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Cancers (Basel). 2019;12(1):cancers12010086.

Conversion Surgery in Metastatic Gastric Cancer and Cancer Dormancy as a Prognostic Biomarker.

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제1저자 최훈지 · 교신저자 김진원, 이혜승

소속 (5)
  1. Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea.
  2. Department of Pathology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea.
  3. Department of Pathology, Dong-A University Hospital, Dong-A University College of Medicine, Busan 49201, Korea.
  4. Department of Surgery, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam 13620, Korea.
  5. Department of Surgery, Seoul National University Hospital, Seoul National University College of Medicine, Seoul 03080, Korea.

Abstract

The role of conversion surgery in metastatic gastric cancer remains unclear. Cancer dormancy markers might have a role in predicting the survival in patients with conversion surgery. We identified 26 patients who went through conversion surgery, i.e., a curative-intent gastrectomy with metastasectomy after chemotherapy in initially metastatic gastric cancer. As controls, 114 potential candidates for conversion surgery who only received chemotherapy were included for the propensity score matching. Conversion surgery showed a significantly longer overall survival (OS) compared with only palliative chemotherapy (median-43.6 vs. 14.0 months, respectively, p < 0.001). This better survival in the conversion surgery group persisted even after propensity matching (p < 0.001), and also when compared to patients with tumor response over 5.1 months in the chemotherapy only group (p = 0.005). In the conversion surgery group, OS was longer in patients with R0 resection (22/26, 84.6%) than without R0 resection (4/26, 15.4%) (median-not reached vs 22.1 months, respectively, p = 0.005). Although it should be interpreted with caution due to the primitive analysis in a small population, the positive expression of NR2F1 showed a longer duration of disease-free survival (DFS) after conversion surgery (p = 0.016). In conclusion, conversion surgery showed a durable OS even in patients with initially metastatic gastric cancer when R0 resection was achieved after chemotherapy.

Keywords

cancer dormancyconversion surgerygastric cancernuclear receptor NR2F1

Figures

Figure 1
Figure 1 Kaplan–Meier curve for overall survival (OS) in patients who received conversion surgery and only chemotherapy. (a) Comparison of OS after chemotherapy in patients who received conversion surgery (n = 26) and those that only received chemotherapy (n = 114) (p < 0.001). (b) Comparison of OS after chemotherapy in patients who received conversion surgery (n = 26) vs. subgroup of patients in the chemotherapy only group whose tumor responded to or were stabilized with chemotherapy for 5.1 or more months (n = 61) (p = 0.005). (c) Comparison of OS in patients who received R0 resection (n = 22) vs. noncurative resection in conversion surgery (n = 4) (p = 0.005). (d) Comparison of OS after chemotherapy in patients who received noncurative resection in conversion surgery (n = 4) vs. only chemotherapy (n = 114) (p = 0.642). (e) After propensity score matching, comparison of OS after chemotherapy in patients who received conversion surgery (n = 26) vs. only chemotherapy (n = 52) after propensity score matching (p < 0.001). (f) After propensity score matching, comparison of OS after chemotherapy in patients who received conversion surgery (n = 26) vs. subgroup of patients with tumor response of 5.1 or more months after propensity score matching (n = 31) (p = 0.002).
Figure 2
Figure 2 Consort diagram of the study.
Figure 3
Figure 3 Tissue microarray (TMA) core of the cancer dormancy markers. (a) Negative expression of the NR2F1. (b) Positive expression of the NR2F1. (c) Negative expression of the NANOG. (d) Positive expression of the NANOG. (e) Negative expression of the MIG6. (f) Positive expression of the MIG6. (g) Negative expression of the PERK. (h) Positive expression of the PERK.

그림 출처: PubMed Central 공개 논문 (PMC7016667)

Conflict of interest statement

There is no conflict of interest to disclose.

그 밖의 정보
출판 형태
Journal Article
저널
Cancers · ISSN 2072-6694
전자 출판
2019-12-30
참고문헌
27편