History of the early development of aromatase inhibitors for treatment of breast cancer.

PURPOSE: To review the early history of the development of aromatase inhibitors for treatment of breast cancer by the Penn State Hershey collaborative group and to acknowledge the support and advice of Dr. William L. McGuire in the studies conducted.

METHODS

The historical information reported here reflect the memories of Drs. Richard J. Santen and Laurence L. Demers and comprehensive documentation provided in the literature references cited.

RESULTS

The project of development of aromatase inhibitors began with the mis-assumption that the regimen of aminoglutethimide and hydrocortisone represented a "medical adrenalectomy" and primarily represented the blockade of adrenal steroidogenesis. Later studies demonstrated that aminoglutethimide blocked the aromatase enzyme by 95-98%. A key research step involved isotopic kinetic studies in post-menopausal women using 3H-androstenedione and 14C estrone to precisely measure aromatase under equilibrium conditions. Dr. William L. McGuire provided major advice to the investigators, suggested enlistment of key collaborators, provided laboratory assistance in measuring ER levels, and facilitated funding for the studies. Observational studies involved 147 patients treated with the AG/HC regimen and the results demonstrated efficacy of the regimen. Later, randomized controlled trials demonstrated the equivalence of this regimen to surgical adrenalectomy and tamoxifen. In order eliminate the need for HC, three selective inhibitors of aromatase were developed and shown to induce remissions statistically significantly greater than achieved with the anti-estrogen, tamoxifen.

CONCLUSION

These studies provided definitive evidence of the superiority of aromatase inhibitors over tamoxifen in postmenopausal women with hormone responsive breast cancer.