- Open Access
The role of surgical treatment in isolated organ recurrence of esophageal cancer—a systematic review of the literature
- Dimitrios Schizas†1Email authorView ORCID ID profile,
- Ioannis I. Lazaridis†2,
- Demetrios Moris1,
- Aikaterini Mastoraki3,
- Lazaros-Dimitrios Lazaridis4,
- Diamantis I. Tsilimigras5,
- Nikolaos Charalampakis6 and
- Theodore Liakakos1
© The Author(s). 2018
- Received: 22 August 2017
- Accepted: 6 March 2018
- Published: 14 March 2018
Despite the improvements in the early detection and treatment of non-metastatic esophageal cancer, more than half of patients undergoing a curative treatment for esophageal cancer will develop recurrence within three years. The prognosis of these patients is poor. However, a wide range in overall survival has been reported, depending on the pattern of recurrence, and no optimal treatment strategy following recurrence has yet been uniformly accepted.
In this article, we aimed to systematically review the literature for the role of surgical resection of metachronous distant metastasis following primary treatment of esophageal cancer. Furthermore, we discuss possible factors that could possibly predict which patients may benefit from a surgical approach. A comprehensive literature search was conducted in PubMed using combinations of keywords.
Patients with recurrence may benefit of a multimodality treatment. Regarding the isolated recurrence of esophageal cancer in solid visceral organs, operative intervention has been proposed as a treatment that may offer a survival benefit in an individual basis. No definitive conclusions regarding the potential survival advantage offered by the surgical treatment of solitary recurrent lesions can be drawn. However, recent improvements in surgical treatment and optimization of perioperative management guarantee an acceptable operative risk, making surgical resection of solitary recurrence lesions a considerable therapeutic option.
It can be conferred from the available studies that the surgical treatment of isolated recurrence from esophageal cancer may offer a survival benefit for properly selected patients. Prospective, multicenter studies might be useful to gain a better insight into those factors that affect selection of patients to take benefit from an operative intervention.
- Esophageal cancer
- Isolated recurrence
- Solitary lesions
- Surgical management
Nearly half of all patients undergoing curative esophagectomy for esophageal cancer develop recurrence, and in approximately half of these patients, the recurrence appears within the first year postoperatively. According to the type of recurrence, the metachronous lesions are classified as locoregional, distant, and of mixed type. Distant recurrences include hematogenous metastasis within a solid organ, abdominal paraortic lymph node metastasis, and peritoneal metastasis . Solid organs presenting distant recurrence are usually the lung, the liver, the brain, the kidneys, and the adrenal glands . The prognosis of patients with locoregional recurrence tends to be better than of those with distant metastasis, while the mixed type has the poorest outcome .
Abate et al. showed that survival is considerably improved in patients undergoing therapy for their recurrence . However, there is no consensus concerning the type of treatment to be followed in case of recurrence. Regarding the patients with isolated tumor recurrence, salvage therapeutic options include systemic chemotherapy, irradiation, surgical resection, or a combination of the above. Because of poor prognosis, only a few retrospective studies with small series of selected patients and several case reports showing the results of surgical treatment exist. Therefore, the benefit of surgical resection as a part of multimodality treatment to patients with isolated distant recurrence in solid organs is controversial. The aim of this study is to review the outcomes of surgical management of such lesions and to discover which patients’ characteristics may predict a better outcome after surgical resection.
Search strategy and data sources
The review was conducted in line with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines . A study protocol was agreed by all authors. Identification of eligible studies was performed through search of PubMed (MEDLINE) database until 10 August 2017. The following algorithm was applied: “(surgery OR (surgical treatment) OR metastasectomy) AND ((esophageal or oesophageal) AND (cancer OR carcinoma)) AND (metastasis OR metastases OR recurrence).” Two independent reviewers (DS, IIL) screened the available literature, and discrepancies were resolved by team consensus. Finally, reference lists of eligible studies were manually assessed in order to detect any potential relevant article (“snowball” procedure).
Inclusion and exclusion criteria
Eligible were considered those studies reporting on patients undergoing surgery for metachronous, solitary organ recurrence following primary surgical treatment of esophageal cancer. Neither language nor study sample size restriction was applied. Exclusion criteria were as follows: (1) irrelevant studies, (2) studies reporting on synchronous metastases, (3) reviews and meta-analyses, and (4) editorials and letters to the editors.
Data extraction and tabulation
Two independent authors (DS, IIL) extracted the data. Results were cross-checked by a third reviewer (DIT), and any discrepancies were resolved by team consensus. Variables of interest included general study characteristics (e.g., author, year of publication, number of patients), number of lesions, disease-free interval (DFI) following esophagectomy, type of operation, and survival following resection of recurrence. DFI was defined as the time from primary surgery for esophageal cancer to disease recurrence. Data were tabulated when possible. Due to the nature of the included studies (i.e., case reports) and the high heterogeneity in reporting of outcomes among eligible studies, no cumulative statistical analysis or meta-analysis was attempted. Ultimately, a purely descriptive presentation of available data was adopted.
