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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_639_Библиотеки_им_академика_М_И_Перельмана.pdf
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382 Part III Esophagus
have been developed to seal esophagoairway stulae and pre­vent tumor ingrowth. ree randomized trials were reported comparing the use of metallic stents with plastic prostheses. Perforation, pneumonia, bleeding, or migration rates were signicantly less with metallic stents. Because of the lower morbidity, metallic stents were also more cost-eective
288–290
despite their higher initial cost.
e choice of various metallic stents depends on their individual characteristics, in terms of exibility, tensile force, and degree of shortening on deployment in relation to the site of placement. Compared with more conventional methods of palliation such as laser therapy, patients with SEMS spent less time in the hospital and required less frequent reinterventions.
291
e main problems with SEMS are stent migration, tumor ingrowth or overgrowth, and, if placed across the GEJ, they allow acid reux. Placing uncovered stents across the cardia lessens the chance of migration, and stents have been devel-
292
oped with a one-way ap valve to prevent reux.
It has also been shown that “tumor” ingrowth is sometimes due to granulation tissue or hyperplastic reaction by the esophageal
293
mucosa.
Patency can be achieved again by laser, argon beam application, or sometimes placement of a second stent within the rst. One recent randomized trial compared the use of the Ultraex stent (Boston Scientic, MA) with the Polyex stent (Boston Scientic, MA), and the Niti-S double stent (Taewoong Medical, Seoul, Korea). e Polyex stent is a sili­cone device with an encapsulated monolament braid made of polyester. e silicone and polyester material is designed to lessen nontumoral tissue overgrowth, a problem common with SEMS. e Niti-S stent has an inner polyurethane layer over its entire length, and an outer uncovered nitinol wire tube to allow the mesh to embed itself in the esophageal wall. Success rates were similar for all three stents, but recur­rent dysphagia was more common with the Ultraex stent, because of tissue ingrowth and overgrowth, and, to lesser degree, the Niti-S stent. Polyex stent had a higher chance of migration, not surprisingly, because the stent is also designed to be removable in benign esophageal stenosis.
294
Another problem of stent insertion is for placement near to the upper esophageal sphincter. Foreign body sensation, pain, odynophagia, and airway compression can be troublesome and demand accurate placement. is is illustrated in the situ­ation when recurrent disease is found at the anastomosis or in the esophageal remnant after subtotal esophagectomy. Place­ment of SEMS is still possible and achieves good palliation.
295
SUMMARY AND FUTURE PERSPECTIVES
Advances have been made in the management of esophageal cancer; survival of patients has improved. the most appropriate combination for individual patients. Surgeons play a central role in directing management treatment of this disease by advising on how best to integrate surgi­cal resection with nonoperative programs. Surgeons should aim at improving their results further, so that low mortality
296
e key is to select
rates for resections are used to compare with seemingly safer therapies. e technique and extent of surgical resection may change when more information is made available, and should vary with patients and disease stage. MIE will be more widely practiced; it should achieve the same radicality of operation with less morbidity. Chemoradiation therapy has made a real
296
impact on current management strategies,
but perhaps its overenthusiastic adoption and its presumed benet have to be balanced against the lack of clear evidence of superiority over
297
surgery.
Distant failure remains a major problem, and search for more eective systemic drugs as well as our ability to predict responders with precision must be therapeutic targets. Manage­ment strategies are going to evolve further, with improvements in molecular techniques, imaging methods, and introduction of more novel tumoricidal agents. e challenge for the future is for us to critically test our strategies in a scientic, unbiased manner, and to explore other innovative treatments.
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289. - anzano C. Plastic prosthesis versus expandable metal stents for palliation of inoperable esophageal thoracic carcinoma: a controlled prospective study. Gastrointest Endosc. 1996;43(5):478–482.
290. Siersema PD, Hop WCJ, Dees J, Tilanus HW, van Blankenstein M. Coated self-expanding metal stents versus latex prostheses for esophago­gastric cancer with special reference to prior radiation and chemotherapy: a controlled, prospective study. Gastrointest Endosc. 1998;47:113–120.
291.       e cost eectiveness of metal oesophageal stenting in malignant disease compared with conventional therapy. Clin Radiol. 1999;54(4):212–215.
