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Volume 2013 (2013), Article ID 672027, 8 pages
Decreasing Frequency of Osteonecrosis of the Jaw in Cancer and Myeloma Patients Treated with Bisphosphonates: The Experience of the Oncology Network of Piedmont and Aosta Valley (North-Western Italy)
1Medical Oncology Unit, Department of Oncology and Hematology, Ospedale SS Antonio e Biagio e C Arrigo, Via Venezia 16, 15121 Alessandria, Italy
2Unit of Cancer Epidemiology, S. Giovanni Battista-Molinette and CPO-Corso Bramante 88, 10126 Piedmont, Turin, Italy
3Oncology Unit, University of Brescia, Spedali Civili Hospital, Piazzale Spedali Civili 1, 25123 Brescia, Italy
4Oncology Unit, IRCC Candiolo, Strada Provinciale 142, 10060 Candiolo, Turin, Italy
5Oncology Unit, S. Giovanni Battista, Molinette, Corso Bramante 88, 10126 Turin, Italy
6Oral Surgery Unit, S. Giovanni Battista, Molinette, Corso Bramante 88, 10126 Turin, Italy
7Oral Care Unit, Mauriziano Hospital, Via Magellano 1, 10126 Turin, Italy
8Dental Clinic, Department of Health Science, University of Eastern Piedmont “A. Avogadro”, Via Solaroli 17, 28100 Novara, Italy
9Hematology Unit, Department of Oncology and Hematology, Ospedale SS Antonio e Biagio e Cesare Arrigo Hospital, Via Venezia 16, 15121 Alessandria, Italy
10Hematology Unit, Turin University, Corso Bramante 88, 10126 Turin, Italy
11“Rete Oncologica di Piemonte e Valle d’Aosta” Oncology Network, Azienda Ospedaliero Universitaria San Giovanni Battista-Presidio San Lazzaro, Via Cherasco 23, 10126 Turin, Italy
Received 28 December 2012; Accepted 18 January 2013
Academic Editors: Z. S. Guo and V. Lorusso
Copyright © 2013 Vittorio Fusco et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background. Data concerning frequency of Osteonecrosis of Jaws (ONJ) are mostly based on single center experiences. Patients and Methods. Since 2005 a multidisciplinary study group collected data of cases of ONJ in patients treated with Bisphosphonates (BP) and observed in oncology and hematology centers of a regional network. Results. By December 2008, 221 cases were registered. We report details of 200 cases, identified after cross-checking reports from centres of medical oncology, haematology, and oral care. Primary neoplasm was breast cancer (39%), myeloma (32%), prostate cancer (16%), and other types of cancer (8%). In about 50% of the cases a history of dental extraction was present. Zoledronic acid was administered (alone or with other BP) to 178 patients (89%). Median time from first infusion to ONJ diagnosis was 21.0 (zoledronic acid only) and 39.0 months (pamidronate only). The number of ONJ cases per year was 3 in 2003, 21 in 2004, 58 in 2005, 60 in 2006, 37 in 2007, and 21 in 2008. Conclusion. The number of new ONJ cases in cancer and myeloma patients increased until 2006 and then reduced. The possible reasons of this trend (introduction of zoledronic acid; increase of ONJ awareness; diffusion of preventive dental measures; late modifications of BP prescription) are herein discussed.
Bisphosphonates (BPs) are widely prescribed at different doses, way of administration (oral versus IV) and treatment durations, for a range of bone diseases including cancer-induced bone disease, osteoporosis, and Paget’s disease. Most of IV prescriptions of more potent BPs are written for patients affected by myeloma or bone metastases from solid cancer . Despite the optimal duration of treatment with BPs is unknown, several recommendations and position papers suggested in the past that administration of BP should be carried on indefinitely [2–4].
Osteonecrosis of the Jaws (ONJ) was first reported in patients treated with BPs in North American literature in 2003 [5, 6]. Ever since a large amount of case reports and case series have been published worldwide [6, 7], although, quite surprisingly, no cases were reported in previously published randomized controlled trials (RCT) that led to the introduction of BP in the therapy armamentarium.
