Preoperative embolization of primary bone tumors: A case control study

Abstract

AIM: To study the safety and effectiveness of preoperative embolization of primary bone tumors in relation to intraoperative blood loss, intraoperative blood transfusion volume and surgical time.

METHODS: Thirty-three patients underwent preoperative embolization of primary tumors of extremities, hip or vertebrae before resection and stabilization. The primary osseous tumors included giant cell tumors, aneurysmal bone cyst, osteoblastoma, chondroblastoma and chondrosarcoma. Twenty-six patients were included for the statistical analysis (embolization group) as they were operated within 0-48 h within preoperative embolization. A control group (non-embolization group, n = 28) with bone tumor having similar histological diagnosis and operated without embolization was retrieved from hospital record for statistical comparison.

RESULTS: The mean intraoperative blood loss was 1300 mL (250-2900 mL), the mean intraoperative blood transfusion was 700 mL (0-1400 mL) and the mean surgical time was 221 ± 76.7 min for embolization group (group I, n = 26). Non-embolization group (group II, n = 28), the mean intraoperative blood loss was 1800 mL (800-6000 mL), the mean intraoperative blood transfusion was 1400 mL (700-8400 mL) and the mean surgical time was 250 ± 69.7 min. On comparison, statistically significant (P < 0.001) difference was found between embolisation group and non-embolisation group for the amount of blood loss and requirement of blood transfusion. There was no statistical difference between the two groups for the surgical time. No patients developed any angiography or embolization related complications.

CONCLUSION: Preoperative embolization of bone tumors is a safe and effective adjunct to the surgical management of primary bone tumors that leads to reduction in intraoperative blood loss and blood transfusion volume.

Core tip: The current study shows that the preoperative embolisation of bone tumors performed 48 h prior to either limb salvage surgery or spinal stabilization leads to decrease in intraoperative blood loss and intraoperative blood transfusion volume. Therefore, would recommend that pre-operative embolisation is a safe procedure and should be used as part of the multi-disciplinary approach to the management of bone tumours in difficult anatomical locations especially those are known to be highly vascular.

INTRODUCTION

Bone tumors include primary and metastatic tumors[1]. They present in several ways, like bone destruction, expansion or, infiltration of periosteum. Bone tumors may be detected as an incidental finding or the patient may present with pain or loss of function, or with a pathological fracture[2]. Though there are many treatment modalities for bone tumors, surgical excision is the treatment of choice and may be coupled with other adjunctive therapies. However, several factors including tumor bulk, vascularity, vicinity to vital structures and potentially inaccessible location of the lesion may make the surgical treatment very difficult if not impossible[1].

Transarterial embolization (TAE) is an important adjuvant treatment modality and it may also be the primary and curative modality in some cases. It has been found that preoperative TAE is effective in both primary and metastatic bone tumors. Preoperative TAE reduces the tumor vascularity and intraoperative blood loss. It also reduces the need for blood transfusion and decreases the incidence of complications associated with surgery. TAE allows better definition of tissue planes at surgery leading to complete excision of the bone tumor, which ultimately leads to decrease tumor recurrence rates[2,3]. Refinement of angiographic techniques and advances in hardwares led to its use in preoperative embolization of both primary and secondary bone tumors[4,5]. The principle behind TAE of primary bone tumors is the precise targeting of the tumor feeding vessels and tumor capillary bed[6]. Non-target embolization and the occlusion of a non-target vessel leading to inadvertent necrosis of normal organ is the major concern during the procedure of trans arterial embolization of bone tumors, however, it can be prevented by careful review of the diagnostic angiograms obtained immediately before embolization and meticulous care during injection of the embolic agent into the selective vessels supplying the tumor.

The common types of bone tumor which usually require TAE are hypervascular in nature such as giant cell tumors (GCT), aneurysmal bone cysts (ABC), telengiactatic osteosarcomas, vertebral hemangiomas, arterio-venous malformations, osteoblastoma and vascular metastatic lesions especially from renal cell or thyroid[7-10].

Studies have documented the use of preoperative embolization as an effective intervention to reduce intraoperative blood loss, transfusion requirements and duration of surgery[11-13]. Many studies conducted worldwide have proved the efficacy of preoperative embolization but most of them were done on secondary bone tumors[14-22]. The aim of our study was to assess the effectiveness and safety of preoperative TAE of primary bone tumors in relation to the amount of intraoperative blood loss, requirement of amount of blood transfusion, surgical time and procedure related complications.

