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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
A
C
Figure 10.2A-C
Setup and Field Arrangement for Conventional Radiotherapy Technique
Marking of shoulders and palpable nodes facilitates portal design.  e patient is immobilized in a supine position with the shoulders pulled down to the maximal extent. Lateral parallel–opposed photon  elds are used to treat the primary tumor and upper and mid neck nodes.
Superior border: a
t the level of the skull base to include the
upper jugular and parapharyngeal lymphatics.
Anterior border: 1-cm fallo .
Posterior border: behind the spinous processes or more
posteriorly in the presence of large nodal mass.
Inferior border: encompasses primary lesion with margin
(as low as possible while avoiding the shoulders).
A matching anterior portal is used to treat the lower neck nodes. It may be necessary to use anterior and inferior tilts for patients with a short neck or because of the inferior extent of
B
the primary tumor or nodal mass. In this case, the supraclav­icular fossae are included in the primary portal (see Fig. 9.11).
For boost volume, reduced lateral  elds are used as follows:
Superior and inferior borders: dep
ends on the extent of the disease; at least include aryepiglottic folds superiorly and cricoid cartilage inferiorly.
Anterior border: 1-cm fallo , except when primary lesion
is con ned to the posterior structures where a small strip of anterior skin may be spared.
Posterior border: midvertebral bodies, or posterior one
third of vertebral bodies when the primary involves posterior pharyngeal wall.
Involved upper and midjugular nodes receive boost dose through lateral  elds along with the primary tumor and lower neck nodes through a reduced anterior portal.
Nodes overlying the spinal cord can receive boost dose
with electron beam(s) or, alternatively, the primary tumor
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175
and ipsilateral node can receive boost dose with oblique pho­ton  elds depending on the location of the node(s).
Intensity-Modulated Radiation Therapy Planning
Most patients are now treated with intensity-modulated radiation therapy (IMRT) to spare parotid function
(Case Study 10-3).  e primary tumor and involved
node(s) with a minimum of 1-cm margin constitutes CTVHD (CTV1). However, because of laryngeal motion, it is prudent to encompass the majority of the larynx in the high-dose target volume. CTVID (CTV2) de nes the neck compartments outside CTVHD with a 2-cm (cranial– caudal) margin .  e remaining nodal levels (II to V) are contoured
Case
Study
10-3
biopsy of which showed squamous cell carcinoma.  ere was no clinical evidence of lymphadenopathy. He received concurrent radiation and chemotherapy. While bulky dis­ease was seen  lling the right pyriform sinus, the disease had signi cant super cial spread.
A 61-year-old male, presented with sore throat, mild odynophagia, and weight loss. Examination revealed an extensive tumor of the oropharyngeal walls extending into the right pyriform sinus and postcricoid region,
as CTVED (CTV3). LevelIb on the side of involved node is included in CTVED.
Dose
Stage I (T1 N0) tumors: 50 Gy in 25 fractions to the initial target volume and then 16 Gy in 8 fractions to the primary tumor. For patients treated with IMRT, a dose of 66 Gy is pre­scribed to CTVHD and 54 Gy to CTVED. An alternative option is to treat with two sequential plans.  e  rst delivers 50 Gy in 25 fractions to CTVHD and CTVED followed by a plan that delivers 16 Gy in 8 fractions to CTV
Stage II (T2 N0) tumors: hyperfractionated or concomi-
tant boost regimen. Hyperfractionation delivers 55.2 Gy in
A PET-CT simulation was performed to assist in de n­ing the targets, particularly the inferior extent of disease that could not be visualized clinically (Fig. 10.3). An axial CT slice with adjacent fused PET image is shown in Figure10.3A.  e high dose CTV (red) and subclinical target (yellow) are shown on the CT scan. A more inferior slice through the postcri­coid region (Fig. 10.3B) did not demonstrate an increase in FDG uptake. A high-dose clinical volume was outlined for boost volume de nition, as this slice was approximately 1 cm below the identi ed gross target volume.