The paucity of data from well-designed prospective trials do not allow to estimate the precise incidence of ONJ among subjects exposed to BPs [8–11]. According to several published reports (cohort studies, case series, usually based on single centre experience), the frequency of ONJ in cancer patients receiving BPs is estimated to vary in a wide range (i.e. from less than 1% to about 50%), suggesting that it can be a common event [12–14]. There are very few data about frequency of ONJ based on systematically collected data in large populations [6, 15].
The risk of ONJ is directly related to the cumulative dose (dose per duration of exposure) and the potency of BPs, with evidence of a greater risk with IV amino-BPs, and in particular with zoledronic acid [12, 16–19]. The role of other possible risk factors is at present unclear ; there are suggestions of an increased risk of ONJ in subjects exposed to antiangiogenic drugs as well [21, 22]. In most of cases, the trigger events leading to ONJ diagnosis are dental extraction, bone surgery, periodontal disease, and denture trauma, even though spontaneous cases are reported in almost all the published case series [16, 17, 23].
We present here the results of a large series of ONJ cases systematically collected at oncology and hematology units and at referral oral care centers of a regional area in North-Western Italy: Piemonte and Valle d’Aosta.
2. Materials and Methods
In November 2005, a regional ONJ Study Group was established by members of a Piemonte and Valle d’Aosta network (Rete Oncologica), encompassing all public oncology and hematology units of two administrative regions in North-Western Italy. The group included maxillofacial surgeons and dental specialists of all referral centers in the regional area.
A data collection form was sent to all oncology and hematology units of the network and to the referral oral care centers (maxillofacial surgery; otolaryngology; hospital oral medicine units) in the region.
We cross-checked data from network centers and specialist units (to integrate data and to avoid double-counting), identifying cases observed before November 2005 with sufficiently detailed forms to be included in a specific data base .
From November 2005 onwards, data about new suspected and recognized ONJ cases were collected prospectively and sent (in case of confirmed ONJ diagnosis) to the study group coordinator (V.Fusco).
One author (A.Loidoris) visited most of the oncology and hematology units and maxillofacial or oral care units, to assure consistency in data collection. Local audit visits have been periodically repeated in the course of subsequent years in the main referral centers.
Cases were confirmed and included in the data base as “ONJ cases” when the following criteria were met: history of BP therapy; intraoral lesion (exposed bone, pus exudates, or fistulae) or extra oral manifestations of swelling or fistulae that fail to heal within 8 weeks; imaging exams identifying jaw bone necrosis in case of absent bone exposure; and no history of radiation therapy that could imply osteo-radionecrosis.
Requested and collected data included the following: (a)demographics: age, sex;(b)cancer and myeloma history: type of primary cancer or myeloma; date of diagnosis (myeloma or primary solid tumor, and metastatic bone lesions); (c)BP therapy: start date, treatment duration, type of BP, dosage, and number of administrations;(d)other cancer and myeloma treatments: chemotherapy (administered prior, concomitantly or after BP therapy), hormone therapy, steroid treatment (massive or occasional), antiangiogenic therapies;(e)possible ONJ risk factors: smoking history, diabetes;(f)site(s) (maxillary versus mandible) and date of ONJ diagnosis;(g)clinical findings at the ONJ diagnosis;(h)dental comorbidities or possible precipitating events, such as teeth extraction, periodontal surgery, dental implants, or traumatic use of dentures;(i)ONJ treatment and evolution.
Continuous data are presented as median (interquartile range, IQR) or mean (Standard Deviation, SD) as appropriate, and categoric data as number (percentage, %). STATA SE version 11.0 (STATA Corp, USA) was used for all analyses.
3.1. Patients Characteristics
We collected individual data of 241 patients identified as ONJ cases by the medical or dental specialists. Twenty patients had ONJ diagnosis after BP therapy of bone disease (osteoporosis and osteopenia, Paget’s disease, etc.) without any clear history of cancer and were therefore beyond the subject of this paper. Twenty-one ONJ cases were excluded due to incomplete data regarding information of interest, that is, cancer history, BP treatment (duration, dose), and dental history.
