Background
Ameloblastoma is a common odontogenic epithelial tumor that can transform into a malignant tumor called ameloblastic carcinoma (AC), which is very rare [
1]. In the latest edition of the 2017 World Health Organization (WHO) classification of odontogenic tumors, AC was defined as a rare odontogenic malignancy that combines the histologic features of ameloblastoma with cytologic atypia, having a 5-year survival rate of 69.1% [
2,
3]. AC occurs mainly in the posterior mandible and presents as two main types: a primary type called de novo
cancer and a secondary type, defined as a malignant transformation from a pre-existing benign ameloblastoma [
3,
4].
Unfortunately, AC has a high recurrence rate after surgery, causing invasive and extensive bone destruction; its clinical diagnosis and treatment are very challenging. Transformation may be closely associated with a long medical history, multiple operations, radiotherapy, and chemotherapy, but the mechanisms of malignant transformation are poorly understood. Therefore, early tumor diagnosis and treatment are crucial.
In recent years, with the rapid development of molecular biology, some studies also reported a
BRAF-V600E mutation rate of approximately 60% in ameloblastoma [
5‐
7]. The
BRAF gene is an important proto-oncogene that plays an important role in tumor cell proliferation, differentiation, and apoptosis. Therefore, the presence of
BRAF-V600E mutation may be a biomarker of a more aggressive clinical course. Despite published reports on AC [
2,
8], the systematic analysis of large samples of clinical, imaging, and pathological features is still lacking. In this study, we analyzed 15 patients with AC with a clear diagnosis and summarized the clinical and biological characteristics of AC.
Discussion
AC is a rare and widely invasive malignant odontogenic epithelial neoplasm with significant proliferation and metastatic potential, requiring radical surgical intervention and close post-operative medical follow-up [
9]. Little is known about the malignant mechanism of AC. A mixture of benign and malignant features may be present within the same tumor. Karakida et al. [
4] inferred that postoperative chronic inflammation may promote its malignant transformation. Slater [
10] proposed that multistep carcinogenesis, as seen in secondary AC, develops from pre-existing benign ameloblastoma before malignant transformation; patients usually experience multiple recurrences and various management courses. Accordingly, its diagnosis and treatment remain challenging. In this study, AC showed a unique biological behavior, different from ameloblastoma, which can not only cause extensive destruction of the jaw bone, but also nerve paralysis and distant metastasis. Imaging and histological features also showed that it had a more aggressive biological behavior.
A wide incidence age range with a mean age of 49 years has been reported [
2]. In this study, the median presentation age was 53 years. The mandible was the most common AC location, closely correlating with earlier findings, which showed the posterior part of the mandible to be the most affected site, followed by the maxilla [
11]. In this study, only two patients presented with cervical lymph nodes and lung metastases. Giridhar et al. [
2] found that the progression-free survival and overall survival of AC were not different for patients with or without neck dissection, and prophylactic neck node dissection should be avoided. In this study, one patient suffered from eight recurrences. For this phenomenon, an important factor may be the maxillary location because of the abundant blood supply and its adjacent location to vital structures including the orbit, cranial base, and pterygomaxillary fossa, which are difficult to access by the surgeon and to obtain clear surgical margins [
12]. The nuclear protein, Ki-67 antigen is a reliable marker reflecting cell proliferation, and Ki-67 is more specific for the proliferation of ameloblastoma and AC [
13]. In this study, immunohistochemistry revealed that the proliferation index of Ki-67 in secondary tumors was higher than that in primary tumors, but radiography revealed that primary tumors were more destructive than secondary tumors, indicating that the increase in the Ki-67 index could not explain the invasiveness and bone destruction of those lesions but could help explain its ability to sustain growth and expansion [
14]. Therefore, using the Ki-67 index increase to illustrate the destructive ability of AC remains a subjective measure [
15]. In this study, one patient had AC accompanied by squamous cell carcinoma. This may be due to the malignant transformation of acanthomatous ameloblastoma, which exhibits extensive squamous metaplasia [
16,
17]. Although AC shows squamous cell differentiation, it is not its main component; therefore, the possibility of AC must be first considered, rather than a primary oral squamous cell carcinoma [
18].
