Literature DB >> 22353421

Learning from experience. Proposal of a refined definition and staging system for bisphosphonate-related osteonecrosis of the jaw (BRONJ).

A Bedogni, V Fusco, A Agrillo, G Campisi.   

Abstract

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Year:  2012        PMID: 22353421      PMCID: PMC3443365          DOI: 10.1111/j.1601-0825.2012.01903.x

Source DB:  PubMed          Journal:  Oral Dis        ISSN: 1354-523X            Impact factor:   3.511


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Dear Editor, It is the authors’ belief that the internationally accepted definition of bisphosphonate-related osteonecrosis of the jaws (BRONJ) (Ruggiero ) has several limitations that prevent clinicians from being confident with the diagnosis of the disease. Following recognition of the non-exposed BRONJ clinical variant (Lazarovici ), we all became aware that the presence of ‘exposed necrotic bone in the oral cavity’, as outlined in the American Association of Oral and Maxillofacial Surgery (AAOMS) case definition, is just one of the possible clinical manifestations of BRONJ and is not found in all BRONJ patients. As ‘bone exposure’ is certainly not the initial sign of BRONJ in most patients and a minimum of 6–8 weeks’ persistence is required to confirm the clinical suspicion, the final diagnosis is usually delayed for several weeks or months. Therefore, to date, it has been almost impossible to study the early phases of BRONJ. This delayed diagnosis can also explain, at least in part, why the disease is often refractory to the medical and surgical treatments commonly used. We believe that clinicians will benefit from a definition of BRONJ that contains only robust information, without considering any definite clinical picture or a binding time-frame (i.e. 6–8 weeks). As qualified members of the Expert Panel of the Italian Society for Maxillofacial Surgery (SICMF) and the Italian Society of Oral Pathology and Medicine (SIPMO) on Bisphosphonate-Related Osteonecrosis of the Jaws, we are submitting to the attention of the scientific community the following definition of BRONJ: ‘bisphosphonate related osteonecrosis of the jaw (BRONJ) is an adverse drug reaction described as the progressive destruction and death of bone that affects the mandible or maxilla of patients exposed to the treatment with nitrogen-containing bisphosphonates, in the absence of a previous radiation treatment’. Along with this new definition of BRONJ, we set up and propose a diagnostic work-up to be used to reach the final diagnosis. Although exposed necrotic bone in the oral cavity still remains the best indicator of BRONJ (Ruggiero ), other non-specific signs and symptoms (Table 1) should raise the suspicion of BRONJ, even in a patient with a well-recognized dental or periodontal disease (Fedele ). In short, BRONJ should be always investigated in a patient taking nitrogen-containing bisphosphonates (NBP), when one or more clinical signs are present. Because BRONJ is primarily a disease that affects the jawbone, we strongly believe that radiological examination is an important step of the diagnosis. However, as the radiological findings may be characteristic not only of BRONJ (Khan ), these findings should always match the clinical picture, in order to progress from the clinical suspicion to the final diagnosis. This is of outmost importance as bone biopsies for histology are still not routinely advised for the risk of worsening the disease process. A schematic approach to the work-up for a diagnosis of BRONJ is proposed (Scheme 1), where computed tomography (CT) currently represents the most useful diagnostic tool because of its widespread use and accessibility for patients (Bianchi ). Structural alteration of trabecular bone is a consistent finding of CT scans performed in patients with BRONJ (Table 2) (Arce ). CT scans can clearly depict the degree of osteosclerosis of the affected site, visible as the loss of contrast definition between the endosteal cortex and the subjacent medullary bone (i.e. trabecular thickening and/or regional or diffuse osteosclerosis), with respect to the uninvolved bone tissue (Hutchinson ). Osteosclerosis seems to characterize the early stages of disease and also precedes the occurrence of frank bone exposure in the oral cavity (Saia ), and thus it should be searched for to provide an early diagnosis.
Table 1

Non-specific clinical signs associated with bisphosphonate-related osteonecrosis of the jaws (BRONJ)

Major clinical sign
 Exposed necrotic bone in the oral cavity
Minor clinical signs and symptoms
 Abscess
 Displaced mandibular stumps
 Extra-oral fistula
 Gross mandible deformity
 Hypoesthesia/paraesthesia of the lipsa
 Mucosal/gengival fistula
 Nasal leakage of fluids
 Nonhealing postextraction socket
 Purulent discharge
 Spontaneous expulsion of sequestra and necrotic bone fragments
 Sudden dental mobility
 Swelling
 Toothache and bone pain
 Trismus

Owing to inferior alveolar nerve/infraorbital nerve involvement.

