Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

Factors Associating with Bone-Only Metastasis in Chinese Breast Cancer Patients in the Absence of Anti-Human Epidermal Growth Factor Receptor 2-Targeted Therapy.

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
  • Additional Information
    • Source:
      Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101627692 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2296-5262 (Electronic) Linking ISSN: 22965270 NLM ISO Abbreviation: Oncol Res Treat Subsets: MEDLINE
    • Publication Information:
      Original Publication: Basel : S. Karger, [2014]-
    • Subject Terms:
    • Abstract:
      Introduction: Bone-only metastasis (BOM) is a distinct clinical phenomenon in which cancer cells disseminate exclusively to the bones, without involvement of other distant organs. We investigated the factors associated with the BOM state versus other states of metastasis in breast cancer patients with bone metastasis (BM) at their first relapse. The results could help tailor the screening and preventive therapy strategies for BM in breast cancer.
      Methods: The study included 231 women who underwent mastectomy for primary unilateral non-metastatic breast cancer in 1997 or later and were subsequently diagnosed with BM at first relapse in 2008-2018 at the Fourth Hospital of Hebei Medical University in China. Factors such as patient age at primary breast cancer diagnosis, tumor clinicopathological characteristics, chemotherapy, radiotherapy, endocrine therapy (ET), time to progression (TTP), and others were analyzed. ET compliance was categorized from medication adherence. Multivariate logistic regressions were used to estimate the odds ratio (OR) and p value.
      Results: Only three (3.8%, 3/79) human epidermal growth factor receptor 2-positive (HER2+) breast cancer patients (n = 79) used anti-HER2-targeted agents in the adjuvant setting. After excluding them, the remaining 228 patients were analyzed. They had an average age of 47.3 years and median TTP 29.4 months at their first relapse. Overall, patients with BOM accounted for 26.8%. The BOM state was similarly presented in the hormone receptor-positive (HR+) patients (n = 182) and in the HR-negative (HR-) patients (n = 45) (28.6% vs. 17.8%, p = 0.142). However, it was significantly lower in the HER2+ patients (n = 76) than in the HER2-negative (HER2-) patients (n = 129) (13.2% vs. 31.8%, p = 0.003). Multivariate analyses showed that the BOM state was not associated with the HR+ (vs. HR-, OR 1.253, p = 0.723) and full ET compliance (vs. no/partial, OR 1.346, p = 0.545) status. Nonetheless, the BOM state was significantly associated with a lower chance in the HER2+ patients overall (OR 0.240, p = 0.008) and in the HR+ patients (OR 0.145, p = 0.005) but not in the HR- patients (OR 1.012, p = 0.991) than one in the HER2- patients. A lower chance of BOM state was also associated with TTP ≥24 months (p < 0.05). There were no other associated factors identified.
      Conclusion: Differently from HR status and other clinicopathological factors, the HER2+ status is associated with a lower chance of the BOM state in breast cancer patients with first BM. Such association appears to be reflected in HR+ patients only.
      Introduction: Bone-only metastasis (BOM) is a distinct clinical phenomenon in which cancer cells disseminate exclusively to the bones, without involvement of other distant organs. We investigated the factors associated with the BOM state versus other states of metastasis in breast cancer patients with bone metastasis (BM) at their first relapse. The results could help tailor the screening and preventive therapy strategies for BM in breast cancer.
      Methods: The study included 231 women who underwent mastectomy for primary unilateral non-metastatic breast cancer in 1997 or later and were subsequently diagnosed with BM at first relapse in 2008-2018 at the Fourth Hospital of Hebei Medical University in China. Factors such as patient age at primary breast cancer diagnosis, tumor clinicopathological characteristics, chemotherapy, radiotherapy, endocrine therapy (ET), time to progression (TTP), and others were analyzed. ET compliance was categorized from medication adherence. Multivariate logistic regressions were used to estimate the odds ratio (OR) and p value.