The characteristics of the 200 ONJ cases included in this study are presented in Table 1.
The median time from diagnosis of the bone metastasis or myeloma to ONJ onset was 34.1 (range 3.5–268.4) and 42.7 months (5.6–203.2), respectively.
3.2. Bisphosphonates: Drug, Duration of Treatment, and Cumulative Dosage
One hundred forty-seven patients (73.5%) were treated with only one type of BP, 53 patients (26.5%) with at least two different drugs, being zoledronic acid the most prescribed drug (90% of total population) (Table 1).
The median time from the first infusion of BP to the diagnosis of ONJ was 27.4 months (range 1.8–203.1), with 20.7 months (range 1.8–74.5) for those receiving zoledronic acid only and 38.6 months (range 5.5–102.7) for those treated with pamidronate only. Among patients who received more than one BP, the median time was 56 months (range 6.5–203.1) with pamidronate/zoledronate sequence. The median duration of BP therapy and median doses of administered drugs are illustrated in Table 2.
3.3. Exposure to Possible Risk Factors and Medical Comorbidities
Among ONJ patients (Table 3), 17.5% were active smokers and 7.5% were ex smokers. About 45% of patients received massive steroids treatment (mostly in myeloma affected patients) and another 20% of patients were occasionally treated with steroids (mainly in association with chemotherapy). Diabetes was reported in 14% of the cases. About medical treatment timing, 15% had been treated with chemotherapy before the infusions of BPs only, 42% received chemotherapy concomitant to BP treatment, 17.5% had both prior and concomitant chemotherapy and 18.5% did not receive chemotherapy. Thirty-eight patients received anti-angiogenic drugs (35 thalidomide, 2 lenalidomide, and 1 bevacizumab). In about 50% of cases a history of dental extraction was present.
3.4. ONJ Clinical Manifestations
The presentation and treatment outcomes of ONJ are resumed in Table 3. The majority of patients (122) had a lesion in the mandible; in 57 patients, ONJ lesions occurred in the maxilla and in 21 patients in both maxilla and mandible. A considerable proportion of patients (48 cases, 24%) had multifocal lesions.
3.5. Followup and Treatment Outcome
The ONJ treatment was substantially uniform among centers. The therapeutic approach to each patient was changed on the basis of patient characteristics (age, Performance Status, comorbidities), disease extension (limited versus extended), expected cancer survival and prognosis.
Patients showing exposed and necrotic bone regions (but not heavily symptomatic) were generally followed and treated conservatively with local wound care and irrigations with/without antibiotics. Surgical procedures included conservative surgery (sequestrectomy or soft debridement), but in some selected cases mandibular resections and maxillectomies were performed.
After a short-term reevaluation (3–6 months after ONJ diagnosis and first treatments), a complete ONJ remission was observed in 11 patients (5.5%), whereas the disease improved in 69 patients (34.5%), did not change in 53 patients (26.5%), and worsened in 46 patients (23.0%). BP treatment was withdrawn in most patients (87.5%) at the ONJ occurrence.
3.6. Changes in Number of ONJ Cases over Time
The pattern of distribution of ONJ cases over time is depicted in Figure 1. It showed an initial increase from 2003 to 2006 and a subsequent decrease in the following 2 years. In particular the number of new diagnoses decreased by 65% in 2008 (21 cases) as compared to 2006 (60 cases) (Figures 1(a) and 1(b)). There was no substantial difference among the main patient groups (breast cancer, myeloma, prostate cancer, and other types of carcinoma) (Figure 1(a)). The drug (or sequence of drugs) administered to patients is shown in Figure 1(b).
Osteonecrosis of jaws (ONJ) is a relatively new disease, recognized since 2003, potentially affecting the quality of life of cancer and myeloma patients ; a largely accepted definition (with accompanying staging system) has been established only in 2007  and revised in 2009 , but the presence of cases without bone exposure enlarged the recognition problem [28, 29]. Incidence of ONJ is possibly underestimated worldwide [6, 7, 30].
