| Home | E-Submission | Sitemap | Editorial Office
top_img
Clin Endosc > Volume 51(3); 2018 > Article
Chhoda, Jain, Surabhi, and Singhal: Contrast Enhanced Harmonic Endoscopic Ultrasound: A Novel Approach for Diagnosis and Management of Gastrointestinal Stromal Tumors

Abstract

The histologic analysis of gastrointestinal stromal tumors (GISTs) is a common method to detect the mitotic activity and to subsequently determine the risk of GISTs for malignancy. The potential false negative error due to inadequate yield of specimens and actual determination of malignancy risk requires analysis of the whole tumor. We aimed to assess the role of contrast enhanced endoscopic ultrasound (CE-EUS) in the management of GISTs. Two authors individually did review of English literatures to identify nine peer-reviewed original articles using keywords- contrast endoscopic ultrasound, GIST and submucosal tumor. Studies were heterogeneous in their aims looking either at differentiating submucosal lesions from GISTs, estimating malignant potential of GISTs with histologic correlation or studying the role of angiogenesis in malignant risk stratification. CE-EUS had moderate to high efficacy in differentiating GISTs from alternative submucosal tumors. CE-EUS had a higher sensitivity than EUS-guided fine needle aspiration, contrast computed tomography and Doppler EUS for detection of neo-vascularity within the GISTs. However, the evidence of abnormal angiogenesis within GIST as a prognostic factor needs further validation. CE-EUS is a non-invasive modality, which can help differentiate GISTs and provide valuable assessment of their perfusion patterns to allow better prediction of their malignant potential but more experience is needed.

INTRODUCTION

Gastrointestinal stromal tumors (GISTs) are mesenchymal tumors originating from interstitial cells of Cajal within the gastrointestinal (GI) tract. They constitute the majority of mesenchymal tumors worldwide with annual incidence of 11–14 per 1,000,000 persons [1,2]. They have variable presentation and many of them are asymptomatic, detected incidentally on routine procedures and imaging. Even though only 10%–30% of these lesions are malignant, all of them have malignant potential [3]. It is important to distinguish GIST from other submucosal tumors and to assess their malignant risk to allow appropriate use of drugs like imatinib, sunitinib and other anti-vascular endothelial growth factor (VEGF) medication as a pre-surgical neo-adjuvant therapy [4]. As a predictive tool, Fletchers classification has been used to determine the risk for malignancy among GIST patients [5]. However, in a pre-operative setting this score has limited utility since whole tumor needs to be resected for determination of mitotic count.
A method of choice for diagnosis, endoscopic ultrasound (EUS) provides good spatial resolution in imaging of upper GI lesions and also guides in acquisition of biopsy specimen. It has been used to distinguish GISTs from submucosal tumors and determine its malignant potential [6]. However, it has a limited role in this regard and is based on subtle differences in the shape, echogenicity and homogeneity [7,8]. Among all the characteristics, abnormal blood vessel have a major role in distinguishing GISTs from other submucosal lesions and also in prediction of malignant risk.
Contrast enhanced harmonic (CEH) imaging has evolved to differentiate GISTs from other submucosal tumors and to assess abnormal angiogenesis within the tumors.
In this article we review the principles of CEH imaging, and evaluate its role in accurate diagnosis of GISTs and prediction of their malignant potential.

PRINCIPLE OF CONTRAST ENHANCED HARMONIC IMAGING

CEH imaging is based on nonlinear acoustic response of tissue or micro-bubble to US signal. The nonlinear response means that on insonation, the resultant signals include sum of insonated frequency and integer multiple (n=1,2,3…) of transmitted frequency, known as harmonics. Received signal when twice of transmission frequency is called as second harmonic [9-11]. For example, transmit at 3 Mhz and receive at 6 Mhz. The higher frequency and the one-way travel of returning signal leads to better resolution of final images. Over the past decade, there has been advent of ultrasound transducers with wider bandwidth and optimal acoustic power. This is coupled with contrast agents, which comprises infusion of air filled micro-bubbles surrounded by surface-active substance. On US insonation micro-bubble contracts and relaxes in response to pressure waves. The mechanical index (MI) is a unitless number calculated by dividing the peak negative pressure (MPascal) by the square root of transmission frequency (Mhz). At low MI the micro-bubbles behave linearly, while in medium range (0.1–0.6) they have asymmetrical expansion and at MI >0.6 they have transient nonlinear scattering followed by micro-bubble destruction [9-11]. Thus while tissues have linear response to insonation at low MI, micro-bubbles produce optimal backscattering of acoustic signals and improve detectability of smaller blood vessels [12].
In harmonic imaging common modalities are utilized like:
Contrast harmonic Doppler US: It is beneficial in detection of blood flow, depending on fast blood flow within the tumor vessels [13]. It has limited role among smaller blood vessels with slower blood flow and is limited by artifacts like over-painting, blooming and flash artifacts from movement of tissues.
Contrast phase inversion mode: This modality (HITACHI system) includes imaging via 2 waves wherein one is inverted as compared to other and thereby linear response will sum up to zero output. But the nonlinear response of micro-bubbles will not be inverted and will add up to produce intense signals as compared to tissues [12-14]. Despite this the system is not able to filter out the nonlinear response from tissues.
Extended Pure Harmonic Detection: In this system (ALOKA system) the signals from micro-bubbles have higher amplitude and phase shift than those from the tissues. The signals from the tissues are filtered out and the machine receives only the signals from the micro-bubbles in the vasculature [15,16]. This gives an accurate estimate of vascularity even among lesions with vascular supply with slow flow.

