Effect of Letrozole Versus Placebo on Bone Mineral Density in Women With Primary Breast Cancer Completing 5 or More Years of Adjuvant Tamoxifen: A Companion Study to NCIC CTG MA.17

  • Edith A. Perez
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Robert G. Josse
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Kathleen I. Pritchard
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • James N. Ingle
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Silvana Martino
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Brian P. Findlay
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Tamara N. Shenkier
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Richard G. Tozer
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Michael J. Palmer
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Lois E. Shepherd
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Shifang Liu
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Dongsheng Tu
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA
  • Paul E. Goss
    From the St Michael's Hospital; Toronto Sunnybrook Regional Cancer Centre, Toronto; Hotel Dieu Health Sciences Hospital, St Catharines; Juravinski Cancer Centre, Hamilton; National Cancer Institute of Canada Clinical Trials Group, Kingston, Ontario; British Columbia Cancer Agency, Vancouver Cancer Clinic, Vancouver, British Columbia, Canada; Mayo Clinic, Jacksonville, FL; Mayo Clinic, Rochester, MN; Cancer Institute Medical Group, Santa Monica, CA; and Massachusetts General Hospital, Boston, MA

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<jats:sec><jats:title>Purpose</jats:title><jats:p> Aromatase inhibition depletes estrogen levels and may be associated with accelerated bone resorption. The National Cancer Institute of Canada Clinical Trials Group (NCIC CTG) study MA.17B evaluated bone turnover markers and bone mineral density (BMD) in postmenopausal women randomly assigned to MA.17, a placebo-controlled trial of letrozole after standard adjuvant tamoxifen. </jats:p></jats:sec><jats:sec><jats:title>Patients and Methods</jats:title><jats:p> Eligible women had a baseline BMD T score of at least 2.0 in either the hip or L2-4 spine; all received calcium 500 mg and vitamin D 400 U daily. Percentage change in BMD (L2-L4 spine and hip) at 12 and 24 months, rate of osteoporosis, and change in markers of bone formation (serum bone alkaline phosphatase) and resorption (serum C-telopeptide and urine N-telopeptide) at 6, 12, and 24 months were compared. </jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p> Two hundred twenty-six patients (122 letrozole, 104 placebo) were enrolled. Baseline characteristics were similar in the two groups, including BMD, median age of 60.7 years (81% < 70 years), and median follow-up of 1.6 years. At 24 months, patients receiving letrozole had a significant decrease in total hip BMD (−3.6% v −0.71%; P = .044) and lumbar spine BMD (−5.35% v −0.70%; P = .008). Letrozole increased urine N-telopeptide at 6, 12, and 24 months (P = .054, < .001, and .016, respectively). No patient went below the threshold for osteoporosis in total hip BMD, whereas at the L2-L4 (posteroanterior view), more women became osteoporotic by BMD while receiving letrozole (4.1% v 0%; P = .064). </jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p> After 5 years of adjuvant tamoxifen, subsequent letrozole causes a modest increase in bone resorption and reduction in bone mineral density in the spine and hip compared to placebo. Further follow-up is necessary to evaluate the long-term clinical implications of this difference. </jats:p></jats:sec>

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