Advances in UrologyVolume 2012 (2012), Article ID 893193, 8 pagesdoi:10.1155/2012/893193

Review Article

Modern Detection of Prostate Cancer's Bone Metastasis: Is the Bone Scan Era Over?

Bertrand Tombal¹ and Frederic Lecouvet²

¹Division of Urology, Cliniques Universitaires Saint Luc, Université Catholique de Louvain, 1200 Brussels, Belgium²Division of Radiology, Cliniques Universitaires Saint Luc, Université Catholique de Louvain, 1200 Brussels, Belgium

Received 13 July 2011; Accepted 11 August 2011

Academic Editor: Steven Joniau

Copyright © 2012 Bertrand Tombal and Frederic Lecouvet. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Prostate cancer cells have an exquisite tropism for bone, which clinically translates into the highest rate of bone metastases amongst male cancers. Although in the latest years there has been an active development of new “bone targeted” therapies, modern diagnostic techniques for bone metastases still relies mostly on bone scanning (BS) and plain X-ray. BS dramatically lacks specificity and sensitivity. Recent publications using modern imaging technologies have clearly pinpointed that BS grossly underestimates the true prevalence of bone metastasis. In addition BS does not allow tumour measurement and is, therefore, not appropriate to monitor response to therapy. This might be extremely important in patients harbouring high-risk localized disease that are eventually candidate for local therapy. Here we reviewed what are the emerging imaging strategies that are likely to supplant BS and to what extent they can be used in the clinic already.

1. Introduction

In men over the age of 50, prostate cancer (PCa) is the most commonly diagnosed cancer and the second leading cause of death by cancer [1]. With the intense use of PSA testing, most PCa are diagnosed at an early stage, and most are candidate to intent-to-cure therapies such as radical prostatectomy, external beam radiation therapy, or seeds implant. Initially essentially intended for low- or intermediate-risk disease, local therapies are now more often indicated in patients with high-risk localized disease and locally advanced disease. Indeed, hormone therapy has failed to demonstrate to increase overall survival when it was not associated with a local treatment [2]. In that high-risk population; however, it is critical to precisely rule out the presence of metastases since as for today it still represents the tipping point for excluding local control.

PCa cells spreading out of the prostate show an exquisite tropism for bone. In most patients, the initial seeding of metastatic deposits occurs in the hematopoietic red marrow of the axial skeleton leading to the formation of bone metastases (BMs). BMs represent the initial and the main metastatic site in about 80% of PCa patients, therefore, being one of the most important prognostic factors [3, 4]. Skeletal complications, most commonly designed as “skeletal-related events (SREs),” account for most of the PCa’s morbidity and mortality [5]. Replacement of hematopoietic tissues in the bone marrow by PCa cells leads to anaemia while abnormal tissue growing in the bone marrow can lead to pain, fractures, and spinal cord compression. As for today, despite the development of bone-targeted strategies, BMs are still considered incurable [6].

The main phenotypic manifestations of PCa BMs are their tropism to the axial skeleton (skull, vertebra, ribs and collar bone, scapula, and proximal femur) and their most often osteoblastic appearance, resulting from the stimulation of osteoblasts [6]. BM, are often associated with increased levels of serum markers of osteoblastic proliferation, such as bone-specific alkaline phosphatase [7].

Interestingly, there has been no major evolution in the diagnostic algorithm for BM in the recent years. Most international guidelines still recognized bone scintigraphy (BS) and plain X-ray radiography as the cornerstone diagnostic techniques to detect and follow BM [8, 9]. Most modern clinical trials still incorporate BS as a major component to define time to progression, although it is recognized as not appropriate to measure tumour response and required serial examinations to define progression [10–12]. There are, however, several technological developments addressing this important diagnostic aspect. Here we will review some of these developments.

