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Is the assessment of the central skeleton sufficient for osseous staging in breast cancer patients? A retrospective approach using bone scans

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Abstract

Objective

By analyzing bone scans we aimed to determine whether the assessment of the central skeleton is sufficient for osseous staging in breast cancer patients. This might be of interest for future staging modalities, especially positron emission tomography/computed tomography, usually sparing the peripheral extremities, as well as the skull.

Materials and methods

In this retrospective study, a total of 837 bone scans for initial staging or restaging of breast cancer were included. A total of 291 bone scans in 172 patients were positive for bone metastases. The localization and distribution of the metastases were re-evaluated by two readers in consensus. The extent of the central skeleton involvement was correlated to the incidence of peripheral metastases.

Results

In all 172 patients bone metastases were seen in the central skeleton (including the proximal third of humerus and femur). In 34 patients (19.8 %) peripheral metastases of the extremities (distally of the proximal third of humerus and femur) could be detected. Sixty-four patients (37.2 %) showed metastases of the skull. Summarizing the metastases of the distal extremities and skull, 79 patients (45.9 %) had peripheral metastases. None of the patients showed peripheral metastases without any affliction of the central skeleton. The incidence of peripheral metastases significantly correlated with the extent of central skeleton involvement (p < 0.001).

Conclusions

Regarding bone scans, an isolated metastatic spread to the peripheral skeleton without any manifestation in the central skeleton seems to be the exception. Thus, the assessment of the central skeleton should be sufficient in osseous breast cancer staging and restaging. However, in case of central metastases, additional imaging of the periphery should be considered for staging and restaging.

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References

  1. Galasko CS. Skeletal metastases and mammary cancer. Ann R Coll Surg Engl. 1972;50:3–28.

    PubMed  CAS  Google Scholar 

  2. Coleman RE, Rubens RD. The clinical course of bone metastases from breast cancer. Br J Cancer. 1987;55:61–6.

    Article  PubMed  CAS  Google Scholar 

  3. Coleman RE, Smith P, Rubens RD. Clinical course and prognostic factors following bone recurrence from breast cancer. Br J Cancer. 1998;77:336–40.

    Article  PubMed  CAS  Google Scholar 

  4. Ahmed A, Glynne-Jones R, Ell PJ. Skeletal scintigraphy in carcinoma of the breast—a ten-year retrospective study of 389 patients. Nucl Med Commun. 1990;11:421–6.

    Article  PubMed  CAS  Google Scholar 

  5. Wikenheiser KA, Silberstein EB. Bone scintigraphy screening in stage I-II breast cancer: is it cost-effective? Cleve Clin J Med. 1996;63:43–7.

    Article  PubMed  CAS  Google Scholar 

  6. Yip CH, Paramsothy M. Value of routine 99mTc-MDP bone scintigraphy in the detection of occult skeletal metastases in women with primary breast cancer. Breast. 1999;8:267–9.

    Article  PubMed  CAS  Google Scholar 

  7. Myers RE, Johnston M, Pritchard K, et al. Baseline staging tests in primary breast cancer: a practice guideline. CMAJ. 2001;164:1439–44.

    PubMed  CAS  Google Scholar 

  8. Dose-Schwarz J, Mahner S, Schirrmacher S, et al. [Detection of metastases in breast cancer patients: comparison of FDG PET with chest X-ray, bone scintigraphy and ultrasound of the abdomen]. Nuklearmedizin. 2008;47:97–103 [in German].

    PubMed  CAS  Google Scholar 

  9. Taira AV, Herfkens RJ, Gambhir SS, Quon A. Detection of bone metastases: assessment of integrated FDG PET/CT imaging. Radiology. 2007;243:204–11.

    Article  PubMed  Google Scholar 

  10. Ghanem N, Altehoefer C, Kelly T, et al. Whole-body MRI in comparison to skeletal scintigraphy in detection of skeletal metastases in patients with solid tumors. In Vivo. 2006;20:173–82.

    PubMed  CAS  Google Scholar 

  11. Hahn S, Heusner T, Kummel S, et al. Comparison of FDG-PET/CT and bone scintigraphy for detection of bone metastases in breast cancer. Acta Radiol. 2011;52:1009–14.

    Article  PubMed  Google Scholar 

  12. Dose J, Bleckmann C, Bachmann S, et al. Comparison of fluorodeoxyglucose positron emission tomography and “conventional diagnostic procedures” for the detection of distant metastases in breast cancer patients. Nucl Med Commun. 2002;23:857–64.