In the present study we describe a large case series of ONJ cases among cancer and myeloma patients in the period 2003–2008. ONJ cases observed in all referenced regional centers have been prospectively collected since 2005, so that we are confident that very few patients could have escaped our registration after this date. Unfortunately, due to the absence of a unique collecting data system for all the patients treated with BPs in our region, we were not able to draw the incidence of ONJ among the exposed (at risk) population, but we could only estimate the crude frequency in the general population. This represents a clear limitation of our study.
Our results show that this adverse event is not rare, since we recorded a total of 221 cases among patients with cancer observed within a 5-6 year time period in a region of 4.3 million population. These numbers appear much higher than those previously reported in Australia (114 new cases in 2 years in a population of 20.3 millions) . To our knowledge, no further data or estimations on large populations have been published. Projecting these data on a national basis and assuming an equivalent use of BPs in cancer patients in all the Italian regions, we could estimate that between 2000 and 3000 new ONJ cases have been observed in Italy (58 millions) from 2003 to 2008. These numbers are much higher than those reported to the Drug Surveillance System of the Italian Medicine Agency (425 cases on June 2009) .
The number of new ONJ diagnoses sharply increased from 2003 to 2006, although active data collection in our region only started in November 2005, and therefore we cannot exclude that some ONJ cases diagnosed before this date could have been missed. From 2003 onwards an increasing number of ONJ reports appeared in dental and oncology literature leading to an enlarging awareness of the disease and preventing new ONJ cases from being misclassified as bone jaw metastasis, myeloma disease sites, osteomyelitis, and so forth, as occurred before [5, 6]. In addition, due to a possible “harvesting” effect, some prevalent cases could have been included as “new” cases in the first years. The increasing number of ONJ cases in our region parallels an increased use of zoledronic acid. In Italy, zoledronic acid, the most potent BP, rapidly and largely replaced pamidronate from 2002 onwards as the first choice BP therapy in myeloma and cancer patients (Figure 2), and many patients already receiving pamidronate were shifted to zoledronic acid. A trend comparable to the one observed in Italy was registered in the Piedmont region for the prescriptions of zoledronic acid.
The decreasing number of ONJ cases observed from 2006 onwards can have several explanations, but two factors appear as the most relevant. Firstly, the awareness of this important adverse event led from late 2005 onwards to the adoption in our region of preventive dental measures including a pretherapy dental assessment (with eventual necessary dental extractions before starting BP treatment, when possible) and limitation of further dental and jaw bone trauma during BP treatment; furthermore, periodical dental visits were recommended, and the patients were alerted to refer to a physician in case of dental problems arising during BP treatment. Secondly, a significant reduction in IV BP prescriptions has been observed in Italy (Figure 2), mainly due to a reduction in the zoledronic acid prescriptions, and there was a similar trend in the Piedmont region. This could be related to a lower number of treated patients or to a lower number of administered doses per single patient (a possible reduction of the individual cumulative dose due, for instance, to a reduced duration of treatment, as suggested by several authors and expert panels since 2006) [32–37], or both.
Both the above-mentioned factors (i.e., implementation of dental preventive measures and reduction in zoledronic acid prescriptions) could have contributed to the decreasing incidence trend of ONJ observed after 2006. However, the design of the present study does not allow to quantify the relative effects of these two factors in the reduction of the ONJ cases.
Two papers firstly reported on the efficacy of preventive dental measures [38, 39]. Both papers showed a reduction (but not the disappearance) of ONJ new cases in the time period in which these measures were adopted as opposed to an earlier period in which this was not done. These papers, however, did not adequately evaluate the contribution of a possible reduction of BP treatment duration and/or BP cumulative dose. Further studies with an appropriate prospective design are necessary to disentangle this point. Moreover, prospective randomized clinical trials (RCTs) are urgently needed to evaluate the risk/benefit ratio of alternative dosing schedules, as already suggested .
