Abstract
Background
This study was performed to identify new significant prognostic factors in breast cancer patients irradiated for metastatic spinal cord compression (MSCC).
Patients and methods
The data of 504 patients with breast cancer patients with MSCC were retrospectively analyzed with respect to posttreatment motor function, local control of MSCC, and survival. The investigated potential prognostic factors included age, Eastern Cooperative Oncology Group (ECOG) performance score, number of involved vertebrae, other bone metastases, visceral metastases, pretreatment ambulatory status, interval from cancer diagnosis to radiotherapy of MSCC, time developing motor deficits before radiotherapy, and the radiation schedule.
Results
On multivariate analysis, better functional outcome was associated with ambulatory status prior to RT (estimate − 1.29, p < 0.001), no visceral metastases (estimate − 0.52, p = 0.020), and slower development of motor deficits (estimate + 2.47, p < 0.001). Improved local control was significantly associated with no other bone metastases (risk ratio (RR) 4.33, 95% confidence interval (CI) 1.36–14.02, p = 0.013) and no visceral metastases (RR 3.02, 95% CI 1.42–6.40, p = 0.005). Improved survival was significantly associated with involvement of only 1–2 vertebrae (RR 1.27, 95% CI 1.01–1.60, p = 0.044), ambulatory status before radiotherapy (RR 1.75, 95% CI 1.23–2.50, p = 0.002), no other bone metastases (RR 1.93, 95% CI 1.18–3.13, p = 0.009), no visceral metastases (RR 7.60, 95% CI 5.39–10.84, p < 0.001), and time developing motor deficits before radiotherapy (RR 1.55, 95% CI 1.30–1.86, p < 0.001).
Conclusion
Several new independent prognostic factors were identified for treatment outcomes. These prognostic factors should be considered in future trials and may be used to develop prognostic scores for breast cancer patients with MSCC.
Zusammenfassung
Hintergrund
Ziel dieser Studie war es, neue Prognosefaktoren bei Brustkrebspatientinnen, die aufgrund einer metastatisch bedingten Rückenmarkskompression (MSCC) bestrahlt wurden, zu identifizieren.
Patienten und Methoden
Die Daten von 504 Brustkrebspatientinnen mit einer MSCC wurden retrospektiv im Hinblick auf die motorische Funktion nach Therapie, die lokale Kontrolle der MSCC und das Gesamtüberleben ausgewertet. Es wurden folgende mögliche Prognosefaktoren untersucht: Alter, Allgemeinzustand („performance score“ der ECOG, Eastern Cooperative Oncology Group), Anzahl befallener Wirbelkörper, Vorhandensein anderer Knochenmetastasen, Vorhandensein von Organmetastasen, Gehfähigkeit vor Therapie, Intervall von der Diagnose der Tumorerkrankung bis zur Strahlentherapie der MSCC, Entwicklungszeit motorischer Defizite vor Strahlentherapie sowie das Strahlentherapieregime.
Ergebnisse
In der Multivarianzanalyse war eine bessere motorische Funktion nach Therapie signifikant mit der Gehfähigkeit vor Strahlentherapie (estimate: − 1,29; p < 0,001), dem Nicht-Vorhandensein von Organmetastasen (estimate: − 0,52; p = 0,020) und einer langsameren Entwicklung motorischer Defizite (estimate: + 2,47; p < 0,001) assoziiert. Eine bessere lokale Kontrolle war signifikant mit dem Nicht-Vorhandensein anderer Knochenmetastasen (Risk Ratio [RR] 4,33; 95% confidence interval [CI] 1,36–14,02; p = 0,013) und dem Nicht-Vorhandensein von Organmetastasen (RR 3,02; 95% CI 1,42–6,40; p = 0,005) assoziiert. Ein besseres Gesamtüberleben war signifikant mit einem Befall von nur 1–2 Wirbelkörpern (RR 1,27; 95% CI 1,01–1,60; p = 0,044), Gehfähigkeit vor Strahlentherapie (RR 1,75; 95% CI 1,23–2,50; p = 0,002), dem Nicht-Vorhandensein anderer Knochenmetastasen (RR 1,93; 95% CI 1,18–3,13; p = 0,009), dem Nicht-Vorhandensein von Organmetastasen (RR 7,60; 95% CI 5,39–10,84; p < 0,001) und einer langsameren Entwicklung motorischer Defizite vor Strahlentherapie (RR 1,55; 95% CI 1,30–1,86; p < 0,001) assoziiert.
