Skip Navigation
Skip to contents

Cancer Res Treat : Cancer Research and Treatment

OPEN ACCESS

Articles

Page Path
HOME > Cancer Res Treat > Volume 44(3); 2012 > Article
Original Article Metachronous Double Primary Cancer after Diagnosis of Gastric Cancer
Jin Young Kim, MD1, Won Young Jang, MD1, Mi Hwa Heo, MD1, Kang Kuk Lee, MD1, Young Rok Do, MD1, Keon Uk Park, MD1, Hong Suk Song, MD1, Yoon Nyun Kim, MD2
Cancer Research and Treatment : Official Journal of Korean Cancer Association 2012;44(3):173-178.
DOI: https://doi.org/10.4143/crt.2012.44.3.173
Published online: September 30, 2012

1Division of Hematology/Oncology, Department of Internal Medicine, Keimyung University Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea.

2Division of Cardiology, Department of Internal Medicine, Keimyung University Dongsan Medical Center, Keimyung University School of Medicine, Daegu, Korea.

Correspondence: Hong Suk Song, MD. Department of Internal Medicine, Keimyung University Dongsan Medical Center, Keimyung University School of Medicine, 56 Dalseong-ro, Jung-gu, Daegu 700-712, Korea.
Tel: 82-53-250-7436, Fax: 82-53-425-6476, shs7436@dsmc.or.kr
• Received: March 7, 2012   • Accepted: June 22, 2012

