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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_4505_Библиотеки_им_академика_М_И_Перельмана

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Part 2 Site-Specifi c Indications and Techniques
Case
Study
12-7
tiated carcinoma. MRI revealed residual disease in the right nasoethmoidal region with extension to the nasopharynx. She was treated with three cycles of cisplatin and etoposide yield­ing a partial response.  is was followed by IMRT using nine  elds and dynamic multileaf collimation.  e gross residual tumor received 70 Gy, the prechemotherapy volume received 60 Gy, and bilateral upper neck nodes received 56 Gy.
A 43-year-old woman presented with right periorbital pain and nasal obstruction. She under­went bilateral endoscopic surgery removing a mass from the right nasal cavity and ethmoids, which was positive for sinonasal-undi eren-
Figure 12.7 shows axial (Fig. 12.7A) and sagittal (Fig.12.7B) isodose distributions.  e residual tumor and prechemotherapy tumor (bright red and pale red) and optic pathways (yellow for chiasm) are shown. Concurrent cispl- atin was administered every 3 weeks. Posttreatment imag­ing revealed a residual mass.  erefore, a resection was performed. Histologic examination revealed  brotic tissue only. She developed a solitary larynx metastasis 2 years later and received radiation and chemotherapy to the lar­ynx only. She is without disease, 4 years from her initial diagnosis.
A B
Figure 12.7A,B
Case
Study
12-8
noma. CT scan revealed a tumor in the right ethmoid sinuses and upper part of the right nasal cavity involv­ing the floor of the right orbit. The tumor was resected through a craniofacial approach. The right antrum and sphenoid sinus were inspected and found free of gross disease, but the mucosal lining was removed.
A 56-year-old man sought medical atten­tion because of nasal stuffiness and pressure discomfort below the right eye. A polypoid mass was removed from the right nasal cav­ity, which was diagnosed as adenocarci-
Histologic examination revealed an adenocarcinoma at the ethmoid sinuses spreading to the mucosa of the nasal septum.
 e patient received postoperative radiotherapy. Figure 12.8 shows anterior  eld (Fig. 12.8A) and right (Fig.12.8B) and le lateral  elds used to treat the surgical bed with 6 MV photons.  e lateral orbital canthi, external auditory canals, oral commissures, and position of the cor­nea of the right eye were marked at simulation.  e thick, straight wire indicated the slope of the face. A dose of 56 Gy was delivered to the isocenter in 28 fractions.
Chapter 12 Paranasal Sinuses
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A B
Figure 12.8A,B
Case
Study
12-9
through the  oor of the anterior cranial fossa in coronal view (Fig. 12.9A—blue arrow). She underwent resection of the mass with an endoscopic approach inferiorly and a bifrontal craniotomy to address the superior aspect of the tumor. Histologic examination revealed an esthesioneuro­blastoma extended through the cribiform plate to involve the duramater. Margins were positive.
She was treated with postoperative IMRT delivered in 30 fractions. CTV structed from the imaging and operative and pathology reports. A small higher-risk volume, at the right ante­rior cranial fossa  oor where the margin was not cleared, was de ned and given 63 Gy. CTVID (57 Gy) covered the additional margin on the cranial fossa  oor, as well as the
 is 47-year-old woman presented with anos­mia and nasal obstruction.
As shown in Figure 12.9, CT scan dem­onstrates a tumor epicentered in the ethmoid sinuses (Fig. 12.9A—green arrows) broken
(60 Gy) covered the vGTV as recon-
HD
remaining sinuses that were uninvolved but were in the surgical bed. Figure 12.9B shows a coronal view through the posterior orbits with an isodose distribution. Note the 63-Gy line at the superior aspect of the surgical cav­ity and the 60-Gy line encompassing the resected ethmoids between the orbits.  e 57-Gy line in this view covers the bilateral maxillary sinuses and nasal cavity. Figure 12.9C shows a sagittal view through midline. Again the 63-Gy line and 60-Gy line are appreciated covering a small por­tion of the inferior aspect of the anterior cranium and the resected tumor bed, respectively.  e 57-Gy line covers the sphenoid sinus. Also note the isodose gradient achieved to keep the optic chiasm within tolerance. Axial isodose distributions are shown at the level of the orbits and optic pathways (Fig. 12.9D), the epicenter of the surgical cavity (Fig. 12.9E), and mid maxillary sinuses (Fig. 12.9F). CTVED (54 Gy) encompassed the retropharyngeal (Fig. 12.9G) and the upper neck (Fig. 12.9H) nodes. She remains without disease 3 years later.