LITERATURE SEARCH

Materials and methods

Two authors individually did review of English literatures from inception through May, 2017. PubMed and Google scholar were used to identify the peer reviewed original and review articles using keywords- contrast endoscopic ultrasound; GIST; submucosal tumor. The references of pertinent studies were manually searched to identify additional relevant studies. The indication, procedural details, clinical outcomes, complications and limitations were reviewed for each study.

Results

We selected nine original studies to be included in this review article; one of them was a prelim study [16], while rest of them were observational human studies [15,17-23]. Most of the studies are from Asia and Europe and were mostly retrospective and observational. The studies aimed at differentiating submucosal lesions from GISTs [18,19,23], estimating malignant potential of GISTs with histologic correlation [17,20,22,23] and studying the role of angiogenesis in malignant risk stratification [21,22].

Prelim study

A study by Kitano et al. revealed the utility of prototype curved endoscope with wide bandwidth transducer in visualization of GI organs post intravenous contrast infusion among in vivo experimental dog subjects (n=12) and evaluation of vascular defects artificially created with radiofrequency ablation in pancreatic tissue (n=6) along with histologic correlation [16]. This was also clinically applied to 2 human patients one of whom had GIST lesion revealing diffuse blood vessels.

Human studies

Patient characteristics

Eight observational human studies included a total of 175 GIST patients [15,17-23]. There was symmetric gender distribution (Male-60 vs. Female-65) among six studies [17-23]. While the inclusion criteria was suspected submucosal lesion and suspected or histologically proven GISTs, the exclusion criteria included morphologic confounders like esophageal varices, extrinsic compressions, lipomas, cysts and/or adenocarcinomas on histology post resection [20]. It also included demographic characters i.e. age <18 years, pregnancy, lactation, severe heart failure, severe chronic obstructive lung disease, or, known allergic disposition [17,19].

Technique

All the studies included routine EUS for localization of sub-epithelial lesions and injecting second-generation contrast agents to define the lesions. The study by Kitano et al. investigated the role of CEH-EUS in perfusion imaging of pancreatic lesions (n=27; lesions=32) [16]. It initially delineated optimal settings for imaging resulting in MI of 0.4 and frame interval of 2 seconds in intermittent imaging and 0.6 MHz in continuous imaging. Furthermore 2 GIST lesions were visualized to reveal diffuse rich vascularity on real time imaging. The image settings and contrast agents utilized are described in the Table 1. The images were obtained in the early arterial phase post injection of contrast material. The sub-epithelial lesions were characterized mostly on the basis of their size and localization of abnormal intra-tumor vessels and additional factors such as necrotic center. They underwent histologic review post acquisition via EUS-guided fine needle aspiration (FNA), trucut biopsy and/or surgical resection. Histologic review were analyzed mostly via hematoxylin and eosin stain while immune-histo-chemisty for C-kit, DESMIN, S-100, CD-34 and DOG was done in certain studies [21]. Only 2 studies utilized marker for angiogenesis (factor VIII and VEGF) for histologic correlation of abnormal vascular structures appreciated in contrast EUS studies [21,22].

Safety

In all the studies contrast agent was well tolerated and there were no adverse events [16-23]. Bleeding was spontaneous in 1 patient [19], but was biopsy-related in 6 patients [19,20]. Endoscopic clipping and fibrin glue injection successfully managed them.

Procedural time

This has been discreetly mentioned only in a few manuscripts and the time for the procedure was not significantly increased due to additional perfusion studies [22].