The physiopathology of ONJ is mostly unknown, but several predisposing factors have been pointed out, such as previous or concomitant treatment with steroids (massive prescriptions, as in myeloma patients) and antiangiogenic drugs. In our series these therapies had been administered in 45% and 19% of patients, respectively. The main apparent “trigger” condition leading to ONJ occurrence or discovery was dental extraction (50% of cases in our series), confirming the literature findings [14, 40, 41]. It has been stated that ONJ often occurs in older medically compromised patients . Our data do not confirm this observation since the mean age of our ONJ patients (68 years) is not different from the expected age of cancer patients.
Most cases (89%) in our series had been treated with zoledronic acid, either alone or after a previous pamidronate therapy. In addition, a shorter latency between the BP start and the ONJ onset has been observed in zoledronic acid treated patients (median: 21 months) as opposed to pamidronate treated patients (median: 39 months). All these findings are confirmatory of literature data [19, 43]. In our regional experience, about 35% of the cases had their ONJ condition improved and in a further 5% the disease achieved a complete remission after a short followup. These data suggest that the conservative therapeutic approaches commonly employed seem efficacious in temporarily controlling the disease in some cases, but better evaluations of surgical treatments are needed, especially monitoring both mucosal and bone defect restoration upon a longer followup.
In conclusion, in this series we confirm that BP-associated ONJ was not a rare event in our region, even though its frequency has sharply decreased after 2006. This appears related to a greater awareness of this relevant adverse event and consequently to the adoption of several measures that include preventive and periodical dental visits, patient’s education, and a reduction of BP cumulative dose. Further evaluations on years 2009–2011 in our regional network are ongoing.
Collaborating CentersAlba-Bra Hospital (Franchini, Faggiuolo) Alessandria Hospital (Fasciolo, Levis, Baraldi, Fusco, Loidoris, Pertino, De Martino) Amedeo di Savoia Hospital, Torino (Pontiglio) Aosta Hospital (Ferrero, Gini, Numico, Alvaro) Asti Hospital (Polastri, Cartoni, Marchetti, Testore, Ferrero) Biella Hospital (Ion, Tonso, Clerico, Vincenti) Borgomanero Hospital (Romaniello) Casale Monferrato Hospital (Botta, Muzio) Chivasso Hospital (Bertoldo) Ciriè Hospital (Guiso, Freilone, Grassi, Montrucchio) Cottolengo Hospital, Torino (Raucci) CPO Epidemiological team, Torino (Merletti, Ciccone, Galassi, Richiardi) Cuneo Hospital (Ruffino, Spada, Grasso, Merlano, Garrone, Occelli, Violante) Fossano Hospital (Genesio) Institute for Cancer Research, Candiolo (Aglietta, Ortega,Vormola, Prati) Ivrea Hospital (Bugni, Prosa, Bretti, Vellani) Martini Hospital, Torino (Succo, Carbonaro) Mauriziano Hospital (Goia, Basano, Gilardino, Chiarelli, Poccardi) Molinette Hospital and University, Torino (Boccadoro, Falco, Gallo, Pregno, Benevolo, Bertetto, Ciuffreda, Donadio, Vandone, Berrone, Ranieri, Diaspro, Mozzati, Scoletta, Gandolfo, Arduino) Moncalieri Hospital (Dongiovanni, Ardine) Novara Hospital and University (Alabiso, Miraglia, Forti, Bertona, Foglio Bonda, Migliario, Benech, Poglio, Stellin, Avanzi, Gaidano, Rossi) Novi Ligure Hospital (Castagneto, Stevani) Orbassano—S.Luigi Hospital and University (Pomatto, Barberis, Saglio, Guglielmelli, Dogliotti, Berruti, Gorzegno, Tucci) Ovada Hospital (Varese) S. Anna Hospital, Torino (Durando) S. Giovanni Antica Sede Hospital, Torino (Airoldi) S. Giovanni Bosco Hospital, Torino (Beatrice, Caldarelli, Madaro, Vietti Ramus, Tonda, Addeo) Tortona Hospital (Simoni, Cosentino) Verbania Hospital (Cozzi, Amodei, Loi, Milani) Vercelli Hospital (Falco, Demarino, Manachino)
Conflict of Interests
The authors declare that they have no conflict of interests.