HD.
A
B
Figure 10.3A,B
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Part 2 Site-Specifi c Indications and Techniques
46 fractions to the initial target volume and then 21.6 Gy in 18 fractions (1.2-Gy fractions, twice daily, 6-hour interval); the spinal cord dose is limited to 44.4 to 45.6 Gy or less, and uninvolved posterior cervical nodes are supplemented with 2Gy daily to approximately 55 Gy. Concomitant boost deliv­ers 1.8-Gy fractions to 54 Gy in 30 fractions to the initial target volume and 1.5-Gy fractions to 15 to 18 Gy given as second daily fractions during the last 2 to 2.5 weeks; the spi­nal cord dose is limited to 45 Gy or less. For patients treated with IMRT, one option is to use the concomitant boost sched­ule, which requires two separate plans.  e  rst plan delivers 54 Gy in 30 fractions to CTVHD and CTVED, and the second plan is for 18 Gy in 10 to 12 fractions to CTVHD (given as sec­ond daily fractions). An alternative choice is to use one plan that delivers 70 Gy to CTVHD and 56 Gy to CTVED. Treatment is given in 35 fractions over 30 treatment days, by delivering 6 fractions a week for 5 weeks with a 6-hour interfraction interval on the day 2 fractions are delivered.
Stage III and IV tumors: in combination with three cycles of concurrent cisplatin, radiation is given in conventional 2-Gy fractions to a dose of 50 Gy to the initial target volume and 70 Gy to the boost volume. Di erential loading may bepreferred
for lateralized lesions with ipsilateral nodal disease only. In this situation, the dose is speci ed at an isodose line with maximal allowable dose heterogeneity of ±2.5%.  e spinal cord dose is limited to 45 Gy or less. For patients treated with IMRT, the commonly prescribed doses are 70 Gy to CTVHD 60 to 63 Gy to CTVID, and 56 to 57 Gy to CTVED, given once daily in 33 to 35 fractions (Case Studies10-4and10-5).
Postoperative Radiotherapy
 e indications, technique, and dose prescriptions are simi­lar to those for supraglottic carcinoma except that the target volume also encompasses the retropharyngeal nodes.  e superior border of the lateral  elds is placed at the level of the base of skull (Case Study 10-6). For IMRT treatment planning, CTVHD (CTV1) encompasses the preoperative tumor bed and involved nodal regions with margin, CTVID (CTV2) the operative bed, and CTVED (CTV3) the undis­sected nodal volumes at risk including the retropharyngeal nodes.  e stoma can be delineated as CTVID or CTVED depending on the risk features. Areas of very high risk (posi­tive margin or extranodal extension) can be delineated sepa­rately, to a prescribed higher dose (e.g., 64 to 66 Gy).
Case
Study
10-4
images (Fig. 10.4B,C) showed the right level II node and the superior aspect of the primary tumor at the vestibule of the right pyriform sinus and the bulk of the primary lesion at the level of the mid-pyriform sinus.  e inferior aspect of the node can be seen abutting the anterior aspect of the sternocleidomastoid muscle. Biopsy of the primary tumor revealed squamous cell carcinoma. He was staged as
A 53-year-old male presented with a right upper neck mass and mild sore throat.
Examination revealed a 2.5 cm upper jugular node and a lesion on the medial wall of the pyriform sinus (Fig. 10.4A). Axial CT
having a T2 N1 M0 and treated with IMRT with three cycles of concurrent high-dose cisplatin.
CTVHD (70 Gy) encompassed the primary tumor and involved node with margins, CTVID (60 Gy) the right pos­terior neck, and CTVED (56 Gy) the le neck (Fig. 10.4D).  e ipsilateral hypopharyngeal wall down to the cricoid level was included in CTVHD, right level III nodal region in CTVID, and le level III, and bilateral level IV, nodes in CTVED (Fig. 10.4E,F). Figure 10.4G shows the sagit­tal isodose distribution through the primary tumor.  e patient had good function without evidence of disease 3 years a er completing treatment.
