Background
After melanoma has grown radially and superficially in the epidermis and on mucosal surfaces, it can metastasize to any organ or tissue such as the lungs and bone, where melanoma metastases are common [ 1 , 2 ]. Melanoma most frequently occurs in fair-skinned Caucasian individuals older than 40 years who have numerous moles [ 3 ]. In most countries, the incidence of melanoma has been increasing recently, with annual incidences reaching 3–7% among fair-skinned populations [ 3 , 4 ]. In the United States, the incidence of melanoma has increased more than that of any other cancer [ 5 ]. An estimated 60,000 new cases of melanoma are diagnosed each year with more than 8,000 annual deaths in the United States; about one in 75 persons will develop this cancer in their lifetime [ 5 , 6 ]. After osseous metastases occur, the patient's survival is usually short-term [ 7 , 8 ]. In addition, bone metastases of melanoma predispose patients to pathological fractures of axial and appendicular skeletons, bone marrow failure and neurological deficits. These complications substantially increase their pain and result in a poor quality of life [ 6 , 7 , 9 ].
Despite its high mortality rate, melanoma is not well studied in Asians, with only a limited number of reported cases [ 10 ]. Acral-lentiginous melanoma (ALM) is the most common subtype of melanoma in Asian populations including Taiwanese [ 11 ]. The diagnosis of this subtype is often delayed [ 11 , 12 ]. We conducted this retrospective chart review in two national medical centers in Taiwan to improve our understanding of the incidence, treatment and outcomes of osseous metastases of melanoma in Asia.
Methods
The hospital records of the National Taiwan University Hospital and the National Cheng Kung University Hospital from January 1983 to December 2006 were surveyed to identify cases of malignant melanoma. We reviewed the charts, medical records, surgical notes, radiological images and pathology records of patients diagnosed with osseous metastases. A total of 11 patients underwent surgical intervention for osseous metastases. Surgical indications in our series included an intractable skin ulcer, mechanical instability due to pathologic fractures, neurological deterioration due to neural compression by metastases, pain unresponsive to nonoperative measures such as radiation and the need for biopsy material for histopathological verification of the diagnosis. The choice of surgical procedure depended on the patients' individual clinical situation, location of the tumor, medical comorbidities and overall prognosis. Surgical treatments included wide excision (four patients), posterior laminectomy for decompression and posterior instrumentation (one patient), below-the-knee amputation (two patients), above-the-knee amputation (one patient), ray amputation (one patient) and intralesional excision plus internal fixation with cement augmentation (two patients) (Tables 1 & 2 ).
Table 1
Clinical, pathological and radiographic data
L, left; R, right; NA, not applicable.
| Patient age (years) | Sex | Primary tumor | Clinical size (cm) | Microscopic classification | Depth (Clark level) | Osseous metastases and complications | Radiographic manifestation | Other metastases | Synchronous tumor |
| 45 | F | Scalp | 1.5 × 1.0 | Malignant melanoma | V | Frontoparietal skull, multiple cervico- thoracolumbar spine (compression fractures of thoracolumbar spine), bone marrow infiltration | Multiple spinal metastases with bony destruction and cord compression | Liver, bone marrow | None |
| 72 | M | L anterior chest wall | 1.5 × 1.5 | Malignant melanoma | IV | 5 th lumbar vertebra, R acetabulum | L5 compression fracture with bony destruction | Lung, Lymph nodes | None |
| 64 | M | R sole | 1.5 × 1.5 | acral lentiginous melanoma | V | L skull base, midcervical, mid thoracolumbar spine | Multiple bony destruction, permeative osteolytic skull lesion | Lung | None |