Copyright © 2012 by the Korean Cancer Association

This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

  • 14,894 Views
  • 96 Download
  • 20 Crossref
  • 23 Scopus
prev next
  • Purpose
    The pattern of double primary cancers after treatment for gastric cancer is important for a patient's survival.
  • Materials and Methods
    We analyzed the clinicopathologic data of 214 gastric cancer patients from October 1996 to November 2007 with regard to metachronous second primary cancers.
  • Results
    Out of 5,778 patients with gastric cancer, metachronous second primary cancers occurred in 214 patients. The median age was 61.8 years, the number of male and female patients was 140 (65.4%), 74 (34.6%), respectively. The median time to the occurrence of second cancers after diagnosis of the first was 39.2 months (standard deviation, 31.2 months). The most common cancer was colorectal cancer, which occurred in 44 patients (20.6%), and lung cancer in 33 patients (15.4%), hepatocellular carcinoma in 26 patients (12.1%), ovarian cancer in 15 patients (7.0%), cervical cancer in 12 patients (7.0%), breast cancer in 11 patients (5.1%), and esophageal cancer in 11 patients (5.1%). The observed/expected (O/E) ratio showed a significant increase in colorectal (1.25), male biliary (1.60), ovarian (8.72), and cervical cancer (3.33) with primary gastric cancer. After five years from diagnosis of gastric cancer, secondary cancer occurred in 50 patients (23.4%), and breast cancer, prostate cancer, laryngeal cancer, lung cancer, and hepatocellular carcinoma were the most frequent.
  • Conclusion
    The O/E ratio showed a significant increase in colorectal, male biliary, ovarian, and cervical cancer with primary gastric cancer, and second primary cancer as the main cause of death for these patients. A follow-up examination for metachronous double primary cancer is needed in order to improve the survival time in patients with gastric cancer.
Incidence of gastric cancer in Korea is very high, and, despite early detection, it continues to be a major health problem. Through achievement of remarkable advances in cancer treatment, the number of patients who survive cancer has shown a significant increase. One problem, however, is that because patients are living longer, they may be at increased risk of developing second primary cancer. The incidence of metachronous dual primary gastric cancer has increased with the concomitant increase in the prevalence of gastric cancer [1]. Patients with metachronous cancer are defined as those with an interval of six months or more after diagnosis of gastric cancer [2]. Some studies of double primary cancer in patients with gastric cancer have reported on prognosis or characteristics of metachronous cancer [3-5]. However, the general pattern of metachronous gastric cancer still needs to be clarified.
Due to the high incidence of gastric cancer in Korea, its surveillance in patients diagnosed with stomach cancer might be of clinical benefit. Although numerous reports on metachronous cancers have been issued, most have been simple case reports, as relatively few studies on the incidence and characteristics of metachronous cancers that develop during the postsurgical follow-up period have been conducted. Studies evaluating the characteristics of synchronous and metachronous cancer are limited, and the incidence of metachronous cancer varies to the extent that the clinical results differ in each study.
Further characterization of metachronous gastric cancer could provide valuable information for use in early diagnosis and treatment of these diseases. The purpose of this study was to investigate the prognosis and clinical features of metachronous gastric cancer.
Between October 1996 and November 2007, 5,778 patients underwent surgical treatment or chemotherapy for gastric cancer at Dongsan Medical Center; however, these patients did not undergo endoscopic resection. Patients who had been diagnosed with new primary cancer developing from other origins were selected from the original group.
Among the 5,778 patients who underwent treatment for gastric cancer, metachronous cancers were diagnosed in 214 patients. The metachronous cancer patients described above could be defined as those with an interval of six months or more after diagnosis of gastric cancer [2].
All patients with gastric cancer underwent routine preoperative upper gastrointestinal endoscopy. The histological diagnosis was established by gastrointestinal endoscopic biopsies and operative specimens. As part of the standard preoperative workup for gastric cancer, the staging workup included a complete physical examination, a complete blood count and biochemical profile, a gastrointestinal contrast study, and a chest and abdominal computed tomography scan. Second primary cancer was confirmed by histologic diagnosis, however, hepatocellular carcinoma, pancreatic cancer, and biliary cancer proved difficult to diagnose using this procedure in cases of poor performance. In such cases, second primary cancer was diagnosed through an imaging examination and tumor markers.
In addition, the age of patients at onset of metachronous cancer, or, the tumor, node and metastasis (TNM) stage, according to the American Joint Committee on Cancer (AJCC) 6th edition, and the presence of factors that could mediate effects on the survival rate were examined retrospectively. Evaluation of the interval from the first gastric surgery to development of second primary cancer, clinical characteristics, and survival rate after the second surgery was based on medical records.
1. Statistical analysis
The Kaplan-Meier method was used for generation of overall survival curves, and the log-rank test was used for comparison of between-group differences. Univariate and multivariate analyses with the Cox proportional hazard model were used for analysis of prognostic factors. The survival curve for patients with metachronous double primary cancer was calculated from the date of diagnosis of the second cancer. A p-value of <0.05 was considered to indicate statistical significance. The SPSS ver. 18.0 (SPSS Inc., Chicago, IL) was used.
Among 5,778 patients with gastric cancer, 209 patients (5.0%) were diagnosed with synchronous double primary cancer and 214 patients (3.7%) were diagnosed with metachronous double primary cancer. The group of patients consisted of 140 men and 74 women. Looking at the age distribution between the groups, the proportion was higher in older patients diagnosed with metachronous double primary cancer (p<0.001) (Table 1). The most common group included patients aged 60 to 70, and the most common metachronous double primary cancer was colorectal cancer, followed by lung, liver (excluding cholangiocarcinoma), ovarian, and cervical cancer.
Table 2 shows the mean age distribution of patients with metachronous double primary cancer. No difference was observed among the types of metachronous double primary cancer. The mean age was 61.8±10.62 years, and the oldest patient, who had lung cancer, was 68.5 years old, and the youngest patient, with breast cancer, was 51.7 years old.
In comparison of sex distribution of patients with metachronous double primary cancer, double primary cancer occurred more frequently in male patients, with the exception of breast, ovary, and cervical cancer (p<0.001) (Table 3). The observed/expected (O/E) ratio was significantly higher in male colorectal (1.25), male biliary (1.60), ovarian (8.72), and cervical cancer (3.33) with primary gastric cancer, compared with double primary cancer.