MATERIALS AND METHODS

The prospective study was performed with the approval of the local ethical committee, 33 patients with primary bone tumors were included in this prospective study from January 2012 to October 2013. Patients with primary bone tumor of extremities amenable for limb salvage surgery and resectable primary vertebral/sacral tumor were included in this study. After obtaining informed consent, preoperative embolization was done in all these 33 patients. Twenty-six patients (15 men, 11 women, age range 14-82 years), who had surgical resection within 0-48 h of TAE, were included for statistical analysis and remaining 7 patients were excluded from the statistical analysis as they were operated after 48 h of embolization.

Among 26 patients who underwent TAE, most common histological type of tumor was GCT comprising of 20 patients (77%) predominantly located in lower limb and the second most common type was ABC and chondrosarcoma in two patients (7%) each, rest each had osteoblastoma and chondroblastoma. Axial skeletal skeleton was affected in 5 patients.

For statistical analysis, 28 patients (16 men, 12 women, age range 10-60 years) with similar histological diagnosis were retrieved from hospital record who were operated in past without preoperative embolization (control group, n = 28). Among these 28 patients, the most common histological type was GCT comprising of 23 patients (82%) followed by ABC and osteoblastoma comprising of 2 patients (7%) each. There was no case of chondrosarcoma in the control group.

Patient demographics and histological diagnosis of tumors of both study group and control group were shown in Table 1.

Table 1.

Patient demography and baseline features of study group and control group

Study group (embolisation group, n = 26)		Control group (non-embolisation group, n = 28)
Characteristics	Number (%)	Characteristics	Number (%)
Age Group		Age Group
0-40 yr	18 (69%)	0-40 yr	18 (64%)
40-80 yr	7 (27%)	40-80 yr	10 (36%)
> 80 yr	1 (4%)
Sex		Sex
Male	15 (58%)	Male	16 (57%)
Female	11 (42%)	Female	12(43%)
Tumor histology		Tumor histology
Giant cell tumor	20 (78%)	Giant cell tumor	23 (82%)
Aneurysmal bone cyst	2 (7%)	Aneurysmal bone cyst	2 (7%)
Chondrosarcoma	2 (7%)	Chondrosarcoma	0 (0%)
Osteoblastoma	1 (4%)	Osteoblastoma	2 (7%)
Chondroblastoma	1 (4%)	Chondroblastoma	1 (4%)

Angiographic and embolization technique

Angiography and embolization was done using state of art, digital substraction angiography unit (Allura Xper FD 20, Philips Medical Systems, Best, The Netherlands), under local anesthesia by a single interventional radiologist with experience of more than 10 years. All the angiographies were performed through transfemoral route, most vessels could be catheterized selectively either with 5 French diagnostic catheter (Picard, Cook, Bloomington, IN, United States) or using coaxial microcatheter system 2.7 F (Progreat, Terumo, Tokyo, Japan) with 0.018 inch wire. Coaxial microcatheter system was used in 20 patients (77%) for superselective cannulation of smaller feeder arteries.

Thirteen embolisations were performed using combination of gelfoam (Gelfoam; Pfizer, New York, NY, United States) and polyvinyl alcohol (PVA, Cook, Bloomington, IN, United States) particles of size 300-500 and 550-700 microns[23], 12 embolisations were performed using only PVA particles and remaining one embolisation was using only gelfoam, following selective catheterisation of individual vessels supplying the tumor as ascertained on angiograms. The choice of embolising material was done on the basis of personal preference, catheter size, position of catheter tip and diameter of the feeding vessel. The embolisation endpoint was decided to be when all major vessels supplying the tumor were embolised and there was essentially near complete obliteration of tumor blush (Figure 1). Percentage of reduction of tumor blush was categorized into three groups as mentioned in previous studies, < 50% reduction, 50%-75% reduction and > 75% reduction[16,24]. More than > 75% reduction of tumor blush was achieved in 24 patients (92%), and 50%-75% in 2 patients (8%).

Figure 1.

