the cancer, the worse it gets.
EDIT2: So, to follow on with GGP's point: "Near perfect accuracy" isn't very specific, but colloquially would imply that if you have a positive test, you have a high chance of actually having cancer. To get that number to 95% you'd need to have only 52 false positives, would require a specificity closer to 99.995%.
EDIT: Fixed some math
[1] https://en.wikipedia.org/wiki/Base_rate_fallacy [2] https://www.cancer.org/cancer/prostate-cancer/about/key-stat...
I just wanted to point out that both "P(Detect | Positive)" and "P(Not Detect | Negative)" are both high, since GP only mentioned one and not the other.
https://www.untrammeledmind.com/2018/01/cancer-screening-an-...
And the criticism section of the WP article is quite long: