Life expectancy stage 4 esophageal cancer spread to liver

In the earliest stages, when it's easiest to treat, esophageal cancer has very few symptoms, so unfortunately it's rarely caught early. As esophageal cancer begins to progress and advance to the later stages, symptoms become more apparent, and the cancer becomes more difficult to treat.

Esophageal Cancer: Stages and Survival Rates

The esophagus is a long, muscular tube that joins your mouth to your stomach. Esophageal cancer is classified into four stages, 0 through IV. In the earliest stage of esophageal cancer, the cancer affects only the lining of the esophagus. At this point, it is generally easy to treat and survival rates are high. But as cancerous cells grow and spread, a larger tumor forms in the esophagus, and often spreads to nearby lymph nodes, tissues, and eventually to other organs in the body. The following is a breakdown of the stages of esophageal cancer:

  • Stage 0. This is the best-case scenario for a person diagnosed with esophageal cancer; in this stage of cancer, the disease has just begun to develop and has not spread beyond the lining of the esophagus. There are typically very few or no symptoms in this stage. Between 80 and 90 percent of esophageal cancer patients diagnosed in stage 0 can expect to survive five years following their treatment.
  • Stage I. At this stage of esophageal cancer, the disease has spread deeper into the tissues of the esophagus, but has not yet affected nearby lymph nodes or organs. The five-year survival rate for people diagnosed with esophageal cancer during this stage is 34 percent.
  • Stage II. By this stage, the cancer has moved into the deeper tissues of the esophageal wall and may now affect lymph nodes near the esophagus. The five-year rate of survival is 17 percent when esophageal cancer is diagnosed at stage II.
  • Stage III. In stage III, the cancer has progressed beyond the wall of the esophagus and nearby lymph nodes to surrounding tissues, but other organs are not yet affected. At this stage, people often complain of throat pain and difficulty swallowing. Twenty to 30 percent of patients in stage III who receive both chemotherapy and radiation are likely to survive between three and five years.
  • Stage IV. In stage IV, the cancer has metastasized, or spread, to other parts of the body. The five-year rate of survival for esophageal cancer patients diagnosed during stage IV drops to 2.8 percent.

Original Article

Introduction

Esophageal cancer is the eighth most common cancer worldwide, with 455,800 new cases estimated in 2012, and the sixth leading cause of death from cancer with 400,200 deaths (1). The prognosis of esophageal cancer patients is dismal, especially those with distant organ metastases (2). Poor outcomes in patients with esophageal cancer are related to the propensity for metastases, even when tumors are superficial (2,3) and lack of effective treatment modality for those with distant metastasis (4). However, there are few studies describing the patterns of distant metastasis in esophageal cancer systematically. In this study, we described demographic and clinical characteristics and overall survival in patients with distant metastatic esophageal cancer using Surveillance Epidemiology and End Results (SEER) database from 2010 to 2013.


Methods

Study population

The SEER program is the largest publicly available cancer database, which collects information on cancer incidence and survival from 17 population-based cancer registries covering approximately 28% of the United States population. We hypothesize that SEER is a good database from which to analyze the distant metastasis pattern for esophageal cancer. However, SEER does not include any information on the location of metastases until 2010. As a result, we can only analyze the data between 2010 and 2013.

The criteria defined for inclusion in this study were primary histologically confirmed esophageal cancer and diagnosed between 2010 and 2013. We excluded a total of 3,222 patients (24%) from those diagnosed with esophageal cancer in the SEER database (n=13,156) mainly because of unknown histologic grade (n=2,680) or pathology type (n=467) of tumor, lack of racial information (n=45) or unstaged tumors (n=1). Patients with ‘blanks’ metastatic site (n=319) should also be excluded. A total of 9,934 patients with esophageal cancer matching the specified criteria were included in the final sample for this analysis (Figure 1).

Life expectancy stage 4 esophageal cancer spread to liver

Figure 1 A flowchart of patient selection from the SEER database

Statistical analysis

Demographic of patients and tumor characteristics were summarized with descriptive statistics. Categorical variables were analyzed by the Pearson Chi square test, and continuous variables were analyzed by the two-sample t test.

Overall survival (OS) was defined as the period from diagnosis to death as a result of any cause. Survival estimation and comparison among different variables were performed using Kaplan-Meier method.

A multivariable logistic regression model was used to calculate odds ratios (OR) for sex, age, anatomical site, and histological type on specific metastases. Proportional hazards regression model was conducted to obtain adjusted hazard ratio (HRs) for different predictors of overall survival.

A two-sided P value of <05 was considered statistically significant. All statistical analyses were performed using SPSS 19.0 (SPSS, Chicago, IL, USA), and the survival curves were drawn with GraphPad Prism 6.0 (GraphPad Software, San Diego, CA, USA).


Results

Patient characteristics

The study group consisted of 9,934 patients with esophageal cancer diagnosed from 2010 to 2013, including 7,979 men (80.3%) and 1,955 women (19.7%). According to UICC TNM classification 7th edition, 32.7% (n=3,245) of the patients were stage IV (Figure 2). Esophageal adenocarcinoma (EAC) was almost twice (61.4% vs. 32.6%) than esophageal squamous cell carcinoma (ESCC) when diagnosed.

Life expectancy stage 4 esophageal cancer spread to liver

Figure 2 Proportions of different stages in selected patients

Clinical features of metastases were as follows (Table1).

Life expectancy stage 4 esophageal cancer spread to liver

Table 1 Clinical characteristics of patients

Full table

Metastasis pattern

According to the database, we had metastatic information related to liver, lung, bone and brain metastases. Patients who had metastasis to at least one of the four sites accounted for 77.3% (2,507/3,245) of stage IV diseases. Proportions of metastases to the four sites above were presented in Figure 3. In the patients of all-stage esophageal cancer, liver (15.6%) was the most common metastatic site among the four sites followed by lung (9.7%) and bone (7.7%). Metastasis to brain (1.6%) was the least among the four sites. In all stage IV patients, the proportion of liver, lung, bone and brain metastasis was 47.6%, 29.8%, 23.6%, and 4.8%, respectively. The sum was over 100% due to multiple metastases in some patients.

Life expectancy stage 4 esophageal cancer spread to liver

Figure 3 Proportions of metastasis to different sites in all-stage esophageal cancer patients (A) and stage IV patients (B).

We found that histology type was one of the independent factors for metastatic diseases (Table 2). ESCC had a higher incidence rate of lung metastasis (11.4% vs. 9.1% (EAC), P<0.001), while EAC had a higher incidence rate of liver (19.3% vs. 8.9%, P<0.001), bone (8.6% vs. 5.6%, P<0.001) and brain (2.2% vs. 0.6%, P<0.001) metastasis than ESCC (Table 1). The characteristics of lung metastasis might be different from other sites.

Life expectancy stage 4 esophageal cancer spread to liver

Table 2 Multivariate logistic regression model for odds of specific metastases in esophageal cancer

Full table

As for sex, men had a higher incidence rate than women in terms of most of metastatic sites [liver (16.9% vs. 10.2%, P<0.001), lung, (10.0% vs. 8.6%, P=0.048) and bone (8.2% vs. 5.5%, P<0.001)] (Tables 1,2). For most of the metastatic sites (liver, bone and brain), we found that there was a significant difference (P<0.001) in age between patients with and without metastasis and age was also an independent risk factor for metastatic diseases above. Younger patients were more likely to suffer from metastatic diseases (Table 1).

Besides, histologic grade of tumor was also an independent risk factor for metastatic disease (Table 2). In most of the metastatic sites, it could be seen that poorer differentiation was independently associated with higher incidence of metastasis (Table 1).