Preoperative embolisation of giant cell tumor of upper end of tibia. A-F: Antero-posterior (A) and lateral (B) plain radiographs of right knee show expansile lytic destructive lesion involving proximal end of right tibia reaching up to subarticular location suggestive of giant cell tumor; Axial (C) T2-weighted fat saturated magnetic resonance image show heterogeneously hyperintense lesion with blood-fluid levels within it suggestive of secondary aneurysmal bone cysts formation (arrow); Pre embolisation non-selective DSA (D) image of left SFA show multiple feeders arising from distal SFA and proximal anterior tibial artery supplying the tumor with marked tumor blush; Post embolisation non-selective DSA (E) image show > 90% reduction in tumor blush (arrow); Postoperative AP plain radiograph of right knee (F) show replacement of bony defect following tumor curettage with combined autograft (iliac crest) and allograft. DSA: Digital substraction angiography; SFA: Superficial femoral artery.

All the patients underwent tumor resection and stabilization within 0-48 h of embolization. Three orthopedic surgeons having experience of more than 15 years performed all surgical procedures. Intraoperative blood loss was derived from operative a note which was calculated by the surgical team with use of standard surgical assessment like weighing of blood soaked gauze pieces and measuring the collected blood in the drain (Figure 2). Similarly intraoperative blood transfusion volume and surgical time taken were also noted from the surgical note. Any adverse events related to angiography or embolization and related to surgery were noted up to 48 h of postoperative period. We also recorded the same parameters from the surgical notes of the 28 patients of the control group operated in past without undergoing any preoperative embolization.

Figure 2.

Photograph of gauze pieces and suction bottle used to measure blood loss during the study. Operative photograph (A) show blood soaked gauze pieces that were weighed to calculate blood loss and photograph of suction bottle (B) show collected blood during surgery.

Statistical analysis

It was performed using Stata 11.2 software. Statistical comparison was done between the study population - embolisation group and the control group - non-embolisation group (data retrieved from the hospital medical record). To compare the difference between the two groups (embolization and non embolization group) and to calculate the P-value, Student’s t test was applied.

RESULTS

All 26 embolisation procedures were technically and clinically successful. All the tumors were hypervascular on angiograms (Figures 3 and 4). Following embolisation, more than > 75% reduction of tumor blush was achieved in 24 patients (92%) and reduction was in the range of 50%-75% in 2 patients (8%).

Figure 3.

Preopertaive embolisation of spinal aneurysmal bone cyst. Antero-posterior (A) plain radiograph of lumbo-sacral spine show expansile lytic lesion involving the posterior elements of L4 vertebra suggestive of aneurysmal bone cyst; Sagittal (B) 3D-reformatted non-contrast computed tomography of lumbo-sacral spine show lytic expansile destructive lesion involving posterior elements of L4 vertebra; Sagittal (C) and axial (D) T2-weighted fat saturated magnetic resonance images show T2 hyperintense lesion involving posterior element of L4 vertebra with blood-fluid levels (arrow); Pre embolisation non-selective digital substraction angiography (DSA) (E) image of L3 lumbar artery showmultiple feeders supplying the tumor with tumor blush; Post embolisation DSA (F) image show more than 90% reduction in tumor blush (asterix).

Figure 4.

Preoperative embolisation of aneurysmal bone cyst of humerus. Antero-posterior (A) plain radiograph of right shoulder show expansile lytic destructive lesion involving proximal end ofright humerus, suggestive of aneurysmal bone cyst; Axial (B) T2-weighted fat suppressed magnetic resonance image showlesion is hyperintense with fluid-fluid levels within it (arrow); Digital substraction angiography (C) image of right circumflex humeral artery show multiple feeders supplying the tumor with marked tumor blush; Post embolisation angiogram (D) of circumflex humeral artery show near complete reduction of tumor blush.

None of the patients developed any major complications related to either angiography or embolization during the procedure or during observation period. Minor complications like local site pain, shivering were noted in 4 patients which did not warrant any medical treatment. None of the patients had postembolization syndrome.

The type of surgical procedures performed in study group included, tumor resection in 7 patients, curettage and bone grafting in 8 patients, tumor resection, bone grafting and fixation using compression plate in 7 patients and tumor resection with posterior element fixation and cage placement in 4 patients.

Embolisation group (n = 26)

The mean intraoperative blood loss was 1300 mL (range 250-2900 mL), with mean requirement of intraoperative blood transfusion of 700 mL (range 0-1400 mL). Five patients did not require any blood transfusion. The mean surgical time was 221 min (range 115-450 min).