Table 4 shows the yearly diagnostic period for metachronous double primary cancer, and does not indicate any notable difference in incidence from year to year. The most common period of occurrence was 1-2 years (n=60, 40.8%). Subjective symptoms were observed in three patients after 10 years. These patients were diagnosed with hepatocellular carcinoma, lung cancer, and cervical cancer. The mean diagnostic period was 39.2±31.2 months. No significant differences were observed among sex and cancer groups. Bladder cancer and esophageal cancer were diagnosed earlier, compared to other cancers (Table 5).
Table 6 shows development of metachronous double primary cancer over a period of fiveyears, after diagnosis of gastric cancer. Development of breast cancer (54.5%), prostate cancer (50.0%), and laryngeal cancer (40.0%) occurred much more frequently after five years from diagnosis of gastric cancer.
The mean follow-up period was 35.5 months for metachronous cancers. The median survival period for metachronous double primary cancer after diagnosis of second primary cancer was 19.8±3.33 months (Table 7). The four year survival rate for patients with double primary gastric cancer was 4%, however, the rate without second primary cancer was 61.1% (Fig. 1). The median survival period for patients with breast, laryngeal, cervical, and colorectal cancers was longer than that of other cancers, however, no survival difference was observed according to gastric cancer stage (Table 8).
The first study of synchronous and metachronous cancer in patients with gastric cancer was reported by Yoshino et al. [6]. Results of the study, conducted in Japan, showed an incidence of synchronous and metachronous cancer in patients with gastric cancer of 2.0%. Other studies have since reported incidence rates of 1.1-4.7% [3-10]. In this study, the incidence was 3.7%, which appears to be overestimated, as it included patients who had not been diagnosed with pathologic confirmation due to their physical condition and/or had difficulty in receiving a pathologic diagnosis.
In this study, the most common double primary cancer was colorectal cancer, followed by lung, liver (excluding cholangiocarcinoma), ovary, and cervical cancer. Comparing this result with the general cancer incidence in Korea, the incidence of colorectal cancer is higher than expected. That is, although colorectal cancer is the third most common cancer in the general population, it is the most common double primary cancer. This result has been observed not only in Korea, but also in Japan, China, and Australia. In the general population, colorectal cancer is the fifth most common cancer in China and the third most common cancer in Australia; however, it is the most common double primary cancer in both countries [4,11,12]. Many papers have evaluated genetic and environmental relationships between gastric and colorectal cancer [13,14]. Therefore, performance of regular colonoscopies on patients who have been diagnosed with gastric cancer is important, particularly for those who are over sixty. The median age for secondary gastric cancer was 63.0 years; the number of males was 137, the number of females was 59. Hepatocellular carcinoma (30 in 2,481 cases, 1.21%), esophageal cancer (24 in 518 cases, 4.63%), and lung cancer (20 in 2,814 cases, 0.71%) were reported as common types of primary cancers.
A comparison of clinicopathological characteristics among patients with other primary cancers and patients without them was conducted by Kato et al. [15] and Lee et al. [9]. Statistical differences in age, sex, and gastric cancer staging were observed in these previous studies. That is, the mean age, sex ratio, and proportion of early gastric cancer was higher in patients with other primary cancers than in those without. This study reported similar results, except with regard to gastric cancer staging; no significant difference was observed in gastric cancer staging, compared to the statistics.
The incidences of most cancers are higher in males than in females and tend to increase with age. Patients with metachronous cancer of ovary or breast were younger than those with other cancers, which means that female patients with metachronous double primary cancer tend to be younger than male patients. In this study, the O/E ratio was found to be significantly higher in colorectal, biliary, ovarian, and cervical cancer with primary gastric cancer. In order to enhance detection and survival rate, conduct of a large scale prospective study is necessary for investigation of the efficacy of colonoscopies, abdomen and pelvic computed tomographys, and PAP smears.
Previous studies have reported that the majority of double primary malignancies develop within a period of three years, and that surveillance gastroscopy is commonly recommended for a period of three years after surgery for treatment of colorectal cancer [16]. However, there was no exact surveillance colonoscopy recommendation period or surveillance tool for detection of colon cancer after gastric cancer surgery. A higher percentage of metachronous cancers was confirmed for both colorectal and lung cancer. Ikeda et al. [4] reported that metachronous lung cancer showed a high incidence of advanced-stage disease and was a major cause of death in patients with metachronous double primary cancers. Therefore, close attention should be paid and regular checkups should be performed on patients who have undergone surgery for treatment of gastric cancer.
Patients who have not been diagnosed with secondary cancers within five years after gastric cancer surgery are usually regarded as having been cured. In this study, metachronous double primary cancer was found to occur after 10 years; therefore, performance of regular checkups for a longer period of time on patients who have undergone surgery for treatment of gastric cancer is important.
Survival rates of patients with a metachronous or synchronous cancer were analyzed by Maehara et al. [5], Furukawa et al. [17], and Ikeda et al. [4]. According to the study reported by Ikeda et al. [4], the 10-year survival rate was 69.3% for gastric cancer patients without a double primary cancer, 40.1% for patients with synchronous double primary cancer, and 75.2% for patients with metachronous double primary cancer. In this study, the median survival time for patients with metachronous double primary cancer after diagnosis of second primary cancer was 19.8 months, and 55.2 months after diagnosis of gastric cancer. Survival rates for patients withpancreatic cancer and hepato-biliary cancer were very low, indicating a strong relationship of survival rate with the type of double primary cancer. Other prognostic factors should be evaluated in order to demonstrate the difference in median survival rate of patients with metachronous double primary cancer.
Patients with gastric cancer develop double primary cancers either synchronously or metachronously, and, in the present study, second primary cancer was the main cause of death for these patients. The O/E ratio showed a significant increase in colorectal, male biliary, ovarian, and cervical cancer with primary gastric cancer, and second primary cancer was the main cause of death for these patients. A follow-up examination for metachronous double primary cancer is needed in order to improve the survival time in patients with gastric cancer.
Acknowledgements
This study was supported by a grant from the Korea Health technology R&D Project, Ministry of Health & Welfare, Republic of Korea (A091326).