Scheme 1

Diagnostic work-up for BRONJ. VAS, visual analogic scale

Table 2

Non-specific computed tomography (CT) findings associated with bisphosphonate-related osteonecrosis of the jaws (BRONJ)

Early signsLate signs
Cortical disruptionDiffuse osteosclerosisb
Focal bone marrow sclerosisaOro-antral fistula
Markedly thickened and sclerotic lamina duraOsteolysis extending to the sinus floor
Persisting alveolar socketOsteosclerosis of adjacent bones (zygoma, hard palate)
Trabecular thickeningaPathologic fracture
Periosteal reaction
Prominence of the inferior alveolar nerve canal
Sequestra formationSinusitis

Density in the sclerotic areas is limited to the alveolar bone region and ranges from little to fully sclerotic with irregular compact and disorganized trabeculation.

Reduced or complete loss of contrast definition between the endosteal cortex and subjacent medullary bone (density confluence), involving both the alveolar bone and the basal bone of the mandible and maxilla.

Non-specific clinical signs associated with bisphosphonate-related osteonecrosis of the jaws (BRONJ) Owing to inferior alveolar nerve/infraorbital nerve involvement. Diagnostic work-up for BRONJ. VAS, visual analogic scale Non-specific computed tomography (CT) findings associated with bisphosphonate-related osteonecrosis of the jaws (BRONJ) Density in the sclerotic areas is limited to the alveolar bone region and ranges from little to fully sclerotic with irregular compact and disorganized trabeculation. Reduced or complete loss of contrast definition between the endosteal cortex and subjacent medullary bone (density confluence), involving both the alveolar bone and the basal bone of the mandible and maxilla. Even though magnetic resonance imaging (MRI) provides more detailed information than CT on focal bone marrow alterations (Bisdas ), the former could provide non-diagnostic results owing to magnetic artifacts caused by the presence of dental casting alloys (Shafiei ) as well as to motion artifacts caused by the prolonged time necessary to scan the head and neck region (Lenz ). The majority of BRONJ cases could be diagnosed and staged correctly by the combined use of clinical methods and CT, the latter method currently being more cost-effective and easily accessible than MRI. On the other hand, we believe that MRI should be used to evaluate cases difficult to identify with CT and to establish the real extent of jawbone and soft-tissue involvement in BRONJ patients who are candidates for surgical resection. The staging system of a bone disease that relies on the use of radiologic imaging for its diagnosis should also be based on the common radiologic features of the disease. The current AAOMS staging system (Ruggiero ; Migliorati ), which assigns patients to different stages of disease on the basis almost exclusively of clinical criteria, fails, in our opinion, to consider this important aspect. In this regard, we set up a combined clinical and radiological staging system with the aim of pooling BRONJ patients in different groups also based on the radiological extent of the disease. The staging system we propose (Table 3) differs from the 2009 AAOMS classification as follows:
Table 3

Clinical and radiological staging system of bisphosphonate-related osteonecrosis of the jaws (BRONJ)

Stage 1Focal BRONJ
Clinical signs and symptoms: bone exposure; sudden dental mobility; nonhealing postextraction socket; mucosal fistula; swelling; abscess formation; trismus; gross mandibular deformity and/or hypoesthesia/paraesthesia of the lips
CT findings: increased bone density limited to the alveolar bone region (trabecular thickening and/or focal osteosclerosis ), with or without the following signs: markedly thickened and sclerotic lamina dura; persisting alveolar socket; and/orcortical disruption
1a. Asymptomatic
1b. Symptomatic (pain and purulent discharge)
Stage 2Diffuse BRONJ
Clinical signs and symptoms: same as Stage 1
CT findings: increased bone density extended to the basal bone (diffuse osteosclerosis), with or without the following signs: prominence of the inferior alveolar nerve canal; periosteal reaction; sinusitis; sequestra formation; and/or oro-antral fistula
2a. Asymptomatic
2b. Symptomatic (pain and purulent discharge)
Stage 3Complicated BRONJ
Same as Stage 2, with one or more of the following:
clinical signs and symptoms: extra-oral fistula; displaced mandibular stumps; nasal leakage of fluids
CT findings: osteosclerosis of adjacent bones (zygoma, hard palate); pathologic mandibular fracture; and/or osteolysis extending to the sinus floor

CT, computed tomography.

