The Position Paper of the American Association of Oral and Maxillofacial Surgeons and the Guidelines of Multinational Association of Supportive Care in Cancer/International Society of Oral Oncology (MASCC/ISOO) state that conservative therapies, such as administration of antibiotics and gargling with antiseptic mouthwash, are the first choice of treatments for MRONJ [1, 2]. Surgical therapy can be performed for refractory cases. Conversely, many investigators have reported the superiority of surgical therapy over conservative therapy [4–6]. In a multi-center observational study using propensity score matching analysis, we previously reported that the treatment outcomes were significantly better in patients undergoing surgery than in those undergoing conservative therapy [7].
The quality of life (QOL) of patients with MRONJ decreases as the MRONJ stage progresses [8]. The prognosis for life may not be very long, because many MRONJ patients are elderly or have cancer with distant metastases. Therefore, when choosing a treatment for MRONJ, it is necessary to consider the cure of the disease and the QOL of patients. Persistent pain and pus discharge during the remaining survival period can be very distressing for the patient. We believe that “terminal care” for MRONJ patients, which aims to maintain and improve the QOL by relieving the patients’ physical and mental pain, is necessary to choose the treatment method. For this reason, segmental mandibulectomy should be included as an option in the treatment of elderly patients and cancer-bearing patients, as it is more likely to be curative.
Hanasono et al. reported no recurrence in 13 patients with MRONJ who underwent segmental mandibulectomy and free flap reconstruction [3]. In the current study, we focused on segmental mandibulectomy for MRONJ. The results showed that the healing rate was higher in segmental mandibulectomy than in marginal mandibulectomy. There was only one recurrence in which the cortical bone of the extraction socket of a tooth was left behind. That patient was cured by additional resection. Of course, because segmental mandibulectomy is highly invasive, marginal mandibulectomy should be performed if the lesion can be controlled. However, conservative therapy and marginal mandibulectomy were performed for more than a year without cure; segmental mandibulectomy was eventually performed in some cases. Therefore, it is necessary to consider the indications for conservative therapy and marginal mandibulectomy.
Bone reconstruction is generally performed because segmental mandibulectomy breaks the continuity of the mandible, resulting in facial deformity and malocclusion. Of the 13 segmental mandibulectomy cases in this study, free fibula flaps and reconstruction plates were transplanted in two and four cases involving the anterior part of the mandible, respectively. Reconstruction was not performed in the remaining seven cases involving the posterior part of the mandible after consultation with the patient, because reconstructive surgery increases the surgical invasion and poses a risk of postoperative infection and reoperation. If bone reconstruction is not performed, malocclusion may lead to masticatory disturbance. In this study, some patients had a worse diet after surgery than before surgery. However, others had a better diet postoperatively than before surgery, and all patients could eat after surgery. The improvement in feeding status despite segmental resection may be due to the relief from symptoms such as pain. As mentioned above, we believe that segmental mandibulectomy is a treatment option for patients with intolerable physical and mental pain or persistent discomfort due to pus discharge despite conservative therapy or marginal mandibulectomy.
The resection range for segmental mandibulectomy was also examined. Marx et al. recommend performing resection until some bone marrow remains, bone color is normal, and bleeding is noted [9]. Nocini et al. reviewed the pathological characteristics of patients who underwent segmental mandibulectomy and found that only one patient had a residual lesion in the resection specimen. The patient experienced a recurrence of MRONJ within 6 months [10]. Similarly, Bedogni et al. analyzed 32 jaws resected for MRONJ and reported that the presence of osteomyelitis at the pathological resection edge was a strong predictor of BRONJ recurrence [11]. However, this is only a diagnosis of pathological specimens and intraoperative findings, and not a preoperative diagnosis. We examined factors for preoperatively assuming the resection range of segmental mandibulectomy. We examined osteolytic lesions, PR, osteosclerosis, TCB, and TCW. Osteolytic lesions and PR can be adequately removed by segmental mandibulectomy. Soutome et al. reported that PR should also be considered when determining the extent of osteotomy [12]. Segmental mandibulectomy seemed more likely to eliminate osteolytic lesions and PR as compared to marginal mandibulectomy.
The osteosclerotic lesion remained in nine cases, but it was not always necessary to include osteosclerosis in the resection field because healing was obtained. We also hypothesized that enlargement of the cortical bone is involved in blood flow disorder when considering blood flow from the periosteal and inferior alveolar arteries. However, there is no apparent relationship between the residual TCB of TCW and the cure rate. Finally, we believe that it is necessary to resect osteolytic lesions and PR when performing segmental mandibulectomy for MRONJ of the mandible.
This study has some limitations. First, this is a retrospective case series of a small number of patients; therefore, it is difficult to generalize the results. Second, because we did not conduct a detailed study of QOL, it was not possible to clarify whether segmental mandibulectomy contributed to improving the patient's QOL. In the future, we would like to examine the decision on the indication for segmental mandibulectomy and verify its effectiveness in a larger number of cases.