A
Figure 10.4A,B
B
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C
E
D
F
G
Figure 10.4C-G
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Part 2 Site-Specifi c Indications and Techniques
Case
Study
10-5
scan revealed tumor extension into the neck (Fig. 10.5A).  ere were multiple ipsilateral lymph nodes. Biopsy of the primary tumor showed squamous cell carcinoma. Stage: T4 N2b M0.
Due to marginal renal function, he received three cycles of carboplatin and paclitaxel with good response. He was subsequently treated with IMRT and concurrent weekly paclitaxel. Figure 10.5B shows CTVHD (70 Gy—red) encompassing the prechemotherapy tumor extent with
A 69-year-old man, with a history of heavy tobacco and alcohol consumption, presented with a large right neck mass.
Examination showed a large primary
tumor of the right pyriform sinus. PET-CT
1-cm margin, CTVID (63 Gy—blue) de ning the uninvolved ipsilateral level V nodes, and CTVED (57 Gy—yellow) cov­ering the uninvolved contralateral neck nodes at the level of the mid pyriform sinus. A fourth volume (orange) was delineated to prescribe a dose of 66 Gy to the anterior tis­sues and the mid-posterior hypopharynx due to the exten­sive neck involvement.  e red circle over the vertebral body is a dosimetric reference point. Figures 10.5C–E show isodose distributions through the isocenter on axial, sagit­tal, and coronal views. Isodose distributions on axial slices at the level of the retropharyngeal nodes (Fig. 10.5F) and low level IV nodes (Fig. 10.5G) are also displayed. Two years a er completion of therapy, he remained free of dis­ease, ate a near normal diet, and had normal speech.
A
C
Figure 10.5A-D
B
D
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E
G
Figure 10.5E-G
Case
Study
10-6
ately di erentiated squamous cell carcinoma. Because of the weight loss and near obstruction of the larynx, a gas­trostomy tube was placed and tracheostomy performed. He subsequently underwent total laryngectomy, partial phar­yngectomy, and bilateral neck dissections.  e defect was repaired with a radial forearm gra . Histologic examina­tion revealed a carcinoma of the le pyriform sinus invad­ing the le aryepiglottic fold and thyroid cartilage.  ere
A 61-year-old man presented with several months of le otalgia and weight loss. Exami­nation showed a large mass  lling the le pyri­form sinus, invading medially into the larynx. Biopsy of the primary tumor revealed moder-
F
was perineural and lymph-vascular space invasion. Two of twenty- ve nodes recovered from the le neck dissec­tion contained metastatic disease without extracapsular extension. Stage: pT4 N2b M0. He received postoperative radiation.
Figure 10.6A shows treatment began with large parallel–opposed  elds that were progressively reduced a er 42 and 56 Gy to administer a total of 60 Gy to the high-risk regions. Figure 10.6B shows an isodose distri­bution through the central axis.  e posterior cervical strips were supplemented with 12 MeV electrons to 56 Gy. Amatching anterior  eld was used to treat the low neck and stoma to 50 Gy.
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Part 2 Site-Specifi c Indications and Techniques
A B
Figure 10.6A,B
Background Data
Table 10.1
Institution
University of Florida T1 (23) 85
University of Texas M.D. T1 (19) 89
Anderson Cancer Center
Massachusetts General Hospital
Japan (10 institutions)
a
Includes all hypopharyngeal sites (69% of patients had pyriform sinus
tumors).
b
Includes all hypopharyngeal sites (70% of patients had pyriform sinus
tumors).
c
Crude local control rate. Adapted from Rabbani A, et al. Defi nitive radiotherapy for T1-T2 squamous cell carcinoma of the pyriform sinus. Int J Radiat Oncol Biol Phys 2008;72:351; Garden AS, et al. Early squamous cell carcinoma of the hypopharynx: outcomes of treatment with radiation alone to the primary disease. Head Neck 1996;18:317; Wang CC. Carcinoma of the hypopharynx. In: Radiotherapy of head and neck neoplasms. New York, NY: Wiley-Liss, 1997:212; and Nakamura K. et al. Multi-institutional analysis of early squamous cell carcinoma of the hypopharynx. Int J Radiat Oncol Biol Phys 2006;65:1045.