Conflict of interest relevant to this article was not reported.

  • 1. Watanabe M, Kochi M, Fujii M, Kaiga T, Mihara Y, Funada T, et al. Dual primary gastric and colorectal cancer: Is the prognosis better for synchronous or metachronous? Am J Clin Oncol. 2011;6. 08[Epub]. http://dx.doi.org/10.1097/COC.0b013e318218585a Article
  • 2. Moertel CG, Bargen JA, Dockerty MB. Multiple carcinomas of the large intestine: a review of the literature and a study of 261 cases. Gastroenterology. 1958;34:85–98. PMID: 13501357ArticlePubMed
  • 3. Eom BW, Lee HJ, Yoo MW, Cho JJ, Kim WH, Yang HK, et al. Synchronous and metachronous cancers in patients with gastric cancer. J Surg Oncol. 2008;98:106–110. PMID: 18452218ArticlePubMed
  • 4. Ikeda Y, Saku M, Kawanaka H, Nonaka M, Yoshida K. Features of second primary cancer in patients with gastric cancer. Oncology. 2003;65:113–117. PMID: 12931016ArticlePubMed
  • 5. Maehara Y, Tomisaki S, Emi Y, Sakaguchi Y, Kusumoto T, Ichiyoshi Y, et al. Clinicopathological features of patients who died with second primary cancer after curative resection for gastric cancer. Anticancer Res. 1995;15:1049–1053. PMID: 7645924PubMed
  • 6. Yoshino K, Asanuma F, Hanatani Y, Otani Y, Kumai K, Ishibiki K. Multiple primary cancers in the stomach and another organ: frequency and the effects on prognosis. Jpn J Clin Oncol. 1985;15(Suppl 1):183–190. PMID: 4009981PubMed
  • 7. Lundegardh G, Hansson LE, Nyren O, Adami HO, Krusemo UB. The risk of gastrointestinal and other primary malignant diseases following gastric cancer. Acta Oncol. 1991;30:1–6. PMID: 2009177Article
  • 8. Lynge E, Jensen OM, Carstensen B. Second cancer following cancer of the digestive system in Denmark, 1943-80. Natl Cancer Inst Monogr. 1985;68:277–308. PMID: 4088303PubMed
  • 9. Lee JH, Bae JS, Ryu KW, Lee JS, Park SR, Kim CG, et al. Gastric cancer patients at high-risk of having synchronous cancer. World J Gastroenterol. 2006;12:2588–2592. PMID: 16688807ArticlePubMedPMC
  • 10. Hiyama T, Hanai A, Fujimoto I. Second primary cancer after diagnosis of stomach cancer in Osaka, Japan. Jpn J Cancer Res. 1991;82:762–770. PMID: 1908843ArticlePubMedPMC
  • 11. Yang L, Parkin DM, Ferlay J, Li L, Chen Y. Estimates of cancer incidence in China for 2000 and projections for 2005. Cancer Epidemiol Biomarkers Prev. 2005;14:243–250. PMID: 15668501ArticlePubMed
  • 12. Heard A, Roder D, Luke C. Multiple primary cancers of separate organ sites: implications for research and cancer control (Australia). Cancer Causes Control. 2005;16:475–481. PMID: 15986102ArticlePubMed
  • 13. Deakin M, Elder J, Hendrickse C, Peckham D, Baldwin D, Pantin C, et al. Glutathione S-transferase GSTT1 genotypes and susceptibility to cancer: studies of interactions with GSTM1 in lung, oral, gastric and colorectal cancers. Carcinogenesis. 1996;17:881–884. PMID: 8625505ArticlePubMed
  • 14. Knekt P, Jarvinen R, Dich J, Hakulinen T. Risk of colorectal and other gastro-intestinal cancers after exposure to nitrate, nitrite and N-nitroso compounds: a follow-up study. Int J Cancer. 1999;80:852–856. PMID: 10074917ArticlePubMed
  • 15. Kato I, Kito T, Nakazato H, Tominaga S. Second malignancy in stomach cancer patients and its possible risk factors. Jpn J Clin Oncol. 1986;16:373–381. PMID: 3795533PubMed
  • 16. Yun HR, Yi LJ, Cho YK, Park JH, Cho YB, Yun SH, et al. Double primary malignancy in colorectal cancer patients: MSI is the useful marker for predicting double primary tumors. Int J Colorectal Dis. 2009;24:369–375. PMID: 18797888ArticlePubMed
  • 17. Furukawa H, Hiratsuka M, Iwanaga T, Imaoka S, Kabuto T, Ishikawa O, et al. Treatments for second malignancies after gastrectomy for stomach cancer. Hepatogastroenterology. 1996;43:194–198. PMID: 8682461PubMed
Fig. 1
Four-year survival rate for gastric cancer patients without double primary cancer.
crt-44-173-g001.jpg
Table 1
Sex and age distribution of patients with metachronous double primary cancer in gastric cancer patients
Age (yr) With second cancera) Without second cancer


Male Female Male Female
20-30 1 (5.3) 0 (0) 18 (94.7) 39 (100)
30-40 1 (0.6) 6 (3.7) 156 (99.4) 158 (96.3)
40-50 8 (1.6) 15 (5.4) 496 (98.4) 264 (94.6)
50-60 22 (2.5) 17 (4.9) 861 (97.5) 329 (95.1)
60-70 69 (5.1) 24 (3.8) 1,278 (94.9) 601 (96.2)
>70 39 (4.5) 12 (2.2) 832 (95.5) 525 (97.8)
Total 140 (3.7) 74 (3.7) 3,641 (96.3) 1,916 (96.3)

Values are presented as number (%). a)Age and sex distribution of metachronous double primary cancer: p<0.001.

