Biochemical markers of bone turnover and clinical outcome in patients with renal cell and bladder carcinoma with bone metastases following treatment with zoledronic acid: The TUGAMO study.

BACKGROUND: Levels of bone turnover markers (BTM) might be correlated with outcome in terms of skeletal-related events (SRE), disease progression, and death in patients with bladder cancer (BC) and renal cell carcinoma (RCC) with bone metastases (BM). We try to evaluate this possible correlation in patients who receive treatment with zoledronic acid (ZOL).
METHODS: This observational, prospective, and multicenter study analysed BTM and clinical outcome in these patients. Serum levels of bone alkaline phosphatase (BALP), procollagen type I amino-terminal propeptide (PINP), and beta-isomer of carboxy-terminal telopeptide of type I collagen (β-CTX) were analysed.
RESULTS: Patients with RCC who died or progressed had higher baseline β-CTX levels and those who experienced SRE during follow-up showed high baseline BALP levels. In BC, a poor rate of survival was related with high baseline β-CTX and BALP levels, and new SRE with increased PINP levels. Cox univariate analysis showed that β-CTX levels were associated with higher mortality and disease progression in RCC and higher mortality in BC. Bone alkaline phosphatase was associated with increased risk of premature SRE appearance in RCC and death in BC.
CONCLUSION: Beta-isomer of carboxy-terminal telopeptide of type I collagen and BALP can be considered a complementary tool for prediction of clinical outcomes in patients with BC and RCC with BM treated with ZOL.

The skeleton is the third most frequent site of tumour metastases, behind lung and liver, and often the only site where metastases of advanced solid tumours develop. Bone metastases (BM) are observed in ∼80% of patients with advanced-stage malignant tumours (Coleman ). Thirty percent of patients with renal cell carcinoma (RCC) are diagnosed with BM, and another one-third of all patients will develop them throughout their disease period, even after undergoing nephrectomy (Wood and Brown, 2012), meaning a majority of RCC patients will suffer BM at some point of time. An estimated 40% of patients with bladder carcinoma (BC) develop BM. As of diagnosis of BM, the median survival of these patients is 12 months in RCC patients and 6–9 months in BC patients (Selvaggi and Scagliotti, 2005).

Bone metastases are associated with skeletal-related events (SRE) such as pathological fractures, spinal cord compression, severe bone pain, and hypercalcemia. Skeletal-related events can dramatically impair quality of life, and therefore appropriate management of cancer patients includes preservation of bone health.

Balance between bone resorption and bone formation is required for maintenance of bone metabolism. This equilibrium is altered by BM, which can produce an increase not only in bone formation but also in the destruction of bone. Bone metastases from RCC and BC are lytic in nature, and the increase in bone resorption is compensated by an increase in bone formation. Bone metabolism can be reflected by bone turnover markers (BTM). Previous studies have demonstrated that some BTM can alert to the existence of BM (Zhao ), but their correlation with clinical outcomes is contradictory in different studies.

Several studies have demonstrated that bisphosphonates can reduce SRE, resulting from BM, as they are bone-targeted agents that inhibit osteoclast-mediated osteolysis and, hence, are currently being recommended as standard therapy. Although several bisphosphonates, which prevent SRE in patients with cancer and BM are available, zoledronic acid (ZOL) is the first such agent with proven efficacy for the prevention of SRE in patients with BM from breast cancer, prostate cancer (PC), and other solid tumours (Saad ). Some authors had stated previously that ZOL could be an effective treatment for reducing morbidity in advanced RCC with BM (Zekri ) and it has been proven in subsequent studies (Lipton ).

The aim of this work was to study levels of two bone formation markers, bone alkaline phosphatase (BALP) and procollagen type I amino-terminal propeptide (PINP), and one marker of bone resorption, beta-isomer of carboxy-terminal telopeptide of type I collagen (β-CTX), in a population of patients with RCC or BC and bone metastases. The markers were studied at baseline and at 3, 6, 9, 12, 15, and 18 months after the beginning of treatment with ZOL. The relationship of these markers with mortality, disease progression, and SRE was also analysed.