292. Kocher M, Dlouhy M, Neoral C, et al. Esophageal stent with antire­ux valve for tumors involving the cardia: work in progress. J Vasc Interv Radiol. 1998;9(6):1007–1010.
293.  - malignant obstruction is a common problem with metal stents in the treat­ment of esophageal cancer. Gastrointest Endosc. 2000;51(5): 556–559.
294.  design esophageal stents for the palliation of dysphagia from esopha­geal or gastric cardia cancer: a randomized trial. Am J Gastroenterol. 2008;103(2):304–312.
295. Law S, Tung PH, Chu KM, Wong J. Self-expanding metallic stents for palliation of recurrent malignant esophageal obstruction after subtotal esophagectomy for cancer. Gastrointest Endosc. 1999;50(3):427–436.
296. Law S, Kwong DL, Kwok KF, et al. Improvement in treatment results and long-term survival of patients with esophageal cancer: impact of chemora­diation and change in treatment strategy. Ann Surg. 2003;238(3): 339–348.
297. Law S. Chemoradiotherapy—panacea for esophageal cancer? Commentary for chemoradiotherapy of locally advanced esophageal cancer. Long-term
JAMA South­east Asia 1999;15(5):9–11.

SURGICAL PROCEDURES TO RESECT AND REPLACE THE ESOPHAGUS

Jon O. Wee • David J. Sugarbaker
18
Billroth and Czerny described the  rst esophageal resections in the 1870s, and they consisted of resections of the cer­vical esophagus without reconstruction. Later, resection of gastroesophageal (GE) junction tumors was performed by laparotomy with gastroesophageal anastomosis to reestab­lish intestinal continuity. Because there were concerns over respiratory compromise, surgeons were hesitant to enter the chest to perform esophageal resection. In 1915, Torek described the  rst transthoracic esophageal resection. used a left thoracotomy to resect the esophagus but did not attempt reconstruction. Instead, a cervical esophagostomy and abdominal gastrostomy were performed. A 3-ft-long external rubber tube was used to connect the ostomies, and it allowed the patient to eat for 17 more years ( Fig. 18-1 ). Turner performed the  rst transhiatal esophagectomy in
2
Oshawa reported the  rst transthoracic resection of
1933. the esophagus with esophagogastric anastomosis in 1933. Knowledge of this procedure did not become widespread in the Western community until Adams and Phemister described the procedure in 1938.
Ivor Lewis is credited with popularizing transthoracic resec­tion of the esophagus. Initially, he performed the procedure in two stages:  rst, mobilizing the stomach via laparotomy and several days later resecting the intrathoracic esophagus and reconstructing with the stomach.  e Ivor Lewis approach, which is an upper midline laparotomy for mobilization of the gastric conduit followed by right thoracotomy for resection and reconstruction, and the transhiatal approach are currently the two most commonly used techniques of esophageal resec­tion. In 1962, McKeown described a tri-incisional approach. He used a right thoracotomy to mobilize the esophagus.  e patient was then repositioned in the supine position, the gas­tric conduit was mobilized by laparotomy, and the anastomo­sis was performed in the neck. for surgical resection have also become increasingly popular. Combined thoracoscopic and laparoscopic techniques in some combination with open techniques have created a wider hybrid experience and are discussed in other chapters.
4
5
Minimally invasive options
1
He
3
6,
7
NEOADJUVANT TREATMENT
Historically, surgery has been the primary mode of treat­ment for localized esophageal cancer. Nonetheless, the long-term results of surgery alone for esophageal cancer are disappointing. posed as a means of improving long-term survival. Eight randomized trials have been performed using preoperative chemoradiation. Although the two largest randomized trials comparing preoperative chemoradiation followed by surgery to surgery alone showed no di erence in survival, smaller randomized trials have been used to support the use of preoperative chemoradiation. Urba and colleagues looked at 100 total patients randomized to preoperative chemora­diation or surgery alone. months in both groups, although there was a trend toward improved survival at 3 years (30 vs 16%; not statistically signi cant). Walsh and associates randomized 113 patients, and at 3 years 32% of those receiving preoperative chemo­radiation were alive versus 6% of those undergoing surgery
12
alone. lack of adequate pretreatment staging as well as a very poor survival in the surgical arm that is far below all other reported series. Hence, although there are no de nitive data to support the use of chemotherapy and radiation in the neoadjuvant setting, it remains widely used.
