feasible.

The agency did, however, suggest two more specific studies that

could provide useful information (10):
1.

Continue to follow (at 5-year intervals) the "SMOKY" cohort previously studied by the CDC/NRC. If the excess leukemia detected was
simply a matter of chance, no excess of other radiogenic cancers
would be expected.

2.

Conduct a mortality study of the veterans who participated in
Operation CROSSROADS pending the results of a General Accounting
Office review of the radiation dose estimates.

In determining the feasibility and desirability of an epidemiological
study or studies, the VA Advisory Board considered the recommendations of the
Caldwell committee, CIRRPC, and OTA.
following:

It also reviewed commentary given in the

the General Accounting Office (GAO) report Operation Crossroads:

Personnel Radiation Exposure Estimates Should Be Improved (8 November 1985),

discussed in section 7.7; the NAS report Review of the Methods Used to Assign
Radiation Doses to Service Personnel at Nuclear Weapons Tests (7 February ¢
1986), discussed in section 7.7; and the hearing held by the Senate Committee
on Veterans Affairs on 11 December 1985 regarding issues pertinent to possible
radiation exposures received by CROSSROADS participants.
During February 1986, the VA Advisory Board listened to presentations by
DNA, GAO, and NAS on dose determination for CROSSROADS participants.

Asa

result of Board recommendations, VA decided that it would not participate ina
mortality study of CROSSROADS veterans but that it would continue the followup
of SMOKY personnel.

The Administrator of Veterans’ Affairs informed OTA of

these decisions in April 1986.
OTA is reviewing the VA decisions and is considering a NAS proposal to
conduct a mortality study of CROSSROADS personnel.

In March 1986, DNA

indicated to the Senate Committee on Veterans Affairs that it would be willing
to provide part of the funding if OTA considered the study feasible and if
Congress decided against appropriating funds specifically for the effort.
decision on this study is expected in late 1986.
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