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UK Team Claims Breakthrough In Universal Cancer Test

An anonymous reader writes UK researchers say they've devised a simple blood test that can be used to diagnose whether people have cancer or not. The Lymphocyte Genome Sensitivity (LGS) test looks at white blood cells and measures the damage caused to their DNA when subjected to different intensities of ultraviolet light (UVA), which is known to damage DNA. The results of the empirical study show a distinction between the damage to the white blood cells from patients with cancer, with pre-cancerous conditions and from healthy patients. "Whilst the numbers of people we tested are, in epidemiological terms, quite small (208), in molecular epidemiological terms, the results are powerful," said the team's lead researcher. "We've identified significant differences between the healthy volunteers, suspected cancer patients and confirmed cancer patients of mixed ages at a statistically significant level .... This means that the possibility of these results happening by chance is 1 in 1000." The research is published online in the FASEB Journal, the U.S. Journal of the Federation of American Societies for Experimental Biology.

8 of 63 comments (clear)

  1. So... by AlCapwn · · Score: 2

    We'll see this technology applied in... 20 years? Reading /. is sometimes painful.

    1. Re:So... by Edis+Krad · · Score: 3, Informative
      From TFA

      The University of Bradford has filed patents for the technology and a spin-out company, Oncascan, has been established to commercialise the research.

      And they already have a website running.

      I'd say under 5 years before we start seeing this applied in the wild.

    2. Re: So... by pla · · Score: 2, Insightful

      Don't do it! Everyone will be diagnosed.

      Bizarre trolling aside, You have the right idea - Virtually everyone over the age of 50 has dozens of "cancerous" cell clusters scattered around their bodies, all more-or-less harmless unless juuust the right combination of environmental conditions triggers a few to start growing (and spreading) uncontrollably.

      I find it easy to believe that a universal test for "cancer" would have a near-perfect success rate, because nearly everyone has it, to some degree. I find the negative side much harder to believe, because it means differentiating between cancer-but-harmless and cancer-gonna-kill-you.

      Or looked at another way, consider recent changes in attitude regarding breast and prostate cancers. 20 years ago, detecting either meant immediately scheduling a radical mastectomy/prostatectomy. Today, unless you have a family history of aggressive cancers, your oncologist will likely suggest watching and waiting for at least a few months to see if it actually does anything more that sit there harmlessly. Yet, even if it does - still cancer. Much like we don't universally vaccinate people against TB because it makes TB antibody tests diagnostically useless, I see this test as having the same issue, accurate but useless.

  2. Cause/Effect? by RyanFenton · · Score: 3, Interesting

    Sounds like generalized damage to white blood cells they're detecting. It's my understanding that "cancers" of a sort kind of exist in pockets in most everyone - they're just not the sort that get aggressive and kill people, because those mutant pockets just don't break enough of the rules of good cell conduct yet to count as a notable risk.

    My big issue with the methodology is that when anyone has already detectable active cancer, they usually are on chemo, or too sick to stop the progress... both of which will cause generalized damage to the body's defenses. If they can reliably distinguish the kinds of damage though, that would be a nice development.

    Even as it is stated, sounds useful to help distinguish some symptoms from cancer perhaps - but it seems this could also correlate with radiation damage or other generalized damage too. Cool study all the same - perhaps may help lead to cheaper or more automated screening at some level.

    Ryan Fenton

  3. Great progress, hasty generalization. by kaliann · · Score: 4, Informative

    This could be a giant step forward in cancer diagnostics, but media reports are - of course - sensationalizing beyond evidence.

    In the study, the types of tumors tested share some similarities that might mean findings true of them would not be true of "all cancers". Specifically, none of the lesions tested were tumors of mesenchymal origin. No sarcomas, no fibromas, no leukemias. That's a broad range to not examine, and it means that generalizing this as a test for "all cancers" is premature. Additionally, none of the tumors tested were types that tend to show up in places that lymphocytes have trouble getting to (like the brain, eye, and portions of the reproductive tract).

    It is good that they tested against COPD (a chronic inflammatory condition), but it does not appear as if they could distinguish between less-aggressive tumors and inflammatory conditions (I can't tell for sure because of the paywall). It may be that this is a test that is a good indicator of chronic inflammation (seen in many cancers as well as other conditions) rather than a cancer-specific test.

    Regardless of the limitations of the preliminary sample set, the findings are very exciting and a potentially amazing discovery in cancer medicine. Kudos to the hardworking scientists involved!

  4. Link to abstract by Michael+Woodhams · · Score: 4, Insightful

    Here is the abstract. The actual paper is behind a paywall.

    "ROC analysis of [the test statistic], for cancers plus precancerous/suspect conditions vs. controls, cancer vs. precancerous/suspect conditions plus controls, and cancer vs. controls, gave areas under the curve of 0.87, 0.89, and 0.93, respectively (P<0.001). Optimization allowed test sensitivity or specificity to approach 100% with acceptable complementary measures."

    The ROC curve has area under it of 1 for a perfect classifier and 0.5 for wild guessing. This is a more useful measurement than the p-value. (E.g. if I look at height vs sex for humans, it won't take too big a sample to get a great p-value for there being a difference, yet classifying people as male/female depending on whether they exceed some height threshold is a very poor diagnostic system.) I don't have much of a feel for how good ROC area of about 0.9 is for a medical test. I'd guess it is good enough to be useful, but you'd not want to rely on that test alone.

    --
    Quattuor res in hoc mundo sanctae sunt: libri, liberi, libertas et liberalitas.
    1. Re:Link to abstract by gringer · · Score: 4, Interesting

      The actual paper is behind a paywall.

      Yay for institute access. Their idea of "approach[ing] 100%" is a little bit loose:

      Based on these calculations, the cutoffs for low (0.10), medium (0.25), and high (0.50) thresholds are 1.47 at a sensitivity of 94.8% and a specificity of 54.7%, 1.73 at a sensitivity of 81% and a specificity of 78.7%, and 1.99 at a sensitivity of 62.1% and a specificity of 94%, respectively

      I have yet to do the calculations using population prevalence, but I'm going to guess that the positive predictive value of these tests are not particularly high.

      --
      Ask me about repetitive DNA
  5. Expect many years before approved in USA by whoever57 · · Score: 2

    Like many medical advances, this will likely take years before it is approved for use in the USA. Apart from the FDA being very slow, this would cut into revenues from colonoscopies.

    Even things like better and safe sunscreen are available in other developed countries but not in the USA. Improved treatments for tooth decay took years before approval in the USA.

    --
    The real "Libtards" are the Libertarians!