2. Why and When Bone Imaging Is Required?

Early BM detection is critical in the management of patients with high-risk PCa. Newly diagnosed patients with localized disease and no metastases may benefit from radical treatment with curative intent. In contrast, most guidelines recognize that patients with BM should be kept away from local therapy to avoid unnecessary side effects and treated with systemic therapy [9]. With modern PSA-based diagnostic strategies, many patients are diagnosed while they are still asymptomatic. In screening trials, BMs are detected at diagnosis in less than 10% of the patients [13]. This means that there is no need to perform an initial BS in every new patient. PSA value and Gleason’s score at diagnostic remain the strongest BM’s indicators. In a study conducted on 60 patients with newly diagnosed PCa, Rana et al. demonstrated that the positive predictive value of a PSA >100 ng/mL was 100% [14]. Together with PSA, cT₃₋₄ stage and a Gleason score >7 are the other predictors of BM; their positive predictive value being, respectively, 71.4% and 81% [14]. Based on this trial and others, the EAU guidelines recommend that [] a staging bone scan may be superfluous if the serum PSA concentration is less than 20 ng/mL in asymptomatic patients with well-, or moderately differentiated tumours. In contrast, in patients with poorly differentiated tumours and locally advanced disease, a staging bone scan should be obtained irrespective of the serum PSA value [] [9]. Briganti et al. have developed a risk stratification tool to select patients requiring initial imaging from a series of 853 consecutive patients [15]. Their classification and regression tree (CART) stratifies patients into low risk (biopsy Gleason ≤7, cT₁₋₃, and PSA <10 ng/mL), intermediate risk (biopsy Gleason ≤7, cT₂₋₃, and PSA >10 ng/mL), and high risk (biopsy Gleason >7) conferring a risk of BM of 1.8%, 8.5%, and 16.4%. Briganti’s regression tree shows higher sensitivity (87.5%) compared to the EAU, AUA, and NCCN guidelines [8, 9, 16].

Later in the course of the disease, BM detection may be discussed in case of PSA recurrence after radical treatment or when the tumour becomes resistant to castration (CRCP). This information may be important to guide initiation of hormone therapy, chemotherapy, or bone-targeted agents. Gomez et al. have evaluated the use of BS in 153 patients presenting with a PSA recurrence after radical prostatectomy. This study demonstrated that it is unlikely to have a positive BS in patients with a serum PSA of <7 ng/mL except in case of skeletal symptoms [17]. Pound et al. have reviewed a large series of radical prostatectomy performed at the Johns Hopkins University and identified 304 patients with a subsequent PSA rise [18]. The median actuarial time to metastases was 8 years from the time of PSA level elevation. In survival analysis, time to biochemical progression ≤2 years (), Gleason’s score ≤8 (), and PSA doubling time ≤10 months (PSADT) () were predictive of the probability and time to the development of metastatic disease. Choueiri et al. have reviewed case notes of 292 patients from CaPSURE who had recurrence and had undergone at least 1 imaging study (BS, computerized tomography (CT), or magnetic resonance imaging (MRI) of the abdomen and the pelvis) [19]. Overall only 11% patients showed a positive imaging study, and this was unlikely to occur when PSA was ≤5 ng/mL or PSADT ≥10 months [19].

Smith et al. have reported the natural history of 201 non-metastatic (M0) CRCP patients consisting of the placebo group of an aborted trial with zoledronic acid [20]. At 2 years, only 33% of patients had developed BM. A baseline PSA level >10 ng/mL and a high PSA velocity independently predicted shorter time to first BM. Patients with a PSADT <6 months were those most likely to rapidly develop BM. More recently, Smith et al. have reported the natural history of placebo group of another M0 CRCP study conducted with the endothelin receptor A inhibitor, atrasentan [21]. Patients included in the atrasentan trial had a shorter PSADT (: months) than those in the zoledronic acid trial (: months) [20, 21]. In multivariate analyses, a baseline PSA ≥13.1 ng/mL was associated with shorter time to the first BM and BM-free survival.

In conclusion, all these data pinpoint at a high Gleason’s score, a high PSA, and a short PSADT being important to decide which patients should receive bone investigation to search for BM. Taken together, these data should help the clinician schedule follow-up examination.

2.1. () Bone Scintigraphy

Today, standard diagnostic algorithms of bone metastases still rely primarily on methylene diphosphonate (MDP) bone scintigraphy (BS). BS has been used for decades as the first-line modality for the screening of PCa bone metastases [22, 23]. -MDP is a nonspecific marker of osteoblastic activity. Studies using microautoradiography have demonstrated that -MDP localizes along mineralization fronts. The isotope is occasionally found in the substance of the osteoid but is absent from the cytoplasm and nuclei of osteoblasts and osteocytes [24]. -MDP accumulates in response not only to tumour but also to degenerative joint disease, benign fractures, and inflammation [25–27]. Therefore, BS detects bone metastases at an advanced stage of tumour infiltration, when osteoblastic reaction to metastatic cell deposit has occurred [28]. Sensitivities reported in the literature range between 62 and 89% and, therefore, could be considered acceptable [28]. BS’s main problem is its low specificity so that its diagnostic effectiveness has been widely questioned in the literature [29, 30]. Indeed, in many cases, regions of increased uptake cannot be definitively characterized negative or positive for malignancy. Routinely, it will end up in reading characterized as “equivocal,” “possible,” “suspicious,” “likely,” “highly suspicious,” “almost certain,” a series of definition encompassing all cases in which imaging findings could not be categorized confidently as metastatic or benign, regardless of the level of incertitude. Usually equivocal BS uptakes will be characterized by targeted X-ray to distinguish benign (fracture, Paget’s, degenerative joint disease, etc.) from malignant (metastatic) origin [31]. This association is imperfect, and the diagnosis may remain equivocal after this workup. In clinical practice, a normal bone radiograph associated with an abnormal scan is highly suggestive of BM [32]. But this conclusion invokes conventional wisdom or suggestion more than it relies on a robust approach. Conventional wisdom may be acceptable in clinical practice to assess a fractures risk; it becomes questionable when it comes to definitive decisions in oncology [33].