Non-embolisation group (n = 28)

The mean intraoperative blood loss was 1800 mL (range 800-6000 mL), with mean requirement of intraoperative blood transfusion of 1400 mL (range 700-8400 mL). The mean surgical time was 250 min (range 145-450 min).

On comparison, statistically significant (P < 0.001) difference was found between embolisation group and non-embolisation group for the amount of blood loss and requirement of blood transfusion. There was no statistical difference between the two groups for the surgical time.

The comparison of intraoperative blood loss, intraoperative blood transfusion and surgical time is depicted in Table 2. In order to extract safer conclusions; we have made two homogenous groups, i.e., GCT in extremities of same grade and underwent same type of operation.

Table 2.

Intraoperative details of patients of study group and control group for entire study population

Parameters	Study group, n = 26	Control group, n = 28	P value
Intraoperative blood loss (mL)
Minimum	250	800
Maximum	2900	6000	< 0.0015
Median	1300	1800
Intraoperative blood transfusion (mL)
Minimum	0	700
Maximum	1400	8400	< 0.0001
Median	700	1400
Surgical time (min)
Minimum	115	145	> 0.14
Maximum	450	450

The comparison of intraoperative blood loss, intraoperative blood transfusion and surgical time for the GCT in extremities between embolisation (study group) and non-embolisation group (control group) is depicted in Table 3.

Table 3.

Intraoperative details of patients of study group and control group only for giant cell tumors of extremities

Parameters	Study group, n = 18	Control group, n = 22	P value
Intraoperative blood loss (mL)
Minimum	250	800
Maximum	2900	6000	< 0.0012
Median	1300	1800
Intraoperative blood transfusion (mL)
Minimum	0	700
Maximum	1400	8400	< 0.0007
Median	525	1400
Surgical time (min)
Minimum	115	145
Maximum	340	450	> 0.0079
Median	210	252.5

GCT in extremities

Embolisation group (n = 18): The mean intraoperative blood loss was 1300 mL (range 250-2900 mL), with mean requirement of intraoperative blood transfusion of 525 mL (range 0-1400 mL). Four patients did not require any blood transfusion. The mean surgical time was 210 min (range 115-340 min).

Non-embolisation group (n = 22): The mean intraoperative blood loss was 1800 mL (range 800-6000 mL), with mean requirement of intraoperative blood transfusion of 1400 mL (range 700-8400 mL). The mean surgical time was 252.5 min (range 145-450 min).

On comparison, statistically significant (P < 0.001) difference was found between embolisation group and non-embolisation group for the GCT in extremities for the amount of blood loss, requirement of blood transfusion and also for surgical time.

Patient demographics, histological diagnosis, location of tumor, blood loss, transfusion requirement and surgical time of study group and control group were shown in Table 4 for entire study population and in Table 5 for GCT in extremities.

Table 4.

Patient demographics, histological diagnosis, location of tumor, blood loss, transfusion requirement and surgical time of study group and control group for the entire study population