Article selection and study demographics
Liver represents a common organ for metastasis for a wide range of tumors. The benefit of liver resection for colorectal and neuroendocrine metastases has been proven and is considered as a standard treatment with curative intention when feasible. Few retrospective studies with > 50 highly selected patients aimed to show the benefit of liver resection for non-colorectal and non-neuroendocrine tumors. In most of them, however, the operative management for metachronous metastases of esophageal cancer represents only a very small part of the mentioned series. Adam et al. reviewed 1452 patients operated for non-colorectal and non-neuroendocrine liver metastases. Among them, 20 patients with liver metastases from esophageal cancer and 25 patients with liver metastases from gastroesophageal junction cancer underwent liver resection, reporting a 3-year survival of 32% and 12%, respectively and a median survival of 16 and 14 months, respectively .
Reported cases of surgical management of liver recurrence for esophageal cancer
Disease-free interval following esophagectomy (months)
Number of patients
Number of lesions
Survival following recurrence resection
Liu et al. 2016
14.15 ± 9.68†
2 left hemihepatectomies, 2 left lateral lobectomies, 2 right hemihepatectomies, 1 right anterior lobectomy, 19 non-anatomical hepatectomies
1- and 2-year cumulative survival rates of 50.8 and 21.2%, respectively
Hiyoshi et al 2015
N/S‡ (solitary or occurred in a localized field)
Huddy et al. 2015
Resection segments 2 and 3, resection segment 5, right hemihepatectomy and extension to segment 4A, central hepatectomy with extension to segment 6
10 months, 21 months, 22 months alive, 92 months alive
Tada et al. 2015 (published in Japanese)
Right hepatic lobectomy
10 months alive
Blom et al. 2013
Iitaka et al. 2013
Ichida et al. 2012
6 (0–14) §
13 months (2–70)§
Ikebe et al. 2012 (published in Japanese)
4 years alive
Tokairin et al. 2009 (published in Japanese)
S8-semi-segmental lobectomy, followed by right hepatic lobectomy and lymphadenectomy
Adam et al. 2006
16 months for esophageal primaries and 14 months for primaries of the gastroesophageal junction§
Nagano et al. 2001 (published in Japanese)
2 years and 3 months alive
Surgical resection is accepted as a treatment modality for resectable pulmonary metastases arising from various solid tumors, in the absence of other extrapulmonary metastasis. Several retrospective studies have intended to investigate its benefit in the case of metachronous, pulmonary metastasis after surgical treatment of esophageal cancer. Ichikawa et al. reported a retrospective series of 23 patients with pulmonary oligometastatic disease after curative treatment of esophageal cancer (esophagectomy ± neoadjuvant or adjuvant chemotherapy or definitive chemoradiotherapy). The lungs were the initial recurrence site in 19 patients. All patients underwent surgical resection, including wedge resection, segmentectomy, and lobectomy, and the predicted overall 5-year survival rate was 43.5% with a median survival time of 28.7 months (range 4.9–214.5 months). The authors suggested that the group of patients with pulmonary metastasis as initial recurrence had a significantly longer survival (median survival 63 months) in comparison to the patients with antecedent extrapulmonary metastasis (11 months, p = 0.0411) . Kobayashi et al. reviewed 30 pulmonary metastasectomies of 23 patients who presented pulmonary recurrence after definitive treatment of SCC (17 patients underwent esophagectomy, 5 patients definitive chemoradiotherapy, and 1 patient endoscopic submucosal dissection). Among these surgical resections, 26 concerned solitary metastasis including recurring metastases, 2 were undertaken at patients with two metastatic lesions, and 2 at patients with three metastases. The cumulative survival for patients without a history of extrapulmonary metastasis between initial treatment and pulmonal recurrence was 40.7% at 5 years, while the patients with well and moderately differentiated SCC had significantly prolonged survival compared to those with poor differentiated primaries (p < 0.01). DFI of > 12 months was showed as another favorable prognostic factor (median survival with DFI > 12 months and DFI < 12 months was 43.7 and 24.7 months, respectively, p = 0.02) . The largest published series is the one reported by Shiono et al., including 49 patients who underwent metastasectomy (48 cases with SCC, 1 case with adenocarcinoma), 39 of whom with solitary metastases. The authors identified DFI of less than 12 months to be an independent prognostic factor (p = 0.04) for significantly worse prognosis, thus concluding that pulmonary metastasectomy for esophageal cancer should be considered for selected patients with a DFI of 12 months or more . Kanamori et al. published recently a series of 33 patients undergoing pulmonary metastasectomy, 27 of whom with single pulmonary lesions and 22 of them having the lungs as first recurrence site. The overall median survival time was 17.9 months. Significant unfavorable prognostic factors identified with univariate analysis were DFI < 16 months and nodal status of esophageal carcinoma, but multivariate analysis failed to identify these factors to be significant. Again, in this study, most primary tumors histology was SCC .