Clinical and radiological staging system of bisphosphonate-related osteonecrosis of the jaws (BRONJ) CT, computed tomography. The absence of Stage 0, so that BRONJ patients with exposed and non-exposed necrotic bone simply represent distinct clinical pictures within the same disease stage. The description of three stages (1–3) based on clinical and CT findings, ‘where Stage 1 includes patients with focal (alveolar bone) osteosclerosis, Stage 2 includes patients with diffuse (alveolar and basal bone) osteosclerosis and Stage 3 includes patients with clinical and radiological signs of advanced and complicated disease. Pain and purulent discharge are no longer used to distinguish between different disease stages. As these symptoms define only asymptomatic (a) and symptomatic (b) forms of BRONJ in patients within the same stage, exclusion of pain and purulent discharge as criteria would limit the ‘ping-pong’ effect (the migration of patients from Stage 1 to Stage 2, and vice versa) that we all experienced when using the AAOMS classification, as a result of the repeated use of antibiotic therapies to treat recurrent bone infections and associated pain. The presence of clinically detectable sequestra is no longer regarded as a sign of complicated disease, as it is for AAOMS Stage 3. In fact, it is a common experience that the spontaneous expulsion or surgical removal of bony sequestra often leads to dramatic, albeit somewhat temporary, clinical improvement, with mucosal epithelialization of the affected site (Ferlito ). The definition, work-up and staging system proposed here might, as a whole, provide several practical benefits, in the order: anticipated BRONJ diagnosis and access of patients to therapies; a reduced need for extensive surgical resections with associated long and debilitating postoperative hospitalization; and increased overall efficacy of treatments and patients’ curability. The disadvantage of the additional cost of bone imaging (CT) for the diagnosis would be offset against the overall reduction in treatment costs. When a new disease is found, little is known of its medical features and behavior; this makes it necessary to avoid general definitions that may include potentially healthy patients (resulting in a higher false-positive risk). This also occurred at the start, when the actual BRONJ case definition was adopted. At present, with the growing bulk of research on BRONJ, we believe that it is necessary to enter a new phase where clinicians try to establish the initial stages of the disease process, in order to make an earlier diagnosis and improve treatment effectiveness. Although adjustments and updating will be necessary in the future, the definition, work-up and staging system proposed here could achieve this purpose.
  13 in total

1.  Artifacts from dental casting alloys in magnetic resonance imaging.

Authors:  F Shafiei; E Honda; H Takahashi; T Sasaki
Journal:  J Dent Res       Date:  2003-08       Impact factor: 6.116

2.  Radiographic findings in bisphosphonate-treated patients with stage 0 disease in the absence of bone exposure.

Authors:  Matthew Hutchinson; Felice O'Ryan; Vicente Chavez; Phenius V Lathon; Gabriela Sanchez; David C Hatcher; A Thomas Indresano; Joan C Lo
Journal:  J Oral Maxillofac Surg       Date:  2010-09       Impact factor: 1.895

3.  American Association of Oral and Maxillofacial Surgeons position paper on bisphosphonate-related osteonecrosis of the jaws--2009 update.

Authors:  Salvatore L Ruggiero; Thomas B Dodson; Leon A Assael; Regina Landesberg; Robert E Marx; Bhoomi Mehrotra
Journal:  J Oral Maxillofac Surg       Date:  2009-05       Impact factor: 1.895

4.  Occurrence of bisphosphonate-related osteonecrosis of the jaw after surgical tooth extraction.

Authors:  Giorgia Saia; Stella Blandamura; Giordana Bettini; Anita Tronchet; Andrea Totola; Giorgio Bedogni; Giuseppe Ferronato; Pier Francesco Nocini; Alberto Bedogni
Journal:  J Oral Maxillofac Surg       Date:  2010-04       Impact factor: 1.895

5.  Oropharynx, oral cavity, floor of the mouth: CT and MRI.

Authors:  M Lenz; H Greess; U Baum; M Dobritz; B Kersting-Sommerhoff
Journal:  Eur J Radiol       Date:  2000-03       Impact factor: 3.528

6.  Canadian consensus practice guidelines for bisphosphonate associated osteonecrosis of the jaw.

Authors:  Aliya A Khan; George K B Sándor; Edward Dore; Archibald D Morrison; Mazen Alsahli; Faizan Amin; Edmund Peters; David A Hanley; Sultan R Chaudry; David W Dempster; Francis H Glorieux; Alan J Neville; Reena M Talwar; Cameron M Clokie; Majd Al Mardini; Terri Paul; Sundeep Khosla; Robert G Josse; Susan Sutherland; David K Lam; Robert P Carmichael; Nick Blanas; David Kendler; Steven Petak; Louis Georges St-Marie; Jacques Brown; A Wayne Evans; Lorena Rios; Juliet E Compston
Journal:  J Rheumatol       Date:  2008-06-01       Impact factor: 4.666

7.  Biphosphonate-induced osteonecrosis of the jaws: CT and MRI spectrum of findings in 32 patients.

Authors:  S Bisdas; N Chambron Pinho; A Smolarz; R Sader; T J Vogl; M G Mack
Journal:  Clin Radiol       Date:  2007-10-22       Impact factor: 2.350

Review 8.  Imaging findings in bisphosphonate-related osteonecrosis of jaws.

