18 Years of Medication-Related Osteonecrosis of the Jaw (MRONJ) Research: Where Are We Now?—An Umbrella Review

: Background : Osteonecrosis of the jaw (ONJ) is a condition affecting patients exposed to medications used to treat benign and malignant conditions of bone tissue. Many studies have highlighted that ONJ is a severe condition, which is very challenging to manage, especially in individuals with oncologic disease. The aim of this umbrella review is to analyze all available interventional and non-interventional systematic reviews published on medication-related osteonecrosis of the jaw (MRONJ) and summarize this evidence. Material and methods : A multi-database search (PubMed, MEDLINE, EMBASE and CINAHL) was performed to identify related multi-language papers published from January 2003 until June 2021. An additional manual search was also performed in systematic review registries (PROSPERO, INPLASY, JBI and OFS) to identify possible missing reviews. Data were extracted from relevant papers and analyzed according to the outcomes selected in this review. Results: The search generated 25 systematic reviews eligible for the analysis. The total number of patients included in the analysis was 80,840. Of the reviews, 64% ( n = 16) were non-interventional and 36% ( n = 9) were interventional. Study designs included case series 20.50% ( n = 140), retrospective cohort studies 12.30% ( n = 84) and case reports 12.20% ( n = 83). It was unclear what study design was used for 277 studies included in the 25 systematic reviews. Conclusions: The data reviewed conﬁrmed that the knowledge underpinning MRONJ in the last 20 years is still based on weak evidence. This umbrella review highlighted a widespread low-level quality of studies and many poorly designed reviews. prospective (PR); retrospective (RE); case series (CS); case report (CR); prospective case-controlled study (P-CCS); retrospective case-controlled study (R-CCS); case-controlled study (CCS); cross-sectional study (CSS); letter to the editor (LE).


Introduction
Medication-related osteonecrosis of the jaw (MRONJ) is an irreversible adverse event related principally to antiresorptive medications (e.g., bisphosphonates and receptor activator of nuclear factor Kappa-B ligand inhibitors) and angiogenesis inhibitors [1,2]. These types of drug therapies are used for the treatment of the skeletal manifestation of malignancies and/or bone metastases, and in the management of osteoporosis, Paget's disease or hypercalcaemia [3,4].
Since the first clinical study of bisphosphonate-related osteonecrosis of the jaw (BRONJ) was published in 2003, a growing number of scientific articles have documented similar complications connected with other medications, such as monoclonal antibodies, tumor necrosis factor-α (TNF-α) inhibitors drugs and recreational drugs [5][6][7]. Due to the number of medications linked with the development of ONJ, in a 2014 positional paper, the American Association of Oral and Maxillofacial Surgeons (AAOMS) developed and defined the medical term MRONJ [8].
This AAOMS position paper outlined that patients should be considered to have MRONJ if all of the following three characteristics are present: (1) Current or previous treatment with antiresorptive or antiangiogenic agents; exposed bone or bone that can be probed through an intraoral or extraoral fistula in the maxillofacial region that has persisted for longer than 8 weeks; (2) No history of radiation therapy to the jaws or obvious metastatic disease to the jaws [8].
Patients often present with exposed bone associated with a sequela of symptoms: pain, swelling, infection, tooth/teeth mobility, neuropathic pain and in some cases, pathological fracture [8]. Interestingly, approximately 25% of patients present with the aforementioned catalogue of symptoms without frank bone exposure [9].
The pathogenesis of MRONJ remains unclear, however a number of risk factors have been identified that are associated with an increased likelihood of MRONJ development. These risk factors have been recognized in multiple independent studies and include the potency and route of administration of the antiresorptive agent (intravenous bisphosphonate vs. oral), the underlying disease (cancer vs. osteoporosis), the duration and cumulative dosage of antiresorptive therapy, dentoalveolar surgery and dental infections [10][11][12][13][14]. The incidence of MRONJ can also vary based on other factors such as medical history, drug therapy, duration of therapy and type of dental treatments [8]. Researches have reported that for cancer patients treated with intravenous bisphosphonates the incidence of MRONJ following tooth extraction is expected to range from 1.6-14.8% with a mean incidence of 7% [8,15].
This compares to a 1.8% incidence for oncology patients receiving denosumab and an incidence of MRONJ of 0.5% for patients taking oral bisphosphonates [8,[16][17][18]. Furthermore, the use of antiangiogenic agents in combination with antiresorptive drugs is known to increase the risk of MRONJ development with an estimate of 16% of recurrent rates [17].
Studies have reported that dental extractions are the most common cause of MRONJ with figures ranging from 48.5% to up to 80% [19]. In a recent study, the trigger of MRONJ was found to be independent of the administration routes, with 61.7% caused by tooth extraction, 14.8% by spontaneous onset and 7.4% by ill-fitting dentures [20]. There is however, limited information about the generating factors for denosumab-related MRONJ.
Many additional factors have been reported in the literature as being associated with accelerated development and/or increased severity of the condition, but for most of these it remains unclear whether or not they are causative factors [21][22][23]. These include the use of corticosteroids, the presence of concomitant diseases or conditions (e.g., preexisting dental infections, anemia, diabetes-mellitus and immunosuppression or renal failure), poor oral hygiene and smoking [21][22][23][24]. The role of genetic factors in MRONJ is also being investigated in order to help to identify patients at increased risk of MRONJ; however, a robust association between MRONJ risk and a specific genetic variant has not yet been identified [25].
An umbrella review on MRONJ was published in 2020 [37]. However, this review presented deficiencies in many aspects, from the quality assessment strategy to the omission of an analysis of the systematic reviews related to epidemiological, diagnostic and preventive strategies studies (non-interventional studies). Hence the aim of this umbrella review is to summarize and assess quality in a comprehensive and complete manner all available evidence in published systematic reviews on MRONJ and report the strength and the deficiencies associated with studies included.

