International Journal of Radiation Oncology*Biology*Physics
Clinical InvestigationPretreatment Primary Tumor SUVmax Measured by FDG-PET and Pathologic Tumor Depth Predict for Poor Outcomes in Patients With Oral Cavity Squamous Cell Carcinoma and Pathologically Positive Lymph Nodes
Introduction
Taiwan is an endemic betel quid chewing area, and oral cavity cancer remains a leading cause of morbidity and mortality in our country. According to the 2008 Department of Health statistics, oral cavity cancer is the sixth leading cancer in the Taiwanese general population. In men, oral cavity cancer is fourth leading form of cancer and the fourth leading cause of death (1). In this context, we sought to gain a better insight of the potential prognostic factors in this clinical entity that might hold promise to improve patient outcomes. It is well-known that the characteristics of the deep invasive front area of oral cavity squamous cell carcinoma (OSCC) can reflect the tumor prognosis better than other parts of the tumor 2, 3, 4. Tumor depth represents a variable that defines tumor quantity but that at the same time introduces a qualitative aspect with regard to the aggressiveness of local infiltration. In this regard, tumor depth is a strong predictor of the probabilities of regional lymph node metastases, the likelihood of involvement of distant node groups, and the risk of distant metastases 5, 6, 7, 8, 9, 10, 11.
We have previously shown that tumor depth is of greater prognostic value than tumor stage (pT1-pT2 vs. pT3-pT4) in predicting locoregional control and survival among OSCC patients 5, 6, 7. Moreover, the presence of pathologically positive lymph nodes indicates a poor prognosis in this patient group 5, 6, 7, 8, 9, 10, 11, 12. The identification of objective pathologic prognostic determinants in OSCC might enable better patient selection for adjuvant therapy. Some OSCC patients with pathologically positive lymph nodes have a poor outcome even after radical surgery or composite resection with neck dissection (ND). In this context, the identification of OSCC patients at high risk of relapse after radical surgery would have major clinical implications for patient treatment.
Positron emission tomography (PET) using 2-deoxy-2[(18)F]fluoro-d-glucose (FDG) has been widely used in the treatment planning process of head-and-neck cancer patients 13, 14, 15, 16, 17, 18. It is unclear, however, whether high pretreatment uptake of FDG detected by PET measured at the primary tumor predicts poor outcomes for OSCC patients undergoing radical surgery and ND.
The aim of this prospective study was to investigate the prognostic value of the preoperative maximal standardized uptake value (SUVmax) at the primary tumor and other clinicopathologic characteristics in relation to local control (LC) and survival in OSCC patients with pathologically positive lymph nodes.
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Study patients
The institutional review board for Human Research of Chang Gung Memorial Hospital (Taoyuan, Taiwan) approved the study. All patients provided written informed consent. The common eligibility criteria were a histologic diagnosis of node-positive OSCC; previously untreated tumor scheduled for radical surgery and ND; no other suspected distant metastatic lesions detected by imaging (including magnetic resonance imaging/computed tomography and FDG-PET); and a willingness to undergo computed
Patients
Between August 2001 and January 2006, a total of 254 consecutive patients with previously untreated OSCC were scheduled for radical surgery and ND. Of the 254 patients, 109 with pathological lymph node metastases were deemed eligible for this study. The clinicopathologic characteristics of the 109 study participants are listed in Table 1. Of the 109 OSCC patients, the mean SUVmax value was 11.9 (median, 11.2; range, 2.9–27.3; standard deviation, 5.5). Of the 109 patients, 97 (89%) had a SUVmax
Discussion
The biologic behavior of the primary tumor is the chief determinant of the prognosis for OSCC patients. The SUVmax of the primary tumor mass has been previously related to differences in cellular grade and tumor aggressiveness 14, 15, 16, 18. Although it is our policy to perform postoperative adjuvant therapy for all OSCC patients with one or more risk factors 5, 6, 7, 8, 9, 10, 11, 12, some patients continue to face a dismal prognosis. Also, regional lymph node metastases increase the
Conclusion
Taken together, our data have shown that a primary tumor SUVmax of ≥19.3 and tumor depth of ≥12 mm predict for 5-year LC and survival in OSCC patients with pathologically positive lymph nodes. Our findings could have potential implications in the treatment planning process of OSCC patients.
References (25)
- et al.
Multivariate predictors of occult neck metastasis in early oral tongue cancer
Otolaryngol Head Neck Surg
(2004) - et al.
Good tumor control and survivals of squamous cell carcinoma of buccal mucosa treated with radical surgery with or without neck dissection in Taiwan
Oral Oncol
(2006) - et al.
Higher distant failure in young age tongue cancer patients
Oral Oncol
(2006) - et al.
T4b oral cavity cancer below the mandibular notch is resectable with a favorable outcome
Oral Oncol
(2007) - et al.
Prediction of outcome in head-and-neck cancer patients using the standardized uptake value of 2-[18F]fluoro-2-deoxy-d-glucose
Int J Radiat Oncol Biol Phys
(2004) - et al.
Combined postoperative radiotherapy and weekly cisplatin infusion for locally advanced head and neck carcinoma: Final report of a randomized trial
Int J Radiat Oncol Biol Phys
(1996) - Taiwan cancer registry, 2008 annual report. Available from: <http://crs.cph.ntu.edu.tw/>. Accessed April 11,...
- et al.
Prognostic factors of clinically stage I and II oral tongue carcinoma—A comparative study of stage, thickness, shape, growth pattern, invasive front malignancy grading, Martinez-Gimeno score, and pathologic features
Head Neck
(2002) - et al.
The high prognostic value of the histologic grade at the deep invasive front of tongue squamous cell carcinoma
J Oral Pathol Med
(2005) - et al.
Analysis of risk factors of predictive local tumor control in oral cavity cancer
Ann Surg Oncol
(2008)
Survival in squamous cell carcinoma of the oral cavity: Differences between pT4N0 and other stage IVA categories
Cancer
Salvage therapy in relapsed squamous cell carcinoma of the oral cavity: How and when?
Cancer
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Supported by Grants CMRPG361051 and CMRPG370061, Chang Gung Memorial Hospital at Linko.
Conflict of interest: none.