2.2. SPECT and SPECT CT

Noteworthy, guidelines do not provide technical recommendations for BS. In many centres BS is limited to anterior and posterior planar images. Standard planar BS can be improved by single-photon emission computerized tomography (SPECT) on selected areas such as the lower thoracic and lumbar spine region or even on the entire axial skeleton (Whole-body SPECT) [33–35]. In cancer patients in general and in PCa in particular, SPECT enhances both sensitivity and specificity for the detection of BM [34–36]. Even-Sapir et al. have compared BM detection by BS, SPECT, ¹⁸F-Fluoride PET, and ¹⁸F-Fluoride PET/CT in 44 patients with high-risk PCa, including 23 (52%) with BM [36]. The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of planar BS were 70%, 57%, 64%, and 55%, respectively, and of SPECT were 92%, 82%, 86%, and 90%, respectively. SPECT identified 62% of the lesions overlooked by planar BS. The major advantage of SPECT is that the added benefit of tomographic imaging required few extra radiation dose and only slight added cost, since most modern cameras now offer the possibility of whole-body SPECT [33]. Nozaki et al. have assessed the value of SPECT in the detection of PCa BM in the lumbar vertebrae in 39 patients, all of them having increased uptake on BS [37]. Definitive diagnosis of BM was established by MRI. Sensitivity, specificity, PPV, and NPV of bone SPECT were 95.9%, 73.1%, 72.3%, and 96.1%, respectively. Helyar et al. have investigated the additional value of SPECT/CT over Tc-99m BS and SPECT on 50 lesions detected by BS in 40 patients [38]. On reporting the planar study and SPECT scans, reviewers rated 61% of lesions as equivocal. On reporting the SPECT/CT scans, only 8% of lesions were rated as equivocal, 24% were rated as malignant, and 68% as benign.

As a conclusion, SPECT and SPECT/CT provide better accuracy than Tc99m BS in differential diagnosis of lumbar BM. Because whole-body SPECT is time-consuming and not widely available, it is not yet recognized as the “optimal state-of-the art” screening technique, although it is available on most standard BS machine and can be performed at minimal cost increased.

2.3. Metabolic Imaging, PET, and PET/CT

Tumour detection, using positron emission tomography (PET) and PET/CT, has emerged as a standard imaging techniques in oncology, since PET/CT has demonstrated higher sensitivity for the early detection of metastases, including BM, in various malignancies [39–41]. Unfortunately, the most widely used metabolic marker, ¹⁸F-FDG PET, has little or even no interest in PCa patients. Ghanem et al. have demonstrated that ¹⁸F-FDG-PET alone or using PET-CT image fusion, is less sensitive than MRI in the detection of bone metastases [42]. ¹⁸F-(Sodium) Fluoride is a high affinity bone-seeking agent usually considered as a promising substitute for -MDP. In the aforementioned series of 44 high-risk PCa, Even-Sapir et al. has reported sensitivity, specificity, PPV, and NPV of, respectively, 100%, 62%, 74%, and 100% for ¹⁸F-Fluoride PET and of 100% for all parameters for ¹⁸F-Fluoride PET/CT [36]. Of the 156 bone lesions detected by ¹⁸F-Fluoride, 81 lesions (52%), including 34 metastases, were overlooked with normal appearance on planar BS. In contrast, the other aforementioned trial by Ghanem et al. failed to show superiority of ¹⁸F-Fluoride PET over MRI in BM detection [42].