Materials and methods

Study group

The TUGAMO study (‘Tumores UroGenitales Avanzados y Marcadores Óseos', or advanced urogenital tumours and BTM) was performed in patients with PC, BC, and RCC with bone metastases between 2009 and 2011. This article is a sub-analysis of this study about BC and RCC patients. This was an observational, prospective, and national multicenter study. The study enroled patients ⩾18 years of age with histologically confirmed BC or RCC, and at least one diagnosed bone lesion confirmed by scintigraphy. Patients were excluded from the study if they presented with concomitant pathologies that could interfere in the evaluation of BTM, such as bone metabolic disorders, Paget's disease of bone, hyperparathyroidism, thyroid abnormalities, abnormal intestinal absorption, or hepatic or renal dysfunction. Patients treated with bisphosphonates prior to their inclusion in the study and those with dental infection or diagnosis of osteonecrosis of the jaw were also excluded.

A follow-up of the patients was performed over 18 months. Baseline values (visit 0, v0) were those obtained when a patient initiated treatment with ZOL (Zometa, Novartis Pharma, Basel, Switzerland), 4 mg intravenous every 4 weeks for over 18 months. In all cases, anticancer treatment could be changed as clinically indicated throughout the course of the study. Data were collected at v0, v1 (3 months), v2 (6 months), v3 (9 months), v4 (12 months), v5 (15 months), and v6 (18 months). The definition of SRE was the first of any of the following events: pathological fractures, severe pain (which needed major analgesics, radiotherapy or surgery for its treatment), hypercalcemia, and spinal cord compression. Patients were also evaluated for disease progression by physical examination, and Eastern Cooperative Oncology Group performance status and pain score.

This study was conducted in accordance with the guidelines of the Declaration of Helsinki and Good Clinical Practice Guidelines and the protocol was approved by the Ethics Committee of the Hospital Clínico of Barcelona (Spain). Patients were given verbal and written information and gave their informed consent to participate in the study.

Analytical methods

Bone turnover markers were determined in serum. Blood was collected between 0800 and 1000 hours in a fasting state. Serum was kept at −80 °C until the moment of markers determination.

Bone alkaline phosphatase was determined by ELISA (IDS, Tyne & Wear, UK). Assay sensitivity was 0.7 μg  l−1. The normal range for healthy adult men was ⩽15 UI l−1.

Procollagen type I amino-terminal propeptide was determined by electrochemiluminescence (Elecsys, Roche, Mannheim, Germany). Assay sensitivity was 5 μg  l−1. The normal range for healthy adult men was ⩽62 ng ml−1.

Beta-isomer of carboxy-terminal telopeptide of type I collagen was determined by electrochemiluminescence (Elecsys, Roche). Assay sensitivity was 0.07 ng ml−1. The normal range for healthy adult men was ⩽0.548 ng ml−1.

Statistical analyses

Bone marker values were presented in terms of mean, standard deviation, median, and quartiles. Absolute and relative changes in bone markers as compared with baseline and previous visit were assessed at each visit. Absolute changes were summarised by mean and standard deviation, and their statistical significance was assessed using the Wilcoxon test for paired samples. Log transformation was performed for the relative changes obtained, and these were summarised by geometric mean and standard deviation. Statistical significance was assessed using the Student's t-test for paired samples. Receiver operating characteristic (ROC) curves were used to assess the predictive power of BTM levels for mortality, SRE, and progression. Specifically, baseline levels and relative changes at 3 months from baseline were taken as potential predictors. To assess the association between these potential predictors and time to death, time to first SRE and time to progression, a survival analysis was performed using the Kaplan–Meier method and comparisons were performed using the log-rank test. Finally, Cox regression models were fitted to quantify the degree of association between potential predictors and mortality, occurrence of SRE, and progression according to Kaplan–Meier results. The models were summarised by hazard ratio estimate, standard error, and 95% confidence interval for hazard ratio. Also, the P-value obtained from hypothesis testing of the hazard ratio was shown. The significance level was set at 0.05 for all tests.

