Radiosensitivity of Laryngopharyngeal Cancer
Yes, laryngopharyngeal cancers are highly radiosensitive, with radiation therapy achieving local control rates exceeding 90% in early-stage disease and serving as the cornerstone of organ-preservation strategies in advanced disease. 1
Evidence for Radiosensitivity in Early-Stage Disease
Radiation therapy alone achieves excellent tumor control in T1-T2 laryngeal cancers, demonstrating the inherent radiosensitivity of these tumors:
- For T1 glottic cancer, radiation therapy yields 5-year survival rates of 80-90% with complete larynx preservation 2
- Local control rates after radiation therapy are high for both T1-T2 glottic and supraglottic cancers, with functional outcomes often superior to surgery 1
- Early laryngeal cancer treated with definitive radiotherapy achieves an overall locoregional control rate of 84%, with 5-year disease-specific survival of 91% 3
- The radiosensitivity is so pronounced that single-modality radiation therapy is the standard approach for favorable T1-T2 lesions 1, 2
Evidence for Radiosensitivity in Advanced Disease
The radiosensitivity of laryngopharyngeal cancers forms the biological basis for successful organ-preservation strategies in locally advanced disease:
- Concurrent chemoradiation achieves 3-year larynx preservation with local control in 83% of patients and 5-year rates of 77% 4
- The EORTC Hypopharynx Trial demonstrated that induction chemotherapy followed by radiation therapy in responders achieved survival equivalent to primary laryngopharyngectomy, with successful larynx preservation in responding patients 1
- Hypoxic radiosensitizers improve locoregional control and disease-specific survival after radiation therapy, further demonstrating the radiosensitive nature of these tumors 1
- For T3-T4 cancers, concurrent chemoradiation offers the highest rate of larynx preservation compared to other radiation-based approaches, without compromising overall survival when salvage surgery is incorporated 1
Clinical Implications of Radiosensitivity
The radiosensitivity of laryngopharyngeal cancers allows radiation-based treatment to compete with surgery across all disease stages:
- For early-stage disease (T1-T2), radiation therapy and surgery achieve similar survival outcomes, making treatment selection dependent on functional considerations rather than oncologic efficacy 2
- For advanced disease (T3-T4), concurrent cisplatin-based chemoradiation is the standard organ-preservation approach, with local control rates comparable to total laryngectomy 1, 4
- The complete response rate to induction chemotherapy correlates with T stage (82% for T2, 48% for T3), demonstrating maintained radiosensitivity even in larger tumors 1
Important Caveats Regarding Radiosensitivity
While laryngopharyngeal cancers are radiosensitive, certain tumor characteristics predict poorer radiation response:
- Significant invasion of major cartilaginous structures (thyroid or cricoid cartilage) is the most accepted criterion for predicting negative outcomes with radiation therapy 1
- Patients with nonfunctional larynx or tumor penetration through cartilage into surrounding soft tissues are poor candidates for radiation-based organ preservation and should receive primary surgery 1, 2
- T4a tumors with extensive cartilage destruction have less favorable results with radiation-based approaches, though some trials report encouraging results even in selected T4a cases 1
- Continued cigarette smoking is associated with worse outcomes after radiation therapy, suggesting that tumor hypoxia from smoking may reduce radiosensitivity 2, 4
Enhancing Radiosensitivity
Multiple strategies exploit the radiosensitivity of laryngopharyngeal cancers:
- High-dose cisplatin (100 mg/m² every 3 weeks) concurrent with radiation is the only radiosensitizing agent with strong evidence support 1, 4
- Hypoxic radiosensitizers improve locoregional control regardless of radiation fractionation regimen 1
- Altered fractionation radiation therapy (hyperfractionation or accelerated fractionation) results in significant increases in locoregional control, though at the cost of increased acute toxicity 1