Volume 46 | Number 6pt1 | December 2011

Abstract List

David H. Howard Ph.D., Carolyn Kenline, Hillard M. Lazarus, Charles F. LeMaistre, Richard T. Maziarz, Philip L. McCarthy Jr., Susan K. Parsons, David Szwajcer, James Douglas Rizzo, Navneet S. Majhail


Objective

In 1999, three randomized controlled trials concluded that high‐dose chemotherapy followed by autologous hematopoietic stem cell transplantation (HDC/HCT) is no better than conventional chemotherapy for women with breast cancer. This study documents the impact of the trials on use of HDC/HCT and describes how hospitals reacted to the trials.


Data Source

We used patient‐level data on 15,847 HDC/HCTs reported to the Center for International Blood and Marrow Transplant Research between 1994 and 2005.


Study Design

We report trends in total HDC/HCT procedure volume, compare the time to hospitals' exit from the HDC/HCT market between research and nonresearch hospitals, and document trends in hospital‐specific volumes in the 2 years before exit.


Principal Findings

HDC/HCT volume declined from 3,108 in 1998 to 1,363 the year after trial results were released. In 2002, only 76 procedures were performed. Teaching hospitals and the hospitals that participated in the trials were no slower to discontinue the procedure compared with nonteaching, nonparticipating hospitals. At the hospital level, volume declined steadily in the months before abandonment.


Conclusion

The results suggest that comparative effectiveness research studies that report negative results can reduce spending, but specialists may be reluctant to relinquish cutting‐edge technologies.