Data were analysed with SAS, version 9.1.3. for Windows (SAS Analytics, Madrid, Spain) and STATA, 4.0 for Windows (StataCorp, London, UK).

Results

Patient demographics

Thirty-nine patients with RCC and BM, and thirty-four patients with BC and BM were included in the study. Table 1 shows the demographics and baseline disease characteristics of the patients studied.

Table 1

Baseline characteristics of RCC and BC patients

Baseline characteristics	RCC patients (n=39)	BC patients (n=34)
Mean age (years)	65.1 (43–82)	64.4 (44–77)
Sex (%)
Men	69.2	85.3
Women	30.8	14.7
ECOG performance status (%)
0	21.1	18.8
1	47.4	40.6
2	21.1	28.1
3	10.5	9.4
4	0	3.1
TNM stage (%)
I	0	6.7
II	5.7	16.7
III	34.3	6.7
IV	60	70
Previous surgery (%)	87.2	85.3
Mean time since bone metastases diagnosed (months)	6.2 (0–59.1)	2.4 (0–34.6)
Previous SRE (%)	56.4	50
Analgesic treatment (%)	84.6	94.1
Antineoplasic treatment (%)
Chemotherapy	5.1	29.4
Antiangiogenic	61.5	2.9
mTOR inhibitors	20.5	0
Radiotherapy (%)	30.8	32.4

Abbreviations: BC=bladder cancer; ECOG=Eastern Cooperative Oncology Group; mTOR=mammalian target of rapamycin; RCC=renal cell carcinoma; SRE=skeletal-related events; TNM=tumour, nodes, metastasis.

Global survival, defined as the time between the beginning of the 18-month ZOL treatment and death, showed a median value of 10 months in RCC (2.4–17.5) and 8.9 months in BC (2.6–15.3). Thirty-nine patients commenced RCC study and thirty-four patients began BC study; out of them five and three patients completed it, respectively. Losses of participants (RCC/BC) were due to death (21/19), loss of informed consent (0/1), loss to follow-up (1/1), clinical criteria (5/2), and others (e.g., change of address, renal insufficiency, and progression—1/2). No patients presented with osteonecrosis of the jaw or other severe secondary effects during follow-up.

Evolution of bone markers

The correlation among the markers in RCC (β-CTX, PINP, and BALP) was strong at v1 and v2 (P<0.007), decreasing all values. In BC, β-CTX and BALP showed a strong correlation at v1 (P=0.02), BALP and PINP at v0 (P=0.03), and β-CTX and PINP at v1, v2, and v3 (P<0.03).

Most patients with abnormal BTM levels showed a decrease in levels after ZOL treatment. During the first six months, levels of BTM tended to decrease significantly in both patient groups (Figures 1 and 2).

Figure 1

Bone turnover marker evolution during follow-up in RCC patients. (A) Beta-isomer of carboxy-terminal telopeptide of collagen I (β-CTX); (B) bone alkaline phosphatase (BALP); (C) procollagen type I amino-terminal propeptide (PINP). Values (y-axis) are shown as median and standard deviation (BALP and PINP in μg l−1, and β-CTX in ng ml−1). At x-axis, time of follow-up (months) and number of patients alive (n) are shown. **Statistically significant differences with respect to baseline levels (P<0.05).

Figure 2

Bone turnover marker evolution during follow-up in BC patients. (A) Beta-isomer of carboxy-terminal telopeptide of collagen I (β-CTX); (B) bone alkaline phosphatase (BALP); (C) procollagen type I amino-terminal propeptide (PINP). Values (y-axis) are shown as median and standard deviation (BALP and PINP in μg l−1, and β-CTX in ng ml−1). At x-axis, time of follow-up (months) and number of patients alive (n) are shown. **Statistically significant differences with respect to baseline levels (P<0.05).

In RCC, β-CTX was the marker which experienced the greatest decrease and all patients showed normalisation in v1 (P=0.007). All patients remained normal during follow-up, except one patient who got a change for the worse in v3 and died. Bone alkaline phosphatase showed normalisation in v2 in 76.5% of patients (P=0.04), but six patients still showed abnormal values and one patient got a change for the worse and died. Changes in PINP values were not statistically significant in v1, with five patients with abnormal values and four patients with worse values.

