Use of Adjuvant Bisphosphonates and Other Bone-Modifying Agents in Breast Cancer: ASCO-OH (CCO) Guideline Update

Author:

Eisen Andrea1,Somerfield Mark R.2ORCID,Accordino Melissa K.3ORCID,Blanchette Phillip S.4,Clemons Mark J.5ORCID,Dhesy-Thind Sukhbinder6,Dillmon Melissa S.7ORCID,D'Oronzo Stella8ORCID,Fletcher Glenn G.9ORCID,Frank Elizabeth S.10,Hallmeyer Sigrun11,Makhoul Issam12ORCID,Moy Beverly13,Thawer Alia1ORCID,Wu Joy Y.14ORCID,Van Poznak Catherine H.15ORCID

Affiliation:

1. Sunnybrook Odette Cancer Centre; Ontario Health, Toronto, ON, Canada

2. American Society of Clinical Oncology, Alexandria, VA

3. Columbia University HICCC, New York, NY

4. London Health Sciences Centre, London, ON, Canada

5. The Ottawa Hospital Cancer Centre, Ottawa, ON, Canada

6. Juravinski Cancer Centre, Hamilton, ON, Canada

7. Harbin Clinic LLC, Rome, GA

8. University of Bari “Aldo Moro,” Bari, Italy

9. McMaster University, Hamilton, ON, Canada

10. Brookline, MA

11. Advocate Lutheran General Hospital, Prospect Heights, IL

12. University of Arkansas for Medical Sciences, Little Rock, AR

13. Massachusetts General Hospital, Boston, MA

14. Stanford University, Palo Alto, CA

15. University of Michigan, Ann Arbor, MI

Abstract

PURPOSE To update recommendations of the American Society of Clinical Oncology (ASCO)-Ontario Health (Cancer Care Ontario [CCO]) adjuvant bone-modifying agents in breast cancer guideline. METHODS An Expert Panel conducted a systematic review to identify new, potentially practice-changing data. RESULTS Four articles met eligibility criteria and form the evidentiary basis for revision of the previous recommendations. RECOMMENDATIONS Adjuvant bisphosphonate therapy should be discussed with all postmenopausal patients (natural or therapy-induced) with primary breast cancer, irrespective of hormone receptor status and human epidermal growth factor receptor 2 status, who are candidates to receive adjuvant systemic therapy. Adjuvant bisphosphonates, if used, are not substitutes for standard anticancer modalities. The benefit of adjuvant bisphosphonate therapy will vary depending on the underlying risk of recurrence and is associated with a modest improvement in overall survival. The NHS PREDICT tool provides estimates of the benefit of adjuvant bisphosphonate therapy and may aid in decision making. Factors influencing the decision to recommend adjuvant bisphosphonate use should include patients' risk of recurrence, risk of side effects, financial toxicity, drug availability, patient preferences, comorbidities, and life expectancy. When an adjuvant bisphosphonate is used to prevent breast cancer recurrence, the therapeutic options recommended by the Panel include oral clodronate, oral ibandronate, and intravenous zoledronic acid. The Panel supports starting bisphosphonate therapy early, consistent with the points outlined in the parent CCO-ASCO guideline; this is a consensus recommendation. The Panel does not recommend adjuvant denosumab to prevent breast cancer recurrence, because studies did not show a consistent reduction of breast cancer recurrence in any subset of those with early-stage breast cancer. Additional information can be found at www.asco.org/breast-cancer-guideline .

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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