| 79 | M | L sole | 1.0 × 1.0 | acral lentiginous melanoma | III | R scapular, thoracolumbar spine (L2 compression fracture), L sacroiliac joint, pelvic rim and bilateral femurs | Multiple bony destruction with periosteal reaction and dystrophic calcifications | Lymph nodes | Lung cancer |
| 62 | M | L sole | 2.3 × 2.1 | acral lentiginous melanoma | IV | L ninth rib, thoracolumbar spine | Sclerotic lesions in thoracolumbar spine | Liver | Thyroid papillary carcinoma, renal cell carcinoma |
| 67 | F | R heel | 3.5 × 1.0 | acral lentiginous melanoma | V | R femoral pathological fracture, R knee, L mid femur, R scapular, rib | Permeative osteolytic change | Lymph node, lung, liver | None |
| 70 | F | L lower leg | 1.0 × 1.0 | Malignant melanoma | IV | L femoral subtrochanteric fracture | Osteolytic bony destruction | Liver, spleen | Renal cell carcinoma |
| 67 | M | R foot | 7.0 × 6.0 | acral lentiginous melanoma | V | R tibia, proximal femur | Increased tracer uptake over R proximal femur | Lung, lymph nodes | None |
| 39 | F | L subungual | 1.1 × 0.9 | acral lentiginous melanoma | V | Skull, thoracolumbar spine, thoracic cage, pelvic rim | Osteolytic bony destruction | Liver, lung, lymph nodes, brain | None |
| 74 | F | L lower limb | 1.0 × 0.8 | Malignant melanoma | V | L midtibial pathological fracture, sacroiliac joint | Osteolytic bony destruction | Lung | Cervical cancer |
| 51 | M | Unknown | NA | Malignant melanoma | NA | R navicular pathological fracture | Comminuted fracture | Liver, lung, lymph nodes | None |
Table 2
Surgical treatments and outcomes
BCG, Bacillus Calmette-Guérin; ORIF, open reduction and internal fixation. *Diagnosed with fine-needle biopsy.
| Patient age (years) | Sex | Surgical treatment | Therapy | Time (months) | ||
| Diagnosis to bone metastases | Diagnosis to death | Bone metastases to death | ||||
| 45 | F | Wide excision | Radiotherapy | 1.77 | 7.44 | 5.67 |
| 72 | M | Posterior laminectomy for decompression, vertebroplasty with PMMA cement, posterior instrumentation | Radiotherapy, chemotherapy, IL-2 | 16 | 17.27 | 1.27 |
| 64 | M | Below-knee amputation | Radiotherapy, BCG, chemotherapy | 14.00 | 18.27 | 4.27 |
| 79 | M | Wide excision, transposition flap, lymph node dissection | Radiotherapy | 15.90 | 21.87 | 5.97 |
| 62 | M | Wide excision | None | 0.70 | 16.40 | 15.70 |
| 67 | F | Wide excision, groin dissection, ORIF with Küntscher nailing and cement augmentation | Radiotherapy | 37.80 | 38.97 | 1.17 |
| 70 | F | ORIF with CHS and bone cement augmentation | Chemotherapy | 8.87 | 13.67 | 4.80 |
| 67 | M | Below-knee amputation | Chemotherapy | 3.57 | 7.77 | 4.20 |
| 39 | F | Ray amputation | Interferon and tamoxifen | 6.20 | 7.30 | 1.10 |
| 74 | F | Above-knee amputation | Chemotherapy | 2.43 | 10.76 | 8.33 |
| 51 | M | None* | Chemotherapy | 0.00 | 9.87 | 9.87 |
All patients had histopathological proof of bone metastases. Table 1 lists the locations of their osseous metastases, and Table 2 shows the operations performed. Adjuvant therapies after surgical treatment varied depending on the patient's age, the sites and number of metastases, disease progression, the patient's overall medical condition and the patient's intentions for further management. Table 2 lists the adjuvant therapies including chemotherapy with or without tamoxifen (six patients), radiotherapy (five patients) and immunotherapy with Bacillus Calmette-Guérin (BCG), interferon alpha or IL-2 (three patients).
We compiled data on the age and sex distribution of these patients, their primary lesions, clinical sizes, microscopic classification with depth of invasion (Clark level), bone metastases and complications, radiographic manifestations, other metastases, synchronous tumors, usages of analgesic medications, interval from initial diagnosis to occurrence of osseous metastases, interval from diagnosis to death and survival after the occurrence of bone metastases.
