Open AccessRisk Factors for Developing Skeletal‐Related Events in Breast Cancer Patients With Bone Metastases Undergoing Treatment With Bone‐Modifying Agents
Author(s) -
Tanaka Ryota,
Yonemori Kan,
Hirakawa Akihiro,
Kinoshita Fumie,
Takahashi Naoki,
Hashimoto Jun,
Kodaira Makoto,
Yamamoto Harukaze,
Yunokawa Mayu,
Shimizu Chikako,
Fujimoto Manabu,
Fujiwara Yasuhiro,
Tamura Kenji
Publication year - 2016
Publication title -
the oncologist
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.176
H-Index - 164
eISSN - 1549-490X
pISSN - 1083-7159
DOI - 10.1634/theoncologist.2015-0377
Subject(s) - medicine , breast cancer , spinal cord compression , incidence (geometry) , pathologic fracture , radiation therapy , proportional hazards model , oncology , cancer , surgery , radiology , spinal cord , physics , optics , psychiatry
Background. Bone‐modifying agents (BMAs) reduce the incidence of skeletal‐related events (SREs) and are thus recommended for breast cancer patients with bone metastases. However, the risk factors for SREs during BMA treatment are not well‐understood. This study evaluated the number and timing of SREs from case studies to identify these factors. Methods. The medical records of 534 women with breast cancer who developed bone metastases between 1999 and 2011 were reviewed. SREs were defined as a pathologic fracture, spinal cord compression, or the need for bone irradiation or surgery. Multiple variables were assessed and were analyzed by using the Cox proportional hazard analyses and the Andersen and Gill method. Results. Multivariate analyses for both the time to the first SRE and the primary and subsequent SRE frequency demonstrated that significant baseline risk factors included luminal B type disease, a history of palliative radiation therapy, BMA treatment within 2 years, and elevated serum calcium levels at the time of the initial BMA dose. Additionally, for the time to the first SRE and for the primary and subsequent SRE frequency, the presence of extraskeletal metastases and BMA administration initiation ≥6 months after the detection of bone metastases were also significant risk factors, respectively. Conclusion. In breast cancer patients with bone metastases, more vigilant observation should be considered for patients with the identified risk factors. To reduce the risk for SRE, BMAs should be administered within 6 months of bone metastases diagnosis and before palliative radiation therapy. Implications for Practice: Retrospectively, risk factors were identified for skeletal‐related events (SREs) in breast cancer patients with bone metastasis who were treated with bone‐modifying agents (BMAs). For the time to the first SRE and for the SRE frequency, presence of extraskeletal metastases and BMA initiation ≥6 months after the detection of bone metastases were risk factors, respectively. Luminal B type disease, a history of palliative radiation therapy, BMA treatment within 2 years, and elevated serum calcium levels at initial BMA dose were risk factors for both first SRE and SRE frequency. More vigilant observation should be considered for patients with these risk factors.