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Sci Rep. 2021;11(1):296.

Prospective evaluation of metabolic intratumoral heterogeneity in patients with advanced gastric cancer receiving palliative chemotherapy.

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제1저자 유신혜, 강서영 · 교신저자 오도연

소속 (6)
  1. Department of Internal Medicine, Seoul National University Hospital, 101 Daehak-ro, Jongno-gu, Seoul, 03080, South Korea.
  2. Department of Nuclear Medicine, Seoul National University Hospital, Seoul, South Korea.
  3. Department of Molecular Medicine and Biopharmaceutical Science, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, South Korea.
  4. Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea.
  5. Department of Internal Medicine, Seoul National University Hospital, 101 Daehak-ro, Jongno-gu, Seoul, 03080, South Korea. ohdoyoun@snu.ac.kr.
  6. Cancer Research Institute, Seoul National University College of Medicine, Seoul, South Korea. ohdoyoun@snu.ac.kr.

Abstract

Although metabolic intratumoral heterogeneity (ITH) gives important value on treatment responses and prognoses, its association with treatment outcomes have not been reported in gastric cancer (GC). We aimed to evaluate temporal changes in metabolic ITH and the associations with treatment responses, progression-free survival (PFS), and overall survival (OS) in advanced GC patients. Eighty-five patients with unresectable, locally advanced, or metastatic GC were prospectively enrolled before the first-line palliative chemotherapy and underwent [18F]FDG PET at baseline (TP1) and the first response follow-up evaluation (TP2). Standardized uptake values (SUVs), volumetric parameters, and textural features were evaluated in primary gastric tumor at TP1 and TP2. Of 85 patients, 44 had partial response, 33 had stable disease, and 8 progressed. From TP1 to TP2, metabolic ITH was significantly reduced (P < 0.01), and the degree of the decrease was greater in responders than in non-responders (P < 0.01). Using multiple Cox regression analyses, a low SUVmax at TP2, a high kurtosis at TP2 and larger decreases in the coefficient of variance were associated with better PFS. A low SUVmax at TP2, larger decreases in the metabolic tumor volume and larger decreased in the energy were associated with better OS. Age older than 60 years and responders also showed better OS. An early reduction in metabolic ITH is useful to predict treatment outcomes in advanced GC patients.

Figures

Figure 1
Figure 1 Flow chart of study participant enrollment.
Figure 2
Figure 2 The percentage of changes in metabolic parameters that relate to best responses: SUVmax (a), CoV (b), MTV (c), compacity (d), entropyHisto (e), energy (f), dissimilarity (g), and coarseness (h). CoVcoefficient of variance, Histohistogram, SUVstandardized uptake value, MTVmetabolic tumor volume.
Figure 3
Figure 3 Kaplan–Meier survival curves for progression-free survival according to SUVmax at TP2 (a) and the percent change in CoV (b). SUVstandardized uptake value, CoVcoefficient of variance;
Figure 4
Figure 4 Kaplan–Meier survival curves for overall survival according to the SUVmax at TP2 (a) and percent change in MTV (b). SUVstandardized uptake value, MTVmetabolic tumor volume.
Figure 5
Figure 5 Representative cases showing clinical significance of metabolic ITH changes from [18F]FDG-PET-CT. Case (a) is a 74-year-old male patient with PFS of 19.5 months and OS of 19.8 months. The histogram and AUC-CSH showed decreased metabolic ITH after palliative chemotherapy. Case (b) is a 72-year-old male patient with PFS of 1.1 months and OS of 2.3 months, suggesting very poor prognosis. The histogram and AUC-CSH represent no significant change of metabolic ITH after palliative chemotherapy. AUC-CSHarea under the curve of the cumulative standardized uptake value volume histogram, [18F]FDG-PET-CT[18F]fluoro-2-deoxy-d-glucose positron emission tomography-computed tomography, ITHintratumoral heterogeneity, OSoverall survival, PFSprogression free survival, ROIregion of interest.

그림 출처: PubMed Central 공개 논문 (PMC7804009)

Conflict of interest statement

The authors declare no competing interests.

그 밖의 정보
출판 형태
Journal Article, Research Support, Non-U.S. Gov't
저널
Scientific reports · eISSN 2045-2322
전자 출판
2021-01-12
MeSH
Adult · Aged · Aged, 80 and over · Drug Therapy · Female · Fluorodeoxyglucose F18 / pharmacokinetics · Humans · Kaplan-Meier Estimate · Male · Middle Aged · Palliative Care* · Positron Emission Tomography Computed Tomography · Prospective Studies · Radiopharmaceuticals / pharmacokinetics · Stomach Neoplasms / diagnostic imaging / drug therapy / metabolism / pathology · Treatment Outcome · Tumor Burden / drug effects / physiology · Tumor Microenvironment / drug effects / physiology
Substances
Radiopharmaceuticals · Fluorodeoxyglucose F18
참고문헌
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