Table 2
Cancer type and mean age distribution of metachronous double primary cancer in gastric cancer patients
Cancer type No. (%) Double primary cancer

Age (mean±SD, yr)
Colorectum 44 (20.6) 61.8±8.61
Lung 33 (15.4) 68.5±7.07
Liver 26 (12.1) 60.0±10.22
Ovary 15 (7.0) 54.6±12.45
Cervix 12 (5.6) 60.2±5.42
Breast 11 (5.1) 51.7±11.30
Esophagus 11 (5.1) 63.7±12.96
Biliary 8 (3.7) 67.6±7.73
Pancreas 7 (3.3) 58.6±8.94
Bladder 6 (2.8) 67.2±5.42
Skin 5 (2.3) 67.0±9.70
Larynx 5 (2.3) 67.2±10.18
Others 31 (14.5) 61.1±10.72
Total 214 (100) 61.8±10.62

SD, standard deviation.

Table 3
Type of metachronous double primary cancera) in gastric cancer patients according to sexb)
Cancer type Male (n=3,787) Female (n=1,991) Total (n=5,778)a)
Colorectum 34 (0.90)b) 10 (0.05) 44 (0.76)
Lung 28 (0.74) 5 (0.25) 33 (0.57)
Liver 23 (0.61) 3 (0.15) 26 (0.44)
Ovary 0 (0) 15 (0.75)b) 15 (0.26)
Cervix 0 (0) 12 (0.60)b) 12 (0.21)
Breast 0 (0) 11 (0.55) 11 (0.19)
Esophagus 11 (0.29) 0 (0) 11 (0.19)
Biliary 7 (0.18)b) 1 (0.05) 8 (0.14)
Others 37 (0.98) 17 (0.85) 54 (0.93)
Total 140 (3.70) 74 (3.72) 214 (3.70)

Values are presented as number (%). a)Sex distribution of metachronous double primary cancer: p<0.001, b)Observed/expected (O/E) ratio was significantly different compared with single primary cancer (O/E ratio: male colorectal, 1.25; male biliary, 1.60; ovary, 8.72; cervix, 3.33).

Table 4
Diagnostic period of metachronous double primary cancer in patients with gastric cancer
Diagnostic period (yr) No.
  <1 37
  1-2 60
  2-3 28
  3-4 24
  4-5 15
  5-6 13
  6-7 9
  7-8 10
  8-9 10
  9-10 5
  >10 3
  Total 214
Table 5
Mean diagnostic period of metachronous double primary cancer in gastric cancer patients
Cancer type Male Female Total
Colorectum 34.9±24.3 49.7±32.8 38.2±26.8
Lung 43.2±35.9 45.1±43.1 43.4±36.3
Liver 41.2±31.3 64.5±47.7 44.8±33.1
Ovary 34.0±28.1 34.0±28.1
Breast 59.0±35.2 59.0±35.2
Cervix 37.8±32.7 37.8±32.7
Esophagus 24.5±27.7 24.5±27.7
Biliary 50.8±31.1 36.0 48.9±29.2
Pancreas 39.7±21.6 27.9±15.2 34.7±18.7
Bladder 24.0±13.4 17.3±12.3 22.9±12.3
Skin 36.3±35.2 9.5 36.9±34.6
Larynx 43.7±38.7 43.7±38.7
Total 38.5±30.8 40.7±32.1 39.2±31.2

Values are presented as mean±SD (mo).

Table 6
Diagnosis of metachronous double primary cancer after five years from diagnosis of gastric cancer
Cancer type No. (%) Total
Colorectum 10 (22.7) 44
Lung 10 (30.3) 33
Liver 7 (26.9) 26
Breast 6 (54.5) 11
Cervix 2 (16.7) 12
Biliary 2 (25.0) 8
Larynx 2 (40.0) 5
Ovary 2 (13.3) 15
Prostate 2 (50.0) 4
Others 7 (12.5) 56
Total 50 (23.4) 214
Table 7
Median survival after diagnosis of metachronous double primary cancer in patients with gastric cancer
Cancer type No. Survival (median±SD, mo)a)
Colorectum 44 25.5±3.85
Lung 33 13.3±5.73
HCC 26 9.6±12.54
Ovary 15 17.4±5.13
Cervix 12 30.6±21.22
Breast 11 53.1±13.73
Esophagus 11 19.3±22.36
Biliary 8 8.8±6.21
Pancreas 7 3.0±3.37
Bladder 6 15.5±39.14
Skin 5 25.0±12.60
Larynx 5 32.6±13.77
Others 31 9.2±3.90
Total 214 19.8±3.33

HCC, hepatocellular carcinoma. a)Median survival according to metachronous double primary cancer: p=0.015.