Survival

Survival in metastatic esophageal cancer was shown in Figure 4. Among the four sites of distant metastases, there was no significant difference in OS (P=0.078) (Figure 4A), irrespective of number of metastatic sites. However, we found a decrease in OS with the increase of number of metastatic sites. The median OS of one, two, three and four metastatic sites were 5.0, 4.0, 3.0 and 2.0 months, respectively and there was a significant difference (P<0.001) (Figure 4B). Among stage IV patients, there were also significant differences in OS between different histologic grades (P<0.001) (Figure 5A) and histology types (P=0.012) (Figure 5B). However, OS had no significant difference between men and women (P=0.455) (Figure 5C).

Life expectancy stage 4 esophageal cancer spread to liver

Figure 4 Survival curves of overall survival (OS) for (A) specific metastatic site (P=0.078) and (B) different number of metastatic sites (P<0.001).

Life expectancy stage 4 esophageal cancer spread to liver

Figure 5 Survival curves of overall survival (OS) for (A) different histologic grades (P<0.001); (B) different histology type (P=0.012); (C) women and men (P=0.455).

According to the result of multivariate analysis, age, histology type and number of metastatic sites were independent prognostic factors of overall survival and histologic grade tended to be another prognostic factor (Table 3). Patients with younger age, poorer differentiation, adenoma type and more metastatic sites were more likely to decrease life expectancy.

Life expectancy stage 4 esophageal cancer spread to liver

Table 3 Multivariate analysis for survival in stage IV esophageal cancer

Full table


Discussion

In this paper, we investigated patterns of distant organ metastases in esophageal cancer and presented results from SEER database. The relation between metastatic sites and clinical characteristics, including sex, age, race, histology type, histologic grade, was also discussed in this article, which would provide references for diagnosis and treatment.

With the development of diagnostic techniques, we found more metastatic diseases than ever before. From SEER database, the proportion of metastasis was growing over the past 20 years and it was 43.3% in patients without any prior treatment between 2009 and 2013. In our study, liver was the most common metastatic site among four sites, followed by lung, bone and brain, and the proportions were in consistent with autopsy findings.(5) In autopsy findings, lung (31%), liver (23%) and bone (13%) were also the most common sites and brain metastasis was still rare (less than 5%). Proportions of metastases from autopsy findings were much higher than our study due to the inclusion of recurrence and metastasis after treatment when autopsy, but the distribution pattern of metastatic sites was similar.

We found some relations between clinical characteristics and metastatic sites. Younger patients were more likely to suffer from metastatic diseases and had poorer prognosis, which was confirmed by an autopsy study. Barz H and Barz D (6) have demonstrated that the frequency of metastases from 5,708 cancers of various types, confirmed on autopsies, gradually decreases among patients beyond the age of 60. Cases without metastases have been found three times more in elderly people than in younger people and the sclerosis of capillaries may be an important factor for the reduction of distant organ metastases in elderly people.

Moreover, histologic grade might be another risk factor for metastatic diseases in our study. Quantities of studies have indicated that histologic grade should be regarded as a strong predictor of survival and survival always decreases monotonically according to histologic grade (7,8). The relation between histologic grade, metastatic disease and survival may result from the biological behavior of tumor, which still needs further research.

Prognosis of metastatic esophageal cancer is always dismal, and 5-year relative survival is 4.5% (9), which is much lower when compared with other high-incidence metastatic cancer, like breast cancer (26.3%) (10) and colorectal cancer (13.5%) (11). The main reasons are malignant biological behaviors and lack of effective systemic treatment. The objective response rates of 5-fluorouracil/cisplatin and paclitaxel/cisplatin, recommended regimens from NCCN guideline, are only 30–40% (12,13), which has limited influence on survival. No effective targeted therapy has been applied in metastatic esophageal cancer except for trastuzumab in HER2-neu overexpressing metastatic adenocarcinoma (14), which is rare among all patients (15).

In our study, there was no significant difference among four metastatic sites. However, OS was related to number of metastatic sites. Hellman and Weichselbaum (16) have proposed that a state of oligometastases and patients with oligometastases may benefit from local aggressive therapy and prolong their survival (17).