Future studies will focus on newer markers such as ¹¹C- or ¹⁸F-labeled choline and acetate, ¹¹C-methionine, and ¹⁸F-fluorodihydrotestosterone [26, 36, 40–44]. Kotzerke et al. have compared ¹¹C-acetate and ¹¹C-choline uptake in 12 PCa patients and concluded that the ability of both radiotracers to detect known BM was identical, although interindividual variation was high [45]. Yu et al. have tested the feasibility of ¹¹C-acetate and ¹⁸F-FDG for the detection and measurement of response to therapy in 8 patients detected with ≥3 BM diagnosed by BS. ¹¹C-acetate PET detected BM in all 8 patients, whereas ¹⁸F-FDG PET detected lesions in 6 of the 7 imaged patients [46]. Beheshti et al. have prospectively compared the potential value of ¹⁸F-fluorocholine and ¹⁸F-fluoride PET/CT for BM detection in 38 PCa patients [47]. In case of discrepant results, follow-up was used as validator. Overall, 321 lesions were evaluated in this study. Sixteen malignant osteoblastic lesions were negative with both ¹⁸F-fluorocholine and ¹⁸F-fluoride PET/CT. The sensitivity, specificity, and accuracy of PET/CT for PCa BM detection was 81%, 93%, and 86% for ¹⁸F-fluoride and 74% (), 99% (), and 85% for ¹⁸F-fluorocholine PET/CT, respectively. In a later study on 70 patients, Beheshti et al. have calculated that the sensitivity, specificity, and accuracy of ¹⁸F-fluorcholine PET/CT in detecting PCa BM was 79%, 97%, and 84%, respectively [48]. Eschmann et al. have published a small study on 42 patients aiming to compare the diagnostic accuracy of ¹¹C-Choline PET/CT and whole-body WB-MRI [49]. After validation by histology, follow-up, or consensus reading, 88/103 detected lesions were considered as malignant including 44 BMs. Sensitivity, specificity, and accuracy for ¹¹C-choline PET/CT were 96.6%, 76.5%, and 93.3%, respectively, and for WB-MRI 78.4%, 94.1%, and 81.0%, respectively. Interestingly, however; whole-body MRI was performed without diffusion reading, thus, lowering its performance.

3. CT Scanner

CT scanner imaging is central in the diagnosis of musculoskeletal disorders. In bone malignancies, it is not used as a screening test but as a second-line imaging technique to clear-up abnormal BS uptakes remaining unexplained after standard X-ray or to image suspicion of neurological disorders.

Recently, the development of multidetector spiral technology has reawakened the potential interest of CT for early detection of BMs. In a recent analysis, Groves et al. have investigated the value of this technique in BM assessment [50]. They have compared BS and bone imaging from the cranium vertex to the knee by 16-slices CT in 43 patients with known malignancy. BS detected BM in 14/43 and CT in 13/43 patients. There were, however, several discordances. Based on their preliminary analysis, Groves et al. concluded that CT with its present performance is unlikely to replace BS for BM screening. In addition, the total accumulated radiation dose required by whole spine CT precludes the systematic use of this technique for the determination of therapeutic response in clinical trials.

4. Magnetic Resonance Imaging (MRI) of the Skeleton

MRI is highly sensitive for detecting BM in cancer patients [25, 31, 51–53]. Its superiority over BS has been repeatedly demonstrated [54–56]. It has been used as a “gold standard” to evaluate PET for detecting BM and more recently to quantify PCa metastases and measure tumour response to therapy [30, 57]. However, the use of MRI in first line is often presented as “not feasible” putting forward its limited availability, costs, or limitations of published series validating the method [30].

MRI characteristics of malignant involvement of the bone marrow are well documented [25, 36, 57–59]. The different MRI patterns of bone marrow involvement in neoplastic disease have been precisely described, so that discriminating metastatic lesions from benign marrow abnormalities such as marrow hyperplasia induced by chemotherapy can easily be made by trained radiologists. MRI appearance of the spinal and pelvi-femoral can be categorized into simple well-defined categories [58, 60]: normal appearance, focal metastatic lesions (focal marrow replacement pattern), which are nodular areas that can be measured, and diffuse marrow infiltration (Figure 1).

(a)

(b)

(c)

(d)

Figure 1: Example of a 55 years old patient diagnosed with high-risk localized disease. bone scan shows an area of uptake in the body of the 3rd lumbar vertebra ((a) and (b)). Confirmatory X-ray is read as normal (c) although MRI of the axial skeleton (T1 sequence, (d)) shows a large focal area of malignant replacement of the bone marrow.

