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©2014 Baishideng Publishing Group Inc.
World J Clin Oncol. Dec 10, 2014; 5(5): 973-981
Published online Dec 10, 2014. doi: 10.5306/wjco.v5.i5.973
Published online Dec 10, 2014. doi: 10.5306/wjco.v5.i5.973
Table 1 Summary of key findings
| With improved oncologic outcomes, RIS are increasingly seen in long-term survivors of head and neck cancers |
| There is no subsite predilection; They can arise in any irradiated tissue of mesenchymal origin |
| Common histologic subtypes parallel their de novo counterparts |
| Imaging features of RIS are not pathognomonic but large size, extensive local invasion with bony destruction, and marked enhancement within a prior radiotherapy field are suggestive of a diagnosis of RIS |
| RIS development may be influenced by factors such as radiation dose, age at initial exposure, exposure to chemotherapeutic agents, and genetic tendency |
| Precise pathogenetic mechanisms of RIS are poorly understood |
| Management is challenging, entailing surgery in irradiated tissue and limited scope for further radiotherapy and chemotherapy |
| RIS is associated with significantly poorer outcomes than stage-matched de novo sarcomas |
| Surgical resection with clear margins appears to offer the best chance for cure |
Table 2 Advantages and disadvantages of computed tomography and magnetic resonance imaging in head and neck oncologic imaging
| CT | MRI |
| Advantages | |
| Fast | Superior soft tissue resolution including better assessment of perineural invasion, intracranial extension of disease, marrow infiltration |
| Well tolerated | Multi-planar imaging capability, better definition of cradiocaudal extent |
| Relatively inexpensive | Less image degradation caused by artifacts arising from dental amalgam |
| Provides assessment of tissue composition (vascularity, lipid content etc.) | Does not involve ionizing radiation |
| Ideal at demonstrating cortical bone erosion | Contrast material is less likely to produce allergic reaction |
| Disadvantages | |
| Involves exposure to small amounts of radiation | May take more time to perform |
| Inferior soft tissue resolution compared with MRI | More expensive |
| Higher risk of allergic reactions and nephrotoxicity associated with the use of iodinated contrast agents | Lower patient tolerance; Claustrophobic patients may need sedation |
| Contraindicated in patients with pacemakers and other implanted metallic devices which may malfunction following exposure to strong magnetic fields | |
| More susceptible to motion artefact |
Table 3 TNM staging for soft tissue sarcoma
| Primary tumor (T) | ||||
| TX | Primary tumor cannot be assessed | |||
| T0 | No evidence of primary tumor | |||
| T1 | Tumor 5 cm or less in greatest dimension | |||
| T1a | Superficial tumor | |||
| T1b | Deep tumor | |||
| T2 | Tumor more than 5 cm in greatest dimension | |||
| T2a | Superficial tumor | |||
| T2b | Deep tumor | |||
| Regional lymph nodes (N) | ||||
| NX | Regional lymph nodes cannot be assessed | |||
| N0 | No regional lymph node metastasis | |||
| N1 | Regional lymph node metastasis | |||
| Distant metastasis (M) | ||||
| M0 | No distant metastasis | |||
| M1 | Distant metastasis | |||
| Histologic grade (G)Δ | ||||
| GX | Grade cannot be assessed | |||
| G1 | Grade 1 | |||
| G2 | Grade 2 | |||
| G3 | Grade 3 | |||
| Anatomic stage/prognostic groups | ||||
| Stage IA | T1a | N0 | M0 | G1, GX |
| T1b | N0 | M0 | G1, GX | |
| Stage IB | T2a | N0 | M0 | G1, GX |
| T2b | N0 | M0 | G1, GX | |
| Stage IIA | T1a | N0 | M0 | G2, G3 |
| T1b | N0 | M0 | G2, G3 | |
| Stage IIB | T2a | N0 | M0 | G2 |
| T2b | N0 | M0 | G2 | |
| Stage III | T2a, T2b | N0 | M0 | G3 |
| Any T | N1 | M0 | Any G | |
| Stage IV | Any T | Any N | M1 | Any G |
Table 4 TNM staging for bone tumors other than lymphoma and myeloma
| Primary tumor (T) | ||||
| TX | Primary tumor cannot be assessed | |||
| T0 | No evidence of primary tumor | |||
| T1 | Tumor 8 cm or less in greatest dimension | |||
| T2 | Tumor more than 8 cm in greatest dimension | |||
| T3 | Discontinuous tumors in the primary bone site | |||
| Regional lymph nodes (N) | ||||
| NX | Regional lymph nodes cannot be assessed | |||
| N0 | No regional lymph node metastasis | |||
| N1 | Regional lymph node metastasis | |||
| Distant metastasis (M) | ||||
| M0 | No distant metastasis | |||
| M1 | Distant metastasis | |||
| M1a | Lung | |||
| M1b | Other distant sites | |||
| Histologic grade (G) | ||||
| Grade is reported in registry systems by the grade value. A two-grade, three-grade, or four-grade system may be used. If a grading system is not specified, generally the following system is used: | ||||
| GX | Grade cannot be assessed | |||
| G1 | Well differentiated-low grade | |||
| G2 | Moderately differentiated-low grade | |||
| G3 | Poorly differentiated-high grade | |||
| G4 | Undifferentiated-high grade | |||
| Anatomic stage/prognostic groups | ||||
| Stage IA | T1 | N0 | M0 | G1, 2 Low grade, GX |
| Stage IB | T2 | N0 | M0 | G1, 2 Low grade, GX |
| T3 | N0 | M0 | G1, 2 Low grade, GX | |
| Stage IIA | T1 | N0 | M0 | G3, 4 High grade |
| Stage IIB | T2 | N0 | M0 | G3, 4 High grade |
| Stage III | T3 | N0 | M0 | G3, 4 High grade |
| Stage IVA | Any T | N0 | M1a | Any G |
| Stage IVB | Any T | N1 | Any M | Any G |
| Any T | Any N | M1b | Any G | |
Table 5 TNM staging system for rhabdomyosarcoma
| Stage | Sites | Tumor stage invasiveness | T stage size | N | M |
| 1 | Orbit Head and neck Genitourinary Biliary tract | T1 or T2 | a or b | Any N | M0 |
| 2 | Bladder/prostate Extremity Cranial parameningeal OtherΔ | T1 or T2 | a | N0 or NX | M0 |
| 3 | Bladder/prostate Extremity Cranial parameningeal OtherΔ | T1 or T2 | a b | N1 Any N | M0 |
| 4 | All | T1 or T2 | a or b | N0 or N1 | M1 |
- Citation: Thiagarajan A, Iyer NG. Radiation-induced sarcomas of the head and neck. World J Clin Oncol 2014; 5(5): 973-981
- URL: https://www.wjgnet.com/2218-4333/full/v5/i5/973.htm
- DOI: https://dx.doi.org/10.5306/wjco.v5.i5.973
