Relationship of Barrett’s esophagus, gastroesophageal reflux disease, and
esophageal adenocarcinoma
Barrett’s esophagus (BE) represents the morphological premalignant manifestation of
gastroesophageal reflux disease (GERD), which develops as a consequence of the
dysfunction and failure of the antireflux mechanism
. BE involves the formation of intestinal metaplasia (IM) from the squamous
epithelium of the esophagus, which is a reparative response to reflux-induced
damage
. Although the prevalence in Western countries is about 1-2% in the general
population and about 10% in population who report acid reflux symptoms, the accurate
prevalence of BE in the general population is difficult to determine as the majority
of individuals with BE are not diagnosed
,
. Epidemiological and histopathological evidence indicate that many cases of
esophageal adenocarcinoma (EAC) arise in individuals with BE by the progression of
IM (nondysplastic Barrett’s esophagus [NDBE]) and indefinite for dysplasia (IND) to
dysplasia (including low-grade dysplasia [LGD] and high-grade dysplasia [HGD]) and
finally to neoplasia
. To date, dysplasia remains the best available marker of cancer risk in
patients with BE.Since BE is considered a complication of chronic GERD, it is perhaps not surprising
that risk factors for gastric reflux are also strongly associated with BE
,
. Reflux-induced injury has been linked to cellular and molecular changes in
the esophagus
,
. Symptoms of heartburn and regurgitation are strongly associated with the
presence of BE, and duration of GERD symptoms may also be a risk factor for BE
. Although GERD is a strong risk factor for both BE and EAC, 40-50% of
patients with these disorders do not report chronic reflux symptoms, suggesting that
silent reflux or other risk factors such as male sex
, age 50 or older
, white race
, central obesity
, and cigarette smoking
also likely play a role in the pathogenesis of BE and EAC.Although BE is well-established precursor for EAC, the assumption that all patients
who develop EAC go through the same reflux-induced response leading to
adenocarcinoma was challenged by a retrospective analysis that found that only 46%
of patients with EAC presented with endoscopic confirmation of BE and
histopathological evidence of IM
. Furthermore, comparison of patients with EAC who had confirmed BE at
presentation to those without BE suggested the existence of two EAC phenotypes with
different tumor behavior and response to therapy
. These findings raise the question of whether EAC always develops through
the IM-dysplasia-EAC sequence.
Current management of Barrett’s esophagus
Accepting that a controversy exists, the natural course of progression to dysplasia
and cancer in BE in the majority of patients is thought to be stepwise from NDBE to
LGD to HGD and cancer. The annual cancer risk depends on the degree of dysplasia,
such as 0.33% if there is no dysplasia, 0.54% with LGD, and 7% with HGD
. Thus, the management is based on disease stages.
1. Nondysplastic Barrett’s esophagus
Proton-pump inhibitor (PPI) therapy is recommended to control reflux symptoms in
patients with NDBE. The American College of Gastroenterology (ACG)
, American Gastroenterological Association (AGA)
, and American Society for Gastrointestinal Endoscopy (ASGE)
all recommend that surveillance endoscopy with four-quadrant biopsies at
2-cm intervals every 3-5 years for NDBE. PPI therapy is associated with a 71%
decrease in the risk of developing HGD and EAC in patients with BE
. Long-term therapy (>2-3 years) has a higher protective effect
. Chemoprevention to inhibit the progression to cancer in patients with
BE is currently being assessed. Various medications such as aspirin, metformin,
and statins have been studied. A randomized controlled trial indicated that the
combination of high-dose esomeprazole plus aspirin had the strongest protective
effect compared with low-dose esomeprazole without aspirin at a median follow-up
of 8.9 years
. However, the ACG guidelines do not currently recommend chemoprevention
for all patients with BE, but suggest it should be considered in patients with
BE who are appropriate candidates for aspirin use for cardioprotection
.
2. Indefinite for dysplasia
In BE IND, either the epithelial abnormalities are insufficient for a diagnosis
of dysplasia, or the nature of the epithelial abnormalities is uncertain due to
inflammation or technical difficulties with specimen processing. The risk of HGD
or cancer within 1 year of the diagnosis of IND varies between 1.9% and 15%
. The recommendation from ACG
for management is to optimize acid suppressive therapy for 3-6 months
and then to repeat esophagogastroduodenoscopy (EGD). If indefinite dysplasia is
noted again, repeat endoscopy in 12 months is recommended
.