Local Control of Radiation for Early (T1 To T2) Squamous Cell Carcinoma of the Pyriform Sinus (Literature Review)
Stage (No.
Patients)
5-yr Actuarial Control (%)
T2 (100) 85
a
T2 (63) 70
T1 (24) T2 (51)
b
T1 (39) T2 (76)
74 76
85
68
c
Table 10.2
Distribution of Initial Failures in Patients with Early Stage (T1 To T2) Carcinoma of the Hypopharynx Treated with Radiation Therapy
Type of Recurrence
T1
(n = 58)
T2
(n = 139)
Total
(n = 197)
Primary relapse (P) 8 32 40
Nodal recurrence (N) 3 11 16
P + N 0 7 7
P + D 1 0 1
N + D 0 5 5
P + N + D 0 1 1
Distant metastasis (D) 3 8 10
Failure above clavicles
12 (21%) 50 (36%) 62 (31%)
without D
Total failures 15 (26%) 58 (42%) 73 (37%)
Modifi ed from Garden AS, et al. Early squamous cell carcinoma of the hypopharynx: outcomes of treatment with radiation alone to the primary disease. Head Neck 1996;18:317 and Nakamura K. et al. Multi-institutional analysis of early squamous cell carcinoma of the hypopharynx. Int J Radiat Oncol Biol Phys 2006;65:1045.
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Table 10.3
Stage No. of Patients
T1–T2
N0 N1b N3 Total
T3
N0
N1b
N2b
N3
Total
Overall total 434 119 (27) 70 (16) 40 (9) 229/434 (53)
Minimal follow-up 2 years. P, primary; N, node; P + N, primary + node. Modifi ed from Bataini, et al. Int J Radiat Oncol Biol Phys 1982;8:1277.
Table 10.4
Type of Complications No. of Patients
Death related to therapy Total 11/434 (2.5%)
Hemorrhage 7
Cachexia 2
Asphyxia due to laryngeal edema 1
Aspiration pneumonia 1
Major but nonfatal (in 114 patients alive at 3 yr):
Total 12/114 (11%)
Tracheostomy 6
Gastrostomy 1
Tracheostomy + gastrostomy 1
Soft tissue necrosis (treated
conservatively)
Modifi ed from Bataini, et al. Int J Radiat Oncol Biol Phys 1982;8:1277.
Cancer of the Pyriform Sinus Treated by Radical Radiotherapy: Loco-Regional Failures According to Stage of Primary and Nodal Disease
Recurrences
P: No. (%) P + N: No. (%) N: No. (%) Total: No. (%)
33 21 36 90
90
105
9 140 344
Cancer of the Pyriform Sinus Treated by Radical Radiotherapy: Radiotherapy Complications in 434 Patients
10
6 7
23 (26)
27 30
5 34 96 (28)
1 5 6 (7)
6 15 — 42 64 (19)
2 9
11 (12)
3
11
6/9 15 29 (8)
setting, the combination of conventional radiation frac­tionation(70 Gy in 35 fractions over 7 weeks) with cisplatin
2
(100mg/m
given on days, 1, 22, and 43 of radiotherapy) is rec-
10/33 (33)
9/21 (43) 21/36 (58) 40/90 (44)
36/90 (40) 56/105 (53)
91/140 (65)
189/344 (55)
ommended. Neck dissection is indicated in patients who have residual neck mass 6 to 10 weeks a er completion of therapy.