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A
C
B
D
E
Figure 12.9A-F
F
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G
Figure 12.9G,H
Intensity-Modulated Radiation Therapy Planning
 e patient is immobilized in a supine position, with an extended head and shoulder thermoplastic mask.  in-cut CT scans are obtained in treatment position.  e target volumes are outlined for dosimetric planning.
Gross Target Volume
GTV represents all areas determined from clinical examina­tion and imaging studies to contain gross disease.  ere is no actual GTV a er complete surgical tumor resection. How­ever, it can be useful to formulate a vGTV to facilitate target volume de nition in the postoperative setting.  e vGTV is the best approximation of the tissues having high likelihood of harboring microscopic tumor reconstructed based on  ndings of preoperative clinical examination, imaging stud­ies, and surgical–pathologic assessment.
Clinical Target Volume
 ree CTVs are generally delineated.
H
CTVHD delineates volumes to receive the highest dose.
 is includes the primary and nodal GTVs (or vGTVin the postoperative setting) with 0.5- to 1-cm margins.
CTVID delineates volumes to receive an intermediate dose,
which includes a 0.5- to 1-cm margin around CTVHD. In the node-positive neck, CTVID covers the involved nodal bed outside CTVHD and additional 1 to 2 cm in cranial– caudal directions.
CTVED delineates volumes to receive an elective dose for
subclinical disease. If not already included in higher dose targets (rare), CTVED should cover the entire sinus, the medial orbital wall, sphenoid sinus, nasal cavity, medial aspect of the maxillary sinus (or sinuses for bilateral disease) and  oor of the anterior cranial fossa. In clinically N0 neck (except for low-grade tumors), CTVED encompasses levels I and II nodes. If level I or II node is involved, CTVED cov­ers levels III and IV regions. Alternatively, levels III and IV regions can be irradiated with a separate matched anterior beam with an isocenter placed above the thyroid cartilage.
Background Data
Table 12.1
Variables No. of Patients Local 5-yr Control (%)
Pathologic T stage T1 + T2 T3 T4
N stage N0 N1–N2
Infl uence of Disease and Therapy Variables on the Treatment Outcome
Regional 5-yr Control (%)
a
22 47 77
126
20
73 84 68
73 79
76 82 84
83 75
5-yr Overall Survival (%)
66 57 50
56 44
(Continued )
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Table 12.1
Variables No. of Patients Local 5-yr Control (%)
Infl uence of Disease and Therapy Variables on the Treatment Outcome
(Continued )
Regional 5-yr Control (%)
5-yr Overall Survival (%)
Histologic fi ndings SCC Undifferentiated Adenocarcinoma Adenoid cystic carcinoma Other
Nerve invasion
a
No Yes
Margin of resection
a
Negative/close Positive Elective nodal treatment
a
Patients with unknown status excluded. Bristol IJ, Ahamad A, Garden AS, et al. Postoperative radiotherapy for maxillary sinus cancer: long-term outcomes and toxicities of treatment. Int J Radiat Oncol Biol Phys 2007;68:719, with permission.