In BC, following ZOL treatment, 65% of patients exhibited improved β-CTX and two patients got worse (P=0.02) in v1. Bone alkaline phosphatase had improved in 53% of patients at v1 (P=0.01) and three patients remained with abnormal values. Procollagen type I amino-terminal propeptide did not show statistically significant changes. Only the three first visits were analysed because the number of patients was too low at subsequent visits. Levels of PINP and β-CTX at v2 decreased by 73 and 75%, respectively (P<0.003). Bone alkaline phosphatase showed a decrease of 44% at v1 (P=0.02).

Bone markers as predictors of mortality risk, disease progression, and SRE appearance

Receiver operating characteristic analyses were performed to evaluate BTM as predictors of mortality risk, disease progression, and SRE appearance. Two different values were used as a cutoff point: baseline BTM levels and respective changes between v0 and v1 BTM levels. The sensitivity, specificity, and positive and negative predictive values of each BTM in each disease was found. The areas under the curve (AUC) were low for prediction mortality risk in RCC patients (<0.6), but AUC was 0.769 for basal β-CTX levels for prediction of disease progression and 0.719 for basal PINP levels for prediction of SRE. For BC patients, AUC for basal BALP levels was 0.801 for prediction of mortality risk and 0.716 for prediction of SRE. The other AUC were too low.

Kaplan–Meier curves (KMc) were performed with four categories:

Baseline BTM normal or abnormal (defined as higher than the upper limit of normality).

Basal BTM ‘higher' or ‘equal to or less than' the cutoff obtained in the ROC curves (ROC cutoff or ROC-CO).

Relative changes between v0 and v1 (v1/v0) ‘higher than' or ‘equal to or less than' ROC-CO.

Presence or absence of a normal BTM level at v1.

In RCC patients, KMc showed a significantly diminished survival rate in patients with abnormal baseline β-CTX and in those with higher β-CTX values than ROC-CO. Both groups also exhibited an increase in disease progression. Baseline BALP levels higher than ROC-CO showed a close relation with lesser time until SRE appearance. Statistically significant KMc are shown in Figure 3.

Figure 3

Kaplan–Meier analysis after the completion of treatment (18 months) with ZOL in RCC patients. (A) β-isomer of carboxy-terminal telopeptide of collagen I (β-CTX) and overall survival. Stratification was performed using ‘normal or abnormal baseline marker values' against death. (B) β-CTX and overall survival. Stratification was performed using the cutoff point obtained from the ROC curves of ‘baseline values of biomarkers at the beginning of the study' against death. (C) β-CTX and disease progression. Stratification was performed using ‘normal or abnormal baseline marker values' against death. (D) β-CTX and disease progression. Stratification was performed using the cutoff point obtained from the ROC curves of ‘baseline values of biomarkers at the beginning of the study' against death. (E) Bone alkaline phosphatase (BALP) and new SRE. Stratification was performed using the cutoff point obtained from the ROC curves of ‘baseline values of biomarkers at the beginning of the study' against death.

Moreover, in BC patients, KMc showed a different survival rate in patients with higher β-CTX and BALP levels using ROC-CO. Patients whose PINP levels changed relatively between v0 and v1 had a KMc that showed a lower time until new SRE appearance. No significant differences were found in KMc regarding progression. These statistically significant results are shown in Figure 4.

Figure 4

Kaplan–Meier analysis after the completion of treatment (18 months) with ZOL in BC patients. (A) β-isomer of carboxy-terminal telopeptide of collagen I (β-CTX) and overall survival. Stratification was performed using the cutoff point obtained from the ROC curves of ‘baseline values of biomarkers at the beginning of the study' against death. (B) Bone alkaline phosphatase (BALP) and overall survival. Stratification was performed using the cutoff point obtained from the ROC curves of ‘baseline values of biomarkers at the beginning of the study' against death. (C) Amino-terminal propeptide of procollagen I (PINP) and new SRE. Stratification was performed using relative changes between visit 0 and visit 1 (v1/v0) in relation to cutoff point obtained from the ROC curves against death.

