Survival and prognostic factors of salivary gland malignant mixed tumor-not otherwise specified: A population-based analysis

Malignant mixed tumors of the salivary gland are a group of neoplasms comprised of carcinoma-ex-pleomorphic adenoma, carcinosarcoma, and metastasizing pleomorphic adenoma. An alternative classification, malignant mixed tumor-not otherwise (MMT-NOS), is a diagnosis of exclusion for neoplasms that do...

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Published inAmerican journal of otolaryngology Vol. 42; no. 6; p. 103135
Main Authors Soffer, Justin M., Nassif, Samih J., Von Plato, Michael, Chisholm, Jaime, O'Leary, Miriam A.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.11.2021
Elsevier Limited
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Abstract Malignant mixed tumors of the salivary gland are a group of neoplasms comprised of carcinoma-ex-pleomorphic adenoma, carcinosarcoma, and metastasizing pleomorphic adenoma. An alternative classification, malignant mixed tumor-not otherwise (MMT-NOS), is a diagnosis of exclusion for neoplasms that do not fit the previous histologically profiled subtypes. The objective was to provide a comprehensive assessment of MMT-NOS and determine prognostic factors. This retrospective cohort study queried the Surveillance, Epidemiology, and End Results database for patient and tumor characteristics of US patients with MMT-NOS of the major salivary glands from 1973 to 2016. Kaplan-Meier and Cox regression analysis were performed to determine 5-year survival and prognostic factors. 434 patients were identified with a mean age at diagnosis of 61.5 years. The majority of neoplasms were high grade and stage (70.8% grade III/IV; 63.8% stage III/IV). Extraparenchymal extension (40.6%) and lymph node involvement (28.5%) were common; distant metastases (2.4%) were rare. Treatment included surgery (93.0%), radiation (51.6%), and chemotherapy (10.4%). Facial nerve sacrifice was common (50.8%). Median survival was 66.5 months. 5-year overall and disease-specific survival were 65.7% and 83.0%, respectively. In multivariate analysis, nodal involvement (HR 7.0; P < 0.001), surgery-radiation-chemotherapy (HR 6.1; P = 0.02), extraparenchymal extension (HR 2.50; P = 0.04), and tumor size >4 cm (HR 1.3; P = 0.03) were prognostic factors. Despite high stage and grade at diagnosis, MMT-NOS portends a good 5-year prognosis and low rate of distant metastasis. Prognostic factors were nodal involvement, tumor size, and extraparenchymal extension.
AbstractList ObjectiveMalignant mixed tumors of the salivary gland are a group of neoplasms comprised of carcinoma-ex-pleomorphic adenoma, carcinosarcoma, and metastasizing pleomorphic adenoma. An alternative classification, malignant mixed tumor-not otherwise (MMT-NOS), is a diagnosis of exclusion for neoplasms that do not fit the previous histologically profiled subtypes. The objective was to provide a comprehensive assessment of MMT-NOS and determine prognostic factors.MethodsThis retrospective cohort study queried the Surveillance, Epidemiology, and End Results database for patient and tumor characteristics of US patients with MMT-NOS of the major salivary glands from 1973 to 2016. Kaplan-Meier and Cox regression analysis were performed to determine 5-year survival and prognostic factors.Results434 patients were identified with a mean age at diagnosis of 61.5 years. The majority of neoplasms were high grade and stage (70.8% grade III/IV; 63.8% stage III/IV). Extraparenchymal extension (40.6%) and lymph node involvement (28.5%) were common; distant metastases (2.4%) were rare. Treatment included surgery (93.0%), radiation (51.6%), and chemotherapy (10.4%). Facial nerve sacrifice was common (50.8%). Median survival was 66.5 months. 5-year overall and disease-specific survival were 65.7% and 83.0%, respectively. In multivariate analysis, nodal involvement (HR 7.0; P < 0.001), surgery-radiation-chemotherapy (HR 6.1; P = 0.02), extraparenchymal extension (HR 2.50; P = 0.04), and tumor size >4 cm (HR 1.3; P = 0.03) were prognostic factors.ConclusionDespite high stage and grade at diagnosis, MMT-NOS portends a good 5-year prognosis and low rate of distant metastasis. Prognostic factors were nodal involvement, tumor size, and extraparenchymal extension.
