more about more life

2
and Markman do not present any coun- terargument. Second, they claim that we erred in describing the randomized trial compar- ing St. John’s Wort, sertraline, and placebo as contrary to clinical equipoise. Although there remains some theoreti- cal debate in the literature whether anti- depressants are superior to placebo, the Food and Drug Administration has ap- proved several antidepressant drugs based on the results of placebo-con- trolled trials. To be sure, in particular trials, standard antidepressants often fail to beat placebo. However, a recent meta-analysis of depression trials in the FDA database, encompassing thousands of patients, indicated a significant differ- ence between standard drugs and place- bo (A. Khan et al., “Symptom Reduc- tion and Suicide Risk in Patients Treated with Placebo in Antidepressant Clinical Trials: An Analysis of the Food and Drug Administration Database,” Archives of General Psychiatry 57 (2000): 311-17). Therefore, we see the inclusion of placebo in the St. John’s Wort trial as violating clinical equipoise, which pre- vents physician-investigators from ran- domizing patients to treatments known, on the basis of the preponderance of the evidence, to be inferior. As we indicated in our article, Charles Weijer, a leading advocate of clinical equipoise, has criti- cized placebo-controlled trials in depres- sion as violating this standard. Finally, DeMarco and Markman sug- gest that clinical equipoise should be modified to “include reference to assay sensitivity and to trials without signifi- cant risk.” It is possible to do so, but it is unclear how such a revised doctrine of clinical equipoise would be formulated. We doubt that the moral transparency and integrity of clinical equipoise can be preserved when exceptions relating to scientific methodology and the level of risk are built into its definition. If it is acceptable within the meaning of clini- cal equipoise to randomize patients to placebo despite the existence of proven effective treatment, provided that use of placebo is required for producing valid trial results or the risks are not signifi- cant, then the moral force of clinical equipoise appears vitiated. This effort to save clinical equipoise reinforces our ar- gument that this standard is unnecessary to provide adequate guidance for the ethics of clinical trials. More about More Life To the Editor: Fearing the worst upon seeing the title “Is More Life Al- ways Better?” (HCR, July-August, 2003), I was glad to find that David Gems offers a sophisticated critical dis- cussion rather than a paean to the won- ders of mortality. Still, I think he over- rates the dangers of anti-aging therapies and greatly increased longevity. His fear of the “chilling. . . prospect of power concentrated relentlessly into the hands of a few undying individuals—and par- ticularly into the hands of tyrants” in- vites objections. First, a similar fear could have been used against any poten- tially life-extending medical advance, in- cluding chemotherapy and antibiotics. Surely, a tyrant who dies of an infection at thirty will do less harm than one who lives vigorously into his eighties. But it seems cruel to deny medical advances to everyone for fear that such advances might prolong the active lives of some dreadful people. Moreover, such denial would hardly be an effective way to combat tyranny, for one tyrant can re- place another and often does. Particular- ly inappropriate for his argument is Gems’ admonition, “Remember the words of O’Brien to Winston Smith in Orwell’s 1984: ‘If you want a picture of the future, imagine a boot stamping on a human face—forever.’” No increased longevity was envisioned in 1984; tyran- ny arose from a totalitarian system. Gems also worries that “access to life extension technology might be consid- ered a fundamental human right, like that of access to education,” even though we might not want to offer life extension technology to murderers. But (regardless of whether society should offer life extension technology to mur- derers) it seems clear that considering something a fundamental human right does not preclude denying it to murder- ers. After all, we consider liberty a fun- damental human right but deny it to murderers. Felicia Nimue Ackerman Brown University Gems replies: Felicia Ackerman raises an interesting point when she compares life extension due to conventional medicine (such as antibiotics) to that resulting from treat- ments for aging. I have heard it argued that ethically there is little difference be- tween these two forms of life extension. In my view, this is not correct, at least where the possibility of large increases in lifespan are concerned (that is, on the order of decades). Yes, life expectancy from birth has increased greatly during the last century; yet the ripe old age of three score and ten that most aspired to in former times has increased only slightly. By contrast, an increase in mean lifespan of, say, 50 percent (as seen in many animal experiments) would repre- sent a major qualitative change in human existence. As for tyrants: I imagine that Alexan- der Fleming would have winced had he been present when, say, Adolf Hitler’s life was saved by penicillin after the Stauffenberg bomb plot (if it was). He might see a hundred thousand corpses in that pill bottle, but I doubt that he would regret his discovery. Nor did I mean to suggest that the danger of long- lived tyrants was a reason to abjure anti- aging medicine. Yet this says nothing against the fact that totalitarianism and an effective treatment for aging could be a terrible combination. My comment about whether Charles Manson should be given anti-aging treatment was really just an aside. I wonder to what extent convicts are actu- ally denied life-saving medical treat- ment? But given anti-aging therapies as HASTINGS CENTER REPORT 5 November-December 2003

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Page 1: More about More Life

and Markman do not present any coun-terargument.