Univariate Cox regression was derived from the above-mentioned KMc. Table 2 shows the hazard ratios for RCC patients and Table 3 shows the hazard ratios for BC patients. In RCC, higher β-CTX levels were related with death and a poor prognosis for disease progression. Higher levels of BALP were associated with premature SRE. In BC, higher β-CTX and BALP levels were also related with death. The Cox regression regarding progression could not be made because no significant differences were found in KMc. Procollagen type I amino-terminal propeptide did not show being associated with outcomes.

Table 2

Univariate Cox regression analysis of bone markers in renal cell carcinoma after 18 months of ZOL treatment

Variable	HR	95% CI (HR)	P-value
Death
Abnormal baseline β-CTX levels (>0.548 ng ml−1)	2.834	1.076–7.465	0.035a
High baseline β-CTX levels (>0.7 ng ml−1, ROC cutoff)	6.146	2.223–16.990	<0.001a
No normalisation of β-CTX levels in v1b	—	—	—
Abnormal baseline BALP levels (>15 UI l−1)	1.226	0.475–3.165	0.674
High baseline BALP levels (>17.9 UI l−1, ROC cutoff)	0.886	0.35–2.24	0.798
No normalisation of BALP levels in v1	2.283	0.54–9.662	0.262
Abnormal baseline PINP levels (>62 ng ml−1)	1.644	0.655–4.123	0.29
High baseline PINP levels (>110.3 ng ml−1, ROC cutoff)	2.810	0.903–8.747	0.074
No normalisation of PINP levels in v1	2.511	0.614–10.275	0.2
Disease progression
Abnormal baseline β-CTX levels (>0.548 ng ml−1)	4.036	1.364–11.938	0.012a
High baseline β-CTX levels (>0.641 ng ml−1, ROC cutoff)	8.055	2.524–25.71	<0.001a
No normalisation of β-CTX levels in v1b	—	—	—
Abnormal baseline BALP levels (>15 UI l−1)	1.028	0.355–2.976	0.96
High baseline BALP levels (>12.4 UI l−1, ROC cutoff)	1.981	0.549–7.151	0.296
No normalisation of BALP levels in v1	1.097	0.227–5.315	0.908
Abnormal baseline PINP levels (>62 ng ml−1)	1.681	0.589–4.793	0.331
High baseline PINP levels (>87.5 ng ml−1, ROC cutoff)	1.723	0.599–4.957	0.312
No normalisation of PINP levels in v1	2.523	0.709–8.982	0.153
Skeletal-related events
Abnormal baseline β-CTX levels (>0.548 ng ml−1)	0.881	0.268–2.897	0.834
High baseline β-CTX levels (>0.157 ng ml−1, ROC cutoff)	2.992	0.386–23.211	0.294
No normalisation of β-CTX levels in v1b	—	—	—
Abnormal baseline BALP levels (>15 UI l−1)	2.107	0.694–6.393	0.188
High baseline BALP levels (>95.1 UI l−1, ROC cutoff)	3.634	1.071–12.323	0.038a
No normalisation of BALP levels in v1	3.050	0.699–13.303	0.138
Abnormal baseline PINP levels (>62 ng ml−1)	3.155	0.91–10.934	0.070
High baseline PINP levels (>53 ng ml−1, ROC cutoff)	3.253	0.886–11.939	0.075
No normalisation of PINP levels in v1	1.99	0.559–7.079	0.288

Abbreviations: BALP=bone alkaline phosphatase; β-CTX=beta-isomer of carboxy-terminal telopeptide of type I collagen; CI=confidence interval; HR=hazard ratio; PINP=procollagen type I amino-terminal propeptide; ROC=receiver operating characteristic; v1=visit 1; ZOL=zoledronic acid.

Relative changes between v1 and v0 did not show statistically significant results, and they are not shown.

Statistically significant results.

There were no patients with abnormal levels in v1.