Results
The 11 patients (six men and five women) ranged in age from 39–79 years (mean 61.8 years) at the time of diagnosis of melanoma. Six patients had the ALM subtype. The metastases of the melanoma were correlated with the severity of the primary cutaneous lesions (Table 1 ). One patient who did not possess a primary cutaneous lesion had a melanoma of the navicular bone (Fig. 1 ), with an initial presentation of dull pain in the right midfoot that lasted six months. Most patients had pain and weakness in the involved regions. Osteolytic bone lesions were radiographically detected in 10 patients. Osteosclerosis of the thoracolumbar spine was also found (Table 1 ). Most lesions in the long bones were multiple, eccentric and oval, with clinically significant cortical erosion (Fig. 2 ). Two patients had permeated osteolytic lesions; such a pattern was characterized by numerous, tiny radiolucencies between the trabeculae of the residual bones. Periosteal reactions and dystrophic calcifications were found in one patient with multiple sites of bony destruction in the ileum and sacrum.


The osseous metastases were in the axial skeleton in eight patients, six of whom had spinal metastases. Two patients had osseous metastases to the cervical spine, four to the thoracic spine, six to the lumbar spine, two to the scapula, three to the ribs, four to the pelvis and three to the skull. Compression fractures with epidural compression occurred in three patients with spinal metastases. One patient received posterior laminectomy for decompression and posterior instrumentation because of progressive muscle power weakness of right lower limb (Fig. 3 ). The other two patients received irradiation instead of laminectomy because of their poor medical condition. The appendicular skeletons were involved in six patients, with bone metastases to the femur in four patients, to the tibia in two and to the navicular bone in one. Four patients had pathological fractures including one each in the subtrochanteric region of the femur, the midshaft of the femur, the midshaft of the tibia, and the navicular bone. Two patients with femoral fractures were successfully treated with intralesional excision and internal fixation with compression hip screws and Küntscher nailing augmented with cement fixation. The patient with the tibia fracture was treated with above-the-knee amputation because of multiple skin lesions and ulcers. The patient with the navicular fracture underwent conservative treatment with chemotherapy alone because of the coexistence of several distant metastases.

All 11 patients had metastases other than osseous metastases from their melanomas. Four patients had a synchronous malignancy including one lung cancer, one thyroid papillary carcinoma, two renal cell carcinomas and one cervical cancer. The synchronous malignancy usually occurred first and then co-existed with the melanoma (Table 1 ). The use of analgesic medications was decreased after the operations, and most patients reported significant alleviation of pain after surgical intervention. Dramatic pain relief was achieved in three patients with pathological fractures who received internal fixation.
The interval from the diagnosis of melanoma to the detection of osseous metastases varied from 0–37.8 months (mean 9.75 months) (Table 2 ). The prognosis of patients with melanoma and osseous metastases was generally poor. After osseous metastasis had been diagnosed, the mean survival was only 5.67 months (Table 2 ). We found no significant differences in prognosis between the axial and appendicular osseous metastases (mean survival 5.44 and5.72 months, respectively). The average survival time of males (6.88 months) was longer than females (4.21 months). There was no obvious correlation between age and survival. The survival time of six patients with the ALM subtype averaged 5.40 months, which was only slightly shorter than that of the other five patients (5.99 months). Even in patients with a synchronous tumor, the prognosis did not deteriorate. There were no distinct differences in survival among patients receiving chemotherapy, radiotherapy and/or immunotherapy.
Discussion
Osseous metastases of malignant melanoma are rare among Asians [ 10 , 11 ]. Six of our patients had ALM, which has the predilection to occur on the palms, soles and subungual nail beds. Such a distribution usually delays diagnosis and patients accordingly have worsened prognoses. Indeed, presently we found that the survival time of ALM patients (5.4 months) was slightly shorter than that of other subtypes (5.99 months). Osseous metastases from malignant melanoma usually occur in patients with relatively advanced primary lesions and multiple bony lesions at the time of diagnosis [ 12 - 14 ], as shown in the histopathological findings of our series with a Clark level of III, IV or V. Until now, there has not been evidence to support the conclusion that the surgical treatment contributes to the survival of metastatic melanoma patients [ 1 , 8 , 15 ]. Therefore, management is directed towards the relief of symptoms and the maintenance of a good quality of life in patients with osseous metastases of melanoma.