Reported cases of surgical management of lung recurrence for esophageal cancer
Disease-free interval following esophagectomy (months)
Number of patients
Number of lesions
Survival following recurrence resection
Kanamori et al. 2017
27 patients with solitary tumors, 2 patients with 2 tumors, 4 patients with 3 or more
20 wedge resections, 6 segmentectomies, 7 lobectomies
Hiyoshi et al. 2015
N/S† (solitary or occurred in a localized field)
4 partial pulmonary resections, 1 partial pulmonary resection with chest well resection, 1 bilateral pulmonary resection with chest wall resection
Kozu et al. 2015
11 wedge resections, 2 segmentectomies, 2 lobectomies
Kosaka et al. 2014
Thoracoscopic partial lung resection
12 months alive
Kobayashi et al. 2014
25 wedge resections, 2 segmentectomies, 2 lobectomies
Ichida et al. 2013
Takemura et al. 2012
5 wedge resections
48 (6–124) at the time of follow-up
Ichikawa et al. 2011
17 wedge resections, 3 segmentectomies, 3 lobectomies
Shiono et al. 2008
23 wedge resections, 16 lobectomies, 8 segmentectomies, 2 bilobectomies
Chen et al. 2008
2 wedge resections, 3 segmentectomies
24 (11–90) at the follow-up
The incidence of brain metastasis from esophageal carcinoma reported in the literature is 0–2% .The prognosis of these patients is poor, and a median survival of 3.8 months after the diagnosis of brain metastases has been reported . Brain recurrences tend to occur in patients with large primary tumors and findings of local invasion and lymph node metastasis by CT scan and/or microscopic examination . Moreover, in contrary to other primary tumors, a low incidence of lung metastasis at the time brain metastasis appears has been reported in patients with brain metastases from esophageal carcinoma . In a single-center retrospective study, the outcome of surgical resection followed by whole-brain radiotherapy (WBRT) for brain metastases from esophageal carcinoma has been compared to radiation or palliative treatment. Five out of 26 patients with brain metastases from esophageal carcinoma underwent surgery followed by WBRT. Three patients presented a single cerebral lesion and 2 patients had 2 lesions. The median survival of these patients was 7.0 months, while patients who underwent radiation therapy and chemotherapy survived for 4.0 and 1.8 months, respectively. The authors concluded that surgical intervention, the presence of a single lesion, Karnofsky Performance Status (KPS), and extracranial disease status had a statistically significant impact on survival. However, the median time from the diagnosis of esophageal carcinoma to the diagnosis of brain metastasis was 10.2 months (0.0–39.2 months), indicating that patients with synchronous metastases undergoing palliative therapy have been included. Furthermore, no data about the initial treatment of the primary tumor are mentioned . Ogawa et al. reported the outcomes of 36 patients with brain metastases from esophageal cancer treated in a single institution, 8 of whom had no active extracranial disease and controlled primary tumor (primary tumor in complete remission after surgical resection, radical radiotherapy/radiochemotherapy, or a combination therapy). Seventeen patients had a single cerebral metastasis. The median survival was 9.6 months for patients who underwent surgery and radiotherapy and 1.8 months for patients treated only with radiotherapy. Treatment modality, KPS, and extracranial disease status had a statistically significant impact on survival . In another series of 27 patients with brain metastases (13 patients had a single brain lesion), the longest survival was seen in patients with single brain lesions who underwent resection followed by WBRT (median survival, 9.6 months; P = 0.02 compared with all other treatments). The median time from diagnosis of primary tumor was 5.6 months (range 0.0–36.5 months), and 19 patients suffered from systemic metastasis as well . The most recent case series was reported in 2007. Out of 17 patients treated for brain metastasis (median time from diagnosis of primary tumor 12.3 months, range 2.1–36.2 months), 3 patients treated with resection and WBRT had a median survival of 65.6 months (range 2.3–90.6 months), and in all treatment categories, patients with single cerebral metastasis had a better outcome than those with multiple metastases (median survival 38.2 and 16.4 months, respectively). Again, in that case, authors do not mention what kind of therapeutic regime was followed for the primary tumor, but as authors of previous studies, they conclude that an aggressive strategy with neurosurgery followed by radiation offers favorable results in patients with good KPS .
