Korean J Radiol.  2019 Mar;20(3):449-458. 10.3348/kjr.2018.0469.

Evaluation of Early Response to Treatment of Hepatocellular Carcinoma with Yttrium-90 Radioembolization Using Quantitative Computed Tomography Analysis

Affiliations
  • 1Department of Radiology, Severance Hospital, Research Institute of Radiological Science and Center for Clinical Imaging Data Science, Yonsei University College of Medicine, Seoul, Korea. gafield2@yuhs.ac
  • 2Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.

Abstract


OBJECTIVE
To identify an imaging predictor for the assessment of early treatment response to yttrium-90 transarterial radioembolization (TARE) in patients with hepatocellular carcinoma (HCC), using a quantitative assessment of dynamic computed tomography (CT) images.
MATERIALS AND METHODS
Dynamic contrast-enhanced CT was obtained pre- and 4 weeks post-TARE in 44 patients (34 men, 10 women; mean age, 60 years) with HCC. Computer software was developed for measuring the percentage increase in the combined delayed-enhancing area and necrotic area (pD + N) and the percentage increase in the necrotic area (pNI) in the tumor-containing segments pre- and post-TARE. Local progression-free survival (PFS) was compared between patient groups using Cox regression and Kaplan-Meier analyses.
RESULTS
Post-TARE HCC with pD + N ≥ 35.5% showed significantly longer PFS than those with pD + N < 35.5% (p = 0.001). The local tumor progression hazard ratio was 17.3 (p = 0.009) for pD + N < 35.5% versus pD + N ≥ 35.5% groups. HCCs with a high pNI tended to have longer PFS, although this difference did not reach statistical significance.
CONCLUSION
HCCs with a larger pD + N are less likely to develop local progression after TARE.

Keyword

Hepatocellular carcinoma; Computed tomography; Treatment outcome; Response; Yttrium radioisotopes; Quantitative analysis

MeSH Terms

Carcinoma, Hepatocellular*
Disease-Free Survival
Female
Humans
Male
Tomography, X-Ray Computed
Treatment Outcome
Yttrium Radioisotopes
Yttrium Radioisotopes

Figure

  • Fig. 1 Flowchart shows inclusion and exclusion criteria for present study.*SIR-Spheres; Sirtex Medical. CT = computed tomography, HCC = hepatocellular carcinoma, TARE = transarterial radioembolization, 90Y = yttrium-90

  • Fig. 2 Serial steps in quantitative measurement of pD + N pre- and post-TARE, pre-treatment images (A–E), post-treatment images (F–J).(A, F) Pre-contrast, (B, G) delayed phase, (C, H) subtraction image from pre-contrast and delayed phase images, (D, I) map of delayed enhancement after removing area below threshold. Freehand-drawn ROI (yellow dot line) was placed along boundary of tumor-containing hepatic segments in map of delayed enhancement (C, H), then software automatically selected same regions in other processed images (D, E, I, J). This ROI was commonly used to measure combined delayed-enhancing area and necrotic area in each map. (E, J) map of non–enhancing area. pD + N = percentage increase in combined delayed-enhancing area and necrotic area, ROI = region of interest

  • Fig. 3 PFS curves according to parameters of quantitative analysis.DAE = largest diameter of arterial enhancing portion, PFS = local progression-free survival, pNI = percentage increase in necrotic area

  • Fig. 4 Liver CT images of 53-year-old woman with HCC before TARE (A–D) and 4 weeks after treatment (E–H).(A, E) Delayed phase, (B, F) subtraction image from pre-contrast and delayed phase images, (C, G) map of delayed enhancement. (D, H) map of necrosis. Measured value of pD + N in tumor-containing segments was 94.9%. Maximal diameter of tumor and maximal DAE in tumor were decreased only 1.9% and 2.1%, respectively. Tumor did not recur until 19 months.


