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Nuclear Medicine and Molecular Imaging

, Volume 51, Issue 2, pp 147–153 | Cite as

Comparison of Quantitative Methods on FDG PET/CT for Treatment Response Evaluation of Metastatic Colorectal Cancer

  • Ji-In Bang
  • Yoojoo Lim
  • Jin Chul PaengEmail author
  • Sae-Won HanEmail author
  • Sohyun Park
  • Jung Min Lee
  • Hyun Joo Kim
  • Gi Jeong Cheon
  • Dong Soo Lee
  • June-Key Chung
  • Tae-You Kim
  • Keon Wook Kang
Original Article

Abstract

Purpose

FDG PET is effective in treatment response evaluation of cancer. However, there is no standard method for quantitative evaluation of FDG PET, particularly regarding cytostatic drugs. We compared various FDG PET quantitative methods in terms of response determination.

Methods

A total of 39 refractory metastatic colorectal cancer patients who received a multikinase inhibitor treatment were included. Baseline and posttreatment FDG PET/CT scans were performed before and two cycles after treatment. Standardized uptake value (SUV) and total lesion glycolysis (TLG) values using various margin thresholds (30–70 % of maximum SUV with increment 10 %, twice mean SUV of blood pool, SUV 3.0, and SUV 4.0) were measured, with measurement target of the hottest lesion or a maximum of five hottest lesions. Treatment response by the PERCIST criteria was also determined. Predictive values of the PET indexes were evaluated in terms of the treatment response determined by the RECIST 1.1 criteria.

Results

The agreement rate was 38 % between response determined by the PERCIST and the RECIST criteria (κ = 0.381). When patients were classified into disease control group (PR, SD) and non-control group (PD) by the RECIST criteria, percent changes of TLG with various margin thresholds (particularly, 30–50 % of maximum SUV) exhibited significant differences between the two groups, and high diagnostic power for the response by the RECIST criteria. TLG-based criteria, which used a margin threshold of 50 % of maximum SUV, exhibited a high agreement with the RECIST criteria compared with the PERCIST criteria (κ = 0.606).

Conclusion

In metastatic colorectal cancer, FDG PET/CT could be effective for treatment response evaluation by using TLG measured by margin thresholds of 30–50 % of maximum SUV. Further studies are warranted regarding the optimal cutoff values for this method.

Keywords

Colorectal neoplasm Fluorodeoxyglucose F18 Positron-emission tomography Therapy 

Notes

Acknowledgments

This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (009–0093820).

Compliance with Ethical Standards

Conflict of Interest

Ji-In Bang, Yoojoo Lim, Jin Chul Paeng, Sae-Won Han, Sohyun Park, Jung Min Lee, Hyun Joo Kim, Gi Jeong Cheon, Dong Soo Lee, June-Key Chung, Tae-You Kim, and Keon Wook Kang declare that they have no conflict of interest.

Ethical Approval

All procedures followed were performed in accordance with the ethical standards of the responsible committee on human experimentation and with the Helsinki Declaration of 1975, as revised in 2013. The study design of the prospective clinical tiral was approved by the Institutional Review Board of the Seoul National University Hospital and all subjects in the study gave written informed consent (IRB number: 1307-144-507). The study design of the retrospective analysis and exemption of informed consent were approved by the Institutional Review Board of the Seoul National University Hospital (H-1605-063-761).

This manuscript has not been published before or is not under consideration for publication anywhere else and has been approved by all co-authors.

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Copyright information

© Korean Society of Nuclear Medicine 2016

Authors and Affiliations

  • Ji-In Bang
    • 1
  • Yoojoo Lim
    • 2
  • Jin Chul Paeng
    • 1
    Email author
  • Sae-Won Han
    • 2
    Email author
  • Sohyun Park
    • 1
  • Jung Min Lee
    • 1
  • Hyun Joo Kim
    • 1
  • Gi Jeong Cheon
    • 1
  • Dong Soo Lee
    • 1
  • June-Key Chung
    • 1
  • Tae-You Kim
    • 2
  • Keon Wook Kang
    • 1
  1. 1.Department of Nuclear MedicineSeoul National University HospitalSeoulKorea
  2. 2.Department of Internal MedicineSeoul National University HospitalSeoulKorea

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