Table 12.2
Infl uence of Disease and Therapy Variables on the Treatment Outcome of 34 Patients Irradiated for
89 11
6
33
7
82 60
107
37 51
68 91 80 85 64
81 66
74 73 69
80 73 75 96 80
83 82
84 77 93
49 40 37 69 71
61 45
59 41 47
Carcinoma of the Ethmoid Sinuses
Variables No. of Patients
5-yr Actuarial Local Control (%)
5-yr Actuarial Disease-Specifi c Survival (%)
T stage T1 T2 T3
Dura invasion
a
No Yes
Histologic fi ndings
6 13 15
13
5
b
100
79 53
100
30
100
62 51
83 40
Undifferentiated carcinoma 12 82 72
Squamous cell carcinoma Adenoid cystic and
8 13
53 73
70 50
adenocarcinoma
Local treatment Surgery + radiation Radiation alone
21 13
74 64
68 56
Chemotherapy No Yes
a
Patients treated with postoperative irradiation only.
b
Excludes one patient with transitional cell carcinoma. Modifi ed from Jiang GL, Morrison WH, Garden AS, et al. Ethmoid sinus carcinomas: natural history and treatment results. Radiother Oncol 1998;49:21–27, with permission.
25
80
9
50
62 67
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Table 12.3
Histology Patient No.
Esthesioneuroblastoma 31 4 9 0
Neuroendocrine carcinoma 18 27 13 12
Sinonasal-undifferentiated carcinoma 16 21 16 25
Small cell carcinoma 7 33 44 75
a
5-y actuarial rates. Data from the M.D. Anderson Cancer Center. Modifi ed from Rosenthal DI, Barker JL Jr, El-Naggar AK, et al. Sinonasal malignancies with neuroendocrine differentiation: patterns of failure according to histologic phenotype. Cancer 2004;101:2567, with permission.
Table 12.4
First Author (yr) Patient Number % Patients Treated Postoperatively 2-yr Local Control (%)
Combs (2006) 46 ND 81
Daly (2007) 36 89 62
Hoppe (2008) 37 100 75
Madani (2009) 84 89 71
Dirix (2010) 40 100 76
ND, not described. Data from Combs SE, et al. Radiat Oncolog 2006;1:23; Daly ME, et al. Int J Radiat Oncol Biol Phys 2007;67:151; Hoppe BS, et al. Head Neck 2008;30:925; Madani I, Bonte K, Vakaet L, et al. Intensity-modulated radiotherapy for sinonasal tumors: Ghent Univerisity Hospital update. Int J Radiat Oncol Biol Phys 2009;73:424; and Dirix P, et al. Int J Radiat Oncol Biol Phys 2010;78:998.
Patterns of Failure in Patients with Sinonasal Carcinomas with Neuroendocrine Differentiation
Local
a
Failure
Local Control of Paranasal Sinus Malignancies Treated With IMRT
(%)
Regional Failurea (%)
Distant Failurea (%)
SPHENOID AND FRONTAL SINUSES
Treatment Strategy
Cancers of the sphenoid sinus and frontal sinuses are very rare. Treatment is individualized and modalities are cho­sen based on the extent of disease and the histologic type. Radiation is o en recommended either as an adjunct to surgery or as a frontline therapy in patients with inoperable
Case
Study
12-10
chemotherapy yielding a partial response.
He was then treated with IMRT with concurrent chemotherapy. Target delineation was done by fusing the prechemotherapy MRI onto the postchemotherapy plan­ning CT set. CTVHD encompassed the prechemotherapy gross disease. Margin was only added anteriorly into the ethmoids where it was deemed safe. Figure 12.10 shows
A 66-year-old man presented with headache.
An MRI showed a mass (green arrow) in the sphenoid sinus (Fig. 12.10A). An endoscopic biopsy revealed squamous cell carcinoma. He was treated with induction
tumor or with tumor type that is thought to be (chemo) radiosensitive.
Nodal disease is uncommon. Radiation targets are the pri­mary site with margin. IMRT is preferred due to the proximity to the optic structures and brain. Examples of treatment of a patient with sphenoid sinus cancer with frontline radiotherapy
(Case Study 12-10) and a case with frontal sinus cancer treated
th postoperative radiation (Case Study 12-11) are shown.
wi
a sagittal view of isodose distribution through midline (Fig.12.10B) with the optic chiasm highlighted by yellow colorwash and arrow.
