Prognostic factors for survival of women with unstable spinal bone metastases from breast cancer

Abstract

Background

Bone metastases are an important clinical issue in women with breast cancer. Particularly, unstable spinal bone metastases (SBM) are a major cause of severe morbidity and reduced quality of life (QoL) due to frequent immobilization. Radiotherapy (RT) is the major treatment modality and is capable of promoting re-ossification and improving stability. Since local therapy response is excellent, survival of these patients with unstable SBM is of high clinical importance. We therefore conducted this analysis to assess survival and to determine prognostic factors for bone survival (BS) in women with breast cancer and unstable SBM.

Methods

A total population of 92 women with unstable SBM from breast cancer who were treated with RT at our department between January 2000 and January 2012 was retrospectively investigated. We calculated overall survival (OS) and BS (time between first diagnosis of bone metastases until death) with the Kaplan-Meier method and assessed prognostic factors for BS with a Cox regression model.

Results

Mean age at first diagnosis of breast cancer was 60.8 years ± SD 12.4 years. OS after 1, 2 and 5 years was 84.8, 66.3 and 50 %, respectively. BS after 1, 2 and 5 years was 62.0, 33.7 and 12 %, respectively. An age > 50 years (p < .001; HR 1.036 [CI 1.015–1.057]), the presence of a single bone metastasis (p = .002; HR 0.469 [CI 0.292–0.753]) and triple negative phenotype (p < .001; HR 1.068 [CI 0.933–1.125]) were identified as independent prognostic factors for BS.

Conclusions

Our analysis demonstrated a short survival of women with breast cancer and unstable SBM. Age, presence of a solitary SBM and triple-negative phenotype correlated with survival. Our results may have an impact on therapeutic decisions in the future and offer a rationale for future prospective investigations.

Background

Metastases in women with breast cancer most frequently occur in the skeleton [1]. Up to 2.6 % of all breast cancer patients already present with bone metastases at initial diagnosis and up to 15 % will develop bone metastases within 15 years [2, 3]. Particularly, metastases of the spinal column are a major cause of severe morbidity and reduced quality of life due to severe pain, pathological fractures, spinal cord compression and hypercalcemia [4, 5]. Additionally patients with unstable spinal bone metastases (SBM) are often immobilized or prescribed an orthopedic corset for the prevention of vertebral fractures and possible spinal cord compression. Treatment of SBM is multimodal including radiotherapy (RT), surgery and systemic treatments such as bisphosphonates [6]. Most commonly patients are treated with RT [7, 8] and a frequent treatment indication is instability [9]. In previous studies we were able to show that RT is capable of promoting re-ossification leading to increased stability of SBM. In those studies the analyzed patients showed only minor cancer-related morbidity during follow-up and reached comparably high survival rates. Additionally, we showed that the use of a validated scoring system to assess the stability of spinal bone metastases may prevent physicians from overdiagnosis of instability [10–12]. Since local therapy response is excellent, survival represents a major clinical interest in these patients with unstable SBM. Therefore, we conducted this analysis to assess survival and to determine prognostic factors for bone survival (BS) in women with unstable SBM from breast cancer.

Methods

A total population of 92 patients with histologically diagnosed breast cancer and unstable SBM were treated with RT at the University Hospital Heidelberg between January 2000 and January 2012. All patients were included in this retrospective analysis. Inclusion criteria were an osteolytic phenotype, unstable vertebral body, location in the thoracic or lumbar spine and a minimum duration of follow-up treatment of six months. A total of 344 bone lesions in the thoracic and lumbar spine were identified in these patients. Bone metastases diagnoses were verified by computed tomography (CT). Many patients exhibited more than one treated lesion; only one lesion per vertebral body was included in the analysis. Bone metastases distal to the irradiated site were not included. The patients’ data were taken from the Heidelberg NCT Cancer Registry and are summarized in Table 1. Performance status was expressed using the Karnofsky Performance Status score (KPS) [13]. The specifications for an unstable vertebral body were tumor occupancy of more than 60 % of the vertebral body and pedicle destruction [14]. This study was approved by the Heidelberg Ethics Committee on 22 October 2012 (# S-513/2012).