3. Low-grade dysplasia
Most patients with an initial diagnosis of LGD (73%) are downstaged to NDBE or to
IND after review by expert gastrointestinal pathologists
. Patients with confirmed and persistent LGD are at higher risk of
progression
. Once LGD is confirmed by a second gastrointestinal pathologist, the
patient should be considered for endoscopic ablation. A landmark study
demonstrated the benefit of radiofrequency ablation in achieving complete
eradication of dysplasia (90.5% vs. 22.7% for a sham procedure) and complete
eradication of IM (77.4% vs. 2.3% for a sham procedure)
. Patients with confirmed LGD who do not undergo eradication therapy
should have surveillance endoscopy every 6-12 months.
4. High-grade dysplasia
As with LGD, the diagnosis of HGD needs to be confirmed by a second pathologist
with gastrointestinal expertise. In the past, the treatment was esophagectomy,
but due to demonstrated lower morbidity and equivalent efficacy of
radiofrequency ablation, the current treatment of choice is endoscopic mucosal
resection (EMR) of raised lesions, followed by radiofrequency ablation of the
entire affected segment
. Pathology is best assessed by EMR, especially in areas of nodularity
and ulceration. A randomized controlled study of 42 patients with HGD was
randomized between radiofrequency ablation and sham procedure. Complete
eradication of dysplasia was achieved in 81% of ablation patients versus 19%
with the sham procedure
. Eradication of IM was achieved in 77% of ablation patients versus 2% of
patients with the sham therapy
. Results of 3-year follow-up from the same cohort showed complete
eradication of dysplasia in 98% and of IM in 91%
. Endoscopic eradication therapy is recommended for all patients with BE
and HGD without the potential comorbidity and side effects associated with
esophageal resection. Short segment Barrett’s (<3 cm) with HGD can also be
assessed for complete ablation with EMR alone. Alternatively, surveillance every
3 months is an option if the patient does not wish to undergo eradication
therapy
.
What is the role of antireflux surgery in the treatment of Barrett’s
esophagus?
Because dysplasia in BE carries an increased risk of progression to cancer, the
current standard of care in these patients is EMR of visible lesions, followed by
ablation of the flat mucosa, with the aim of achieving complete eradication of
IM
,
. A key part of treatment during this time is maximal acid suppression with
continuous PPI treatment
.PPIs are today the main component of medical treatment for GERD, because they are the
most effective medications to decrease gastric acid production, leading to healing
of esophagitis and relief of symptoms
. However, PPIs only change the pH of the refluxate, without modifying the
occurrence and the number of reflux episodes
. Therefore, symptoms tend to recur after discontinuation of PPIs, and some
patients on PPIs have refractory symptoms due to ongoing reflux.Successful elimination of reflux symptoms does not guarantee control of acid reflux.
Often, BE patients do not experience heartburn due to the reduced sensitivity of the
columnar mucosa to the acidic and bilious refluxate
. In addition, while PPI stops acid reflux, patients may still have
regurgitation as a consequence of an incompetent lower esophageal sphincter
(LES)
and the quality of esophageal peristalsis
. Potentially most significantly, PPIs do not eliminate the reflux of bile, a
major contributor to the pathogenesis of BE
,
,
.As many as 40% of patients with heartburn have either an incomplete or complete lack
of response to once-daily PPIs
. The proportion of patients with persistent troublesome heartburn despite
once-daily PPI use was 32% in randomized trials and 17% in nonrandomized trials; the
proportion of patients with persistent regurgitation was 28% in randomized and
nonrandomized trials
. In addition, increasing evidence has highlighted the risk of adverse events
and side effects after long-term PPI treatment, including kidney disease and
injury
, Clostridium difficile infection
, community-acquired pneumonia
, fractures due to osteoporosis
, gastric cancer
, and increased risk of COVID-19
.Antireflux surgery (ARS) aims to repair the antireflux barrier, which is defective in
patients with BE
. As a result, the function of the LES is improved, the gastroesophageal flap
valve is restored, and acid or duodenal reflux into the esophagus is decreased
compared to medical treatment alone
. The most common indication for ARS is refractory symptoms or persistent
esophagitis that is not responding to medical therapy
. The most commonly performed surgical procedure for GERD is laparoscopic
fundoplication, which enhances the esophagogastric junction ability to prevent
reflux into the esophagus