Figures 12.10C–F show two matched pairs of contours as shown on the prechemotherapy MRI and isodose dis­tributions on the planning CT. CTVHD (red contour) was prescribed 70 Gy. A third matched pair (Fig. 12.10G,H) shows axial views below the optic pathways. CTVED (blue) provided an additional 0.5-cm margin on the ethmoids and was prescribed 60 Gy.  e patient remains well over 2 years from treatment without disease, and there was no vision impairment.
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Part 2 Site-Specifi c Indications and Techniques
A
C
B
D
E
Figure 12.10A-F
F
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221
G
Figure 12.10G,H
Case
Study
12-11
di erentiated squamous cell carcinoma. Restaging revealed no gross residual disease, so it was elected to treat him with postoperative IMRT as the multidisciplinary team did not believe further surgery would be of bene t.
IMRT was designed to address the primary tumor bed
only with two target volumes. Because he had a debulking
A 71-year-old man presented with headache.
An MRI showed changes that were thought to be consistent with a mucocele of the le frontal sinus. He underwent resection, and histologic examination revealed poorly
H
rather than an oncologic surgical approach, CTVHD encom­passing the le frontal sinus was prescribed 66 Gy. CTVED added additional 0.5- to 1-cm margins, more generous margin into the right frontal sinus, and was prescribed 60Gy.
Figure 12.11 shows contours (orange colorwash for CTVHD and aqua for CTVED) and isodose distributions on a coronal view (Fig. 12.11A) and three axial views through the sinus (Fig. 12.11B–D).  e patient is without disease at the last follow-up.
A
Figure 12.11A,B
B
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Part 2 Site-Specifi c Indications and Techniques
C
Figure 12.11C,D
SUGGESTED READINGS
Bristol IJ, Ahamad A, Garden AS, et al. Postoperative radiotherapy for maxillary sinus cancer: long-term outcomes and toxicities of treatment. Int J Radiat Oncol Biol Phys 2007;68:719.
Claus F, De Gersem W, De Wagter C, et al. An implementa­tion strategy for IMRT of ethmoid sinus cancer with bilateral spar­ing of the optic pathways. Int J Radiat Oncol Biol Phys 2001;51:318.
Demonte F, Ginsberg LE, Clayman GL. Primary malignant tumors of the sphenoidal sinus. Neurosurgery 2000;46:1084.
Fletcher GH, Goepfert H, Jesse RH. Nasal and paranasal sinus carcinoma. In: Fletcher GH, ed. Textbook of radiotherapy, 3rd ed. Philadelphia, PA: Lea & Febiger, 1980.
Jesse RH, Goepfert H, Lindberg RD. Carcinoma of the sinuses: a review of treatment. In: Chambers RG, Janssen de Limpens AM, Jaques DA, et al. eds. Cancer of the head and neck. Amsterdam,  e Netherlands: Excerpta Medica, 1975.
Jiang GL, Morrison WH, Garden AS, et al. Ethmoid sinus carcinomas: natural history and treatment results. Radiother Oncol 1998;49:21.
Klintenberg C, Olofsson J, Hellquist H, et al. Adenocarci­noma of the ethmoid sinuses. A review of 28 cases with special ref­erence to wood dust exposure. Cancer 1984;54:482.
Le QT, Fu KK, Kaplan M, et al. Treatment of maxillary sinus carcinoma: a comparison of the 1997 and 1977 American Joint Committee on cancer staging systems. Cancer 1999;86:1700.
Le QT, Fu KK, Kaplan MJ, et al. Lymph node metastasis in maxillary sinus carcinoma. Int J Radiat Oncol Biol Phys 2000;46:541.
Logue JP, Slevin NJ. Carcinoma of the nasal cavity and parana­sal sinuses: an analysis of radical radiotherapy. Clin Oncol 1991;3:84.