Schlussfolgerung
Es wurden verschiedene neue unabhängige Prognosefaktoren identifiziert. Diese Prognosefaktoren sollten in zukünftigen Studien berücksichtigt werden und können bei der Entwicklung von Prognose-Scores für Brustkrebspatientinnen mit MSCC hilfreich sein.
References
Freundt K, Meyners T, Bajrovic A et al (2010) Radiotherapy for oligometastatic disease in patients with spinal cord compression (MSCC) from relatively radioresistant tumors. Strahlenther Onkol 186:218–23
Inoue T, Oh RJ, Shiomi H (2011) New approach for treatment of vertebral metastases using intensity-modulated radiotherapy. Strahlenther Onkol 187:108–113
Kaplan EL, Meier P (1958) Non parametric estimation from incomplete observations. J Am Stat Assoc 53:457–481
Kato A, Ushio Y, Hayakawa T et al (1985) Circulatory disturbance of the spinal cord with epidural neoplasm in rats. J Neurosurg 63:260–265
Loblaw DA, Laperriere NJ (1998) Emergency treatment of malignant extradural spinal cord compression: an evidence-based guideline. J Clin Oncol 16:1613–1624
Manabe S, Tanaka H, Higo Y et al (1989) Experimental analysis of the spinal cord compressed by spinal metastasis. Spine 14:1308–1315
Maranzano E, Latini P, Perrucci E et al (1997) Short-course radiotherapy (8 Gyx2) in metastatic spinal cord compression: an effective and feasible treatment. Int J Radiat Oncol Biol Phys 38:1037–1044
Patchell R, Tibbs PA, Regine WF et al (2005) Direct decompressive surgical resection in the treatment of spinal cord compression caused by metastatic cancer: a randomised trial. Lancet 366:643–648
Rades D, Abrahm JL (2010) The role of radiotherapy for metastatic epidural spinal cord compression. Nat Rev Clin Oncol 7:590–598
Rades D, Heidenreich F, Karstens JH (2002) Final results of a prospective study for the prognostic value of the time of developing motor deficits before irradiation in metastatic spinal cord compression. Int J Radiat Oncol Biol Phys 53:975–979
Rades D, Huttenlocher S, Bajrovic A et al (2011) Surgery followed by radiotherapy versus radiotherapy alone for metastatic spinal cord compression from unfavorable tumors. Int J Radiat Oncol Biol Phys 81:e861–868
Rades D, Huttenlocher S, Dunst J et al (2010) Matched pair analysis comparing surgery followed by radiotherapy and radiotherapy alone for metastatic spinal cord compression. J Clin Oncol 28:3597–604
Rades D, Veninga T, Stalpers LJA et al (2006) Prognostic factors predicting functional outcomes, recurrence-free survival, and overall survival after radiotherapy for metastatic spinal cord compression in breast cancer patients. Int J Radiat Oncol Biol Phys 64:182–188
Sørensen PS, Børgesen SE, Rohde K et al (1990) Metastatic epidural spinal cord compression. Cancer 65:1502–1508
Stieler F, Wolff D, Bauer L et al (2011) Reirradiation of spinal column metastases: comparison of several treatment techniques and dosimetric validation for the use of VMAT. Strahlenther Onkol 187:406–415
Tomita T, Galicich JH, Sundaresan N (1983) Radiation therapy for spinal epidural metastases with complete block. Acta Radiol Oncol 22:135–143
Turner S, Marosszeky B, Timms I et al (1993) Malignant spinal cord compression: a prospective evaluation. Int J Radiat Oncol Biol Phys 26:141–146
Uhl M, Sterzing F, Habl G et al (2011) CT-myelography for high-dose irradiation of spinal and paraspinal tumors with helical tomotherapy: revival of an old tool. Strahlenther Onkol 187:416–420
Conflict of interest
The corresponding author states the following: speaker’s honoraria were received from Amgen, Novartis Oncology, MerckSerono, and AstraZeneca. Travel grants were received from MerckSerono, and research funds were provided by Novartis Oncology and MerckSerono. Relations with MerckSerono and AstraZeneca were not related to the topic of this paper.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Rades, D., Douglas, S., Veninga, T. et al. Prognostic factors in a series of 504 breast cancer patients with metastatic spinal cord compression. Strahlenther Onkol 188, 340–345 (2012). https://doi.org/10.1007/s00066-011-0061-4
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00066-011-0061-4