Materials and Methods
This umbrella review was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [38].
The protocol of this review was registered in the International Platform of Registered Systematic Review and Meta-analysis Protocols (INPLASY) under the number IN-PLASY202160061.
The following four databases were explored: PubMed, MEDLINE, EMBASE and CINAHL. A three-stage screening approach was used to ensure precision and safeguard the quality of the search. The screening of titles and abstracts was carried out independently by five authors (RS, JW, OO, EK and OA) to eliminate any irrelevant materials (i.e., reviews, animal studies, non-clinical studies). Disagreements were resolved by discussion until a consensus was reached.
A data screening and abstraction form was used to: • Verify the study eligibility derived from the inclusion/exclusion criteria. Carry out the methodological quality assessment. • Extract data on study characteristics and outcomes for the included studies ( Figure 1). The authors of any studies eligible for inclusion in the review with insufficient information were contacted directly to provide further information. The inclusion criteria was based on a PICO(S) strategy [39].
Focused question and PICO strategy What is the current state of evidence related to MRONJ after 18 years of study? A search strategy for all databases was developed as follows: 1 and 2 and 3.
The search strategy included appropriate changes in the keywords and followed the syntax rules of each database.

Types of Studies
The authors of this umbrella review considered both interventional and non-interventional reviews. The search strategy for this study focused on published systematic reviews and/or meta-analysis. Articles were obtained from January 2003 to June 2021. No language restrictions were imposed on the search. Narrative reviews, reviews not following PRISMA guidelines (after 2009), reviews without registration, animal reviews, and those reviews which included patients with a previous history of radiation therapy to the head and/or neck regions were excluded.

Types of Participants
The review considered studies involving patients who developed MRONJ after having taken antiresorptive, antiangiogenic and/or any drug therapy associated with osteonecrosis of the jaw. No restriction of age, gender or ethnic origin was applied. There was also no restriction on the minimum number of studies or type of studies included in the systematic reviews and/or meta-analysis.

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Type of studies included in the reviews; • Number of patients included in the review; • Patients' demographic; • Type of patient groups (Oncology vs. Non-oncology).

Data Extracted
All selected papers were carefully read by four independent review authors (RS, OA, JW and JY) and data were extracted using a research report form. The number of included studies, design of the studies, number of patients, results, quality of the evidence and recommendation was recorded. In case of missing information, authors were contacted and given 6 weeks to respond. If the information was not provided, the missing data was recorded as "Not Reported (NR)" in the text and in the tables. A total of 25 systematic reviews were included in this study .

Review Quality Assessment Criteria
Three independent review authors (RS, AA and MDCM) appraised the included studies. The methodological quality of each review was evaluated using the Confidence in Evidence from Reviews of Qualitative (CERQual) research tool recommended by the Grading of Recommendations Assessment, Development and Evaluation Working Group (GRADE). The CERQual evaluation tool enabled the authors to evaluate the included studies, according to four key domains: (1) The methodological limitations of the individual qualitative studies contributing to a review finding; (2) The coherence of the review finding; (3) The adequacy of data supporting a review finding; (4) The relevance of the data from the primary studies supporting a review finding to the context (perspective or population, phenomenon of interest and/or setting) specified in the review question [65].
Any disagreements in risk of bias assessments were referred to the third author of the review team (JY) and subsequently resolved by discussion.