The superiority of MRI lies in its ability to detect early tumour cells seeding into the hematopoietic compartment, leading to replacement of the normal hematopoietic marrow and of its fat cells. This technique, thus, identifies BM at an early stage, before host reaction of the osteoblasts becomes visible on BS and X-ray, therefore, increasing sensitivity [25, 28]. Already in 1993, Turner et al. reported on using MRI in 18 PCa patients to resolve conflicting evidence of BM found on bone scans and X-ray [61]. MRI ruled out metastatic disease in 2 of the 8 positive BS and revealed BM in 5 negative BS. All 5 equivocal BS demonstrated no osseous lesions on MRI. In addition, in 6 patients with evidence of BM serial MRI scans following ADT demonstrated radiographic and clinical improvement. In 2000, Walker et al. evaluated whole-body STIR-MRI to detect metastases to liver, brain, and bone as a single examination in women with breast cancer [62]. BM were identified in 11/17 patients, with correlation between findings at whole-body MRI and scintigraphy in 15/17 patients. Daldrup-Link et al. have compared the diagnostic accuracy of whole-body MRI, Tc-99m BS, and FDG-PET for the detection of bone metastases in 39 children aged 2 to 19 years old with various malignancies [28]. Sensitivities for the detection of bone metastases were 90% for FDG-PET, 82% for MRI, and 71% for skeletal scintigraphy. But FDG-PET also produced most false-positive lesions. More recently, our group has evaluated the diagnostic performance and impact on therapy of one-step MRI of the axial skeleton (MRIas) for detecting BM in 66 patients with high-risk PCa [63]. MRIas has been compared to a routine workup based on BS completed with targeted X-ray in cases of equivocal BS findings and with MRI “on request” (MRIor) in case of inconclusive BS/X-ray findings. Sensitivities were 46% for Tc-99m BS alone, 63% for BS/X-ray, 83% for BS/X-rays/MRI, and 100% for MRIas. Corresponding specificities were 32%, 64%, 100%, and 88%. MRIas was significantly more sensitive than any other approach (, McNemar). MRIas correctly identified metastases in 7/23 (30%) patients considered negative, and 8/17 (47%) considered equivocal by other strategies, which resulted in altering the initially planned therapy. This increased sensitivity has clearly an added value in routine practice, both in newly diagnosed PCa, to avoid unnecessary radical therapy, and later on in the disease to enable early initiation of treatment with the hope to prevent or delay the complications of metastases.

Are these results sufficient to definitively state that MRI will replace BS as initial and sole imaging modality for staging all PCa patients? The answer is no. The access to MRI technology still needs to be improved and the available MRI machine to be increased. Indeed, it is not often acceptable to delay treatment in high-risk patients waiting to rule out BM. In addition, many authors still advocate the use of BS on the assumption that MRI would be too costy [25, 26, 39]. These data, however, demonstrate that MRI surpasses the current imaging strategy used for bone staging in a high-risk patient population. There is place for large multicentric studies in well-defined groups of patients to assess and confirm the clinical efficacy of MRI as the initial tool for bone staging in PCa.

Further development will focus on whole-body MRI (WBMRI). Hardware and software advances have enabled the acquisition of WBMRI, including conventional sequence (T1, STIR) images covering the entire skeleton, and more recently diffusion-weighted images (DWIs), which facilitates the detection of BM, especially in skeletal areas that are difficult to evaluate on conventional sequences, such as ribs [64–68]. In addition, this allows envisioning an all-in-one metastatic workup (visceral and osseous). Eschmann et al. have compared the diagnostic accuracy of ¹¹C-Choline PET/CT to whole-body MRI for the staging workup of PCa in 42 patients [44]. Sensitivity, specificity, and accuracy for ¹¹C-Choline PET/CT were 96.6%, 76.5%, and 93.3%, respectively, and for MRI 78.4%, 94.1%, and 81.0%. Interestingly, 3 BMs had initially been missed by ¹¹C-Choline PET/CT and were found retrospectively. The author concluded that strength of MRI is excellent image quality providing detailed anatomical information whereas the advantage of Choline PET/CT is high image contrast of pathological foci (Figure 2).

(a)

(b)

(c)

Figure 2: Consecutive series of three bone scans (BS) and MRI acquired three months apart on a patient included in a clinical trial designed for M0 CRPC. Only the third BS is adjudicated as positive by the central review although he was already progressive on MRI at the second metastatic workup.

5. Conclusion

Correct diagnosis of BM has emerged as major challenge for those who are developing new therapeutic strategies, including those who advocate aggressive local treatment of high-risk localized and locally advanced disease. Tc-99m BS may not be over, but the time when patients would be treated on suspicion rather than on robust evidences is passed. Many technologies including metabolic imaging by PET and MRI are indeed rapidly gaining interest in the everyday management of PCa patients. As it is for modern treatments, the diagnosis strategies will be multidisciplinary by nature and involve crossfertilization between nuclearists, urologists, and radiation oncologists.

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