    Article  PubMed  CAS  Google Scholar 

  13. Liu T, Cheng T, Xu W, et al. A meta-analysis of 18FDG-PET, MRI and bone scintigraphy for diagnosis of bone metastases in patients with breast cancer. Skeletal Radiol. 2011;40:523–31.

    Article  PubMed  Google Scholar 

  14. Hamaoka T, Madewell JE, Podoloff DA, et al. Bone imaging in metastatic breast cancer. J Clin Oncol. 2004;22:2942–53.

    Article  PubMed  Google Scholar 

  15. Costelloe CM, Rohren EM, Madewell JE, et al. Imaging bone metastases in breast cancer: techniques and recommendations for diagnosis. Lancet Oncol. 2009;10:606–14.

    Article  PubMed  Google Scholar 

  16. Shie P, Cardarelli R, Brandon D, et al. Meta-analysis: comparison of F-18 fluorodeoxyglucose-positron emission tomography and bone scintigraphy in the detection of bone metastases in patients with breast cancer. Clin Nucl Med. 2008;33:97–101.

    Article  PubMed  Google Scholar 

  17. Heusner TA, Kuemmel S, Hahn S, et al. Diagnostic value of full-dose FDG PET/CT for axillary lymph node staging in breast cancer patients. Eur J Nucl Med Mol Imaging. 2009;36:1543–50.

    Article  PubMed  CAS  Google Scholar 

  18. Hausmann D, Kern C, Schroder MT, et al. [Whole-body MRI in preoperative diagnostics of breast cancer–a comparison with [corrected] staging methods according to the S 3 guidelines]. Rofo. 2011;183:1130–7 [in German].

    Article  PubMed  CAS  Google Scholar 

  19. Du Y, Cullum I, Illidge TM, Ell PJ. Fusion of metabolic function and morphology: sequential [18F]fluorodeoxyglucose positron-emission tomography/computed tomography studies yield new insights into the natural history of bone metastases in breast cancer. J Clin Oncol. 2007;25:3440–7.

    Article  PubMed  Google Scholar 

  20. Koolen BB, Vrancken Peeters MJ, Aukema TS, et al. 18F-FDG PET/CT as a staging procedure in primary stage II and III breast cancer: comparison with conventional imaging techniques. Breast Cancer Res Treat. 2012;131:117–26.

    Article  PubMed  Google Scholar 

  21. Riegger C, Herrmann J, Nagarajah J, et al. Whole-body FDG PET/CT is more accurate than conventional imaging for staging primary breast cancer patients. Eur J Nucl Med Mol Imaging. 2012;39(5):852–63

    Google Scholar 

  22. Delbeke D, Coleman RE, Guiberteau MJ, et al. Procedure guideline for tumor imaging with 18F-FDG PET/CT 1.0. J Nucl Med. 2006;47:885–95.

    PubMed  Google Scholar 

  23. Boxer DI, Todd CE, Coleman R, Fogelman I. Bone secondaries in breast cancer: the solitary metastasis. J Nucl Med. 1989;30:1318–20.

    PubMed  CAS  Google Scholar 

  24. Koizumi M, Yoshimoto M, Kasumi F, Ogata E. Comparison between solitary and multiple skeletal metastatic lesions of breast cancer patients. Ann Oncol. 2003;14:1234–40.

    Article  PubMed  CAS  Google Scholar 

  25. Krasnow AZ, Hellman RS, Timins ME, et al. Diagnostic bone scanning in oncology. Semin Nucl Med. 1997;27:107–41.

    Article  PubMed  CAS  Google Scholar 

  26. Kardamakis D, Vassiliou V, Chow E. Pathophysiology of bone metastases. In: Kardamakis D, Vassiliou V, Chow E, editors. Bone metastases: A translational and clinical approach: 12 (cancer metastasis - biology and treatment). chapter 4.3. Netherlands: Springer; 2009. pp. 80–5.

  27. Ribatti D, Mangialardi G, Vacca A. Stephen Paget and the ‘seed and soil’ theory of metastatic dissemination. Clin Exp Med. 2006;6:145–9.

    Article  PubMed  CAS  Google Scholar 

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The authors declare that there are no conflicts of interest.

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Correspondence to Julia Krammer.

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Krammer, J., Engel, D., Schnitzer, A. et al. Is the assessment of the central skeleton sufficient for osseous staging in breast cancer patients? A retrospective approach using bone scans. Skeletal Radiol 42, 787–791 (2013). https://doi.org/10.1007/s00256-012-1562-7

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  • DOI: https://doi.org/10.1007/s00256-012-1562-7

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