Madani I, Bonte K, Vakaet L, et al. Intensity-modulated radi­otherapy for sinonasal tumors: Ghent Univerisity Hospital update. Int J Radiat Oncol Biol Phys 2009;73:424.
D
McNicoll W, Hopkin N, Dalley VM, et al. Cancer of the paranasal sinuses and nasal cavities. Part II. Results of treatment. JLaryngol Otol 1984;98:707.
Mendenhall WM, Amdur RJ, Morris CG, et al. Carcinoma of the nasal cavity and paranasal sinuses. Laryngoscope 2009; 119:899.
Mock U, Georg D, Bogner J, et al. Treatment planning com­parison of conventional, 3D conformal and intensity-modulated photon (IMRT) and proton therapy for paranasal sinus carcinoma. Int J Radiat Oncol Biol Phys 2004;58:147.
Paulino AC, Fisher SG, Marks JE. Is prophylactic neck irra­diation indicated in patients with squamous cell carcinoma of the maxillary sinus? Int J Radiat Oncol Biol Phys 1997;39:283.
Paulino AC, Marks JE, Bricker P, et al. Results of treatment of patients with maxillary sinus carcinoma. Cancer 1998;83:457.
Pommier P, Ginestet C, Sunyach M, et al. Conformal radiotherapy for paranasal sinus and nasal cavity tumors: three­dimensional treatment planning and preliminary results in 40patients. Int J Radiat Oncol Biol Phys 2000;48:485.
Rosenthal DI, Barker JL Jr, El-Naggar AK, et al. Sinona­sal malignancies with neuroendocrine differentiation: patterns of failure according to histologic phenotype. Cancer 2004;101:
2567.
Tsien C, Eisbruch A, McShan D, et al. Intensity-modulated radiation therapy (IMRT) for locally advanced paranasal sinus tumors: incorporating clinical decisions in the optimization process. Int J Radiat Oncol Biol Phys 2003;55:776.
Waldron JN, O’Sullivan B, Gullane P, et al. Carcinoma of the maxillary antrum: a retrospective analysis of 110 cases.
O
ncol 2000;57:167.
Waldron JN, O’Sullivan B, Warde P, et al. Ethmoid sinus can­cer: twenty-nine cases managed with primary radiation therapy. Int
J Radiat Oncol Biol Phys 1998;41:361.
Radiother
Salivary Glands
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Key points
Salivary neoplasms originate mostly from major
salivary glands (parotid, submandibular, and sublin­gual glands) but can arise from thousands of minor glands spread throughout the mucosa of the head and neck.
 e most common neoplasm is benign pleomorphic
adenoma. Malignant tumors are uncommon but com­prise a wide variety of histologic types, with mucoepi­dermoid carcinoma, adenoid cystic carcinoma (ACC), and salivary ductal carcinoma leading the list.
Histologic grade of di erentiation is a strong prog-
nostic factor. Distant metastases are more common in patients with high-grade tumors.
Surgery is the recommended frontline treatment for
resectable salivary gland cancers. Many of these
13
tumors are locally in ltrative with ill-de ned borders.
Surgical section margins are o en close or positive.
Adjuvant radiation is o en recommended. Indications
for radiation include extraglandular extension, close or positive surgical margins, nodal involvement, high­grade histology, and perineural spread.
Due to perineural spread, particularly with ACC,
radiation volumes o en include the nerve pathways from the primary tumor to the skull base.
Primary radiotherapy is reserved for inoperable
tumors. Neutron therapy may be advantageous in this situation, particularly for ACC.
 e role of combination of chemotherapy and radia-
tion for the treatment of high-risk salivary cancers is being investigated.
Despite the realization of the diverse natural history and variation of radiation technique by speci c site of origin, the rarity of salivary cancers led many investigators to report
treatment outcomes in aggregate.  erefore, this chapter begins by summarizing the general background outcome data before addressing individual subsites.
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