Table 8
Median survival of metachronous cancer according to gastric cancer stage
Cancer stage No. After gastric cancer diagnosis (mo) After double primary cancera) (mo)
I 114 62.03 23.90
II 54 111.83 33.70
III 32 44.90 25.50
IV 2 124.93 14.87
I-II 168 67.40 25.30
III-IV 34 44.9 17.37

a)Median survival according to gastric cancer stage was not significant (p=0.703).

Figure & Data

REFERENCES

    Citations

    Citations to this article as recorded by  
    • Multiple Primary Malignancies in Patients With Gastric Cancer: A Retrospective Study in National Cancer Center of China
      Guiling Zhu, Yutong Li, Bingzhi Wang, Liyan Xue, Yuchen Jiao, Xiaobing Wang, Chunxia Du
      Cancer Innovation.2026;[Epub]     CrossRef
    • Deciphering the risk of developing liver cancer following gastric cancer diagnosis with genetic evidence: a Mendelian randomization analysis in an East Asian population
      Jiansheng Chen, Aiming Zeng, Yunzhe Yu, Liqun Liao, Siwei Huang, Sida Sun, Weijie Wu
      Discover Oncology.2025;[Epub]     CrossRef
    • Gastric Metastasis Mimicking Early Gastric Cancer from Invasive Ductal Carcinoma of the Breast: Case Report and Literature Review
      Kwon Cheol Yoo, Dae Hoon Kim, Sungmin Park, HyoYung Yun, Dong Hee Ryu, Jisun Lee, Seung-Myoung Son
      Medicina.2024; 60(6): 980.     CrossRef
    • Synchronous gastric and ovarian cancer successfully treated with FOLFOX therapy: a case report and review of the literature
      Makiko So, Aya Shimoji, Yoko Iemura, Ai Suizu, Shuichiro Iwami, Masahito Hoki, Shinsuke Shibuya
      International Cancer Conference Journal.2024; 13(4): 427.     CrossRef
    • Incidence and pattern of second primary cancer in patients diagnosed with primary cancer
      Jong Sung, Ae Ahn, Ho Park, Kyu Jang, Woo Moon, Ju-Hyung Lee, Kyoung Kim, Myoung Chung
      Oncology Letters.2024;[Epub]     CrossRef
    • The risk and distribution of second primary cancers according to subsite of primary stomach cancer: a retrospective cohort population-based study
      Ali Hemade, Souheil Hallit
      Annals of Medicine & Surgery.2024; 86(12): 6944.     CrossRef
    • Features of synchronous and metachronous dual primary gastric and colorectal cancer
      Yi-Jia Lin, Hua-Xian Chen, Feng-Xiang Zhang, Xian-Sheng Hu, Hai-Juan Huang, Jian-Hua Lu, Ye-Zi Cheng, Jun-Sheng Peng, Lei Lian
      World Journal of Gastrointestinal Oncology.2023; 15(11): 1864.     CrossRef
    • Secondary Primary Cancer after Primary Gastric Cancer: Literature Review and Big Data Analysis Using the Health Insurance Review and Assessment Service (HIRA) Database of Republic of Korea
      Jeong Ho Song, Yeonkyoung Lee, Jaesung Heo, Sang-Yong Son, Hoon Hur, Sang-Uk Han
      Cancers.2022; 14(24): 6165.     CrossRef
    • Simultaneous gastric cancer and breast cancer metastases to the stomach with lymph node collision tumor: a case report
      Takeshi Okamoto, Hidekazu Suzuki, Katsuyuki Fukuda
      BMC Gastroenterology.2021;[Epub]     CrossRef
    • The contribution of second primary cancers to the mortality of patients with a gastric first primary cancer
      Samantha Morais, Luís Antunes, Maria J. Bento, Nuno Lunet
      European Journal of Gastroenterology & Hepatology.2019; 31(4): 471.     CrossRef
    • Second Primary Cancer after Treating Gastrointestinal Cancer
      Jeong Youp Park
      The Korean Journal of Gastroenterology.2019; 74(4): 193.     CrossRef
    • Gastric cancer and intrahepatic cholangiocarcinoma
      Alex Emmanuel Elobu, Ashok Thorat, Vianney Kweyamba, Rakesh Rai
      Formosan Journal of Surgery.2019; 52(3): 107.     CrossRef
    • Occurrence of metachronous multiple primary cancers occurred in different parts of the stomach with 2 pathologic features
      Yan Song, Ningning Zhao, Kui Jiang, Zhongqing Zheng, Bangmao Wang, Dalu Kong, Shu Li
      Medicine.2018; 97(20): e10803.     CrossRef
    • Surgical Strategy and Outcome in Patients Undergoing Pancreaticoduodenectomy After Gastric Resection: A Three‐Center Experience with 39 Patients
      Dooin Lee, Jae Hoon Lee, Dongho Choi, Chang Moo Kang, Jae Uk Chong, Song‐Chul Kim, Kyeong Geun Lee
      World Journal of Surgery.2017; 41(2): 552.     CrossRef
    • Risk of second primary cancers among patients with a first primary gastric cancer: A population-based study in North Portugal
      Samantha Morais, Luís Antunes, Maria José Bento, Nuno Lunet
      Cancer Epidemiology.2017; 50: 85.     CrossRef
    • Incidence of Gastric Cancer in Patients with Laryngeal Cancer
      Ji-Hyun Seo, Hyun-Jin Kim, Jung Je Park, Ok-Jae Lee, Jin Pyeong Kim, Seong-Ki Ahn, Jeong Seok Hwa, Jong Sil Lee, Hee-Shang Youn
      The Korean Journal of Helicobacter and Upper Gastrointestinal Research.2017; 17(4): 190.     CrossRef
    • Second primary malignancy risk among patients with gastric cancer: a nationwide population-based study in Taiwan
      San-Chi Chen, Chia-Jen Liu, Yu-Wen Hu, Chiu-Mei Yeh, Li-Yu Hu, Yen-Po Wang, Yi-Ping Hung, Cheng-Hwai Tzeng, Tzeon-Jye Chiou, Tzeng-Ji Chen, Chung-Jen Teng
      Gastric Cancer.2016; 19(2): 490.     CrossRef
    • Secondary Primary Malignancy Risk in Patients With Ovarian Cancer in Taiwan
      Yi-Ping Hung, Chia-Jen Liu, Yu-Wen Hu, Min-Huang Chen, Chun-Pin Li, Chiu-Mei Yeh, Tzeon-Jye Chiou, Tzeng-Ji Chen, Muh-Hwa Yang, Yee Chao
      Medicine.2015; 94(38): e1626.     CrossRef
    • Role of Ki‐67 Proliferation Index in the Assessment of Patients with Neuroendocrine Neoplasias Regarding the Stage of Disease
      H. C. Miller, P. Drymousis, R. Flora, R. Goldin, D. Spalding, A. Frilling
      World Journal of Surgery.2014; 38(6): 1353.     CrossRef
    • Prediction of metachronous multiple primary cancers following the curative resection of gastric cancer
      Chan Kim, Hong Jae Chon, Beodeul Kang, Kiyeol Kim, Hei-Cheul Jeung, Hyun Cheol Chung, Sung Hoon Noh, Sun Young Rha
      BMC Cancer.2013;[Epub]     CrossRef