Reference

1. Kennedy A, Coldwell D, Sangro B, Wasan H, Salem R. Integrating radioembolization ((90)Y microspheres) into current treatment options for liver tumors: introduction to the international working group report. Am J Clin Oncol. 2012; 35:81–90. PMID: 20938320.
2. Kennedy A, Nag S, Salem R, Murthy R, McEwan AJ, Nutting C, et al. Recommendations for radioembolization of hepatic malignancies using yttrium-90 microsphere brachytherapy: a consensus panel report from the radioembolization brachytherapy oncology consortium. Int J Radiat Oncol Biol Phys. 2007; 68:13–23. PMID: 17448867.
Article
3. Sangro B, Iñarrairaegui M, Bilbao JI. Radioembolization for hepatocellular carcinoma. J Hepatol. 2012; 56:464–473. PMID: 21816126.
Article
4. Therasse P, Arbuck SG, Eisenhauer EA, Wanders J, Kaplan RS, Rubinstein L, et al. New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada. J Natl Cancer Inst. 2000; 92:205–216. PMID: 10655437.
5. Lencioni R, Llovet JM. Modified RECIST (mRECIST) assessment for hepatocellular carcinoma. Semin Liver Dis. 2010; 30:52–60. PMID: 20175033.
Article
6. Keppke AL, Salem R, Reddy D, Huang J, Jin J, Larson AC, et al. Imaging of hepatocellular carcinoma after treatment with yttrium-90 microspheres. AJR Am J Roentgenol. 2007; 188:768–775. PMID: 17312067.
Article
7. Riaz A, Kulik L, Lewandowski RJ, Ryu RK, Giakoumis Spear G, Mulcahy MF, et al. Radiologic-pathologic correlation of hepatocellular carcinoma treated with internal radiation using yttrium-90 microspheres. Hepatology. 2009; 49:1185–1193. PMID: 19133645.
Article
8. Herfarth KK, Hof H, Bahner ML, Lohr F, Höss A, van Kaick G, et al. Assessment of focal liver reaction by multiphasic CT after stereotactic single-dose radiotherapy of liver tumors. Int J Radiat Oncol Biol Phys. 2003; 57:444–451. PMID: 12957256.
Article
9. Maturen KE, Feng MU, Wasnik AP, Azar SF, Appelman HD, Francis IR, et al. Imaging effects of radiation therapy in the abdomen and pelvis: evaluating "innocent bystander" tissues. Radiographics. 2013; 33:599–619. PMID: 23479716.
Article
10. Gulec SA, Mesoloras G, Stabin M. Dosimetric techniques in 90Y-microsphere therapy of liver cancer: the MIRD equations for dose calculations. J Nucl Med. 2006; 47:1209–1211. PMID: 16818957.
11. Tsuji Y, Takahashi N, Fletcher JG, Hough DM, McMenomy BP, Lewis DM, et al. Subtraction color map of contrast-enhanced and unenhanced CT for the prediction of pancreatic necrosis in early stage of acute pancreatitis. AJR Am J Roentgenol. 2014; 202:W349–W356. PMID: 24660733.
Article
12. Prionas ND, Lindfors KK, Ray S, Huang SY, Beckett LA, Monsky WL, et al. Contrast-enhanced dedicated breast CT: initial clinical experience. Radiology. 2010; 256:714–723. PMID: 20720067.
Article
13. Contal C, O'Quigley J. An application of changepoint methods in studying the effect of age on survival in breast cancer. Computational Statistics & Data Analysis. 1999; 30:253–270.
Article
14. Chen BB, Hsu CY, Yu CW, Hou HA, Liu CY, Wei SY, et al. Dynamic contrast-enhanced MR imaging measurement of vertebral bone marrow perfusion may be indicator of outcome of acute myeloid leukemia patients in remission. Radiology. 2011; 258:821–831. PMID: 21212370.
Article
15. Shrout PE, Fleiss JL. Intraclass correlations: uses in assessing rater reliability. Psychol Bull. 1979; 86:420–428. PMID: 18839484.
Article
16. Büsing KA, Kilian AK, Schaible T, Debus A, Weiss C, Neff KW. Reliability and validity of MR image lung volume measurement in fetuses with congenital diaphragmatic hernia and in vitro lung models. Radiology. 2008; 246:553–561. PMID: 18055874.
Article
17. Wong CY, Salem R, Raman S, Gates VL, Dworkin HJ. Evaluating 90Y-glass microsphere treatment response of unresectable colorectal liver metastases by [18F]FDG PET: a comparison with CT or MRI. Eur J Nucl Med Mol Imaging. 2002; 29:815–820. PMID: 12029557.
18. Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009; 45:228–247. PMID: 19097774.
Article
19. Miller AB, Hoogstraten B, Staquet M, Winkler A. Reporting results of cancer treatment. Cancer. 1981; 47:207–214. PMID: 7459811.
Article
20. Reiner CS, Morsbach F, Sah BR, Puippe G, Schaefer N, Pfammatter T, et al. Early treatment response evaluation after yttrium-90 radioembolization of liver malignancy with CT perfusion. J Vasc Interv Radiol. 2014; 25:747–759. PMID: 24630751.
Article
21. Shim JH, Lee HC, Kim SO, Shin YM, Kim KM, Lim YS, et al. Which response criteria best help predict survival of patients with hepatocellular carcinoma following chemoembolization? A validation study of old and new models. Radiology. 2012; 262:708–718. PMID: 22187634.
Article
22. Li Z, Bonekamp S, Halappa VG, Corona-Villalobos CP, Pawlik T, Bhagat N, et al. Islet cell liver metastases: assessment of volumetric early response with functional MR imaging after transarterial chemoembolization. Radiology. 2012; 264:97–109. PMID: 22627602.
Article
23. Gowdra Halappa V, Corona-Villalobos CP, Bonekamp S, Li Z, Reyes D, Cosgrove D, et al. Neuroendocrine liver metastasis treated by using intraarterial therapy: volumetric functional imaging biomarkers of early tumor response and survival. Radiology. 2013; 266:502–513. PMID: 23192780.
Article
24. Miller FH, Keppke AL, Reddy D, Huang J, Jin J, Mulcahy MF, et al. Response of liver metastases after treatment with yttrium-90 microspheres: role of size, necrosis, and PET. AJR Am J Roentgenol. 2007; 188:776–783. PMID: 17312068.
Article
25. Arslanoglu A, Chalian H, Sodagari F, Seyal AR, Töre HG, Salem R, et al. Threshold for enhancement in treated hepatocellular carcinoma on MDCT: effect on necrosis quantification. AJR Am J Roentgenol. 2016; 206:536–543. PMID: 26901009.
Article
26. Blazic IM, Lilic GB, Gajic MM. Quantitative assessment of rectal cancer response to neoadjuvant combined chemotherapy and radiation therapy: comparison of three methods of positioning region of interest for ADC measurements at diffusion-weighted MR imaging. Radiology. 2017; 282:418–428. PMID: 27253423.
Article
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