Results
Initially considered to be potentially eligible for inclusion were 104 studies but after inspection of the full papers, 79 were excluded for not meeting the inclusion criteria for this umbrella review. Results were expressed as descriptive statistics because of the significant heterogeneity in the published data. A total of 25 systematic reviews were therefore included in this study. The included systematic reviews involved a total of 80,840 patients. All the published data described patients evaluated from 2006 to 2021 (Table 2).  Is there any evidence that orthodontic treatment induces ONJ or other adverse outcomes inpatients treated with antiresorptive drug therapy?

Non-Oncology SR
The types of systematic review included in this research were: systematic reviews (n = 21; 84%) and meta-analysis reviews (n = 4; 16%). Of these reviews n = 16 (64%) were non-interventional and n = 9 (36%) were interventional. The general characteristics of the studies included are shown in Tables 2 and 3. Table 3. Type of studies and patients included within respective systematic reviews. Randomized controlled trial (RCT); prospective (PR); retrospective (RE); case series (CS); case report (CR); prospective case-controlled study (P-CCS); retrospective case-controlled study (R-CCS); case-controlled study (CCS); cross-sectional study (CSS); letter to the editor (LE).

Type of Drug Therapy Used
Aljohani et al. (2017)   The most common design of review was a non-interventional epidemiological design (n = 13; 52%) (incidence, frequency and associated risks of MRONJ) followed by an interventional design n = 6 (24%).
The most common drug type therapy investigated in the reviews included in this study were bisphosphonates 60%, while antiangiogenic drug therapy was investigated in 4% of the studies.
The most frequent type of articles included in the reviews included in this study were case series (n = 140; 20.5%) followed by retrospective cohort studies (n = 84; 12.3%) and case report (n = 83; 12.2%). Regarding their study design, 277 articles (40.5%) were unable to be categorized.
The reviews included in the study predominantly analyzed the evidence related to MRONJ in both oncology and non-oncologic patients (n = 14; 56%). A small number considered only oncologic patients (n = 5; 20%) ( Table 3 and Figure 2).
A number of reviews included in this study did not report a formal risk of bias quality analysis (n = 5; 20%), likely due to the year of article publications (antecedent to the PRISMA checklist guidance methodology).
All the results presented in the reviews included in this study were highlighted as having a lack of evidence or providing any conclusive suggestions (Table 4).

Figure 2.
Overview of the study characteristics: (a) type of the disease analyzed in the reviews included in the study; (b) type of drugs analyzed in the reviews included in the study; (c) type of studies analyzed in the reviews included in the study; (d) type of reviews included in the study. Table 4. Results from included reviews.

Author Result
Aljohani et al. (2017) [40] The mean age of MRONJ osteoporosis patients in our study was 69.7 ± 5.2 years. The mandible was the most common site (394, 70.6%), followed by maxilla (152 case, 27.2%) and then in both of them (only 12 cases, 2.2%). The ratio of mandible to maxilla and both jaws involvement was 2.4:1. There was variability in the duration of BPs therapy, which ranged from 2 weeks to 93 months, with a mean duration of 51.9 ± 18 months. Extraction was the most frequently reported preceding event (244 patients, 48.5%).

Cabras et al. (2021) [42]
The data acquired from the moderate/high risk of bias studies suggested that 2-3 g of amoxicillin daily, either alone or in combination with clavulanate, for 6-7 days is the most commonly used antibiotic treatment to minimize risk of MRONJ in patients requiring a dental extraction, which could provide reduction of MRONJ risk.
Dal Prá et al. (2017) [43] All eight of the selected studies found that CTX levels were not predictive of the development of BRONJ. In conclusion, this systematic review indicates that the CTX test has no predictive value in determining the risk of osteonecrosis in patients taking bisphosphonates.
Duarte et al. (2020) [44] Although no cases of osteonecrosis were identified, all studies had weaknesses such as a limited sample size or the absence of risk factors for the development of osteonecrosis. However, it is believed that patients with secondary osteoporosis who use bisphosphonates continuously should be followed up during adulthood, since bone turnover decreases over the years. MRONJ appears to be associated with an increase in prevalence of periodontal disease. However, the lack of scientific evidence in this matter does not allow clear conclusions to be drawn.