      Results: Only three (3.8%, 3/79) human epidermal growth factor receptor 2-positive (HER2+) breast cancer patients (n = 79) used anti-HER2-targeted agents in the adjuvant setting. After excluding them, the remaining 228 patients were analyzed. They had an average age of 47.3 years and median TTP 29.4 months at their first relapse. Overall, patients with BOM accounted for 26.8%. The BOM state was similarly presented in the hormone receptor-positive (HR+) patients (n = 182) and in the HR-negative (HR-) patients (n = 45) (28.6% vs. 17.8%, p = 0.142). However, it was significantly lower in the HER2+ patients (n = 76) than in the HER2-negative (HER2-) patients (n = 129) (13.2% vs. 31.8%, p = 0.003). Multivariate analyses showed that the BOM state was not associated with the HR+ (vs. HR-, OR 1.253, p = 0.723) and full ET compliance (vs. no/partial, OR 1.346, p = 0.545) status. Nonetheless, the BOM state was significantly associated with a lower chance in the HER2+ patients overall (OR 0.240, p = 0.008) and in the HR+ patients (OR 0.145, p = 0.005) but not in the HR- patients (OR 1.012, p = 0.991) than one in the HER2- patients. A lower chance of BOM state was also associated with TTP ≥24 months (p < 0.05). There were no other associated factors identified.
      Conclusion: Differently from HR status and other clinicopathological factors, the HER2+ status is associated with a lower chance of the BOM state in breast cancer patients with first BM. Such association appears to be reflected in HR+ patients only.
      (© 2024 The Author(s). Published by S. Karger AG, Basel.)
    • References:
      Ann Oncol. 2021 Dec;32(12):1475-1495. (PMID: 34678411)
      Chin Clin Oncol. 2016 Jun;5(3):41. (PMID: 27265303)
      Oncologist. 2018 Nov;23(11):1282-1288. (PMID: 30120166)
      Eur J Cancer. 2017 Jul;79:139-148. (PMID: 28494404)
      Nat Rev Dis Primers. 2020 Oct 15;6(1):83. (PMID: 33060614)
      J Clin Oncol. 2010 Jul 10;28(20):3271-7. (PMID: 20498394)
      Ann Oncol. 2020 Dec;31(12):1650-1663. (PMID: 32801018)
      Crit Rev Oncol Hematol. 2017 Jul;115:67-80. (PMID: 28602171)
      Front Oncol. 2022 Aug 26;12:977226. (PMID: 36091103)
      BMC Cancer. 2016 May 12;16:307. (PMID: 27175930)
      Cancers (Basel). 2021 Aug 26;13(17):. (PMID: 34503118)
      Cancer Manag Res. 2022 Aug 23;14:2519-2531. (PMID: 36039341)
      J Natl Compr Canc Netw. 2022 Jun;20(6):691-722. (PMID: 35714673)
      Cancer Treat Res Commun. 2023;37:100764. (PMID: 37769530)
      World J Surg Oncol. 2012 Jan 08;10:4. (PMID: 22226178)
      BMC Cancer. 2020 Nov 13;20(1):1102. (PMID: 33187507)
      Breast Cancer Res Treat. 2015 Apr;150(3):621-9. (PMID: 25783184)
      Yonsei Med J. 2013 Sep;54(5):1168-77. (PMID: 23918566)
      Lancet Oncol. 2014 Jun;15(7):e279-89. (PMID: 24872111)
      J Pathol. 2019 Sep;249(1):6-18. (PMID: 31095738)
      Ecancermedicalscience. 2017 Jan 24;11:715. (PMID: 28194227)
      Breast Cancer Res Treat. 2016 Apr;156(3):587-595. (PMID: 27083181)
      Breast Cancer Res Treat. 2013 Jan;137(2):449-55. (PMID: 23225147)
      NPJ Breast Cancer. 2018 Jan 25;4:2. (PMID: 29387785)
      Lancet Oncol. 2014 Aug;15(9):997-1006. (PMID: 25035292)
      Lancet. 2015 Oct 3;386(10001):1353-1361. (PMID: 26211824)
      Am J Clin Pathol. 2015 Apr;143(4):471-8. (PMID: 25779997)
      Ann Oncol. 2019 Aug 1;30(8):1194-1220. (PMID: 31161190)
    • Contributed Indexing:
      Keywords: Bone metastasis; Bone-only metastasis; Breast cancer; Endocrine therapy; HER2; Hormone receptor
    • Accession Number:
      EC 2.7.10.1 (Erb-b2 Receptor Tyrosine Kinases)
      EC 2.7.10.1 (ERBB2 protein, human)
    • Publication Date:
      Date Created: 20241216 Date Completed: 20250428 Latest Revision: 20260127
    • Publication Date:
      20260130
    • Accession Number:
      PMC11878413
    • Accession Number:
      10.1159/000543137
    • Accession Number:
      39681104