Occasionally, advanced tumors (T4) are treated with surgery and postoperative radiotherapy. Carcinoma of the postcricoid region is very rare and is usually treated with surgery with or without postoperative radiotherapy.
Primary Radiotherapy
Target Volume
 e initial target volume encompasses the primary with at least 2- to 3-cm margins (of note is that submucosal spread can be extensive) and level II to V and retropharyngeal nodes
(Case Study 10-7).  e boost volume encompasses primary
tumor and involved nodes with 1- to 2-cm margins.
4
IMRT target volumes are similar to those described for pyriform sinus cancers. CTVHD should, however, include 3 to 5 mm of the anterior vertebral bodies even without demonstrable bone invasion. CTVID is o en more gener­ous, 2 to 3cm in the cranial and caudal dimensions, because
POSTERIOR HYPOPHARYNGEAL WALL
of the risk of submucosal lymphatic spread through the retropharyngeal space.
Treatment Strategy
Primary radiotherapy is preferred for T1 to T2 tumors. Com­bination of radiation with chemotherapy is the treatment of choice for T3 or N2 to N3 tumors. Outside protocol study
Setup and Field Arrangement for Conventional Radiotherapy T
echnique
Marking of palpable nodes and shoulders facilitates portal design.  e patient is immobilized in a supine position with
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Part 2 Site-Specifi c Indications and Techniques
a thermoplastic mask with the shoulders pulled down as far as possible. Lateral parallel–opposed photon  elds are used for treatment of the primary tumor and upper neck nodes
(see Case Study 10-7).
Superior border: a
geal lymphatics and upper jugular nodes.
Anterior border: at least 2 cm anterior to the known
extent of the tumor, but when feasible short of fallo anteriorly.
Posterior border: just behind the spinous processes or more
posteriorly in the presence of large nodal masses. A er o -cord reduction, the posterior portal margin is at the posterior one third of vertebral bodies to include the ret­ropharyngeal nodes and provide margin for the posterior pharyngeal wall.
Inferior border: encompasses primary lesion with 3-cm or
greater margin when possible.
An anterior appositional portal is used for treating lower neck nodes. It may be necessary to use anterior and infe­rior tilts for patients with a short neck or because of the
t the base of skull to cover parapharyn-
inferior extent of the primary tumor or nodal mass. In this case, the supraclavicular fossae are included in the pri­mary portal.
For boost volume, the lateral  elds are reduced:
Superior and inferior borders: depends on extent of the
primary tumor.
Anterior border: short of fallo .
Posterior border: posterior one third of vertebral bodies.
Involved level II and III nodes are encompassed in lateral  elds and lower neck nodes in a reduced anterior portal.
Nodes overlying the spinal cord can be boosted with electron beam(s) or, alternatively, the primary tumor and ipsilateral node can be boosted with oblique photon  elds.
Intensity-Modulated Radiation Therapy Planning
IMRT is best suited for treating tumors extending to the par­a
vertebral region without overdosing the spinal cord because this technique can produce a horseshoe-shaped isodose dis­tribution.  e patient is immobilized in a supine position with an extended thermoplastic mask.  in-cut computed
Case
Study
10-7
pable neck nodes. A CT scan con rmed the physical  nd­ings and in addition showed some thickening of the le aryepiglottic fold. Biopsy showed moderately di erentiated squamous cell carcinoma. Stage: T2 N0 M0.  is patient received radiotherapy with a hyperfractionation schedule.