The adrenal glands are a frequent site of recurrence of esophageal neoplasms: esophagus is the third most frequent site of origin of adrenal metastases. Although adrenalectomy is a clear indication for the treatment of adrenal metastases from some cancers (lung cancer, renal cell cancer, and melanoma), there are very few case reports of adrenalectomy for recurrence of esophageal cancer following esophagectomy in the literature and thus there are no clear indications on how to treat patients with adrenal metastases from esophageal cancers. In a case series of 5 patients, only one 79-year-old patient presented with no signs of other metastasis and was treated, 13 months after esophagectomy for a Siewert type 2 carcinoma of the esophagogastric junction, with a laparoscopic left adrenalectomy. He died with progressive disease 28 months later . O’Sullivan et al. reported a case of a 50-year-old man who was submitted to an open right adrenalectomy 4 years after a two-stage esophagectomy for a Siewert type 1 cancer of the esophagogastric junction and remained disease-free for over 4 years postadrenalectomy . In another case, a 71-year-old patient underwent a right adrenalectomy for a solitary adrenal metastasis that appeared 22 months after a subtotal esophagectomy with two-field lymphadenectomy for esophageal adenocarcinoma. The patient was free of recurrence for the next 5 years and 11 months .
The kidney is the fourth or fifth most common visceral metastatic site for a primary esophageal carcinoma, but a solitary, unilateral metastasis is rare and often found accidentally, since the patients are mostly asymptomatic. There are only very few case reports of surgical resection of renal recurrence of esophageal cancer after primary surgical treatment. Lim et al. reported a case of solitary recurrence 2 years after an esophagectomy for a SCC, which was treated with radical nephrectomy. The follow-up revealed suspicious paraaortic lymphadenopathy that decreased in extent after admission of palliative chemotherapy, but no data concerning the survival are mentioned . A 57-year-old patient, treated with radiation therapy for esophageal cancer, showed a recurrence in the right kidney accompanied with a tumor thrombus in the inferior vena cava 1 year after. He was treated with right nephrectomy with thrombus resection and died 2 months later . Sun et al. reported also a case of nephrectomy for a solitary renal metastasis 9 months after an esophagectomy for a SCC (stage pT2N0M0), and the patient died 3 months later .
Reported cases of resected solitary recurrence from esophageal cancer in other sites
Author and year
Initial TNM stage
Disease-free interval following esophagectomy
Overall survival following recurrence resection
Sun et al. 2014
O’Sullivan et al. 2013
4 years alive
Fumagalli et al. 2010
Cho et al. 2007
42 months alive
Sanyal et al. 2005
7 months alive
Lim et al. 2004
Saito et al. 2010 (published in Japanese)
1 year and 10 months
5 years and 11 months
Hata et al. 2000 (published in Japanese)
14 months alive
Miyoshi et al. 1997
Shimada et al. 1992 (published in Japanese)
18 months alive
Our study showed that there are only sporadic cases of surgical treatment of distant recurrence of esophageal cancer in visceral organs. The few case series and comparative studies include highly selected patients and are therefore subjected to selection bias. Large-scale randomized multicenter trials are unlikely to be feasible. Hiyoshi et al. reported a study comparing surgical and non-surgical treatment of distant recurrence. Among 14 patients that underwent surgical treatment, 6 patients underwent partial pulmonary resection, 1 patient underwent partial hepatectomy, and 1 patient resection of brain recurrence. The surgery group showed a more favorable prognosis in terms of both survival after esophagectomy and survival after initial recurrence . The largest retrospective study comparing different treatment options for different subtypes of recurrence of esophageal cancer following curative surgical resection (anastomotic, locoregional, single solid organ metastasis, single metastasis at another location, multiple hematogenic metastasis, or mixed-type recurrence) has been conducted by Depypere et al. Regarding the subgroup of patients with single solid organ metastasis (liver, brain, lung, and adrenal), the authors found that the surgically treated patients, with or without systematic chemotherapy (n = 20), had a significantly better survival in comparison with the non-surgically treated patients (n = 63), with a median survival after diagnosis of recurrence of 54.8 months (5-year survival of 43.9%) and 11.6 months (5-year survival of 4.6%), respectively (p = 0.0004) . However, in comparative studies, various prognostic variables are unevenly distributed among the surgical and non-surgical groups. For that reason, no definitive conclusions regarding the potential survival advantage offered by the surgical treatment of solitary recurrent lesions can be drawn.