S.No	Study group (embolisation group), n = 26							Control group (non-embolisation group), n = 28
	Age/sex	Diagnosis	Site	Embolising agent	Blood loss (mL)	Transfusion (mL)	Surgical time (min)	Age/sex	Diagnosis	Site	Blood loss (mL)	Transfusion (mL)	Surgical time (min)
1	52 M	GCT	LL	PVA + GEL FOAM	2900	1400	230	10 F	ABC	LL	1450	750	170
2	30 M	GCT	LL	PVA + GEL FOAM	1740	700	231	46 F	GCT	LL	1300	1400	240
3	18 M	OB	SPINE	PVA + GEL FOAM	1650	700	240	58 M	GCT	LL	1600	1450	230
4	17 M	ABC	SPINE	PVA + GEL FOAM	1600	700	355	20 F	ABC	UL	1800	1400	195
5	42 M	GCT	LL	PVA + GEL FOAM	1500	700	340	28 F	OB	SPINE	2500	1750	195
6	14 F	ABC	SPINE	PVA + GEL FOAM	1200	700	230	31 M	GCT	LL	1250	1050	220
7	34 M	CS	ILIUM	GEL FOAM	1900	1400	450	21 M	GCT	LL	2500	1050	145
8	39 F	GCT	LL	PVA + GEL FOAM	1600	700	240	34 M	GCT	SPINE	2500	1400	295
9	45 F	GCT	LL	PVA + GEL FOAM	1300	350	180	34 F	GCT	LL	1800	1400	150
10	31 M	GCT	LL	PVA	250	0	115	60 F	GCT	LL	1200	700	150
11	20 F	GCT	UL	PVA + GEL FOAM	1300	700	250	20 M	GCT	LL	6000	8400	450
12	25 F	GCT	SPINE	PVA	1300	700	230	28 M	OB	SPINE	1300	700	230
13	48 M	GCT	SACRUM	PVA	1400	700	240	30 M	GCT	LL	2000	2100	350
14	15 M	GCT	UL	PVA + GEL FOAM	500	350	170	45 F	GCT	LL	1500	1400	225
15	32 F	GCT	LL	PVA + GEL FOAM	1600	700	260	22 M	GCT	LL	4300	2100	315
16	30 F	GCT	UL	PVA	350	0	135	40 F	GCT	LL	1800	1400	245
17	28 F	GCT	LL	PVA + GEL FOAM	1400	700	240	24 F	GCT	LL	800	700	290
18	32 M	GCT	LL	PVA	400	350	190	16 M	CB	LL	1400	1050	185
19	45 F	GCT	UL	PVA	2100	1050	245	17 M	GCT	UL	1800	700	180
20	20 M	GCT	LL	PVA	600	0	125	22 F	GCT	LL	1500	1050	260
21	20 F	GCT	LL	PVA	800	350	145	34 M	GCT	UL	900	700	245
22	82 M	GCT	LL	PVA	900	350	155	29 F	GCT	LL	1500	1400	270
23	15 M	CB	LL	PVA	750	350	135	26 M	GCT	LL	1600	1050	290
24	22 M	GCT	UL	PVA+GEL FOAM	1800	1400	230	27 F	GCT	LL	2600	2100	335
25	52 M	CS	UL	PVA	500	0	250	18 M	GCT	LL	3450	2450	330
26	42 F	GCT	UL	PVA	300	0	140	23 F	GCT	UL	2600	2050	285
27								21 F	GCT	LL	2100	1400	245
28								24 M	GCT	LL	1900	1400	290

GCT: Giant cell tumor; ABC: Aneurysmal bone cyst; OB: Osteoblastoma; CS: Chondrosarcoma; UL: Upper limb; LL: Lower Limb.

Table 5.

Patient demographics, histological diagnosis, location of tumor, blood loss, transfusion requirement and surgical time of study group and control group for the giant cell tumors of extremities

S.No	Study group (embolisation group), n = 18							Control group (non-embolisation group), n = 22
	Age/sex	Diagnosis	Site	Embolising agent	Blood loss (mL)	Transfusion (mL)	Surgical time (min)	Age /sex	Diagnosis	Site	Blood loss (mL)	Transfusion (mL)	Surgical time (min)
1	52 M	GCT	LL	PVA + GEL FOAM	2900	1400	230	46 F	GCT	LL	1300	1400	240
2	30 M	GCT	LL	PVA + GEL FOAM	1740	700	231	58 M	GCT	LL	1600	1450	230
3	42 M	GCT	LL	PVA + GEL FOAM	1500	700	340	31 M	GCT	LL	1250	1050	220
4	39 F	GCT	LL	PVA + GEL FOAM	1600	700	240	21 M	GCT	LL	2500	1050	145
5	45 F	GCT	LL	PVA + GEL FOAM	1300	350	180	34 F	GCT	LL	1800	1400	150
6	31 M	GCT	LL	PVA	250	0	115	60 F	GCT	LL	1200	700	150
7	20 F	GCT	UL	PVA + GEL FOAM	1300	700	250	20 M	GCT	LL	6000	8400	450
8	15 M	GCT	UL	PVA + GEL FOAM	500	350	170	30 M	GCT	LL	2000	2100	350
9	32F	GCT	LL	PVA + GEL FOAM	1600	700	260	45F	GCT	LL	1500	1400	225
10	30 F	GCT	UL	PVA	350	0	135	22 M	GCT	LL	4300	2100	315
11	28 F	GCT	LL	PVA + GEL FOAM	1400	700	240	40 F	GCT	LL	1800	1400	245
12	32 M	GCT	LL	PVA	400	350	190	24 F	GCT	LL	800	700	290
13	45 F	GCT	UL	PVA	2100	1050	245	17 M	GCT	UL	1800	700	180
14	20 M	GCT	LL	PVA	600	0	125	22 F	GCT	LL	1500	1050	260
15	20 F	GCT	LL	PVA	800	350	145	34 M	GCT	UL	900	700	245
16	82 M	GCT	LL	PVA	900	350	155	29 F	GCT	LL	1500	1400	270
17	22 M	GCT	UL	PVA + GEL FOAM	1800	1400	230	26 M	GCT	LL	1600	1050	290
18	42 F	GCT	UL	PVA	300	0	140	27 F	GCT	LL	2600	2100	335
19								18 M	GCT	LL	3450	2450	330
20								23 F	GCT	UL	2600	2050	285
21								21 F	GCT	LL	2100	1400	245
22								24M	GCT	LL	1900	1400	290