This study has been sustained by the oncology network “Rete Oncologica di Piemonte e Valle d’Aosta.” Acknowledgments are due to Dr.ssa Iolanda De Martino and Dr.ssa Lorenza Randi for data managing.
- R. E. Coleman and E. V. McCloskey, “Bisphosphonates in oncology,” Bone, vol. 49, no. 1, pp. 71–76, 2011.
- B. E. Hillner, J. N. Ingle, R. T. Chlebowski et al., “American Society of Clinical Oncology 2003 update on the role of bisphosphonates and bone health issues in women with breast cancer,” Journal of Clinical Oncology, vol. 21, no. 21, pp. 4042–4057, 2003.
- J. R. Berenson, B. E. Hillner, R. A. Kyle et al., “American society of clinical oncology clinical practice guidelines: The role of bisphosphonates in multiple myeloma,” Journal of Clinical Oncology, vol. 20, no. 17, pp. 3719–3736, 2002.
- F. Saad, C. S. Higano, O. Sartor et al., “The role of bisphosphonates in the treatment of prostate cancer: Recommendations from an expert panel,” Clinical Genitourinary Cancer, vol. 4, no. 4, pp. 257–262, 2006.
- R. E. Marx, “Pamidronate (Aredia) and zoledronate (Zometa) induced avascular necrosis of the jaws: a growing epidemic,” Journal of Oral and Maxillofacial Surgery, vol. 61, no. 9, pp. 1115–1117, 2003.
- S. L. Ruggiero, “Bisphosphonate-related osteonecrosis of the jaw (BRONJ): initial discovery and subsequent development,” Journal of Oral and Maxillofacial Surgery, vol. 67, supplement 1, pp. 13–18, 2009.
- B. J. Edwards, M. Gounder, J. M. McKoy et al., “Pharmacovigilance and reporting oversight in US FDA fast-track process: bisphosphonates and osteonecrosis of the jaw,” The Lancet Oncology, vol. 9, no. 12, pp. 1166–1172, 2008.
- F. Saad, J. E. Brown, C. V. Poznak, et al., “Incidence, risk factors, and outcomes of osteonecrosis of the jaw: integrated analysis from three blinded active-controlled phase III trials in cancer patients with bone metastases,” Annals of Oncology, vol. 23, pp. 1341–1347, 2012.
- P. Gimsing, K. Carlson, I. Turesson et al., “Effect of pamidronate 30 mg versus 90 mg on physical function in patients with newly diagnosed multiple myeloma (Nordic Myeloma Study Group): a double-blind, randomised controlled trial,” The Lancet Oncology, vol. 11, no. 10, pp. 973–982, 2010.
- G. J. Morgan, F. E. Davies, W. M. Gregory et al., “First-line treatment with zoledronic acid as compared with clodronic acid in multiple myeloma (MRC Myeloma IX): a randomised controlled trial,” The Lancet, vol. 376, no. 9757, pp. 1989–1999, 2010.
- P. Musto, M. T. Petrucci, S. Bringhen et al., “A multicenter, randomized clinical trial comparing zoledronic acid versus observation in patients with asymptomatic myeloma,” Cancer, vol. 113, no. 7, pp. 1588–1595, 2008.
- S. L. Ruggiero, T. B. Dodson, L. A. Assael, R. Landesberg, R. E. Marx, and B. Mehrotra, “American association of oral and maxillofacial surgeons position paper on bisphosphonate-related osteonecrosis of the jaws-2009 update,” Journal of Oral and Maxillofacial Surgery, vol. 67, supplement 1, pp. 2–12, 2009.
- R. Mhaskar, J. Redzepovic, K. Wheatley, et al., “Bisphosphonates in multiple myeloma,” The Cochrane Database of Systematic Reviews, no. 3, Article ID CD003188, 2010.
- C. A. Migliorati, S. B. Woo, I. Hewson, et al., “A systematic review of bisphosphonate osteonecrosis (BON) in cancer,” Support Care Cancer, vol. 18, pp. 1099–1106, 2010.