However, recent improvements in surgical treatment and optimization of perioperative management guarantee an acceptable operative risk, making surgical resection of solitary recurrence lesions a considerable therapeutic option. Indeed, evidence shows that patients with a single distant recurrence may have a favorable prognosis in comparison to patients with more than one lesions [8, 20]. Taking into account, though the very small number of patients operated with more than one distant metastases, no statistical significance can be noted. Therefore, the choice of treatment modality should be individualized. Certain characteristics of patients with good functional status may indicate which patients could be surgical candidates in case of a technically resectable solitary distant recurrence. Moreover, since metastasectomy is widely accepted as a possible curative treatment modality for recurrences of cancers of various visceral organs, including colorectal cancer, conclusions drawn from the analysis of these primaries could be helpful in the comprehension of the benefit of surgical therapy in the esophageal cancer recurrence. Metastasectomy has been also applied as part of the treatment of highly selected patients with oligometastatic gastric cancer and some retrospective, non-randomized studies suggest that surgical intervention may prolong survival [42–44].
Other uncommon sites of isolated esophageal cancer recurrence include skin, eyes, muscle, heart, jaw, skull, breast, thyroid glands, and gastrointestinal tract. Special anatomic features of the esophagus, such as the absence of serosa, its shared arterial and venous vasculature, and its complex lymphatic drainage may be implicated in this rare distribution pattern of tumor recurrences. A systematic review of the literature of the past four decades has shown that surgical resection has been a part of the management in 44% of these special cases, which presented an overall survival rate of 13 and 6.1 months for synchronous and metachronous metastases, respectively .
DFI between the initial surgical treatment of the primary and the diagnosis of recurrence appears to be an important factor to be considered. Long DFI implicates a less aggressive tumor biology, and in case of a surgical excision of a distant recurrence, a local control of the disease could be possibly better achieved, potentially offering curative treatment. Most patients included in the abovementioned studies and case reports underwent a surgical resection after a DFI of more than 12 months. As discussed before, short DFI is negatively correlated with survival , and long DFI is considered as a favorable prognostic factor for overall survival of both surgical and non-surgical groups . Kobayashi et al. and Shiono et al. suggested a DFI > 12 months as a statistically significant favorable prognostic factor for pulmonary metastasectomy (p < 0.05) [18, 19]. With regard to pulmonary recurrence, long DFI is noted to be a favorable prognostic factor from the International Registry of Lung Metastases, but many different tumor types have been assessed in this study . Regarding surgical resection of liver metastasis of colorectal primary, there is no consensus regarding the impact of DFI on outcomes. Some authors have reported that a short DFI did not impact disease-free or overall survival; however, other investigators consider DFI as a reliable prognostic factor [47, 48].
Primary tumor stage has been also accepted as a significant prognostic factor regarding survival, with advanced tumor stage being associated with a worse survival. Increased depth of tumor invasion and the presence and the mean number of positive nodal metastases are found to correlate with an increased incidence of recurrent disease . Regarding resection of colorectal liver recurrence, positive lymph node status is found to correlate with worse outcome. Between all studies regarding esophageal cancer recurrence mentioned above, only that of Kanamori et al. revealed primary positive nodal status as a significant unfavorable prognostic factor concerning survival after pulmonary metastasectomy . Depth of invasion of the primary tumor could not be identified as an independent prognostic factor. Apparently, accumulation of more patients is again needed to evaluate the significance of these factors.
The size of metastasis is another factor under investigation for its significance regarding survival. In their study , included 138 patients with liver and/or lung recurrence after esophagectomy. The statistical analysis resulted in the identification of the maximum size of metastases as a predictor of survival in patients with hepatic and/or pulmonary metastases (risk ratio of 2.39, 95% 1.10–5.18 for maximum size of metastases ≥ 21 mm, p = 0.029), but the outcome refers to both surgical and non-surgical groups . The abovementioned studies failed to show any significance of the size of distant recurrence for the survival benefit of the surgical resection.
The predominant histologic type of the cases mentioned above is the squamous cell carcinoma whereas the adenocarcinoma represents only a small percentage of all cases. Regarding the histological differentiation, only one study revealed poor differentiation as a prognostic factor influencing prognosis in patients undergoing pulmonary metastasectomy .
The site of the isolated distant recurrence appears to correlate with the location of the primary tumor; tumors located in the cervical and upper thoracic esophagus tend to recur more often in the lungs, while isolated recurrences of the tumors of the lower esophagus tend to appear mostly in the liver . However, no conclusions regarding correlation of the primary tumor location and survival after recurrence resection can be drawn.
Other parameters investigated, such as age, gender, elevated tumor markers, initial curative treatment (esophagectomy or definitive chemoradiotherapy), or the operative procedure followed for the recurrence failed to show any relevance in terms of benefit of surgical resection.