Primary melanoma of the bone has been rarely reported in the literature [ 16 ]. In isolated appendicular osseous metastases of melanoma, survival may be prolonged after aggressive surgical resection of the metastatic bony focus [ 17 ]. Common sites for osseous metastases of melanoma include the vertebrae, skull, pelvis, thoracic cage and proximal parts of the femur [ 18 - 22 ]. Osseous metastases generally occur in the axial skeleton; reflecting this, there were eight cases among the 11 patients presently studied. Spinal metastases may result in vertebral compression fractures, epidural or cord compression (Fig. 3 ) [ 6 , 7 , 9 ]. For patients with neurological deficits such as paraplegia or cauda equina syndrome, the neurological decompression to relieve symptoms and recover functions should be considered as health permits. Moreover, simultaneous instrumentation or vertebroplasty with polymethylmethacrylate (PMMA) cement can provide spinal stability to alleviate back pain in patients with pathological vertebral fractures. Intralesional excision or curettage of osseous metastatic melanoma lesions together with open reduction and internal fixation with PMMA cement augmentation might be an effective strategy for the surgical management of pathological fractures in the appendicular skeleton. Two patients in our series received such an intervention and obtained significant pain relief. Metastatic lesions within the long bones are usually multiple, osteolytic, eccentric and oval, and are associated with clinically significant cortical erosion [ 15 ]; this was evident in our cases (Fig. 2 ). Lesions usually appear first in the medullary cavity, and then spread to destroy the bone trabeculae, extend to the cortex and finally lead to pathological fractures (Fig. 2 ) [ 14 , 15 ]. However, such radiographic features in our patients were similar to those in other cancers.
Because melanoma with osseous metastases is heterogeneous in its biology, treatment plans must be highly individualized. Surgical management is generally followed by adjuvant therapies such as chemotherapy, radiation therapy or immunotherapy. Single or combined chemotherapy does not improve survival in advanced-stage disease, as evident presently and reported previously [ 1 , 8 , 10 ]. External beam radiotherapy is effective in preventing local recurrence of malignant melanoma and can provide palliative treatment for metastatic melanoma [ 23 ]. In our cases, irradiation of the affected areas relieved pain considerably for several months without affecting the growth of tumor, similar to previous reports [ 10 , 15 ]. Significant proportions of melanoma cells express estrogen receptors, which leds to a supportive role for tamoxifen in the treatment of metastatic melanoma [ 8 ]. Given their immunologic effects, low-dose interleukin-2, granulocyte-monocyte colony stimulating factor and interferon alpha-2b produce durable remissions in patients with metastatic melanoma, and they have been used as postoperative adjuvant therapies [ 24 ]. Therefore, the goal of surgical treatment for osseous metastases of melanoma should be directed towards the palliation of symptoms, particularly if the anticipated relief of related symptoms exceeds the potential adverse effects of the therapy. Symptomatic metastases in weight-bearing bones require special consideration. For large lesions or cortical destruction, prophylactic stabilization and irradiation are preferred. Alternatively, the lesion may be treated with radiation alone and patients are monitored for evidence of pathologic fractures. Unless the risk of surgery is high or the expected life span is short, pathologic fractures of weight-bearing bones should be stabilized to maximize the quality of life and decrease hospital costs. Furthermore, surgical resection can produce an immediate decrease in tumor burden at a reasonable expenditure [ 25 ].
Bisphosphonates such as pamidronate and zoledronic acid have been used for palliative therapy in patients with osteolytic lesions metastasized from multiple myeloma or metastatic breast cancer. The aim is to prevent or delay the onset of skeletal complications [ 26 , 27 ]. Moreover, bisphosphonates can reduce bone pain in patients with bony metastases [ 28 ]. Zoledronic acid has demonstrated efficacy in the treatment of bone metastases in patients with prostate cancer, lung cancer or other solid tumors [ 26 ]. The bisphosphonate pamidronate induces apoptosis in human melanoma cells in vitro [ 29 ]. In an in vivo animal study, incadronate inhibited bone resorption by increasing numbers of apoptotic osteoclasts [ 30 ]. In addition, incadronate can substantially suppress the growth of human melanoma cells, increase the numbers of apoptosis of tumor cells and decrease the tumor-associated blood-vessel density [ 30 ]. Therefore, bisphosphonate therapy might be an alternative to surgery or an adjuvant treatment for osseous metastatic melanoma in the future.