Second, they claim that we erred indescribing the randomized trial compar-ing St. John’s Wort, sertraline, andplacebo as contrary to clinical equipoise.Although there remains some theoreti-cal debate in the literature whether anti-depressants are superior to placebo, theFood and Drug Administration has ap-proved several antidepressant drugsbased on the results of placebo-con-trolled trials. To be sure, in particulartrials, standard antidepressants often failto beat placebo. However, a recentmeta-analysis of depression trials in theFDA database, encompassing thousandsof patients, indicated a significant differ-ence between standard drugs and place-bo (A. Khan et al., “Symptom Reduc-tion and Suicide Risk in Patients Treatedwith Placebo in Antidepressant ClinicalTrials: An Analysis of the Food andDrug Administration Database,”Archives of General Psychiatry 57 (2000):311-17). Therefore, we see the inclusionof placebo in the St. John’s Wort trial asviolating clinical equipoise, which pre-vents physician-investigators from ran-domizing patients to treatments known,on the basis of the preponderance of theevidence, to be inferior. As we indicatedin our article, Charles Weijer, a leadingadvocate of clinical equipoise, has criti-cized placebo-controlled trials in depres-sion as violating this standard.

Finally, DeMarco and Markman sug-gest that clinical equipoise should bemodified to “include reference to assaysensitivity and to trials without signifi-cant risk.” It is possible to do so, but it isunclear how such a revised doctrine ofclinical equipoise would be formulated.We doubt that the moral transparencyand integrity of clinical equipoise can bepreserved when exceptions relating toscientific methodology and the level ofrisk are built into its definition. If it isacceptable within the meaning of clini-cal equipoise to randomize patients toplacebo despite the existence of proveneffective treatment, provided that use of

placebo is required for producing validtrial results or the risks are not signifi-cant, then the moral force of clinicalequipoise appears vitiated. This effort tosave clinical equipoise reinforces our ar-gument that this standard is unnecessaryto provide adequate guidance for theethics of clinical trials.

More about More Life

TToo tthhee EEddiittoorr:: Fearing the worstupon seeing the title “Is More Life Al-ways Better?” (HCR, July-August,2003), I was glad to find that DavidGems offers a sophisticated critical dis-cussion rather than a paean to the won-ders of mortality. Still, I think he over-rates the dangers of anti-aging therapiesand greatly increased longevity. His fearof the “chilling. . . prospect of powerconcentrated relentlessly into the handsof a few undying individuals—and par-ticularly into the hands of tyrants” in-vites objections. First, a similar fearcould have been used against any poten-tially life-extending medical advance, in-cluding chemotherapy and antibiotics.Surely, a tyrant who dies of an infectionat thirty will do less harm than one wholives vigorously into his eighties. But itseems cruel to deny medical advances toeveryone for fear that such advancesmight prolong the active lives of somedreadful people. Moreover, such denialwould hardly be an effective way tocombat tyranny, for one tyrant can re-place another and often does. Particular-ly inappropriate for his argument isGems’ admonition, “Remember thewords of O’Brien to Winston Smith inOrwell’s 1984: ‘If you want a picture ofthe future, imagine a boot stamping ona human face—forever.’” No increasedlongevity was envisioned in 1984; tyran-ny arose from a totalitarian system.

Gems also worries that “access to lifeextension technology might be consid-ered a fundamental human right, likethat of access to education,” eventhough we might not want to offer lifeextension technology to murderers. But

(regardless of whether society shouldoffer life extension technology to mur-derers) it seems clear that consideringsomething a fundamental human rightdoes not preclude denying it to murder-ers. After all, we consider liberty a fun-damental human right but deny it tomurderers.