Table 1 Patients’ characteristics

BS was defined as the time from initial diagnosis of SBM until death from any cause. The time of site irradiation was not equal to the time of initial diagnosis of bone metastases. Overall survival (OS) was defined as time from initial diagnosis of breast cancer until death from any cause. We estimated patients’ survival using the Kaplan-Meier method. Patients were censored on the basis of whether or not they were alive. Results were reported as the p-values of the log-rank tests. Multivariate analysis was performed to detect factors independently associated with BS using a Cox proportional hazards model. This regression analysis was performed by including the factors age (>50 years), Karnofsky Performance Status score (≤70 %), chemotherapy (ChT) prior to RT (no ChT), number of metastases (solitary metastasis), local response (response after 3 or 6 months), concomitant bisphosphonates (no bisphosphonates), orthopedic corset (no corset) and pathological fractures (no fracture). The results were reported as p-values, hazard ratios and 95 % confidence intervals (CI). For all analyses, a p-value of 0.05 or less was considered statistically significant. All statistical analyses were done using the SAS software version 9.3 (SAS Institute, Cary, NC, USA).

RT was carried out at the clinic of our department. After CT-assisted three-dimensional-simulation, RT was performed with 2-3 dorsal photon beams in the 6-MV energy range. The planning target volume (PTV) covered the specific vertebral body affected, as well as those immediately above and below it. The median individual dose in all patients was 3 Gy; the median total dose 30 Gy. The respective fraction and total doses were planned separately for each individual patient, depending on tumor histology, the patient’s general state of health, the current staging and respective prognosis.

Results

Mean age at first diagnosis of breast cancer was 60.8 years ± SD 12.4 years. OS rates after 1, 2 and 5 years were 84.8, 66.3 and 50.0 % respectively (Fig. 1). BS was 62.0 % after 1 year, 33.7 % after 2 years and 12.0 % after 5 years respectively (Fig. 2). Among the investigated possible prognostic factors only an age > 50 years (p < .001; HR 1.036 [CI 1.015–1.057]), the presence of a single bone metastasis (p = .002; HR 0.469 [CI 0.292–0.753]) and triple negative phenotype (p < .001; HR 1.068 [CI 0.933–1.125]) affected BS statistically significantly (Table 2). KPS, ChT prior to RT, local response, concomitant bisphosphonates, orthopedic corset and pathological fractures prior to RT did not statistically significantly influence BS (Table 2).

Fig. 1

Overall survival

Fig. 2

Bone survival

Table 2 Cox regression model of prognostic factors for bone survival

Discussion

Breast cancer patients suffering from bone metastases of the spine represent a large patient group at most RT facilities. An important indication for RT treatment in these patients is instability, which is often associated with increased pain, profoundly reduced activity in daily life (ADL) and consequently severely impaired QoL. Unstable SBM may therefore be associated with shortened survival. We found OS and BS to be substantially shorter in our analysis with only 50 and 12 %, respectively, alive after 5 years compared to our previous study on osteolytic SBM in women with breast cancer [12]. Further studies have reported even worse survival rates in women with bone metastases [15], but this may be explained by a selection bias of only including patients with a follow-up of at least 6 months in our study. In an earlier small prospective study we already reported even lower survival rates in a population of patients with unstable metastases from various solid tumors [16]. In another study on patients with metastatic lung cancer we did not find any difference in survival between patients with stable and unstable SBM [17]. We believe that this was due to the extremely short survival time of those patients with metastatic lung cancer. Women with metastatic breast cancer have a more favorable prognosis than those with other solid tumors, e.g. lung cancer, and instability, possibly due to its associated morbidity, seems to be a relevant factor for long-term survival.

We found an age of more than 50 years, the presence of multiple SBM and triple negative phenotype to be associated with a worse prognosis after first diagnosis of bone metastases. In a recent study Bollen et al. [18] reported a median survival time of 22.5 months (95 % CI 18.0–26.9) for the receptor positive category and 6.7 months (95 % CI 2.4–10.9) for the triple negative category (p < 0.001). Therefore, patients with bone metastases from triple negative breast cancer have a significantly worse prognosis than those with a receptor positive phenotype.

According to the literature, another important prognostic factor for survival is the existence of additional extra-skeletal metastases [19]. In our analysis we were only able to demonstrate the prognostic relevance of age, the presence of a solitary metastasis and triple-negative phenotype. We believe this to be due to the small number of women with extra-skeletal metastases in our study cohort.

Conclusions

This analysis demonstrated a short survival of breast cancer patients with unstable SBM. Importantly, we presented a correlation between age, presence of a solitary metastasis, triple-negative phenotype, and survival. This may have an impact on therapeutic decisions in the future. The results offer a rationale for future prospective investigations.