- T. Mavrokokki, A. Cheng, B. Stein, and A. Goss, “Nature and frequency of bisphosphonate-associated osteonecrosis of the jaws in Australia,” Journal of Oral and Maxillofacial Surgery, vol. 65, no. 3, pp. 415–423, 2007.
- S. B. Woo, J. W. Hellstein, and J. R. Kalmar, “Systematic review: bisphosphonates and osteonecrosis of the jaws,” Annals of Internal Medicine, vol. 144, no. 10, pp. 753–761, 2006.
- A. O. Hoff, B. B. Toth, K. Altundag et al., “Frequency and risk factors associated with osteonecrosis of the jaw in cancer patients treated with intravenous bisphosphonates,” Journal of Bone and Mineral Research, vol. 23, no. 6, pp. 826–836, 2008.
- G. S. Wilkinson, Y. F. Kuo, J. L. Freeman, and J. S. Goodwin, “Intravenous bisphosphonate therapy and inflammatory conditions or surgery of the jaw: a population-based analysis,” Journal of the National Cancer Institute, vol. 99, no. 13, pp. 1016–1024, 2007.
- V. Fusco, A. Loidoris, G. Colella, P. Vescovi, and G. Campisi, “Osteonecrosis of the jaw (ONJ) risk in breast cancer patients after zoledronic acid treatment,” Breast, vol. 19, no. 5, pp. 432–433, 2010.
- EMEA (European Medicines Agency), “Opinion of the Committee for medicinal products for human use pursuant to article 5(3) of regulation (EC) 726/2004, on Bisphosphonates and Osteonecrosis of the jaw,” EMEA/CHMP/292474/2009, EMEA/H/A-5(3)/1130, 2012, http://www.ema.europa.eu/pdfs/human/opiniongen/29112509en.pdf and http://www.ema.europa.eu/pdfs/human/opiniongen/29247409en.pdf.
- C. Christodoulou, A. Pervena, G. Klouvas et al., “Combination of bisphosphonates and antiangiogenic factors induces osteonecrosis of the jaw more frequently than bisphosphonates alone,” Oncology, vol. 76, no. 3, pp. 209–211, 2009.
- M. Troeltzsch, T. Woodlock, S. Kriegelstein, et al., “Physiology and pharmacology of nonbisphosphonate drugs implicated in osteonecrosis of the jaw,” Journal of the Canadian Dental Association, vol. 78, article c85, 2012.
- P. Vescovi, G. Campisi, V. Fusco et al., “Surgery-triggered and non surgery-triggered Bisphosphonate-related Osteonecrosis of the Jaws (BRONJ): a retrospective analysis of 567 cases in an Italian multicenter study,” Oral Oncology, vol. 47, no. 3, pp. 191–194, 2011.
- R. Gliklich and J. Wilson, “Epidemiology of bisphosphonate-related osteonecrosis of the jaws: the utility of a national registry,” Journal of Oral and Maxillofacial Surgery, vol. 67, supplement 1, pp. 71–74, 2009.
- V. Fusco, C. Ortega, F. Goia, et al., “Bisphosphonates (BP)-related Osteonecrosis of the Jaw (ONJ): clinical experience of the, "Rete Oncologica di Piemonte e Valle d'Aosta" network,” Journal of Clinical Oncology, vol. 24, supplement 20, Abstract 18584, 2006.
- R. A. Miksad, K. C. Lai, T. B. Dodson et al., “Quality of life implications of bisphosphonate-associated osteonecrosis of the jaw,” Oncologist, vol. 16, no. 1, pp. 121–132, 2011.
- Advisory Task Force on Bisphosphonate-Related Ostenonecrosis of the Jaws, American Association of Oral and Maxillofacial Surgeons, “American association of oral and maxillofacial surgeons position paper on bisphosphonate-related osteonecrosis of the jaws,” Journal of Oral and Maxillofacial Surgery, vol. 65, no. 3, pp. 369–376, 2007.
- G. Colella, G. Campisi, and V. Fusco, “American association of oral and maxillofacial surgeons position paper: bisphosphonate-related osteonecrosis of the jaws-2009 update: the need to refine the BRONJ definition,” Journal of Oral and Maxillofacial Surgery, vol. 67, no. 12, pp. 2698–2699, 2009.