CALGB 9781 (Cancer and Leukemia Group B 9781) was a prospective randomized intergroup trial that evalu­ated patients with stages 1–3 esophageal cancer. Patients were randomized to surgery alone or to preoperative cisplatin and 5-FU with concurrent radiation (50.4 Gy) followed by sur­gery. Poor accrual resulted in premature closure of the study with 56 patients, well short of its goal of 500 patients. None­theless, with median follow-up of 6 years, 5-year survival was 39% for the trimodality group versus 16% for the surgery­alone group. Median survival was 4.5 years for the trimo­dality group versus 1.8 years for the surgery-alone group (p = .02).
8
Preoperative chemoradiation has been pro-
11
Median survival was about 18
 is study, however, has been heavily criticized for its
13
A meta-analysis by Urschel and Vasan in 2003
9,
10 two
389
390 Part III Esophagus
A
FIGURE 18-1 A. Depiction of Torek’s rst patient after esophageal resection. e rubber tube connected the lower end of the esophagus with a
gastrostomy. e patient lived 17 years after the surgery and died at age 80. B. Removable rubber tube conduit with beveled ends. (
permission, from Torek F. e operative treatment of carcinoma of the esophagus. Ann Surg 1915;61:385.)
combined the results of over 1100 patients from nine ran­domized controlled studies comparing neoadjuvant chemo-
B
Reproduced, with
adenocarcinoma, and the regional practice patterns make a
large, randomized study dicult to envision. radiotherapy followed by surgery versus surgery alone. is study did favor neoadjuvant chemoradiotherapy with surgery over surgery alone.
14
STAGING
ere is substantial comparative evidence of the benet of neoadjuvant chemotherapy for locally advanced esopha­geal cancer. e MRC (Medical Research Council) trial of 2002 demonstrated a statistically signicant survival benet (43 vs 34%) in those patients who received preoperative che­motherapy with an increase in median survival from 13.3
15
to 16.8 months.
is report was followed by the MAGIC (Medical Research Council Adjuvant Gastric Infusional Che­motherapy) trial in 2006, which further demonstrated an improved survival in patients with GE junction adenocarci­noma at 2 years (50 vs 41%) and at 5 years (36 vs 23%). A head- to-head comparison of neoadjuvant chemotherapy versus neoadjuvant chemoradiotherapy by the German Esophageal Cancer Study Group did not demonstrate any improved ability to achieve R0 resection with the addition
17
of x-ray therapy (XRT).
e study was underpowered, but there was a trend toward increased mortality in the radiation arm. Paradoxically, there also was a trend toward improved survival with the addition of radiation, although this nd­ing was not statistically signicant. Unfortunately, no clear determination was made regarding which method is better. e relatively low incidence of esophageal cancer, the variable response to treatment between squamous cell carcinoma and
It is important to recognize those patients with stage IV disease because the mean survival in these patients is 6–10 months. In the past, palliative esophagectomy was often thought necessary to restore swallowing and oral nutrition. With advances in photodynamic therapy, expandable endo­scopic stents, and other endoluminal therapies, it is unusual for anyone to require esophageal replacement to reestablish swallowing ability. Hence, stage IV patients should be spared the perioperative mortality, morbidity, and recovery time
16
associated with esophagectomy. e appropriate use of neo­adjuvant treatment requires accurate staging. Patients with nodal involvement, invasion through the esophagus, or pos­sibly even invasion into the muscularis often undergo preop­erative chemoradiation, while patients with simple mucosal involvement generally proceed directly to surgery.
e main staging modalities available today are com­puted tomography (CT) scan, positron emission tomography (PET) scan, and endoscopic ultrasound (EUS). CT scans are used mainly for detecting distant metastases in the lungs, liver, or other remote sites, including the brain. CT scan may be useful for excluding T4 tumors if a fat plane can be dem­onstrated between the adjacent structure and the esophagus.
Chapter 18 Surgical Procedures to Resect and Replace the Esophagus 391
Such staging is often not possible if the patient is severely cachectic or if there are no natural fat planes, such as that between the trachea and esophagus. In regard to nodal status, CT is not as sensitive or as accurate as EUS.