The prognosis of patients with melanoma is related to the extent and the stage of the tumor. Early detection and management of melanoma are the key factors to improve overall survival. The prognosis is poor after melanoma progresses and undergoes osseous metastasis [ 2 , 31 ]. Osseous metastases of melanoma may predispose individuals to pathologic fractures in the axial or appendicular bones or to bone marrow failure and may substantially influence the quality of life and survival expectancy of patients. For Asian patients with melanoma, the mean survival after the diagnosis of osseous metastases was 5.67 months in our series, which was longer than 4.7 months reported in Caucasian populations [ 2 , 7 , 31 ].
Conclusion
In conclusion, osseous metastases of melanoma are rare in Taiwan and the prognoses of patients are as poor as with Caucasians. Surgical intervention is effective in providing pain relief, especially for those with pathological fracture and those receiving internal fixation. Due to the high morbidity and poor survival, surgical treatment should be directed towards pain relief and the prevention of skeletal debilitation in order to maintain a patient's quality of life.
Competing interests
The author(s) declare that they have no competing interests.
Authors' contributions
KYH conceived the study, participated in its design, collected the data, and drafting of the manuscript.
CRW did the data analysis, and revised the manuscript.
RSY assisted in the creation and design of the study, collected the data, advised and assisted drafting of the manuscript.
All authors read and approved the final manuscript.
Pre-publication history
The pre-publication history for this paper can be accessed here:
Atkins MB The treatment of metastatic melanoma with chemotherapy and biologics Curr Opin Oncol 1997 9 205 213 9161801 10.1097/00001622-199703000-00016
Barth A Wanek LA Morton DL Prognostic factors in 1,521 melanoma patients with distant metastases J Am Coll Surg 1995 181 193 201 7670677
Brochez L Naeyaert JM Understanding the trends in melanoma incidence and mortality: where do we stand? Eur J Dermatol 2000 10 71 75 10694303
Hall HI Miller DR Rogers JD Bewerse B Update on the incidence and mortality from melanoma in the United States J Am Acad Dermatol 1999 40 35 42 9922010 10.1016/S0190-9622(99)70562-1
Jemal A Siegel R Samuels A Ward E Murray T Xu J Thun MJ Cancer statistics, 2007 CA Cancer J Clin 2007 57 43 66 17237035 10.3322/canjclin.57.1.43
Chatelain D de Pinieux G Guillemette J Forest M Bone metastasis of a clear cell tumor Ann Pathol 1999 19 139 140 10349481
Motzkin NE Rock MG Wold LE Beabout JW Malignant melanoma metastatic to bone Orthopedics 1992 15 657 659 1589358 10.3928/0147-7447-19920501-18
O'Day SJ Kim CJ Reintgen DS Metastatic melanoma: chemotherapy to biochemotherapy Cancer Control 2002 9 31 38 11907464 10.1177/107327480200900105
Kato N Kimura K Sugawara H Aoyagi S Kondo K Yamashiro K Pedunculated melanoma with pulmonary and bony metastases J Dermatol 2000 27 769 773 11211792 10.1111/j.1346-8138.2000.tb02279.x
Lange JR Sharfman WH Alani RM Balch CM melanoma Clinical Oncology 2004 3 Churchill Livingstone 1561 1583
Chen YJ Wu CY Chen JT Shen JL Chen CC Wang HC Clincopathologic analysis of malignant melanoma in Taiwan J Am Acad Dermatol 1999 41 945 9 10570378 10.1016/S0190-9622(99)70251-3
O'Connell ME Powell BW O'Connell JM Harmer CL Spontaneous regression of multiple bone metastases in malignant melanoma Br J Radiol 1989 62 1095 1100 2605458 10.1259/0007-1285-62-744-1095
Potepan P Spagnoli I Danesini GM Laffranchi A Gadda D Mascheroni L Guzzon A The radiodiagnosis of bone metastases from melanoma Radiol Med 1994 87 741 746 8041925