    • PubReader PubReader
    • ePub LinkePub Link
    • Cite
      CITE
      export Copy Download
      Close
      Download Citation
      Download a citation file in RIS format that can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Reference Manager.

      Format:
      • RIS — For EndNote, ProCite, RefWorks, and most other reference management software
      • BibTeX — For JabRef, BibDesk, and other BibTeX-specific software
      Include:
      • Citation for the content below
      Metachronous Double Primary Cancer after Diagnosis of Gastric Cancer
      Cancer Res Treat. 2012;44(3):173-178.   Published online September 30, 2012
      Close
    • XML DownloadXML Download
    Metachronous Double Primary Cancer after Diagnosis of Gastric Cancer
    Image
    Fig. 1 Four-year survival rate for gastric cancer patients without double primary cancer.
    Metachronous Double Primary Cancer after Diagnosis of Gastric Cancer
    Age (yr) With second cancera) Without second cancer


    Male Female Male Female
    20-30 1 (5.3) 0 (0) 18 (94.7) 39 (100)
    30-40 1 (0.6) 6 (3.7) 156 (99.4) 158 (96.3)
    40-50 8 (1.6) 15 (5.4) 496 (98.4) 264 (94.6)
    50-60 22 (2.5) 17 (4.9) 861 (97.5) 329 (95.1)
    60-70 69 (5.1) 24 (3.8) 1,278 (94.9) 601 (96.2)
    >70 39 (4.5) 12 (2.2) 832 (95.5) 525 (97.8)
    Total 140 (3.7) 74 (3.7) 3,641 (96.3) 1,916 (96.3)
    Cancer type No. (%) Double primary cancer