FFeelliicciiaa NNiimmuuee AAcckkeerrmmaannBrown University

GGeemmss rreepplliieess::Felicia Ackerman raises an interesting

point when she compares life extensiondue to conventional medicine (such asantibiotics) to that resulting from treat-ments for aging. I have heard it arguedthat ethically there is little difference be-tween these two forms of life extension.In my view, this is not correct, at leastwhere the possibility of large increases inlifespan are concerned (that is, on theorder of decades). Yes, life expectancyfrom birth has increased greatly duringthe last century; yet the ripe old age ofthree score and ten that most aspired toin former times has increased onlyslightly. By contrast, an increase in meanlifespan of, say, 50 percent (as seen inmany animal experiments) would repre-sent a major qualitative change inhuman existence.

As for tyrants: I imagine that Alexan-der Fleming would have winced had hebeen present when, say, Adolf Hitler’slife was saved by penicillin after theStauffenberg bomb plot (if it was). Hemight see a hundred thousand corpsesin that pill bottle, but I doubt that hewould regret his discovery. Nor did Imean to suggest that the danger of long-lived tyrants was a reason to abjure anti-aging medicine. Yet this says nothingagainst the fact that totalitarianism andan effective treatment for aging could bea terrible combination.

My comment about whether CharlesManson should be given anti-agingtreatment was really just an aside. Iwonder to what extent convicts are actu-ally denied life-saving medical treat-ment? But given anti-aging therapies as

H A S T I N G S C E N T E R R E P O R T 5November-December 2003

Page 2: More about More Life

6 H A S T I N G S C E N T E R R E P O R T November-December 2003

cheap as antibiotics, it might be difficultto deny them to convicts. One mightimagine mass murderers sentenced tothree life terms in prison having the op-tion of serving their full term.

Conflicts of Interest

TToo tthhee EEddiittoorr:: In “Bioethics, Con-flicts of Interest, the Limits of Trans-parency,” Lynn Jansen and Daniel Sul-masy mischaracterize bioethics experttestimony before juries. They describe itas an activity in which the “only way toestimate the value of what is claimed isto consider the reliability of the source.”Adversarial courtroom contexts arestructured to prevent juries from accept-ing arguments or evidence uncritically.Fostering critical thinking about thesubstance of testimony is as much thepurpose of cross-examination as is creat-ing skepticism about the source by ask-ing about conflicts of interest. The com-mitment to fostering juries’ criticalthinking is also the reason experts arepermitted to testify on both sides ofcases, and the reason one must questionJansen and Sulmasy’s assertion that “theclaims of the bioethicist typically aretaken as authoritative.” Your readers

should understand that juries that arepresented with expert bioethics testimo-ny are expected to assess both the valueof the claims being advanced and thetrustworthiness of the source, and thatthey are aided in these tasks by the rulesand structure of the legal system.

The “no past crimes evidence” rule towhich Jansen and Sulmasy refer in sup-port of their argument that “more infor-mation is not always better” is a rule thatconstrains the state in criminal proceed-ings. Any analogy to information aboutbioethicists’ conflicts of interest is, Ihope, inapt.

BBeetthhaannyy SSppiieellmmaannSouthern Illinois University

JJaannsseenn aanndd SSuullmmaassyy rreeppllyy::Bethany Spielman’s letter is puzzling.

She contests neither the conclusion norany of the arguments in our paper. In-stead, she asserts that we “mischaracter-ize” bioethics expert testimony beforejuries. We claimed while it is possiblethat some members of a jury may beable to assess the claims of a bioethicistcritically, it is likely that many membersof a jury will not have the analytical skillor the motivation to reflect carefully onthe rational value of the claims being

presented. For this reason, we conceded,there is a need for members of a jury tobe informed of any relationships, finan-cial or otherwise, that might substantial-ly compromise the judgment of thebioethicist. We stand by this characteri-zation. It is, of course, fully compatiblewith Spielman’s claim that juries shouldbe encouraged to assess the rationalvalue of the claims presented to them.Indeed, to the extent that we have goodreason to have confidence in the abilityof juries to do so, then the case for dis-closing conflicts of interest in this con-text collapses.

Spielman asserts that the “no pastcrimes” rule is “inapt” as an analogy tobioethicists’ conflict of interest. Whatwe said was that “certain kinds of infor-mation about the background of defen-dants should be withheld from juries.This information, while accurate, candistort a jury’s judgment.” These claimsare plainly true, and they illustrate thegeneral point that having more informa-tion does not always improve our abilityto make good judgments. The failure toappreciate this important point helps ac-count for the current uncritical enthusi-asm for extending disclosure require-ments to all contexts in bioethics.

Letters to the editor may be sent by emailto [email protected], or toEditor, Hastings Center Report, 21 Malcolm Gordon Road, Garrison, NY10524; (845) 424-4931 fax.