GCT: Giant cell tumor; UL: Upper limb; LL: Lower Limb; PVA: Polyvinyl alcohol.

DISCUSSION

The management of primary bone tumors, either benign or malignant, varies with the individual lesions; however, surgical resection remains the main treatment modality. However, heavy, uncontrollable blood loss during surgery has been common problem, leading to massive transfusion requirements. Preoperative embolization has significantly reduced peri-operative blood loss and better delineation of the tumor margins from the surrounding, facilitating the tumor excision with reduced blood transfusion requirement.

Barton et al[24] reported a blood loss of 2000-18500 mL (mean 6800 mL) in 20 patients operated without preoperative embolization, whereas only 500-1500 mL blood loss occurred when PAE was performed and cases were operated within 72 h. For better result, close cooperation between the orthopedic surgeon and interventional radiologist is essential. In our study, we studied the role of PAE in bone tumors where limb salvage surgery was possible.

Majority of the patients in our study had GCT (n = 20, 77%) followed by ABC and chondrosarcoma that comprised of two patients (7%) each. Similarly 23 patients (82%) of our control group had GCT. None of the previous studies from literature comprised of this number of GCT and the most common histology in previous studies was metastatic tumors[16,19,21,22]. In a prospective study done by Lee et al[13] total 6 patients were studied. Out of 6 patients they studied, three patients had GCT and 3 patients had ABC. There are scattered case reports, describing the role of TAE in limb-girdle location where GCT and ABCs were the common histology[25,26,27].

Barton et al[24] also reported that, surgery occurred within 3 d of embolization, blood loss was 500-1500 mL, comparing to 1500-2800 mL at 4-14 d post embolisation, due to re-canalization and angiogenesis. In our study, all the cases were operated within 48 h of embolisation.

In our study, significant number of bone tumors where TAE was performed, were located in appendicular skeleton (n = 24, 76%) than axial skeleton (n = 6, 24%). In contrast, as reported by the previous studies where TAE was performed, spinal column was the most common sites and most of these tumors were metastatic in nature than primary bone tumor[15,16,19,22,28,29]. Retrospective study done by Radeleff et al[17] studied four metastatic lower limb tumors and five metastatic upper limb tumors out of 31 patients.

Majority of the studies from literature suggests that TAE was performed under local anaesthesia as in our study. However, in a study done by Thiex et al[29] all angiograms were done under general anesthesia, since all the angiograms were done for spinal column metastatic lesions.

PVA particles, as an embolising agent is considered as a workhorse in pre-operative TAE[15,23,30]. It was used as sole embolising agent in 12 (46%) patients and both PVA and gelfoam were used in 13 (50%) patients in our study. In a study done by Radeleff et al[17] apart from gelfoam and PVA particles, they have also used embosphere and liquid embolising material like cyanoacrylate-lipoidal mixture and ethibloc. They have also advocated the use of embosphere as a particulate embolising material due to its uniform size. Another study reported by Kobayashi et al[27] used PVA and embosphere as embolising material. In study reported by Lee et al[13] only gelfoam was used for embolization. In few studies coils were also used for embolization[3,18]. We compared the various perioperative findings in the PVA only and PVA with gelfoam groups. There was statistically significant difference (P < 0.005) when only PVA was used as embolizing material as there was lesser intraoperative blood loss, lesser intraoperative and post operative blood transfusion volume.