Lorenzo-pouso et al. (2019) [50]
A total of seven biomarkers were identified and classified into three groups: bone turnover, angiogenesis and endocrine markers. Conflicting results were found in relation to most biomarkers, which suggest that no useful markers are currently available to evaluate BRONJ risk.

Mauri et al. (2009) [52]
Overall, osteonecrosis of the jaw was a rare event, occurring in 13 (0.24%) of the 5312 patients receiving bisphosphonates. Treatment with zoledronic acid was significantly associated with the occurrence of osteonecrosis of the jaw (OR = 3.23, 95% CI = 1.7-8) compared with no use.

McGowan et al. (2018) [53]
A total of 4106 patients with MRONJ were identified, 39 different systemic diseases were implicated, and 14 medical and 11 dental risk factors were reported, although no statistical analysis of the significance of each of these factors was possible. However, the most reported dental risk factor was tooth extraction (45%), followed by periodontal disease (10%).

Migliorati et al. (2010) [54]
• The prevalence results observed were different depending on the type of study design. The overall weighted prevalence of BON included a sample of 39,124 patients with a mean weighted prevalence of 6.1%. The weighted prevalence was 13.3% for studies with documented follow-up. The overall prevalence for patients using zoledronic acid only was 8.6%, for pamidronate 7.3%, and 21% for patients who used both.

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There were no studies evaluating the economic impact of BON.

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The poor reporting of outcomes of treatment did not allow us to determine success or failure rates of the treatment strategies.

Palaska et al. (2009) [56]
• The weighted mean time to event was estimated to be 21.9 months (1.8 years), with a median minimum time of 10 months.

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The weighted mean time to event for pamidronate was found to be 33.8 months (2.8 years), whereas the median value for the minimum duration was estimated to be 18 months.

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The majority of the oral BP users were treated for osteoporosis, weighted mean time to event to be 4.6 years, whereas the median minimum time to event was 3 years.

Author Result
Querrer et al. (2021) [57] An increase in bone sequestra, cortical bone lysis, and bone density was observed in bisphosphonate-related ONJ, while larger bone sequestra, more frequent periosteal reactions, and mandibular canal enhancement were noted in denosumab-related ONJ.

Sacco et al. (2021a) [59]
The data reviewed have confirmed that an invasive procedure is the most common trigger of MRONJ with relatively high frequency of postoperative complications or recurrence following management. However, due to low-quality research available in the literature, it is difficult to ascertain quantitatively the susceptibility of immunosuppressed patients in the development of MRONJ in non-oncology patients.

Sacco et al. (2021b) [60]
Based on the limited data available in literature, it is plausible that not histologically analyzing all ONJ specimens could result in a small amount of undiagnosed and untreated malignant diseases (4.64% based on large cohort studies).

Woolley et al. (2021) [64]
Lack of evidence whether orthodontic treatment can precipitate MRONJ. Moreover, antiresorptive drug therapy has been associated with a sub-optimal treatment outcome. The review reported adverse outcomes including: difficulty achieving root parallelism, difficulty achieving complete space closure, exaggerated mobility post-debond, increased duration of orthodontic treatment beyond expected completion, sclerotic alveolar bone changes seen on post-op radiographic images, an increased amount of root resorption and one case of ONJ.

Author Result
Beth-tasdogan et al. (2017) [41] Available evidence is insufficient to either claim or refute a benefit for hyperbaric oxygen therapy as an adjunct to conventional therapy. There is also insufficient evidence to draw conclusions about autofluorescence-guided versus tetracycline fluorescence-guided bone surgery. Moreover, there is insufficient evidence to conclude that the use of the other interventions investigated would reduce the risk of MRONJ or would improve healing of MRONJ.

Madrid & Sanz (2009) [51]
From the analysis yield in this study, the placement of an implant may be considered a safe procedure in patients taking oral BPs for 5 years with regard to the occurrence of BRONJ since in these studies no BRONJ has been reported.

Ottesen et al. (2020) [55]
There is no evidence for using a drug holiday, but it is also clear that caused by a limited numbers of eligible patients, and a great variation in between these patients, high-level evidence for using an AR drug holiday is almost impossible to obtain this data.

Rollason et al. (2016) [58]
There is a lack of evidence from randomized controlled trials to guide treatment of bisphosphonate-related osteonecrosis of the jaw (BRONJ).