Limitations of the studies mentioned above include their retrospective character, the relatively small number of patients included, leading to non-significant statistically conclusions, the selection bias due to the fact that patients with poor medical condition were generally excluded from any surgical treatment and the heterogeneity of the baseline characteristics of the study populations. Due to the lack of strict guidelines pertaining to the therapeutic approach in each recurrence site, well-organized prospective multicenter studies may offer a possibility to draw firmer conclusions. To this end, we suggest that—when feasible—future prospective studies should randomize patients with solitary distant recurrence and DFI > 12 months after curative esophageal cancer resection into surgery and non-surgery groups so that accumulating evidence can permit the formulation of strict guidelines in each setting in the future.
Patients with isolated distant hematogenous recurrence represent a small subgroup of patients with recurrence after curative treatment of esophageal cancer. Multimodality treatment may improve the prognosis of this patient population. Surgical resection of these lesions as a part of this treatment may offer a survival benefit and should be considered as an acceptable treatment for properly selected patients. Further investigation should focus on the prognostic factors that affect selection of patients who may benefit from an operative intervention.
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DS, IIL, and LDL designed the report. DM, AM, and DIT reviewed the literature. DS and IIL wrote the paper. DM and NC revised the manuscript. TL critically reviewed the manuscript and had scientific supervision. All authors read and approved the final manuscript.
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- Kunisaki C, Makino H, Takagawa R, Yamamoto N, Nagano Y, Fujii S, et al. Surgical outcomes in esophageal cancer patients with tumor recurrence after curative esophagectomy. Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract. 2008;12(5):802–10.View ArticleGoogle Scholar
- Mariette C, Balon JM, Piessen G, Fabre S, Van Seuningen I, Triboulet JP. Pattern of recurrence following complete resection of esophageal carcinoma and factors predictive of recurrent disease. Cancer. 2003;97(7):1616–23.View ArticlePubMedGoogle Scholar
- Sugiyama M, Morita M, Yoshida R, Ando K, Egashira A, Takefumi O, et al. Patterns and time of recurrence after complete resection of esophageal cancer. Surg Today. 2012;42(8):752–8.View ArticlePubMedGoogle Scholar
- Abate E, DeMeester SR, Zehetner J, Oezcelik A, Ayazi S, Costales J, et al. Recurrence after esophagectomy for adenocarcinoma: defining optimal follow-up intervals and testing. J Am Coll Surg. 2010;210(4):428–35.View ArticlePubMedGoogle Scholar
- Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. J Clin Epidemiol. 2009;62(10):1006–12.View ArticlePubMedGoogle Scholar
- Adam R, Chiche L, Aloia T, Elias D, Salmon R, Rivoire M, et al. Hepatic resection for noncolorectal nonendocrine liver metastases: analysis of 1,452 patients and development of a prognostic model. Ann Surg. 2006;244(4):524–35.PubMedPubMed CentralGoogle Scholar
- Liu J, Wei Z, Wang Y, Xia Z, Zhao G. Hepatic resection for post-operative solitary liver metastasis from oesophageal squamous cell carcinoma. ANZ J Surg. 2016;Google Scholar
- Ichida H, Imamura H, Yoshimoto J, Sugo H, Kajiyama Y, Tsurumaru M, et al. Pattern of postoperative recurrence and hepatic and/or pulmonary resection for liver and/or lung metastases from esophageal carcinoma. World J Surg. 2013;37(2):398–407.View ArticlePubMedGoogle Scholar
- Huddy JR, Thomas RL, Worthington TR, Karanjia ND. Liver metastases from esophageal carcinoma: is there a role for surgical resection? Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus. 2015;28(5):483–7.View ArticleGoogle Scholar
- Hiyoshi Y, Morita M, Kawano H, Otsu H, Ando K, Ito S, et al. Clinical significance of surgical resection for the recurrence of esophageal cancer after radical esophagectomy. Ann Surg Oncol. 2015;22(1):240–6.View ArticlePubMedGoogle Scholar
- Tada T, Kikuchi T, Watanabe J, Sato N, Hanayama H, Endo H, et al. Surgical resection for a metachronous liver metastasis of an esophagogastric junction adenocarcinoma. Gan to kagaku ryoho Cancer & chemotherapy. 2015;42(12):1617–9.Google Scholar