Table 3

Univariate Cox regression analysis of bone markers in bladder cancer after 18 months of ZOL treatment

Variable	HR	95% CI (HR)	P-value
Death
Abnormal baseline β-CTX levels (>0.548 ng ml−1)	2.062	0.732–5.813	0.171
High baseline β-CTX levels (>0.9 ng ml−1, ROC cutoff)	3.672	1.353–9.967	0.010a
No normalisation of β-CTX levels in v1b	—	—	—
Abnormal baseline BALP levels (>15 UI l−1)	0.963	0.321–2.888	0.946
High baseline BALP levels (>45.9 UI l−1, ROC cutoff)	2.597	1.08–6.248	0.033a
No normalisation of BALP levels in v1b	—	—	—
Abnormal baseline PINP levels (>62 ng ml−1)	1.096	0.367–3.273	0.869
High baseline PINP levels (>128.7 ng ml−1, ROC cutoff)	1.313	0.54–3.191	0.548
No normalisation of PINP levels in v1	0.963	0.225–4.13	0.96
Disease progression
This analysis was not made because Kaplan–Meier curves showed no statistically significance and it did not comply with assumption of proportional risk	—	—	—
Skeletal-related events
Abnormal baseline β-CTX levels (>0.548 ng ml−1)	1.427	0.387–5.268	0.593
High baseline β-CTX levels (>0.8 ng ml−1, ROC cutoff)	2.714	0.811–9.085	0.105
No normalisation of β-CTX levels in v1b	—	—	—
Abnormal baseline BALP levels (>15 UI l−1)	0.408	0.076–2.178	0.294
High baseline BALP levels (>19.9 UI l−1, ROC cutoff)	2.819	0.727–10.92	0.134
No normalisation of BALP levels in v1	—	—	—
Abnormal baseline PINP levels (>62 ng ml−1)	1.764	0.389–7.993	0.461
High baseline PINP levels (>106.8 ng ml−1, ROC cutoff)	2.418	0.797–7.33	0.119
No normalisation of PINP levels in v1	1.136	0.267–4.837	0.863

Abbreviations: BALP=bone alkaline phosphatase; β-CTX=beta-isomer of carboxy-terminal telopeptide of type I collagen; CI=confidence interval; HR=hazard ratio; PINP=procollagen type I amino-terminal propeptide; ROC=receiver operating characteristic; v1=visit 1; ZOL=zoledronic acid.

Relative changes between v1 and v0 did not show statistically significant results and they are not shown.

Statistically significant results.

There were no patients with abnormal levels in v1.

Discussion

The usefulness of BTM as tool for the diagnosis of BM in many types of cancers has been investigated previously (Coleman ; Huang and Ouyang, 2012). Many studies have analysed their relationship with clinical outcomes (Mountzios ; Kamiya ; Zaghloul ; Coleman ; Jung ; Saad ), as well as their clinical importance (Coleman ; Armstrong ). However, only a few articles have analysed the usefulness of BTM in RCC and less in BC, and there is no consensus among these studies as to which BTM is the ideal marker. Recently, the International Osteoporosis Foundation and the International Federation of Clinical Chemistry and Laboratory Medicine have recommended PINP and β-CTX as reference markers in all clinical studies (Vasikaran ), and we have used them in our study previously to this recommendation. The utility of BTM as markers of the presence of BM before their appearance in the bone scintigraphy has been taken up in many studies (Zhao ). In the case of RCC and BC, BTM utility is more important because early bone metastatic lesions in these tumours may not be easily detected by scintigraphy due to their lytic nature (Wood and Brown, 2012). In one study (Kleipzig , they found that PINP was a good predictor of BM in patients with RCC. In two studies (Ramankulov , 2008), these authors analysed osteopontin (a bone-related protein) and serum amyloid A, finding that both were unspecific markers in relation to the number or localisation of metastatic lesions in patients with RCC. Other authors (Okamura ) found that ICTP (a telopeptide of collagen type I) can detect BM in genitourinary cancers. In a study of BC patients (Zissimopoulos ), PICP (similar to PINP) showed a significant difference between patients with or without BM. In spite of these results, in a recent review (Huang and Ouyang, 2012) they concluded that, currently, no BTM can predict occurrence of BM in the absence of bone imaging techniques, and that more prospective trials are needed to assess this possibility. We are currently unable to answer this question, because all our patients were previously diagnosed with BM. To date, no study has provided a definitive answer to this question about BTM and premature diagnosis of BM in RCC.