Malignant mixed tumors of the salivary gland are a group of neoplasms comprised of carcinoma-ex-pleomorphic adenoma, carcinosarcoma, and metastasizing pleomorphic adenoma. An alternative classification, malignant mixed tumor-not otherwise (MMT-NOS), is a diagnosis of exclusion for neoplasms that do not fit the previous histologically profiled subtypes. The objective was to provide a comprehensive assessment of MMT-NOS and determine prognostic factors. This retrospective cohort study queried the Surveillance, Epidemiology, and End Results database for patient and tumor characteristics of US patients with MMT-NOS of the major salivary glands from 1973 to 2016. Kaplan-Meier and Cox regression analysis were performed to determine 5-year survival and prognostic factors. 434 patients were identified with a mean age at diagnosis of 61.5 years. The majority of neoplasms were high grade and stage (70.8% grade III/IV; 63.8% stage III/IV). Extraparenchymal extension (40.6%) and lymph node involvement (28.5%) were common; distant metastases (2.4%) were rare. Treatment included surgery (93.0%), radiation (51.6%), and chemotherapy (10.4%). Facial nerve sacrifice was common (50.8%). Median survival was 66.5 months. 5-year overall and disease-specific survival were 65.7% and 83.0%, respectively. In multivariate analysis, nodal involvement (HR 7.0; P < 0.001), surgery-radiation-chemotherapy (HR 6.1; P = 0.02), extraparenchymal extension (HR 2.50; P = 0.04), and tumor size >4 cm (HR 1.3; P = 0.03) were prognostic factors. Despite high stage and grade at diagnosis, MMT-NOS portends a good 5-year prognosis and low rate of distant metastasis. Prognostic factors were nodal involvement, tumor size, and extraparenchymal extension.
ArticleNumber 103135
Author Chisholm, Jaime
Soffer, Justin M.
Nassif, Samih J.
O'Leary, Miriam A.
Von Plato, Michael
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  organization: Department of Otolaryngology-Head and Neck Surgery, Tufts Medical Center, 800 Washington St, Boston, MA 02111, United States of America
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crossref_primary_10_3390_cancers14235934
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Issue 6
Keywords Malignant mixed tumor-not otherwise specified
Salivary gland
SEER
Malignant mixed tumor
Survival
Prognostic factors
Language English
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Snippet Malignant mixed tumors of the salivary gland are a group of neoplasms comprised of carcinoma-ex-pleomorphic adenoma, carcinosarcoma, and metastasizing...
ObjectiveMalignant mixed tumors of the salivary gland are a group of neoplasms comprised of carcinoma-ex-pleomorphic adenoma, carcinosarcoma, and metastasizing...
OBJECTIVEMalignant mixed tumors of the salivary gland are a group of neoplasms comprised of carcinoma-ex-pleomorphic adenoma, carcinosarcoma, and metastasizing...
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StartPage 103135
SubjectTerms Adenoma
Adenoma, Pleomorphic - epidemiology
Adenoma, Pleomorphic - mortality
Adenoma, Pleomorphic - pathology
Adenoma, Pleomorphic - therapy
Age
Chemotherapy
Demographics
Diagnosis
Divorce
Epidemiology
Ethnicity
Exocrine glands
Facial nerve
Female
Hispanic people
Humans
Lymph nodes
Lymph Nodes - pathology
Lymphatic system
Male
Malignant mixed tumor
Malignant mixed tumor-not otherwise specified
Medical prognosis
Metastases
Metastasis
Middle Aged
Mixed Tumor, Malignant - epidemiology
Mixed Tumor, Malignant - mortality
Mixed Tumor, Malignant - pathology
Mixed Tumor, Malignant - therapy
Mortality
Multivariate analysis
Neoplasm Staging
Neoplasms
Oral cancer
Otolaryngology
Patients
Prognosis
Prognostic factors
Radiation
Regression analysis
Retrospective Studies
Salivary gland
Salivary Gland Neoplasms - epidemiology
Salivary Gland Neoplasms - mortality
Salivary Gland Neoplasms - pathology
Salivary Gland Neoplasms - therapy
Salivary glands
Salivary Glands - pathology
SEER
SEER Program
Surgery
Survival
Survival analysis
Survival Rate
Tumors
Title Survival and prognostic factors of salivary gland malignant mixed tumor-not otherwise specified: A population-based analysis
URI https://dx.doi.org/10.1016/j.amjoto.2021.103135
https://www.ncbi.nlm.nih.gov/pubmed/34171696
https://www.proquest.com/docview/2576478771/abstract/
https://search.proquest.com/docview/2545593984
Volume 42
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