- Blom RL, Lagarde SM, van Oudenaarde K, Klinkenbijl JH, Hulshof MC, van Laarhoven HW, et al. Survival after recurrent esophageal carcinoma has not improved over the past 18 years. Ann Surg Oncol. 2013;20(8):2693–8.View ArticlePubMedGoogle Scholar
- Iitaka D, Shiozaki A, Fujiwara H, Ichikawa D, Okamoto K, Komatsu S, et al. Case involving long-term survival after esophageal cancer with liver and lung metastases treated by multidisciplinary therapy: report of a case. Surg Today. 2013;43(5):556–61.View ArticlePubMedGoogle Scholar
- Ikebe M, Kitamura M, Saitoh G, Hasegawa H. Multimodality therapy containing hepatic arterial infusion chemotherapy for liver metastasis of esophageal cancer—a case report. Gan to kagaku ryoho Cancer & chemotherapy. 2012;39(10):1555–7.Google Scholar
- Tokairin Y, Kumagai Y, Yamazaki S. A case of postoperative liver metastasis of esophageal cancer remains in progression free after successfully resected. Gan to kagaku ryoho Cancer & chemotherapy. 2009;36(12):2462–4.Google Scholar
- Nagano H, Sakon M, Yasuda T, Dono K, Nakamori S, Yano M, et al. A case of postoperative multiple hepatic metastasis from esophageal cancer successfully treated by surgical resection and hepatic arterial infusion chemotherapy. Gan to kagaku ryoho Cancer & chemotherapy. 2001;28(11):1628–31.Google Scholar
- Ichikawa H, Kosugi S, Nakagawa S, Kanda T, Tsuchida M, Koike T, et al. Operative treatment for metachronous pulmonary metastasis from esophageal carcinoma. Surgery. 2011;149(2):164–70.View ArticlePubMedGoogle Scholar
- Kobayashi N, Kohno T, Haruta S, Fujimori S, Shinohara H, Ueno M, et al. Pulmonary metastasectomy secondary to esophageal carcinoma: long-term survival and prognostic factors. Ann Surg Oncol. 2014;21(Suppl 3):S365–9.View ArticlePubMedGoogle Scholar
- Shiono S, Kawamura M, Sato T, Nakagawa K, Nakajima J, Yoshino I, et al. Disease-free interval length correlates to prognosis of patients who underwent metastasectomy for esophageal lung metastases. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer. 2008;3(9):1046–9.View ArticleGoogle Scholar
- Kanamori J, Aokage K, Hishida T, Yoshida J, Tsuboi M, Fujita T, et al. The role of pulmonary resection in tumors metastatic from esophageal carcinoma. Jpn J Clin Oncol. 2017;47(1):25–31.View ArticlePubMedGoogle Scholar
- Kozu Y, Oh S, Takamochi K, Suzuki K. Surgical outcomes of pulmonary metastases from esophageal carcinoma diagnosed by both pathological and clinical criteria. Surg Today. 2015;45(9):1127–33.View ArticlePubMedGoogle Scholar
- Kosaka T, Mogi A, Yamaki E, Miyazaki T, Kuwano H. Surgical resection of a solitary pulmonary metastasis from basaloid squamous cell carcinoma of the esophagus: a case report. Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia. 2014;20(Suppl):646–9.View ArticleGoogle Scholar
- Takemura M, Sakurai K, Takii M, Yoshida K. Metachronous pulmonary metastasis after radical esophagectomy for esophageal cancer: prognosis and outcome. J Cardiothorac Surg. 2012;7:103.View ArticlePubMedPubMed CentralGoogle Scholar
- Chen F, Sato K, Sakai H, Miyahara R, Bando T, Okubo K, et al. Pulmonary resection for metastasis from esophageal carcinoma. Interact Cardiovasc Thorac Surg. 2008;7(5):809–12.View ArticlePubMedGoogle Scholar
- Go PH, Klaassen Z, Meadows MC, Chamberlain RS. Gastrointestinal cancer and brain metastasis: a rare and ominous sign. Cancer. 2011;117(16):3630–40.View ArticlePubMedGoogle Scholar
- Weinberg JS, Suki D, Hanbali F, Cohen ZR, Lenzi R, Sawaya R. Metastasis of esophageal carcinoma to the brain. Cancer. 2003;98(9):1925–33.View ArticlePubMedGoogle Scholar
- Gabrielsen TO, Eldevik OP, Orringer MB, Marshall BL. Esophageal carcinoma metastatic to the brain: clinical value and cost-effectiveness of routine enhanced head CT before esophagectomy. AJNR Am J Neuroradiol. 1995;16(9):1915–21.PubMedGoogle Scholar
- Ogawa K, Toita T, Sueyama H, Fuwa N, Kakinohana Y, Kamata M, et al. Brain metastases from esophageal carcinoma: natural history, prognostic factors, and outcome. Cancer. 2002;94(3):759–64.View ArticlePubMedGoogle Scholar
- Song Z, Lin B, Shao L, Zhang Y. Brain metastases from esophageal cancer: clinical review of 26 cases. World neurosurgery. 2014;81(1):131–5.View ArticlePubMedGoogle Scholar