The early treatment of ameloblastoma is crucial, and its malignant potential should be considered. The treatment of AC is usually extensive local excision. If the identification of benign or malignant ameloblastoma before surgery is difficult, frozen histological examination should be carried out at multiple tumor boundaries during surgery to discover malignant features in time [
19]. Neck dissection should be considered only when local metastasis is suspected on clinical examination. In this study, radical resection and jaw reconstruction proved effective in reducing the recurrence and improving the quality of life of the patients. Radiotherapy is a classic adjuvant method for treating partially resected tumors; however, its efficacy is still unclear [
8,
20‐
22], as is that of systemic chemotherapy. Currently, various chemotherapeutic drugs, including platinum cyclophosphamide, carboplatin, paclitaxel, and 5-fluorouracil, have been reported useful, although with unsatisfactory therapeutic effects [
23,
24]. In a previous report, an 8-year-old child was diagnosed with AC and systemic metastases and died after 5 cycles of chemotherapy [
24]. The recent development of molecular biotechnology has improved tumor treatment. The incidence of
BRAF-
V600E mutations is high in osteogenic tumors [
5‐
7,
25].
BRAF mutation is also associated with ameloblastoma invasiveness [
26], and our results also demonstrated that
BRAF-V600E is associated with AC. Furthermore, Kaye et al. [
25] once treated a patient with ameloblastoma and pulmonary metastases by using two targeted drugs, dabrafenib and trametinib, which inhibit the effects of
BRAF mutation. After 20 weeks, both the primary oral and pulmonary metastases were responding to treatment, suggesting that
BRAF-V600E may be a therapeutic target for ameloblastoma, and targeted drug therapy may be used for AC with
BRAF-V600E mutations.
There are some limitations to our study. Due to the complex mechanism of malignant transformation in AC, more studies focused on AC samples in various fields, such as molecular pathology and molecular biology, should be performed. Due to its rarity, AC treatment with molecular-targeted drugs are still untested. Thus, more AC cases need be documented.
Methods
This study was approved by the Medical Ethics Review Committee of the First Affiliated Hospital of Zhengzhou University (Approval No: KY-2019-LW-008).
Data of 15 patients with AC from the First Affiliated Hospital of Zhengzhou University from 2014 to 2019 were reviewed. The medical files of all patients from the first consultation to the last medical consultation were collected. Hematoxylin and eosin (H&E) staining was performed on 4 μm histological sections and reviewed by three pathologists with > 5 years of work experience to confirm the original diagnoses, following the 2017 WHO odontogenic tumor guidelines [27]. We recorded the patient age and sex, tumor diameter, primary tumor site, patient symptoms, presence and location of metastases, imaging and pathologic features, treatment applied, follow-up information, and time of the last medical consultation. All patients were histologically examined and confirmed to have AC. Five patients (1, 2, 4, 9 and 11) were tested for the BRAF-V600E mutation. The other patients′ tissue samples were stored for too long and DNA degraded, so they could not be tested.
Immunohistochemical staining
Formalin-fixed, paraffin-embedded tissues from cases of AC were retrieved from the department of pathology, the first affiliated hospital of zhengzhou university. These tissues were cut into 4-μm tissue sections. Antibodies against the following antigens were used in this experiment: cytokeratin(CK) (mouse monoclonal antibody, AE1/AE3, Ready-to-use), P63 (mouse monoclonal antibody, 4A4 + UMAB4, Ready-to-use) from ZSGB-Bio, Beijing, China. Ki-67 (mouse monoclonal antibody, 30–9,Roche, Basel, Switzerland)is detected in Roche automatic immunohistochemistry platform.
Real-time PCR analysis and DNA sequencing
Real-time PCR was performed using an ABI 7300 real-time PCR system (Applied Biosystems, Foster City, CA, USA) and the SYBR Premix Ex Taq reagent kit (Takara Bio, Inc., Shiga, Japan). The forward and reverse primers were 5′-TGCTTGCTCTGATAGGAAAATG-3′ and 5′-CCACAAAATGGATCCAGACA-3′, respectively. The reaction procedure was as follows: pre-denaturation at 95 °C for 3 min; denaturation at 94 °C for 30 s, annealing extension at 60 °C for 30 s, and amplification at 72 °C for 30 s, for a total of 35 cycles. The PCR reaction product was handed over to Wuhan Sevier Biotechnology Co.Ltd (Hubei, China) to complete the DNA sequencing process based on ABI 3730XL sequencer(Applied Biosy-stem Inc, Waltham, Massachusetts,US).
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