Accordingly, early diagnosis is extremely important. Five-year relative survival are 41.3% and 22.8% for localized and regional esophageal cancer (9), respectively, much more than metastatic esophageal cancer. Even when oligometastases, diagnosis as early as possible still could provide a chance for further treatment and better quality of life.

Knowledge of metastatic patterns may be useful in making clinical decisions, including early diagnosis and treatment. Evaluation when diagnosis should be systemic and targeted. Since liver and lung are the most common sites, regular imaging recommended by NCCN guideline (18), such as computed tomography (CT) with contrast for chest or abdomen, should be maintained and imaging of other sites should be applied when patients are with high risk factors for specific site of metastasis.

Diagnosis of metastasis is not only for staging, but also for further treatment. Nowadays, varieties of treatment modalities for oligometastases, including stereotactic body radiotherapy (SBRT), radiofrequency ablation and surgery, have been applied and proved to be effective (17). Our findings provide information on the patterns of distant metastases in esophageal cancer so that patients with metastatic esophageal cancer can be diagnosed and treated properly.

To our knowledge, this is the first SEER based study focusing on the metastatic pattern of esophageal cancer. However, there are still some obvious limitations due to the retrospective background of the study. First of all, it is necessary to mention that the database of the study only provides the data from 2010 to 2013 due to lack of enough information. Moreover, we only have information on metastasis to liver, lung, bone and brain, which may lead to an underestimation of other sites of metastasis. However, the four sites of metastasis could account for more than 70% of stage IV esophageal cancer both in our study and in autopsy findings (5). Furthermore, all information on metastasis is from their first diagnosis and we lack the following information, including treatment modalities and progression or remission after treatment. At last, we do not have the details about metastasis, like sizes, exact metastatic lesion quantity in one specific organ.

In conclusion, based on SEER database, we revealed that liver was the most common metastatic site in the patients of esophageal cancer and followed by lung, bone and brain. Some clinical features, including age, sex, histology type and histologic grade were independent risk factors for different sites of metastasis, which may help in surveillance. Prognosis of metastatic esophageal cancer was dismal, and younger age, poorer differentiation, adenoma type and more metastatic sites might lead to poorer prognosis. Our findings put forward the patterns of metastasis in esophageal cancer, which could help clinicians to identify patients with metastasis and deliver proper treatment.


Acknowledgements

Funding: This study was financially supported by grants from the National Natural Science Foundation of China (No. 21172043 and No. 21441010).


Conflicts of Interest: The authors have no conflicts of interest to declare.