. A 5-year follow-up of 372 patients included in an randomized control trial
comparing the PPI esomeprazole with laparoscopic fundoplication found similar
remission rates in the medication group (92%; 95%CI 89-96%) and surgery group (85%;
95%CI 81-90%), but worse symptoms of acid regurgitation in the medication group
(13%) compared with the surgery group (2%)
. A few studies have compared the effect of ARS on BE with best medical
therapy and indicated that the surgery intervention had significantly less dysplasia
de novo
and a greater probability of BE regression
. Laparoscopic fundoplication is safe and has been associated with a very low
short-term mortality (0.1-0.2%). Complications and, more importantly, side effects
of gas bloat and inability to belch and vomit can occur and should be a component of
counseling and discussion with the patient preoperatively
.Other indications for ARS in patients with BE include younger patients who do not
wish to commit themselves to lifelong PPI therapy. It is particularly important that
these patients are counseled that the surgery is being considered to control their
GERD and decrease their reliance on PPIs, not to eliminate the requirement for
long-term endoscopic Barrett’s follow-up
.The optimum timing of ARS in patients with Barrett’s has not been standardized. Some
reports have suggested that performing ARS at the time of ablative therapy can
decrease the number and improve the efficiency of endoscopic Barrett’s ablation
. Failure of laparoscopic fundoplication can often be linked to applying
incorrect indications of inadequate preoperative assessment
. As a result, accurate preoperative assessment including endoscopy,
high-resolution manometry, and selective application of objective pH testing to
define those who will benefit from the ARS, i.e., those with LES dysfunction and
strong symptom correlation, is recommended. There are recognized advantages of
having the procedures conducted in centers with high volume experience and with the
capability of delivering the full spectrum of diagnostic workup, surgical treatment,
and follow-up of GERD and BE
.Controversies are still present regarding the progression of Barrett’s following ARS.
One study based on a Swedish population showed that ARS failed to prevent the
development of esophageal cancer when compared with the corresponding
population
. Other studies have suggested that successful ARS protects against
progression to malignancy; however, this has not been confirmed in prospective
trials or large cohort studies
,
,
.Increasingly, patients with LGD are undergoing successful endoscopic ablation
. Patients with LGD can be considered for ARS
, and recent reports suggest that fundoplication is superior to medical
therapy in avoiding Barrett’s progression and promoting Barrett’s regression
. There are currently very few data on whether successful ARS decreases the
incidence of recurrence following successful ablation of either LGD or HGD.Antireflux surgery can be considered in patients following successful ablation of
HGD. However, many surgeons would advocate an extended period of stable postablation
endoscopic follow-up before proceeding with ARS. Some practitioners recommend
repeating objective pH testing following ARS in patients with NDBE as well as those
with LGD or HGD postablation
. Whether this testing should be done before medical therapy is discontinued
has not been extensively studied
.
CONCLUSION
The current recommended BE treatment is maximal acid suppression with PPIs and
histamine-2 blockers, while in some cases, fundoplication is required to control
reflux refractory to medical therapy. In our opinion, laparoscopic ARS can be an
appropriate alternative and even a preferred option from medical therapy for highly
selected candidates. Minimal morbidity and near zero mortality in high volume
centers along with multiple studies demonstrating long-term success of antireflux
operations support this approach. However, post-treatment surveillance continues to
be a required component of long-term treatment because the risk of progression to
dysplasia still exists. Nevertheless, a prospective randomized controlled trial is
needed to confirm the therapeutic effect and long-term outcomes of laparoscopic ARS
versus medical therapy plus or minus endoscopic ablation in patients with BE. In
addition, future comparisons of maximal medical therapy versus other surgical
techniques (LINX device) and endoscopic antireflux procedures such as TIF (Transoral
Incisionless Fundoplication) and Stretta are also warranted.
Authors: Stuart J Spechler; Prateek Sharma; Rhonda F Souza; John M Inadomi; Nicholas J Shaheen Journal: Gastroenterology Date: 2011-03 Impact factor: 22.682
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