Sacco et al. (2021c) [61]
The data reviewed confirmed that an invasive procedure is the most common trigger of MRONJ. The overall MRONJ disease recurrence was identified in n = 6 (16.6%) cases. Two (n = 2) recurrences were observed in the conservative treatment group, n = 3 recurrences were recognized in the conservative and antibiotics treatment group of patients and n = 1 was observed in the surgical treatment group. However, due to the low quality of available research in literature, it is difficult to draw a definitive conclusion on the validity of the presented treatment to manage patients affected by MRONJ associated with angiogenic therapy. Over suppression of bone turnover is probably the primary mechanism for the development of this condition, although there may be contributing comorbid factors. All sites of potential jaw infection should be eliminated before bisphosphonate therapy is initiated in these patients to reduce the necessity of subsequent dentoalveolar surgery. Conservative debridement of necrotic bone, pain control, infection management, use of antimicrobial oral rinses, and withdrawal of bisphosphonates are preferable to aggressive surgical measures for treating this condition.

Review Quality Assessment
The assessment of each CERQual component was based on judgements by the review authors and these judgements were described and detailed in CERQual Qualitative Evidence Profile (Table 5).

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Methodological limitations: The extent to which there are problems in the design or conduct of the primary studies that contributed evidence to a review finding. • Relevance: The extent to which the body of evidence from the primary studies supporting a review finding is applicable to the context (perspective or population, phenomenon of interest, setting) specified in the review question. • Coherence: The extent to which the review finding is well grounded in data from the contributing primary studies and provides a convincing explanation for the patterns found in these data. • Adequacy of data: An overall determination of the degree of richness and quantity of data supporting a review finding.
** The CERQual approach-Definitions of levels of confidence in a review finding • High confidence: It is highly likely that the review finding is a reasonable representation of the phenomenon of interest. • Moderate confidence: It is likely that the review finding is a reasonable representation of the phenomenon of interest. • Low confidence: It is possible that the review finding is a reasonable representation of the phenomenon of interest. • Very low confidence: It is not clear whether the review finding is a reasonable representation of the phenomenon of interest.  In summary the authors found that:

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There were minor concerns with respect to the relevance and coherence of the epidemiological type of reviews in all studies. Moderate concerns were noted regarding the methodological limitations in eight studies and serious concerns were highlighted for similar limitations in four studies. Serious concerns were also noted for the adequacy of data of their results in all of the included studies. Due to the high number of serious concerns, particularly regarding methodology and result data, the overall assessment was assessed as very low confidence (lack of clarity whether the review finding is a reasonable representation of the phenomenon of interest).

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Minor concerns were highlighted with respect to the relevance and coherence of management types of reviews. Moderate concerns were raised regarding methodological limitations in three studies and serious concerns in methodological limitations in one study. Serious concerns were raised for one study regarding the adequacy of data in the results. Due to these concerns, the overall assessment regarding the management type was graded as very low confidence (lack of clarity whether the review finding is a reasonable representation of the phenomenon of interest).

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With respect to predicting markers, the reviews were graded as having minor concerns for relevance and coherence, moderate concerns regarding methodological limitations and serious concerns regarding methodological limitations and adequacy of the result data. Due to these concerns, the overall assessment regarding predicting markers was rated as having very low confidence (lack of clarity whether the review finding is a reasonable representation of the phenomenon of interest).

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Relating to dental rehabilitation, reviews were graded with minor concerns for relevance, moderate concerns regarding methodological limitations and coherence, and serious concerns regarding adequacy of result data. This domain again was graded as having very low confidence (lack of clarity whether the review finding is a reasonable representation of the phenomenon of interest).

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Regarding preventive strategy, reviews demonstrated minor concerns for relevance and coherence, moderate concerns regarding methodological limitations and serious concerns regarding adequacy of data results. The overall assessment for preventative strategy was rated as very low confidence (lack of clarity whether the review finding is a reasonable representation of the phenomenon of interest). • Finally, when assessing the diagnostic investigations within the reviews, this review identified minor concerns regarding relevance and coherence, moderate concerns regarding methodological limitations and serious concerns regarding adequacy of the data results. Therefore, with regard to the overall assessment, this domain was graded as very low confidence (lack of clarity whether the reviews found a reasonable representation of the phenomenon of interest).