In the current work, we have demonstrated that patients with RCC and BM and elevated baseline β-CTX levels had a higher risk of death and a higher estimated risk of disease progression than those patients whose levels were normal or lower than ROC-CO. When baseline BALP levels were higher than ROC-CO, the estimated risk of premature SRE was also elevated. Procollagen type I amino-terminal propeptide was not associated with analysed clinical outcomes.

No study has arrived at the same conclusions as these regarding RCC. Some authors (Ramankulov , 2008) have found that osteopontin, serum amyloid A, and presence of distant metastases were independent survival predictors in RCC. Other articles (Vermaat ) found the same results about amyloid A and added to that elevated levels of apolipoprotein-A2 and transthyretin were associated with better prognosis. Other authors (Kume ) collected RCC cases and found an association between total alkaline phosphatase and overall survival. Another one (Jung ) had found that osteoprotegerin was predictive of cancer-specific survival in a multivariate model. In a study with a variety of solid tumours, including RCC, a multicenter study (Coleman ) found that increased values of BALP and NTX (amino-terminal telopeptide of collagen I) were associated with increased risk of death, SRE, and disease progression in patients with breast cancer, PC, myeloma, non-small-cell lung cancer and other solid tumours, treated with bisphosphonates. Similar results had been found by the same authors about NTX in bisphosphonates naive patients (Brown ).

As for patients with BC, an increased risk of death was associated with high baseline β-CTX and BALP levels. Only one similar result has been found previously (López-Carrizosa ), but the lower number of patients (2) made the results of the study unreliable. Other authors (Ang ) had found a relation between osteopontin levels and stage of disease previously. Although the current study is limited by the small number of cases in the study groups, this is the first report in the literature showing a relationship between BTM, BC, and clinical outcome.

As in our study, other authors have found relationships between different tumours, clinical outcomes, and β-CTX. In patients with PC, increased BTM levels (especially PINP and ICTP, a resorption marker) have been related with survival, disease progression, and SRE (Jung ). Other authors (Zhao ) studied patients with PC and lung- and breast carcinoma. According to their data, β-CTX and BALP can be considered to be good markers for detecting BM. In addition, high values of PINP were related with poor rates of survival.

Procollagen type I amino-terminal propeptide did not show a statistically significant relation in either of the two cancers in our study. The findings in KMc about relation between progression and relative changes in PINP values in BC are not corroborated to Cox regression, and it can be explained for low number of patients in this group. Further studies with more patients are necessary to support our findings.

Other markers have been well established as prognostic factors in RCC, such as Motzer criteria (haemoglobin, Karnowsky performance status, time from diagnosis to treatment with interferon-alpha, lactate dehydrogenase, and corrected serum calcium) (Motzer ) or Heng criteria (haemoglobin, time from diagnosis to treatment with interferon-alpha, corrected serum calcium, neutrophils and platelets number) (Heng ). In BC, Eastern Cooperative Oncology Group performance status and the presence of visceral metastasis have been associated with decreased survival (Bellmunt ). The main limitation of our study is the small sample size of each of the groups (39 RCC and 34 BC), which are far too small to do multivariable analysis to determine if the BTM are independently predictive of important clinical outcomes when these known prognostic factors (Bellmunt ; Motzer ; Heng ), history of prior SRE, other bone-associated markers, and treatment effects are considered all together. Future studies will have to address this point.

Conclusions

Beta-isomer of carboxy-terminal telopeptide of type I collagen and BALP can be considered promising prognostic factors of clinical outcome in patients with RCC and BC with BM treated with ZOL and they can be one more tool to those existent previously. Metastatic bone disease in RCC and BC may benefit from greater focus than it has to date, and their use may bring about an important advance in the management of these patients. More studies in larger groups of patients are necessary for further confirmatory research.