Monitoring of neoadjuvant radiation therapy by positron emission tomography in oral squamous cell carcinoma

Citation
M. Kunkel et al., Monitoring of neoadjuvant radiation therapy by positron emission tomography in oral squamous cell carcinoma, STRAH ONKOL, 177(3), 2001, pp. 145-152
Citations number
28
Categorie Soggetti
Oncology
Journal title
STRAHLENTHERAPIE UND ONKOLOGIE
ISSN journal
01797158 → ACNP
Volume
177
Issue
3
Year of publication
2001
Pages
145 - 152
Database
ISI
SICI code
0179-7158(200103)177:3<145:MONRTB>2.0.ZU;2-A
Abstract
Background: Combined protocols of radiation therapy and surgical resection, as applied in advanced oral cancer, rely on objective and early assessment of treatment response to radiation therapy. Non-responders require immedia te radical salvage surgery even in spite of substantial operative risks, wh ile complete or subtotal response may give reasons for continuing the conse rvative approach. Therefore, we investigated radiation response by FDG-PET for early monitoring of oral cancer. Patients and Methods: In 30 patients with advanced stages of oral cancer (T able 1), FDG-PET (Siemens, ECAT EXACT 922) was performed within 4 weeks aft er completion of preoperative radiation therapy (36 Gy). SUV of tumor regio ns were compared to the histologic degree of tumor regression in complete r esection specimens. Statistic evaluation included correlation analysis of S UV vs tumor regression and ROC analysis for SUV cut-off values. Results: While Low FDG accumulation was found in tumors with histological c omplete remission (2.3 +/- 0.4) as well as in cases of residual tumor (3.4 +/- 1.8), high FDG uptake was a rather specific indicator of vital tumor ti ssue (Figure 2). Significant correlation (p = 0.045) between postradiothera peutic FDG-uptake and histological tumor regression was recognized. A SUV > 2.75 as a clinically practicable threshold value for the identification of residual vital tumor resulted in a specificity of 88%, sensitivity of 68%, a positive predictive value of 94% and a negative predictive value of 50% (Figure 3). Based on our actual follow-up data we could not confirm a signi ficant correlation between postradiotherapeutic SUV and patients' survival. Conclusion: Within a standardized protocol, FDG-PET recognize treatment res ponse to radiation therapy in oral squamous cell carcinoma with a reasonabl e specificity and thus provides a basis for further therapeutic decisions. An increased SUV (> 2.75) may be the rational to justify an aggressive surg ical approach even when patients face substantial surgical or anesthesiolog ical risk. However, the posttherapeutic pattern of glucose uptake varies wi th the applied treatment modalities and has to be explored for the protocol applied.