- Yoshida S. Brain metastasis in patients with esophageal carcinoma. Surg Neurol. 2007;67(3):288–90.View ArticlePubMedGoogle Scholar
- Fumagalli U, de Carli S, de Pascale S, Rimassa L, Bignardi M, Rosati R. Adrenal metastases from adenocarcinoma of the esophagogastric junction: adrenalectomy and long-term survival. Updat Surg. 2010;62(1):63–7.View ArticleGoogle Scholar
- O'Sullivan KE, Moriarty AR, Larkin JO, Reynolds JV. Curative surgical management of isolated adrenal recurrence of oesophageal adenocarcinoma. BMJ case reports. 2013;2013Google Scholar
- Saito H, Shuto K, Ota T, Toma T, Ohira G, Natsume T, et al. A case of long-term survival after resection for postoperative solitary adrenal metastasis from esophageal adenocarcinoma. Gan to kagaku ryoho Cancer & chemotherapy. 2010;37(12):2406–8.Google Scholar
- Lim DH, Im YH, Ji SH, Park BB, Oh MJ, Lee J, et al. Esophageal squamous cell carcinoma recurring as a solitary renal mass. Cancer research and treatment : official journal of Korean Cancer Association. 2004;36(4):271–4.View ArticleGoogle Scholar
- Miyoshi Y, Asakura T, Matsuzaki J, Fukuda M, Satomi Y. Metastatic renal tumor originating from esophageal cancer: report of 2 cases. Hinyokika kiyo Acta urologica Japonica. 1997;43(5):347–50.PubMedGoogle Scholar
- Sun Y, Yu X, Zhang Y. Renal metastasis after esophagectomy of esophageal squamous cell carcinoma: a case report and literature review. World journal of surgical oncology. 2014;12:165.View ArticlePubMedPubMed CentralGoogle Scholar
- Sanyal S, Kaman L, Sinha SK. Splenic metastasis from esophageal cancer: report of a case. Surg Today. 2005;35(11):988–90.View ArticlePubMedGoogle Scholar
- Cho MM, Kobayashi K, Aoki T, Nishioka K, Yoshida K, Hatano N, et al. Surgical resection of solitary adrenal metastasis from esophageal carcinoma following esophagectomy. Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus. 2007;20(1):79–81.View ArticleGoogle Scholar
- Hata S, Amano S, Sakurai K. Resection of adrenal metastasis from esophageal carcinoma: a case report. Jpn J Gastroenterol Surg. 2000;33:721–4.View ArticleGoogle Scholar
- Shimada Y, Imamura M, Kanda Y. Resection of adrenal metastasis from esophageal carcinoma after esophagectomy without recurrence for one and half year: a case report. Arch Jpn Chir. 1992;61:86.Google Scholar
- Depypere L, Lerut T, Moons J, Coosemans W, Decker G, Van Veer H, et al. Isolated local recurrence or solitary solid organ metastasis after esophagectomy for cancer is not the end of the road. Diseases of the esophagus: Official Journal of the International Society for Diseases of the Esophagus. 2017;30(1):1–8.Google Scholar
- Mohri Y, Tanaka K, Ohi M, Saigusa S, Yasuda H, Toiyama Y, et al. Identification of prognostic factors and surgical indications for metastatic gastric cancer. BMC Cancer. 2014;14:409.View ArticlePubMedPubMed CentralGoogle Scholar
- Kim KH, Lee KW, Baek SK, Chang HJ, Kim YJ, Park DJ, et al. Survival benefit of gastrectomy +/− metastasectomy in patients with metastatic gastric cancer receiving chemotherapy. Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association. 2011;14(2):130–8.View ArticleGoogle Scholar
- Cheon SH, Rha SY, Jeung HC, Im CK, Kim SH, Kim HR, et al. Survival benefit of combined curative resection of the stomach (D2 resection) and liver in gastric cancer patients with liver metastases. Annals of oncology : official journal of the European Society for Medical Oncology. 2008;19(6):1146–53.View ArticleGoogle Scholar
- Shaheen O, Ghibour A, Alsaid B. Esophageal cancer metastases to unexpected sites: a systematic review. Gastroenterol Res Pract. 2017;2017:13.View ArticleGoogle Scholar
- Pastorino U, Buyse M, Friedel G, Ginsberg RJ, Girard P, Goldstraw P, et al. Long-term results of lung metastasectomy: prognostic analyses based on 5206 cases. J Thorac Cardiovasc Surg. 1997;113(1):37–49.View ArticlePubMedGoogle Scholar
- Mann CD, Metcalfe MS, Leopardi LN, Maddern GJ. The clinical risk score: emerging as a reliable preoperative prognostic index in hepatectomy for colorectal metastases. Arch Surg. 2004;139(11):1168–72.View ArticlePubMedGoogle Scholar
- Fong Y, Fortner J, Sun RL, Brennan MF, Blumgart LH. Clinical score for predicting recurrence after hepatic resection for metastatic colorectal cancer: analysis of 1001 consecutive cases. Ann Surg. 1999;230(3):309–18. discussion 18-21View ArticlePubMedPubMed CentralGoogle Scholar