PET scan is superior to CT scan for detecting distant metastatic disease. In a series of 91 patients, CT scan had a sensitivity of 46%, a specicity of 74%, and an overall accu­racy of 73%. In contrast, PET scan had a sensitivity of 69%, specicity of 93%, and overall accuracy of 84%. All metas­tases that were missed by PET were less than 1 cm in size.
18,19
Other studies have shown similar results.
In addition,
7
PET scan may aid in the diagnosis of primary tumor where it may be dicult to perform biopsy because of obstruction. Conversely, a certain percentage of nonbulky tumors of the esophagus may be PET-negative.
EUS gives detailed images of the esophageal wall and nearby structures (Fig. 18-2). Accurate identication of the layers of the esophageal wall is possible. Muscle layers tend to be hypoechoic with intervening hyperechoic mucosal layers. e rst hyperechoic layer and second hypoechoic layer correspond to the mucosa and muscularis mucosa. e third hyperechoic layer is submucosa. e fourth hypoechoic layer is the muscularis propria, and the fth hyperechoic layer is the outside of the esophagus. Tumor inltration of the wall disrupts the normal-layered appearance, and extent of penetration is usually clearly visible. EUS has an overall accuracy of 80–90% in ascertaining T status. e dieren­tiation between T1 and T2 is most dicult. In addition,
biopsy of deeper layers of tumor not accessible by traditional grasping forceps is possible. It should be noted that EUS is not accurate in dening postneoadjuvant treatment T status because of brosis induced by the chemoradiation.
Nodal status is determined by examining four character­istics. Malignant nodes tend to be round and hypoechoic. ey have discrete borders and are larger than 1 cm in size. Nodes that meet such criteria have a 90% chance of being malignant. Fine-needle aspiration (FNA) further increases the accuracy in determining nodal status. If the tumor is from a node, the cytopathologist should be able to identify lym­phoid tissue in the specimen. False positives can result with FNA if the needle passes through the primary tumor. e accuracy of EUS in N-status staging is between 70 and 80%. EUS is 10–15% more accurate than CT scan.
20
Developments in EUS and PET scanning have lessened the enthusiasm for pre-resection operative staging of esophageal cancer patients. Operative staging involving laparoscopy and thoracoscopy is more invasive but may be superior to EUS. Luketich and associates studied 26 patients and detected N1 disease in a considerable number of patients staged NO by
21
It should be noted, however, that the sensitivity of
EUS. EUS in this series was only 60%, considerably lower than that described in other series. In addition, 15% of patients with no radiographic metastatic disease were found to have liver metastases by laparoscopic staging. e average cost of surgi­cal staging was $20,000–$25,000 versus $2000 for EUS.
A common algorithm used in staging patients includes endoscopy for primary diagnosis, CT scanning with PET to evaluate for metastatic disease, and EUS if the patient is an operative candidate and neoadjuvant therapy is considered. In cases of esophageal obstruction, where EUS scanning is known to be less accurate, the incidence of lymph node metastasis is very high (90%) and neoadjuvant therapy should be considered.
FIGURE 18-2 Endoesophageal ultrasound image of an adenocar-
cinoma of the esophagus (T3) and multiple lymph nodes suspicious for metastatic disease (N1).
J, Sivak MV, Catalano MF, et al. High-grade malignant stricture is predictive of esophageal tumor stage: risks of endosonographic evaluation. Cancer. 1993;May 15: 71(10):2910–2917.)
(Reproduced with permission from Van Dam
APPROACH TO THE CERVICAL LESION
e treatment of a cancer of the cervical esophagus is chal­lenging and requires a multidisciplinary approach involving an otorhinolaryngologist, a thoracic surgeon, and occasion­ally a plastic surgeon. Frequently, radiation will be required preoperatively to maximize margins and spare the larynx, if possible. e neck incision is made along the anterior border of the sternocleidomastoid muscle and can be extended across the midline if additional exposure is needed. If the tumor is xed to the spine or neck vessels, the procedure is aborted and palliative radiotherapy is considered. If the larynx is involved, it is removed en bloc with the upper esophagus along with the upper paraesophageal nodes bilaterally. A radical neck dis­section is not routinely performed. e dissection spares the jugular vein, sternocleidomastoid muscles, and spinal acces­sory nerves. e trachea is transected, leaving enough length to allow construction of a permanent end tracheostomy. e endotracheal tube is inserted into the distal trachea and thehypopharynx is divided sharply.