    Age (mean±SD, yr)
    Colorectum 44 (20.6) 61.8±8.61
    Lung 33 (15.4) 68.5±7.07
    Liver 26 (12.1) 60.0±10.22
    Ovary 15 (7.0) 54.6±12.45
    Cervix 12 (5.6) 60.2±5.42
    Breast 11 (5.1) 51.7±11.30
    Esophagus 11 (5.1) 63.7±12.96
    Biliary 8 (3.7) 67.6±7.73
    Pancreas 7 (3.3) 58.6±8.94
    Bladder 6 (2.8) 67.2±5.42
    Skin 5 (2.3) 67.0±9.70
    Larynx 5 (2.3) 67.2±10.18
    Others 31 (14.5) 61.1±10.72
    Total 214 (100) 61.8±10.62
    Cancer type Male (n=3,787) Female (n=1,991) Total (n=5,778)a)
    Colorectum 34 (0.90)b) 10 (0.05) 44 (0.76)
    Lung 28 (0.74) 5 (0.25) 33 (0.57)
    Liver 23 (0.61) 3 (0.15) 26 (0.44)
    Ovary 0 (0) 15 (0.75)b) 15 (0.26)
    Cervix 0 (0) 12 (0.60)b) 12 (0.21)
    Breast 0 (0) 11 (0.55) 11 (0.19)
    Esophagus 11 (0.29) 0 (0) 11 (0.19)
    Biliary 7 (0.18)b) 1 (0.05) 8 (0.14)
    Others 37 (0.98) 17 (0.85) 54 (0.93)
    Total 140 (3.70) 74 (3.72) 214 (3.70)
    Diagnostic period (yr) No.
      <1 37
      1-2 60
      2-3 28
      3-4 24
      4-5 15
      5-6 13
      6-7 9
      7-8 10
      8-9 10
      9-10 5
      >10 3
      Total 214
    Cancer type Male Female Total
    Colorectum 34.9±24.3 49.7±32.8 38.2±26.8
    Lung 43.2±35.9 45.1±43.1 43.4±36.3
    Liver 41.2±31.3 64.5±47.7 44.8±33.1
    Ovary 34.0±28.1 34.0±28.1
    Breast 59.0±35.2 59.0±35.2
    Cervix 37.8±32.7 37.8±32.7
    Esophagus 24.5±27.7 24.5±27.7
    Biliary 50.8±31.1 36.0 48.9±29.2
    Pancreas 39.7±21.6 27.9±15.2 34.7±18.7
    Bladder 24.0±13.4 17.3±12.3 22.9±12.3
    Skin 36.3±35.2 9.5 36.9±34.6
    Larynx 43.7±38.7 43.7±38.7
    Total 38.5±30.8 40.7±32.1 39.2±31.2
    Cancer type No. (%) Total
    Colorectum 10 (22.7) 44
    Lung 10 (30.3) 33
    Liver 7 (26.9) 26
    Breast 6 (54.5) 11
    Cervix 2 (16.7) 12
    Biliary 2 (25.0) 8
    Larynx 2 (40.0) 5
    Ovary 2 (13.3) 15
    Prostate 2 (50.0) 4
    Others 7 (12.5) 56
    Total 50 (23.4) 214
    Cancer type No. Survival (median±SD, mo)a)
    Colorectum 44 25.5±3.85
    Lung 33 13.3±5.73
    HCC 26 9.6±12.54
    Ovary 15 17.4±5.13
    Cervix 12 30.6±21.22
    Breast 11 53.1±13.73
    Esophagus 11 19.3±22.36
    Biliary 8 8.8±6.21
    Pancreas 7 3.0±3.37
    Bladder 6 15.5±39.14
    Skin 5 25.0±12.60
    Larynx 5 32.6±13.77
    Others 31 9.2±3.90
    Total 214 19.8±3.33
    Cancer stage No. After gastric cancer diagnosis (mo) After double primary cancera) (mo)
    I 114 62.03 23.90
    II 54 111.83 33.70
    III 32 44.90 25.50
    IV 2 124.93 14.87
    I-II 168 67.40 25.30
    III-IV 34 44.9 17.37
    Table 1 Sex and age distribution of patients with metachronous double primary cancer in gastric cancer patients

    Values are presented as number (%). a)Age and sex distribution of metachronous double primary cancer: p<0.001.

    Table 2 Cancer type and mean age distribution of metachronous double primary cancer in gastric cancer patients

    SD, standard deviation.

    Table 3 Type of metachronous double primary cancera) in gastric cancer patients according to sexb)

    Values are presented as number (%). a)Sex distribution of metachronous double primary cancer: p<0.001, b)Observed/expected (O/E) ratio was significantly different compared with single primary cancer (O/E ratio: male colorectal, 1.25; male biliary, 1.60; ovary, 8.72; cervix, 3.33).

    Table 4 Diagnostic period of metachronous double primary cancer in patients with gastric cancer

    Table 5 Mean diagnostic period of metachronous double primary cancer in gastric cancer patients

    Values are presented as mean±SD (mo).

    Table 6 Diagnosis of metachronous double primary cancer after five years from diagnosis of gastric cancer

    Table 7 Median survival after diagnosis of metachronous double primary cancer in patients with gastric cancer

    HCC, hepatocellular carcinoma. a)Median survival according to metachronous double primary cancer: p=0.015.

    Table 8 Median survival of metachronous cancer according to gastric cancer stage

    a)Median survival according to gastric cancer stage was not significant (p=0.703).


    Cancer Res Treat : Cancer Research and Treatment
    Close layer
    TOP