Final angiogram was taken after the completion of TAE and degree of tumor devascularity was assessed subjectively. We achieved reduction of tumor blush by more than > 75% in 24 (92%) patients and in rest, the reduction of tumor blush was in range of 50%-75%. In a study done by Börüban et al[12] they had achieved 80%-100% devascularisation in 5 of 11 patients. In another study done by Sun et al[15], more than 70% reduction in tumor blush (stain) was noted in 12 of 16 patients, while in 2 patients reduction of tumor blush was less than 50%. In comparison, none of our patients had reduction of tumor blush less than 50%. This suggests that our study was comparable with many of the studies from the literature. In our study, statistical analysis between the amount of blood loss and amount of devascularisation could not be done since majority of our patients (n = 24) had > 75% devascularisation and the other group which had 50%-75% devascularisation was very small (n = 2). However, we did not find any significant difference during the surgery.

A known complication of embolisation is the possibility of wound healing problems. Wirbel et al[14] noted that 2 patients in their embolisation group (spinal tumours) had wound problems due to psoas muscle necrosis and subsequent skin necrosis. None of the patients from our study population developed any such complication or any other complications related to angiography and embolization. This is in concordance with previous studies where no major complications were reported[11,30-32].

Our results showed significantly less blood in a variety of surgically resected bone tumours as compared with the pre-embolisation era, and comparable blood loss to other studies[12,27,29].

In a study done by Thiex et al[29] on 104 spinal tumors, the blood loss was found to be in the range of 200-15000 mL. In another study done by Kobayashi et al[27], the blood loss was found to be in the range of 250-11000 mL with a mean of 2554 mL. In a study done by Zhang et al[32], the blood loss was in the range of 60-580 mL with a mean blood loss of 290 mL. The lower blood loss in this study can be attributed to the fact that this study was done on osteosarcomas which is not very vascular tumor except for the telengiactatic form. In other study done by Börüban et al[12] on bone and soft tissue tumors of extremities, the blood loss was in the range of 100-2500 mL with a mean blood loss of 1360 mL. Our study had blood loss in comparison to this study as mean blood loss in the range of 1300 mL.

In a study done by Thiex et al[29], the requirement of perioperative blood transfusion requirement was found to be 0-99 units. In another study done by Kobayashi et al[27] on spinal tumors; the requirement of intraoperative blood transfusion volume was noted in the range of 0-28 units with mean of 7 units. In study done by Zhang et al[32], the volume of blood infusion was noted to be 689 ± 133.89 mL. The intraoperative blood transfusion in our study group was comparable to study done by Zhang et al[32], while lower than the study done by Thiex et al[29] and Kobayashi et al[27]. In our study, mean requirement of intraoperative blood transfusion was 700 mL (range 0-1400 mL).

Many retrospective studies from the literature have shown that intraoperative blood loss is significantly lower in embolization group than non-embolisation group (Table 6). In non-embolisation group, the intraoperative blood loss ranged from 4350-8750 mL vs 300-4300 mL as compared to embolisation group[14,30-36]. In our study, the mean intraoperative blood loss was 1300 mL (range 250-2900 mL), with mean requirement of intraoperative blood transfusion of 700 mL (range 0-1400 mL) in embolisation group as compared to mean intraoperative blood loss was 1800 mL (range 800-6000 mL), with mean requirement of intraoperative blood transfusion of 1400 mL (range 700-8400 mL) in non-embolisation group.

Table 6.

Comparing our results with literature reports

Ref.	Year	No. of patients	Type of study	Result
Thiex et al[29]	2013	104	Retrospective	EBL = 100-15000 mL
				BT = 0-99 units
Ibrahim et al[36]	2013	18	Retrospective	EBL = 1100-2600 mL
				MBL = 1400 mL
				BT = 0-8 units
Kobayashi et al[27]	2012	62	Retrospective	EBL = 250-11000 mL
				MBL = 2554 mL
				BT = 0-28 units
Al-Hadithy et al[20]	2011	26	Retrospective	EBL = 100-1800 mL
				BT = 0-3 units
Zhang et al[32]	2009	47	Retrospective	EBL = 705 ± 120 mL
				BT = 689 ± 133 mL
Lee et al[13]	2008	6	Prospective	EBL = 200-830 mL
				BT = Nil
Our study	2012-2013	26 (study group)	Case control study	For study group
				EBL = 250-2900 mL
				BT = 0-1400 mL
		28 (control group)		For control group
				EBL = 800-6000 mL
				BT = 700-8400 mL
				P < 0.05

EBL: Estimated blood loss; MBL: Mean blood loss; BT: Blood transfusion.