References

  1. Torre LA, Bray F, Siegel RL, et al. Global cancer statistics, 2012. CA Cancer J Clin 2015;65:87-108. [Crossref] [PubMed]
  2. Enzinger PC, Mayer RJ. Esophageal cancer. N Engl J Med 2003;349:2241-52. [Crossref] [PubMed]
  3. Pennathur A, Farkas A, Krasinskas AM, et al. Esophagectomy for T1 esophageal cancer: outcomes in 100 patients and implications for endoscopic therapy. Ann Thorac Surg 2009;87:1048-54; discussion 54-5. [Crossref] [PubMed]
  4. Tanaka T, Fujita H, Matono S, et al. Outcomes of multimodality therapy for stage IVB esophageal cancer with distant organ metastasis (M1-Org). Dis Esophagus 2010;23:646-51. [Crossref] [PubMed]
  5. Mandard AM, Chasle J, Marnay J, et al. Autopsy findings in 111 cases of esophageal cancer. Cancer 1981;48:329-35. [Crossref] [PubMed]
  6. Barz H, Barz D. Arch Geschwulstforsch 1984;54:77-83. [Age dependence of metastases. A study of more than 5000 cases of death from cancer]. [PubMed]
  7. Rice TW, Rusch VW, Apperson-Hansen C, et al. Worldwide esophageal cancer collaboration. Dis Esophagus 2009;22:1-8. [Crossref] [PubMed]
  8. Dickson GH, Singh KK, Escofet X, et al. Validation of a modified GTNM classification in peri-junctional oesophago-gastric carcinoma and its use as a prognostic indicator. Eur J Surg Oncol 2001;27:641-4. [Crossref] [PubMed]
  9. Institute NC. SEER Stat Fact Sheets: Esophageal Cancer. 2016. Avaible online: http://seer.cancer.gov/statfacts/html/esoph.html. Accessed 09.04 2016.
  10. Institute NC. SEER Stat Fact Sheets: Female Breast Cancer. 2016. Accessed 09.04 2016.http://seer.cancer.gov/statfacts/html/breast.html
  11. Institute NC. SEER Stat Fact Sheets: Colon and Rectum Cancer. 2016. Accessed 09.04 2016.http://seer.cancer.gov/statfacts/html/breast.html
  12. Lorenzen S, Schuster T, Porschen R, et al. Cetuximab plus cisplatin-5-fluorouracil versus cisplatin-5-fluorouracil alone in first-line metastatic squamous cell carcinoma of the esophagus: a randomized phase II study of the Arbeitsgemeinschaft Internistische Onkologie. Ann Oncol 2009;20:1667-73. [Crossref] [PubMed]
  13. Petrasch S, Welt A, Reinacher A, et al. Chemotherapy with cisplatin and paclitaxel in patients with locally advanced, recurrent or metastatic oesophageal cancer. Br J Cancer 1998;78:511-4. [Crossref] [PubMed]
  14. Bang YJ, Van Cutsem E, Feyereislova A, et al. Trastuzumab in combination with chemotherapy versus chemotherapy alone for treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer (ToGA): a phase 3, open-label, randomised controlled trial. Lancet 2010;376:687-97. [Crossref] [PubMed]
  15. Sauter ER, Keller SM, Erner S, et al. HER-2/neu: a differentiation marker in adenocarcinoma of the esophagus. Cancer Lett 1993;75:41-4. [Crossref] [PubMed]
  16. Weichselbaum RR, Hellman S. Oligometastases revisited. Nat Rev Clin Oncol 2011;8:378-82. [PubMed]
  17. Lo SS, Moffatt-Bruce SD, Dawson LA, et al. The role of local therapy in the management of lung and liver oligometastases. Nat Rev Clin Oncol 2011;8:405-16. [Crossref] [PubMed]
  18. Network NCC. NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Esophageal and Esophagogastric Junction Cancers. 2016. Available online: https://www.nccn.org/professionals/physician_gls/pdf/esophageal.pdf. Accessed 09.14 2016.

Cite this article as: Ai D, Zhu H, Ren W, Chen Y, Liu Q, Deng J, Ye J, Fan J, Zhao K. Patterns of distant organ metastases in esophageal cancer: a population-based study. J Thorac Dis 2017;9(9):3023-3030. doi: 10.21037/jtd.2017.08.72

What is life expectancy for esophageal cancer that has spread to liver?

The 5-year survival rate of people with cancer located only in the esophagus is 46%. The 5-year survival rate for those with disease that has spread to surrounding tissues or organs and/or the regional lymph nodes is 26%. If it has spread to distant parts of the body, the survival rate is 5%.

How long can you survive with Stage 4 esophageal?

Currently available combination chemotherapy treatment for stage IV cancer results in complete remission in up to 20% of patients, with average survival of 8-12 months.

What is the mortality rate of stage 4 esophageal cancer?

It relates to the number of people who are still alive 1 year after their diagnosis of cancer. Some of these people might live longer than 1 year.) Around 20 out of 100 people (around 20%) with stage 4 oesophageal cancer will survive their cancer for 1 year or more after they are diagnosed.

How long does end stage esophageal cancer last?

At this stage, people often complain of throat pain and difficulty swallowing. Twenty to 30 percent of patients in stage III who receive both chemotherapy and radiation are likely to survive between three and five years.