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Adjuvant Bisphosphonates and Other Bone-Modifying Agents in Breast Cancer

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Treatment Table 1. Complete List of Recommendations a New Recommendations from 2021 ASCO-OH Focused Guideline Update Recommendation Evidence rating e Panel does not recommend the use of adjuvant denosumab. Key evidence: Two Phase III studies of adjuvant denosumab did not show a consistent reduction of breast cancer recurrence in any subset of patients with early- stage breast cancer. e larger study, D-CARE, did not show improvement in cancer outcomes with use of denosumab. Moderate recommendation; EB-B-I Recommendations Unchanged From 2017 CCO-ASCO Guideline Recommendations For purposes of adjuvant bisphosphonate use, the definition of menopause should include both natural menopause (at least 12 months of amenorrhea prior to initiation of chemotherapy or endocrine therapy) and menopause induced by ovarian ablation or suppression (but not the cessation of menses due to chemotherapy alone). In people age ≤60 years with a previous hysterectomy and ovaries le in place, luteinizing hormone, follicle-stimulating hormone, and serum estradiol should be in the postmenopausal range and measured prior to initiation of any systemic therapy to receive adjuvant bisphosphonates. A dental assessment is recommended, where feasible, prior to commencement of bisphosphonates, and any pending dental or oral health problems should be dealt with prior to starting treatment, if possible. Patients should be informed of the risk of developing osteonecrosis of the jaw (ONJ), especially with tooth extractions and other invasive dental procedures. Patients should inform their dental practitioner of their treatment. Patients with suspected ONJ should be referred to a dental practitioner with expertise in treating this condition. Recent guidelines or position papers by groups such as the International Task Force on Osteonecrosis of the Jaw, the American Association of Oral and Maxillofacial Surgeons, and the American Dental Association should be consulted. Patients should have serum calcium measured prior to starting treatment. Patients receiving intravenous bisphosphonates (zoledronic acid) should be monitored for renal function prior to starting this treatment, and for serum calcium and increase in serum creatinine throughout the treatment period. Calcium and vitamin D supplementation is recommended unless otherwise contraindicated. Oral bisphosphonates and calcium should not be taken concurrently; several monographs suggest an interval of at least 2 hours to allow for maximum absorption. Symptoms such as ocular pain or loss of vision may be due to serious inflammatory conditions such as uveitis or scleritis and should be promptly evaluated by an ophthalmologist. a From the 2017 CCO-ASCO Guideline and the ASCO-OH (CCO) 2021 Focused Guideline Update. (cont'd)

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