- A. Bedogni, V. Fusco, A. Agrillo, et al., “Letter to the Editor Learning from experience. Proposal of a refined definition and staging system for BRONJ,” Oral Diseases, vol. 18, no. 6, pp. 621–623, 2012.
- V. Fusco, C. Galassi, A. Berruti et al., “Osteonecrosis of the jaw after zoledronic acid and denosumab treatment,” Journal of Clinical Oncology, vol. 29, no. 17, pp. e521–e522, 2011.
- L. Sottosanti, “Le segnalazioni all’AIFA. I dati della Rete Nazionale di Farmacovigilanza (RNF) sui Bifosfonati e ONJ,” http://www.reteoncologica.it/images/stories/ONJ/Osteonecrosi_mascellari_2009/02-04%20Sottosanti%20Laura.pdf.
- A. Corso, M. Varettoni, P. Zappasodi et al., “A different schedule of zoledronic acid can reduce the risk of the osteonecrosis of the jaw in patients with multiple myeloma,” Leukemia, vol. 21, no. 7, pp. 1545–1548, 2007.
- R. A. Kyle, “American Society of Clinical Oncology 2007: clinical practice guideline update on the role of bisphosphonates in multiple myeoloma,” Journal of Clinical Oncology, vol. 25, pp. 2464–2472, 2007.
- M. Q. Lacy, A. Dispenzieri, M. A. Gertz et al., “Mayo Clinic consensus statement for the use of bisphosphonates in multiple myeloma,” Mayo Clinic Proceedings, vol. 81, no. 8, pp. 1047–1053, 2006.
- K. Imrie Stevens A, J. Makarski, et al., “The role of bisphosphonates in the management of skeletal complications for patients with multiple myeloma: a clinical practice guideline,” 2012, Http://www.cancercare.on.ca/pdf/pebc6-4f.pdf.
- M. Aapro, P. A. Abrahamsson, J. J. Body, et al., “Guidance on the use of bisphosphonates in solid tumors: recommendations of an international expert panel,” Annals of Oncology, vol. 19, pp. 420–432, 2008.
- E. Terpos, O. Sezer, P. I. Croucher et al., “The use of bisphosphonates in multiple myeloma: recommendations of an expert panel on behalf of the European Myeloma Network,” Annals of Oncology, vol. 20, no. 8, pp. 1303–1317, 2009.
- C. I. Ripamonti, M. Maniezzo, T. Campa et al., “Decreased occurrence of osteonecrosis of the jaw after implementation of dental preventive measures in solid tumour patients with bone metastases treated with bisphosphonates. The experience of the National Cancer Institute of Milan,” Annals of Oncology, vol. 20, no. 1, pp. 137–145, 2009.
- M. A. Dimopoulos, E. Kastritis, C. Bamia et al., “Reduction of osteonecrosis of the jaw (ONJ) after implementation of preventive measures in patients with multiple myeloma treated with zoledronic acid,” Annals of Oncology, vol. 20, no. 1, pp. 117–120, 2009.
- M. R. Allen and D. B. Burr, “The pathogenesis of bisphosphonate-related osteonecrosis of the jaw: so many hypotheses, so few data,” Journal of Oral and Maxillofacial Surgery, vol. 67, supplement 1, pp. 61–70, 2009.
- C. A. Migliorati, J. B. Epstein, E. Abt, and J. R. Berenson, “Osteonecrosis of the jaw and bisphosphonates in cancer: a narrative review,” Nature Reviews Endocrinology, vol. 7, no. 1, pp. 34–42, 2011.
- A. Badros, D. Weikel, A. Salama et al., “Osteonecrosis of the jaw in multiple myeloma patients: clinical features and risk factors,” Journal of Clinical Oncology, vol. 24, no. 6, pp. 945–952, 2006.
- P. K. Palaska, V. Cartsos, and A. I. Zavras, “Bisphosphonates and time to osteonecrosis development,” Oncologist, vol. 14, no. 11, pp. 1154–1166, 2009.