Thiagarajan A, Iyer NG. Radiation-induced sarcomas of the head and neck. World J Clin Oncol 2014; 5(5): 973-981 [PMID: 25493233 DOI: 10.5306/wjco.v5.i5.973]
Corresponding Author of This Article
Dr. N Gopalakrishna Iyer, MD, PhD, Department of Surgical Oncology, National Cancer Centre Singapore, 11 Hospital Drive, Singapore 169610, Singapore. gopaliyer@yahoo.com
Research Domain of This Article
Oncology
Article-Type of This Article
Topic Highlight
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
World J Clin Oncol. Dec 10, 2014; 5(5): 973-981 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: