FDG metabolic parameter-based models for predicting recurrence after upfront surgery in synchronous colorectal cancer liver metastasis
Creators
- Lee, Hyo Sang1
- Kwon, Hyun Woo2
- Kim, Hyun Joo2
- Kim, Sungeun2
- Lim, Seok-Byung3
- Kim, Jin Cheon3
- Yu, Chang Sik3
- Hong, Yong Sang4
- Kim, Tae Won4
- Oh, Minyoung5
- Han, Sangwon5
- Kim, Jae Seung5
- Oh, Jae Hwan6
- Park, Sohyun7
- Kim, Tae-Sung7
- Kim, Seok-ki7
- Kwak, Jae Young8
- Oh, Ho-Suk9
- Kwak, Jung-Myun10
- Lee, Ji Sung11
- 1. Department of Nuclear Medicine, GangNeung Asan Hospital, University of Ulsan College of Medicine, 38 Bangdong-gil, Sacheon-myeon, 25440, Gangneung-si, Gangwon-do (Korea, Republic of)
- 2. Department of Nuclear Medicine, Korea University College of Medicine, Seoul (Korea, Republic of)
- 3. Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul (Korea, Republic of)
- 4. Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul (Korea, Republic of)
- 5. Department of Nuclear Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul (Korea, Republic of)
- 6. Center for Colorectal Cancer, Research Institute and Hospital, National Cancer Center, Goyang (Korea, Republic of)
- 7. Department of Nuclear Medicine, Research Institute and Hospital, National Cancer Center, Goyang (Korea, Republic of)
- 8. Department of Surgery, GangNeung Asan Hospital, University of Ulsan College of Medicine, Gangneung (Korea, Republic of)
- 9. Division of Hemato-oncology in the Department of Internal Medicine, GangNeung Asan Hospital, University of Ulsan College of Medicine, Gangneung (Korea, Republic of)
- 10. Department of Surgery, Korea University College of Medicine, Seoul (Korea, Republic of)
- 11. Clinical Research Center in the Asan Institute for Life Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul (Korea, Republic of)
Description
This study aimed to develop and validate post- and preoperative models for predicting recurrence after curative-intent surgery using an FDG PET-CT metabolic parameter to improve the prognosis of patients with synchronous colorectal cancer liver metastasis (SCLM). In this retrospective multicenter study, consecutive patients with resectable SCLM underwent upfront surgery between 2006 and 2015 (development cohort) and between 2006 and 2017 (validation cohort). In the development cohort, we developed and internally validated the post- and preoperative models using multivariable Cox regression with an FDG metabolic parameter (metastasis-to-primary-tumor uptake ratio [M/P ratio]) and clinicopathological variables as predictors. In the validation cohort, the models were externally validated for discrimination, calibration, and clinical usefulness. Model performance was compared with that of Fong's clinical risk score (FCRS). A total of 374 patients (59.1 ± 10.5 years, 254 men) belonged in the development cohort and 151 (60.3 ± 12.0 years, 94 men) in the validation cohort. The M/P ratio and nine clinicopathological predictors were included in the models. Both postoperative and preoperative models showed significantly higher discrimination than FCRS (p < .05) in the external validation (time-dependent AUC = 0.76 [95% CI 0.68-0.84] and 0.76 [0.68-0.84] vs. 0.65 [0.57-0.74], respectively). Calibration plots and decision curve analysis demonstrated that both models were well calibrated and clinically useful. The developed models are presented as a web-based calculator (https://cpmodel.shinyapps.io/SCLM/) and nomograms. FDG metabolic parameter-based prognostic models are well-calibrated recurrence prediction models with good discriminative power. They can be used for accurate risk stratification in patients with SCLM. In this multicenter study, we developed and validated prediction models for recurrence in patients with resectable synchronous colorectal cancer liver metastasis using a metabolic parameter from FDG PET-CT. The developed models showed good predictive performance on external validation, significantly exceeding that of a pre-existing model. The models may be utilized for accurate patient risk stratification, thereby aiding in therapeutic decision-making.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00330-022-09141-3Additional details
Identifiers
Publishing Information
- Journal Title
- European Radiology (Internet)
- Journal Volume
- 33
- Journal Issue
- 3
- Journal Page Range
- p. 1746-1756
- ISSN
- 1432-1084
- CODEN
- EURAE3
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 54032634
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CALCULATORS; CALIBRATION; CARCINOMAS; COMPARATIVE EVALUATIONS; DATA COMPILATION; DECISION MAKING; FLUORINE 18; FLUORODEOXYGLUCOSE; LIVER; METABOLISM; METASTASES; NOMOGRAMS; POSITRON COMPUTED TOMOGRAPHY; RADIOPHARMACEUTICALS; RECTUM; SURGERY; SURVIVAL CURVES; TIME DEPENDENCE; UPTAKE; VALIDATION
- Descriptors DEC
- ANTIMETABOLITES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; COMPUTERIZED TOMOGRAPHY; COMPUTERS; DATA; DATA PROCESSING; DIAGNOSTIC TECHNIQUES; DIAGRAMS; DIGESTIVE SYSTEM; DIGITAL COMPUTERS; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; EVALUATION; FLUORINE ISOTOPES; GASTROINTESTINAL TRACT; GLANDS; HOURS LIVING RADIOISOTOPES; INFORMATION; INTESTINES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LARGE INTESTINE; LIGHT NUCLEI; MATERIALS; MEDICINE; NANOSECONDS LIVING RADIOISOTOPES; NEOPLASMS; NUCLEI; ODD-ODD NUCLEI; ORGANS; PROCESSING; RADIOACTIVE MATERIALS; RADIOISOTOPES; TESTING; TOMOGRAPHY