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Review of Epidemiologic Data on Breast Cancer Screening Evokes Strong Reactions

“As a panel member and an epidemiologist, I was asked to evaluate the benefits and risks associated with mammographic screening among women 40 - 49 years of age... The mortality benefit for women 50 and above is not questioned—the benefit to very young women (i.e. those in their 20’s and 30’s) is not beneficial. But the benefit to women 40 - 49 is uncertain. Do we make a definite recommendation to all women 40 - 49 —all healthy women 40 - 49—when we are not certain? I think not...the panel recommended that each woman should consider her own risk-benefit profile and with the best possible information, make her own decision...I felt and still feel, we arrived at the best conclusion based on the available data.”

So spoke Susan Chu, Seattle based epidemiologist at Group Health Cooperative of Puget Sound, when called to testify before Congress in early February following the presentation of a statement on breast cancer screening by an NIH consensus panel.

The uproar caused by the panel’s recommendation was amply described in the press last month. According to a New York Times account, Leon Gordis, a Johns Hopkins University epidemiologist who chaired the panel, said that nothing had prepared him for the venomous reaction his panel got when it said in a report that it had no reason to recommend routine mammograms for women under 50.

The Panel’s Responsibility

Exactly what did the panel get asked to do? According to the National Cancer Institute’s Richard Klausner, the panel was asked to address the often confusing and sometimes contentious debate that surrounds the question of the age at which a woman should begin getting regular mammography screening. According to Klausner, the best data is from eight randomized clinical trials involving about 180,000 women, including five Swedish studies. Few trials have enough deaths from breast cancer to achieve statistical significance, but using meta-analysis there is about a 15% reduction in mortality. He estimates that over 30,000 women in their forties will be diagnosed with breast cancer this year and a 15% reduction in mortality would mean over 1,600 lives saved.

Despite press accounts that Klausner said he was “shocked” at the time by the conclusions of the NIH panel, he indicated in his testimony to Congress that he agrees with the conclusion of the panel, but “it is my opinion that the draft report of the panel overly minimizes the benefits and overly emphasizes the risks for this population. A balanced statement of the pros and cons of screening is essential for a woman to make an informed decision whether to initiate regular mammography in her forties.”

Among the risks associated with mammography are the occurrence of false positives and the procedures involved in the follow-up of these false positives. Also, the test fails to detect up to one fourth of breast cancer cases in this age group. There is no direct evidence that the levels of radiation used in mammography cause breast cancer.

Why did the benefits not seem strong or clear enough? According to Chu, not all the randomized trials showed the reduction in mortality. Two studies showed a significant benefit and two studies showed no significant benefit. “We should not create certainty where there is none to reassure the public or to ‘please the audience’. Our task was to objectively weigh the health benefits and risks of an universal screening program for women 40 - 49. I feel we met that task,” she said.

Why the Strong Reaction?

Several potential reasons for the strong reactions to the panel’s recommendation have been mentioned in the press accounts about this report. One reason involves the marketing of mammography—by instrument makers, medical centers, and even the American Cancer Society—as a way to ease the fears women have about breast cancer. Because it has been touted as a way to find early-stage tumors and therefore strongly influence a women’s chances of a positive outcome, “few want to hear that its much touted effectiveness may be in doubt for women under age 50” (NYT, January 28, 1997).

Reaction to the panel’s recommendations have been so strong that even Congress has jumped into the act. Olympia Snowe (R-Maine) introduced a resolution urging the NCI advisory panel to consider reissuing guidelines recommending that women in their forties seek routine mammograms. “Good science dictates that mammography for women in their forties saves lives,” she insisted.

Not the Senate’s Business

Others are questioning the appropriateness of having politicians involved in the evaluation of scientific evidence. According to a Washington Post article (February 10, 1997) by Jessica Matthews, senior fellow at the Council on Foreign Relations, “the Senate is once again trespassing where it has no business to be. On the basis of some mysteriously acquired epidemiological insight, 98 senators...recently concluded that women in their forties benefit from routine mammograms...The National Cancer Institute is under no illusion as to the source of its funding. The chilling effect of a debacle like this one is not lost on those in Bethesda and around the country whose research is funded by the various National Institutes of Health. Sadly, for some, (including often the most conscientious researchers) the lesson is to stay away from any highly controversial issue. The larger result is to make the NIH and the government’s other health-related agencies, whose job is to evaluate data dispassionately, into less valuable protectors of Americans’ health.”

[Editor’s note: The current controversy is only the latest flare up in a long-standing disagreement about the value of breast cancer screening for women in their forties. For a detailed account of the history behind this debate, see Gary Taubes’s recent article in Science, (February 21). Believe it or not, epidemiologists are not painted in negative terms.]

Published March 1997  v

 

 
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