Discussion
Medication-related osteonecrosis of the jaw (MRONJ) is a rare but disabling disease [1,8,66]. Currently, the aetiopathogenesis of MRONJ has not been well explained despite a large number of patients suffering from this severe adverse event [8].
At present there are three key theories proposed for the pathogenesis of MRONJ; bone turnover suppression, cellular toxicity and infection. Whereas circumstantial studies underpin the hypothesis that antiresorptive drugs reduce bone formation and promote necrosis, physiological and radiological research suggest different findings. The hypotheses of drug-related cellular toxicity affecting epithelial cells and macrophages causing limited immune defence as a result of impaired functions has been purported by many ex vivo and in vivo studies. Infection is believed to be an important contributing factor to the disease as it can encourage extreme bone resorption. Whether it is the generating factor or the result of the disease process still remains unclear [67]. Additional studies are necessary to confirm the exact pathological process of anti-angiogenic drugs as their drug actions are different from bisphosphonates and denosumab.
Despite the great collaborative effort in the past decades in investigating MRONJ, there are many unanswered questions and a lack of a common agreement among researchers and investigators.
Although there are many systematic reviews on the subject, there is still no unanimous consensus on many aspects of MRONJ from preventive strategy, to the management of the disease [41]. Despite the limited evidence available, many countries have established guidelines in the attempt to improve the care of these vulnerable patients.
Using the Oxford Centre for Evidence-Based Medicine (1a, 2a and 3a), the present umbrella review looked at the current highest available evidence published in the last 20 years on drug-induced ONJ in the attempt to highlight the current state of the quality of research [68].
Among the systematic reviews and meta-analysis included in this study, we noticed a very broad inclusion criteria adopted by authors of the many reviews. This is evident from the study numbers included in the reviews, which varied from 1 article [58] to 219 articles [53]. Except for the few meta-analyses included in this review, most of the included articles were often weak, low ranked and demonstrated a high risk of bias [41,52]. These methodological inadequacies have undoubtedly increased the risk of inconsistency of the general guidelines worldwide, resulting in lack of effectiveness in handling patients at risk or affected by MRONJ.
The authors have discovered that the majority of the reviews feature predominantly case reports, case series, and observational studies. For this reason, the findings of these reviews should be interpreted cautiously [48,56,[59][60][61]64]. This review also revealed that a large number of systematic reviews in the literature (excluded in this article) do not follow the recognized PRISMA checklist guidance, which inevitably increases the chances of methodological errors and reporting bias.
In the future, systematic reviews or meta-analysis should outline a clear protocol before conducting the study; with the foresight that these pieces of research are often fundamental tools used to implement clinical practice in the form of guidelines. Unusually, systematic reviews have clear protocols. However, we have noticed that many of the 24 included reviews did not perform a comprehensive search for studies, report funding for included studies or conduct a satisfactory risk bias analysis [56,63]. These shortcomings are likely to have increased the issues surrounding the adequacy of their results, resulting in low strength of evidence in the published conclusions.
Despite the large number of systematic reviews on MRONJ, there is still discordant thought without a unanimous consensus on many aspects of MRONJ, from preventive strategy to the management of the disease.
In the future, it is essential to conduct studies with improved quality, including randomized-controlled trials that support evidence-based treatment protocols. In general, the authors advocate that the following rules should be applied for future MRONJ research studies:

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Sample size calculation should be established and employed for all the RCTs. Large RCTs should be carried out and described in sufficient detail to allow precise assessment, management and/or epidemiological findings. • Risk stratification should be applied for any clinical studies in order to minimize the effect modification and/or confounding factors that could potentially affect the final result/s. • Common, quantifiable and clinically relevant endpoints (time to complete wound healing, pain, specific investigations, treatment acceptability and participant satisfaction) should be described in sufficient detail particularly in patients undergoing to any type of intervention including preventive strategies. • An adequate follow-up period is essential if MRONJ treatment or preventive strategy is studied in order to evaluate the long-term effects on this group of patients. • A predictable special investigation, such as CT, CBCT or MRI should be used for any of the observational and interventional studies at diagnosis and during the follow-up.

Conclusions
Through this umbrella review, it has become clear that there is limited high strength evidence to support many of the current recommendations surrounding medication-related osteonecrosis of the jaw. The low quality systematic reviews and meta-analyses highlighted by this study show no insightful therapeutic recommendations, preventive strategies, risk reduction or standards that can be applied for this debilitating disease. A number of higher quality clinical studies are necessary to make evidence-based decisions on MRONJ therapies.

Data Availability Statement:
The data used to support the findings of this study are included within the article.