We also compared surgical time in our study group and control group. We found that mean surgical time was less in study group (221.19 min) in comparison to the control group (250.35 min), however, we did not found significant correlation (P > 0.14) between preoperative embolization and surgical time.

The important limitations of our study were, first, the sample size of our study was small and study was not randomized according to the tumor size and volume and its effect on blood loss. Second, we did not study osseous metastatic tumors. Third, variables like patient characteristics, tumor characteristics, surgical skill and techniques that can influence perioperative blood loss and BT were not evaluated, as it was not our aim of study. Fourth, no long-term clinical follow up of the patients were available to evaluate the tumor recurrence and survival rates in these patients.

The type, grade and staging of the tumor are important characteristics that affect its “bleeding potential” and type of operation. In our study, we have examined the effectiveness of preoperative embolization in 2 groups with at least 4 different types of tumors or tumor like lesions, unknown staging and grading and different locations, thus these two are heterogeneous group of patients. Comparison of same type of tumor and same location between two groups was not attempted. Since in our study predominant histological pattern was GCT in both study group and control group. Rest of histological pattern was small number and was in different location, hence could not be compared. However in order to extract safer conclusion we have compared the effect of TAE in case of GCT in extremities, who underwent same type of operation. On comparison, we found statistically significant (P < 0.001) difference between embolisation group and non-embolisation group for the GCT in extremities for the amount of blood loss, requirement of blood transfusion and also for surgical time.

In conclusion, the results of the current study show that the preoperative embolisation of bone tumor performed 0-48 prior to either limb salvage surgery or stabilization in vertebral and sacral tumor leads to decrease in intraoperative blood loss and intraoperative blood transfusion volume. We experienced no procedure related complications. Therefore, would recommend that pre-operative embolisation is a safe procedure and should be used as part of the multi-disciplinary approach to the management of bone tumours in difficult anatomical locations and those are known to be highly vascular. Further larger prospective randomized studies are needed to address these issues and generalize it for primary bone tumor resection.

ACKNOWLEDGMENTS

The authors thank Professor Sreenivas V for helping in statistical analysis of the study.

COMMENTS

Background

Preoperative transarterial embolisation (TAE) reduces the tumor vascularity and intraoperative blood loss. It also reduces the need for blood transfusion and decreases the incidence of complications associated with surgery. Many studies conducted worldwide have proved the efficacy of preoperative embolization but most of them were done on secondary bone tumors. The aim of this study was to assess the effectiveness and safety of preoperative TAE of primary bone tumors in relation to the amount of intraoperative blood loss, requirement of amount of blood transfusion, surgical time and procedure related complications.

Research frontiers

Selective TAE was first described by Feldman et al[3] in 1975, since then embolization of tumors has been a widely practiced interventional radiology technique. Refinement of techniques and advances in hardwares led to its use in preoperative embolization of both primary and secondary bone tumors. The principle behind TAE of primary bone tumors is the precise targeting of the tumor feeding vessels and tumor capillary bed, while simultaneously reducing non-target embolisation effects.

Innovations and breakthroughs

The common types of bone tumor which usually require TAE are hypervascular in nature such as giant cell tumors, aneurysmal bone cysts, telengiactatic osteosarcomas, vertebral hemangiomas, arterio-venous malformations, osteoblastoma and vascular metastatic lesions especially from renal cell or thyroid. The management of primary bone tumors, either benign or malignant, varies with the individual lesions; however, surgical resection remains the main treatment modality. However, heavy, uncontrollable blood loss during surgery has been common problem, leading to massive transfusion requirements. Preoperative embolization has significantly reduced peri-operative blood loss and better delineation of the tumor margins from the surrounding, facilitating the tumor excision with reduced blood transfusion requirement. The results of the current study show that the preoperative TAE performed 0-48 h before limb salvage surgery in extremities tumor and tumor resection and stabilization in vertebral and sacral tumor leads to decrease in intraoperative blood loss and intraoperative blood transfusion volume.

Applications

The results of this study suggest that pre-operative embolisation is a safe and effective procedure, could be used as part of the multi-disciplinary approach to the management of bone tumors in difficult anatomical locations and those that are known to be highly vascular.

Terminology

Preoperative TAE reduces the tumor vascularity, intraoperative blood loss, the need for blood transfusion and decreases the incidence of complications associated with surgery.

Peer-review

This is really well designed and written paper regarding the importance of preoperative embolization of primary bone tumors.