Key to Better Outlook in Colorectal Cancer: Earlier Detection
by David W. Sharp

WHAT'S HOT IN MEDICINE...

Rank Paper Citations
This Period
May-June
98
Rank
Last Period
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98
1 F.M. Sacks, et al., "The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels," New Engl. J. Med., 335(14):1001-9, 3 October 1996. [8 U.S. and Canadian institutions] *VL459 51 1 51 1
2 J.W. Mellors, et al., "Prognosis in HIV-1 infection predicted by the quantity of virus in plasma," Science, 272(5265):1167-70, 24 May 1996. [U. Pittsburgh, PA; Chiron Corp., Emeryville, CA] *UM889 36 2 36 2
3 K. Masuko, et al., "Infection with hepatitis GB virus C in patients on maintenance hemodialysis," New Engl. J. Med., 334(23):1485-90, 6 June 1996. [6 Japanese institutions] *UN799 26 10 26 10
4 H.J. Alter, et al., "The incidence of transfusion-associated hepatitis G virus infection and its relation to liver disease," New Engl. J. Med., 336(11):747-54, 13 March 1997. [NIH, Bethesda, MD; Genelabs Technologies, Redwood City, CA] *WM640 26 + 26
5 M.J. Alter, et al., "Acute non-A-E hepatitis in the United States and the role of hepatitis G virus infection," New Engl. J. Med., 336(11):741-6, 13 March 1997. [Ctrs. Disease Control, Atlanta, GA] *WM640 23 + 23
6 P.M. Ridker, et al., "Inflammation, aspirin, and the risk of cardiovascular disease in apparently healthy men," New Engl. J. Med., 336(14):973-9, 3 April 1997. [Harvard Medical Sch., Boston, MA; Harvard Sch. Public Health, Boston; Brigham and Women’s Hosp., Boston, MA; U. Vermont, Burlington] *WR385 22 + 22
7 C.H. Hennekens, et al., "Lack of effect of long-term supplementation with beta carotene on the incidence of malignant neoplasms and cardiovascular disease," New Engl. J. Med., 334(18):1145-9, 2 May 1996. [Brigham and Women’s Hosp., Boston, MA; Harvard Sch. Publ. Hlth., Boston, MA; Harvard Medical Sch., Boston, MA; U. Oxford, U.K.] *UG831 19 7 19
8 A.L. Waldo, et al."Effect of d-sotalol on mortality in patients with left ventricular dysfunction after recent and remote myocardial infarction," The Lancet, 348(9019):7-12, 6 July 1996. [7 institutions worldwide] *UV923 19 + 19
9 L.M. Jarvis, et al., "Infection with hepatitis G virus among recipients of plasma products," The Lancet, 348(9038):1352-5, 16 November 1996. [U. Edinburgh, U.K.; Edinburgh & SE Scotland Blood Transfusion Service, U.K.] *VT332 19 + 19
10 M. Tacke, et al., "Detection of antibodies to a putative hepatitis G virus envelope protein," The Lancet, 349(9048):318-20, 1 February 1997. [Boehringer Mannheim GmbH, Penzberg, Germany; Shinshu U. Sch. Med., Nagano, Japan; Inst. Tropical Med., Berlin, Germany] *WF794 19 + 19

SOURCE: ISI's Hot Papers Database.  Read the full legend.

   Mortality from colorectal cancer has not improved much in the past three decades, and one usual response to such gloomy news is to suggest that the answer lies in earlier detection. There has been much interest lately in the promise of research into the genetics of this tumor, and screening by regular (e.g., every six months) colonoscopy is now offered to individuals in families with a hereditary predisposition. The impact on the general population will be small, however--so what about the rest of us?

   In a commentary in the November 30, 1996 issue of The Lancet, David Lieberman, Oregon Health Sciences University, Portland, and Marvin H. Sleisenger of University of California, San Francisco, wrote: "Health-care policy makers are now confronted with clear evidence that screening can reduce mortality from the second leading cancer killer in Europe and North America," which is what cancer of the colon/rectum is. They were referring specifically to two papers now hovering on the edge of the Top Ten and to an older study, the Minnesota trial (New Engl. J. Med., 328:1365-71, 1993).

   The Nottingham, U.K. randomized study by Jack D. Hardcastle and colleagues (The Lancet, 348:1472-7, 1996; currently at #12 with 19 citations this period and 60 to date) recruited 150,000 people, half of whom were offered screening by testing for fecal occult blood. The simlilarly sized population base for Ole Kronborg’s team was in Funen, Denmark (The Lancet, 348:1467-71, 1996; at #13, with 19 cites this period and 63 to date), and the test method was also the commercial Haemoccult kit for blood in stools. The 18% reduction in mortality from this cancer in the screened group would, the Danish authors say, prevent 360 of that country’s annual mortality of 2,000 for colorectal cancer. In Nottingham the reduction in mortality specific for this cancer was 15% in the group randomized to screening (though not all agreed to the tests); total mortality was not affected, in part, perhaps, because of the higher mortality in those refusing screening.

   Transfer of impressive results--and, though both reports are preliminary and further data are even now accumulating, the studies are impressive--from the research setting to, say, a national screening policy is always difficult. Occult blood testing is cheap and simple but the compliance rate is far from perfect. There will always be false-positives, and that means anxiety for the patient and unnecessary (with hindsight) colonoscopies. Tests would have to be repeated every one or two years. Screening colonoscopy could be done less frequently but compliance with this strategy in the general adult population and the resource implications are largely unexplored. Another worry is the awkward habit of research results not translating exactly into day-to-day healthcare settings.

   In the wake of these papers, the U.K. Department of Health has held two working-parties to review the evidence, and two pilot projects to look at the service implications of such screenings are envisaged.

   Kronberg draws Science Watch readers to recent publications on the implications (Health Economics, 7:1-7, 9-20, 21-29, 1998). In the Danish trial the seventh biennial screen was done in July, 1998, and Kronberg notes that the trial continues to demonstrate "a possible reduction of incidence of colorectal cancer following removal of more large polyps (adenomas) in the test group." The latest cumulative figures show that, among the cancers, 21% in the screened group but only 11% in the controls were Dukes’ stage A (a more favorable prognosis).

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Mr. David W. Sharp, MA (Cambridge), is Deputy Editor of The Lancet, London, U.K.

Science Watch®, September/October 1998, Vol. 9, No. 5
Citing URL: http://www.sciencewatch.com/sept-oct/science-watch_sept-oct98_page5.htm

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