Figure 10.7 shows lateral  elds designed to encom­pass the primary tumor and the majority of neck nodes while sparing a strip of anterior skin.  e posterior border of the o -cord and boost portals at the level of the primary tumor was close to the posterior edge of the vertebral bod­ies to cover the lesion adequately. Supraclavicular nodes were treated with an anterior appositional photon  eld.  e primary tumor received 76.6 Gy in 7weeks (55.2Gy in 46 fractions for 4.6 weeks + 21.6 Gy in 18fractions for 2 weeks); uninvolved upper and midjugular nodes received 55.2 Gy in 4.6weeks and uninvolved posterior cervical nodes 54 Gy in 5 weeks. Supraclavicular nodes received 50 Gy in  ve fractions for 5 weeks. Physical examination 6 months a er radiotherapy revealed full­ness of the le pyriform sinus. Biopsy of this area showed squamous cell carcinoma. He underwent total laryn­gopharyngectomy with le modi ed neck dissection and
A 68-year-old man had a 1-year history of dysphagia. Mirror examination revealed a mass in the le lateral and posterior hypopharyn­geal walls.  e medial wall and apex of the pyriform sinus were free.  ere were no pal-
pharyngeal reconstruction with jejunal free  ap. Second local recurrence occurred 5 months a er surgery, and he died of uncontrolled local disease.
Figure 10.7
Chapter 10 Hypopharynx
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183
tomography (CT) scans are obtained in treatment posi­tion. Clinical target volumes (CTVs), as described for pyri­form sinus carcinomas above, are outlined for dosimetric planning.
Dose
T1 tumors: 50 G then 16 Gy in 8 fractions to the primary tumor.
T2 tumors: hyperfractionated or concomitant boost regimen. Hyperfractionation delivers 55.2 Gy in 46 fractions to the initial target volume and then 21.6 Gy in 18 fractions (1.2-Gy fractions, twice daily, 6-hour interval); the spinal cord dose is limited to 44.4 to 45.6 Gy or less, and uninvolved posterior cervical nodes are supplemented with 2 Gy daily to approximately 55 Gy. Concomitant boost delivers 1.8-Gy fractions to 54 Gy in 30 fractions to the initial target volume and 1.5-Gy fractions to 15 to 18 Gy given as second daily fractions during the last 2 to 2.5 weeks; the spinal cord dose is limited to 45 Gy or less.
Positive nodes, frequently present, receive doses appropriate for the size and the fractionation schedule
Case
Study
10-8
invading the preverterbral muscles (Fig. 10.8B) with le retropharyngeal adenopathy (Fig. 10.8C). He underwent total pharyngolaryngectomy and bilateral neck dissections including resection of the retropharyngeal space followed
y in 25 fractions to the initial target volume
A 60-year-old man presented with dysphagia and was found to have biopsy proven squamous cell carcinoma of the posterior hypopharynx (Fig. 10.8A). Axial CT slices show disease (red arrows) in the posterior hypopharyngeal wall
used, for example, 66 to 70 Gy in 2-Gy fractions, 69 to 72 Gy with concomitant boost, or 74.4 to 79.2 Gy with hyperfractionation.
T3 tumors: in combination with three cycles of concur­rent cisplatin, radiation is given in the conventional 2-Gy fractions to a dose of 50 Gy to the initial target volume and 70 Gy to the boost volume.  e spinal cord dose is limited to 45 Gy or less.
Regimens for IMRT are similar to that described for pyriform sinus tumors.
Postoperative Radiotherapy
Indications and technique for postoperative radiotherapy are similar to those for pyriform sinus cancer with the exception that the posterior border of the o -cord and boost  elds are brought closer to the posterior edge of the vertebral bodies to ensure good coverage of the prevertebral and paraver­tebral tissues (see Case Study 10-8). CTVHD should, how­ever, include 3 to 5 mm of the anterior vertebral bodies even without demonstrable bone invasion.
by a tubed anterolateral thigh free  ap reconstruction. Histologic examination revealed a 7-cm primary tumor,  ve positive nodes in the right neck and eight positive nodes in the le neck, as well as disease in the retropharyngeal space. He was treated with concurrent cisplatin and IMRT deliver­ing 60Gy in 30 fractions to CTVHD. Figure 10.8 D–F show representative isodose distribution on axial, sagittal, and coronal views through isocenter. He developed lung metas­tasis without local-regional relapse <1 year from diagnosis.
A
Figure 10.8A,B
B