Salwen WA Krementz ET Campeau RJ Bone and liver imaging in regionally advanced melanoma J Surg Oncol 1989 42 225 228 2593665 10.1002/jso.2930420405
Brountzos EN Panagiotou IE Bafaloukos D Kelekis DA Bone metastases from malignant melanoma: a retrospective review and analysis of 28 cases Radiol Oncol 2001 35 209 214
Yokoyama R Mukai K Hirota T Beppu Y Fukuma H Primary malignant melanoma (clear cell sarcoma) of bone: report of a case arising in the ulna Cancer 1996 77 2471 2475 8640695 10.1002/(SICI)1097-0142(19960615)77:12<2471::AID-CNCR9>3.0.CO;2-P
DeBoer DK Schwartz HS Thelman S Reynolds VH Heterogeneous survival rates for isolated skeletal metastases from melanoma Clin Orthop 1996 323 277 283 8625592 10.1097/00003086-199602000-00038
Downey MS Lamm BM Metastatic malignant melanoma to the foot and ankle: a review of the literature and case report J Foot Ankle Surg 2000 39 392 401 11131477 10.1016/s1067-2516(00)80076-9
Jaeger HJ Kruegener GH Donovan AG Patellar metastasis from a malignant melanoma Int Orthop 1992 16 282 284 1428344 10.1007/BF00182712
Laredo J Morris DJ Thurer RL Metastatic melanoma to the manubrium sternum Eur J Cardiothorac Surg 1998 14 629 630 9879877 10.1016/S1010-7940(98)00248-6
Tamburri SA Boberg JS Skeletally metastatic malignant melanoma of the foot J Foot Ankle Surg 1994 33 368 372 7951189
Tandogan RN Aydogan U Demirhan B Arican A Yuceturk A Intra-articular metastatic melanoma of the right knee Arthroscopy 1999 15 98 102 10024041 10.1053/ar.1999.v15.0150091
Seegenschmiedt MH Keilholz L Altendorf-Hofmann A Urban A Schell H Hohenberger W Sauer R Palliative radiotherapy for recurrent and metastatic malignant melanoma: prognostic factors for tumor response and long-term outcome: a 20-year experience Int J Radiat Oncol Biol Phys 1999 44 607 18 10348291 10.1016/S0360-3016(99)00066-8
de Gast GC Batchelor D Kersten MJ Vyth-Dreese FA Sein J van de Kasteele WF Nooijen WJ Nieweg OE de Waal MA Boogerd W Temozolomide followed by combined immunotherapy with GM-CSF, low-dose IL2 and IFN alpha in patients with metastatic melanoma Br J Cancer 2003 88 175 180 12610499 10.1038/sj.bjc.6600717 PMC2377058
Young SE Martinez SR Essner R The role of surgery in treatment of stage IV melanoma J Surg Oncol 2006 94 344 51 16917867 10.1002/jso.20303
Berenson JR Recommendations for zoledronic acid treatment of patients with bone metastases Oncologist 2005 10 52 62 15632252 10.1634/theoncologist.10-1-52
Lipton A Theriault RL Hortobagyi GN Simeone J Knight RD Mellars K Reitsma DJ Heffernan M Seaman JJ Pamidronate prevents skeletal complications and is effective palliative treatment in women with breast carcinoma and osteolytic bone metastases: long term follow-up of two randomized, placebo-controlled trials Cancer 2000 88 1082 90 10699899 10.1002/(SICI)1097-0142(20000301)88:5<1082::AID-CNCR20>3.0.CO;2-Z
Wong R Wiffen PJ Bisphosphonates for the relief of pain secondary to bone metastases Cochrane Database Syst Rev 2002 CD002068 12076438 10.1002/14651858.CD002068 PMC6483200
Riebeling C Forsea AM Raisova M Orfanos CE Geilen CC The bisphosphonate pamidronate induces apoptosis in human melanoma cells in vitro Br J Cancer 2002 87 366 71 12177810 10.1038/sj.bjc.6600476 PMC2364216
Kitagawa Y Hiraga T Yura Y Yoneda T Suppression by incadronate of invasion and growth of A-375 human melanoma in mandible in nude mice Oncol Rep 2005 13 211 6 15643500
Reintgen DS Cox C Slingluff CJ Seigler HF Recurrent malignant melanoma: the identification of prognostic factors to predict survival Ann Plast Surg 1992 28 45 49 1642405 10.1097/00000637-199201000-00013