Authors:  Kevin Arce; Leon A Assael; Jane L Weissman; Michael R Markiewicz
Journal:  J Oral Maxillofac Surg       Date:  2009-05       Impact factor: 1.895

9.  Computerized tomographic findings in bisphosphonate-associated osteonecrosis of the jaw in patients with cancer.

Authors:  Silvio Diego Bianchi; Matteo Scoletta; Francesca Bozzalla Cassione; Giuseppe Migliaretti; Marco Mozzati
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod       Date:  2007-06-07

10.  Bisphosphonate-related osteonecrosis of the jaws: a single-center study of 101 patients.

Authors:  Towy Sorel Lazarovici; Ran Yahalom; Shlomo Taicher; Sharon Elad; Izhar Hardan; Noam Yarom
Journal:  J Oral Maxillofac Surg       Date:  2009-04       Impact factor: 1.895

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Review 1.  Bisphosphonate-related osteonecrosis of the jaw: from the sine qua non condition of bone exposure to a non-exposed BRONJ entity.

Authors:  Valesca Sander Koth; Maria Antonia Figueiredo; Fernanda Gonçalves Salum; Karen Cherubini
Journal:  Dentomaxillofac Radiol       Date:  2016-05-31       Impact factor: 2.419

Review 2.  Adjudication of osteonecrosis of the jaw in phase III randomized controlled trials of denosumab: a systematic review.

Authors:  Paul de Boissieu; L Kanagaratnam; R Mahmoudi; A Morel; M Dramé; T Trenque
Journal:  Eur J Clin Pharmacol       Date:  2017-02-10       Impact factor: 2.953

3.  Legal liability in bisphosphonate-related osteonecrosis of the jaw.

Authors:  L Lo Russo; D Ciavarella; C Buccelli; O Di Fede; G Campisi; L Lo Muzio; G Pellegrino; P Di Lorenzo
Journal:  Br Dent J       Date:  2014-09       Impact factor: 1.626

4.  Carcinoma of the lip five years after bone marrow transplantation.

Authors:  M Ardore; M Berrone; G Marchitto; S Gandolfo; M Pentenero
Journal:  Ann Stomatol (Roma)       Date:  2015-12-01

5.  Meaning and Limitation of Cortical Bone Width Measurement with DentaScan in Medication-Related Osteonecrosis of the Jaws.

Authors:  Eiji Iwata; Masaya Akashi; Megumi Kishimoto; Junya Kusumoto; Takumi Hasegawa; Shungo Furudoi; Takahide Komori
Journal:  Kobe J Med Sci       Date:  2017-02-15

6.  Interrelationship of clinical, radiographic and haematological features in patients under bisphosphonate therapy.

Authors:  Valesca S Koth; Maria A Figueiredo; Fernanda G Salum; Karen Cherubini
Journal:  Dentomaxillofac Radiol       Date:  2017-02-17       Impact factor: 2.419

7.  Osteonecrosis of the jaw related to non-antiresorptive medications: a systematic review.

Authors:  Ourania Nicolatou-Galitis; Maria Kouri; Erofili Papadopoulou; Emmanouil Vardas; Dimitra Galiti; Joel B Epstein; Sharon Elad; Giuseppina Campisi; Nikolaos Tsoukalas; Kivanc Bektas-Kayhan; Winston Tan; Jean-Jacques Body; Cesar Migliorati; Rajesh V Lalla
Journal:  Support Care Cancer       Date:  2018-10-23       Impact factor: 3.603

Review 8.  Imaging of Radiation- and Medication-Related Osteonecrosis.

Authors:  Sanjay M Mallya; Sotirios Tetradis
Journal:  Radiol Clin North Am       Date:  2017-10-10       Impact factor: 2.303

Review 9.  Detecting the earliest radiological signs of bisphosphonate-related osteonecrosis.

Authors:  H Devlin; J Greenwall-Cohen; J Benton; T L Goodwin; A Littlewood; K Horner
Journal:  Br Dent J       Date:  2017-11-17       Impact factor: 1.626

10.  A Comparison of the Clinical and Radiological Extent of Denosumab (Xgeva®) Related Osteonecrosis of the Jaw: A Retrospective Study.

Authors:  Zineb Assili; Gilles Dolivet; Julia Salleron; Claire Griffaton-Tallandier; Claire Egloff-Juras; Bérengère Phulpin
Journal:  J Clin Med       Date:  2021-05-28       Impact factor: 4.241

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