Outcomes

The study outcomes included accuracy in distinguishing GISTs from submucosal tumor, grading the malignant risk of GIST lesions and histologic correlation of abnormal angiogenesis. The sensitivity and specificity of CEH-EUS in differentiating GISTS from subepithelial tumors ranged from 53.8% to 100% [18,19,23]. In differentiating low-grade from high-grade malignancy, the range of sensitivity, specificity and accuracy were 75%–100%, 63%–100% and 83%–98% respectively [17,20,23]. Yamashita et al. investigated role of visualization of abnormal intra-tumor blood vessel on CEH-EUS and found significant correlation with VEGF expression (p<0.005) [22]. There was also higher proportion of high-grade malignancy in CEH-EUS positive for neovascularization, which on histologic review revealed large vessels deficient in elastic fibers. Fukuta et al. compared vessel density (vessel count/mm2) among “Poor” (11.0 +/– 1.6/mm2) and “Rich” pattern GISTs (26.7 +/– 3.7/mm2) as visualized on contrast EUS and found significant difference (p<0.01) [21]. In the study by Park et al., the non-enhancing spots were significantly higher among high-grade malignancy as compared to low-grade malignancy (p<0.022) and there was no significant difference in the presence of irregular vessels or heterogeneous perfusion on CEH-EUS [23]. Besides the above, presence of a necrotic center, avascular core and contrast agent arrival time (AAT) were also investigated [18,20]. Sakamoto et al. reported the presence of necrotic center within the lesion as a marker for high-grade malignant lesion (p<0.05) [20]. Contrast AAT was significantly different in GIST as compared to benign lesions per Kannengiesser et al., but it had no role in differentiating benign from malignant lesions [17,19].
CEH-EUS was compared with other modalities in few studies [20,21]. Contrast enhanced computed tomography (CT) failed to demonstrate any neovascularization in study by Fukuta et al. [21] Its sensitivity for detection of blood vessels was 0% in small lesions (<3 cm) and 42% in in large lesions (>3 cm) in the study by Sakamoto et al. [20] In this study EUS-FNA was demonstrated to have sensitivity, specificity and overall accuracy of 92%, 62% and 81% for diagnosis of high-grade malignancy against that of CEH-EUS -100%, 63% and 83%, respectively. Sensitivities with which CEH-EUS and contrast enhanced-CT detected intra-tumor vessels in smaller (<3 cm) high-grade malignancy GISTs were 25%, and 0%, respectively, whereas those values for larger (>3 cm) high-grade malignancy GISTs were 75%, and 42%, respectively.
Figs. 1 to 9 depicts endoscopic, CT with contrast, EUS with Doppler and contrast enhanced US images of a 3 cm submucosal GIST with low malignant risk (based on NIH consensus criteria).

CONCLUSIONS

In conclusion contrast enhanced EUS is a non-invasive modality with valuable assessment of perfusion patterns of GISTs and submucosal tumors. It has a higher sensitivity than EUS–FNA, contrast CT and Doppler EUS for detection of neo-vascularity. The evidence of abnormal angiogenesis within GISTs as a prognostic factor however needs to be evaluated with prospective studies with greater sample size and follow-up periods.

NOTES

Conflicts of Interest:The authors have no financial conflicts of interest.

Fig. 1.
Endoscopic view of submucosal tumor.
ce-2017-170f1.tif
Fig. 2.
Contrast enhanced computed tomography axial image showing a well-circumscribed submucosal lesion along the lesser curvature of the stomach without necrosis.
ce-2017-170f2.tif
Fig. 3.
Endoscopic ultrasound with Doppler showing vascular flow.
ce-2017-170f3.tif
Fig. 4.
Contrast enhanced harmonic endoscopic ultrasound dual image at the start of contrast administration- left image representing contrast image and the right image representing a tissue image.
ce-2017-170f4.tif
Fig. 5.
Contrast enhanced harmonic endoscopic ultrasound images immediately after contrast administration- neo-vascularity (red arrow) in the submucosal lesion.
ce-2017-170f5.tif
Fig. 6.
Contrast enhanced harmonic endoscopic ultrasound images at 30 seconds after contrast administration- intense enhancement of the submucosal lesion.
ce-2017-170f6.tif
Fig. 7.
Contrast enhanced harmonic endoscopic ultrasound images at 39 seconds after contrast administration- further enhancement of the submucosal lesion.
ce-2017-170f7.tif
Fig. 8.
Contrast enhanced harmonic endoscopic ultrasound images depicting focal area of necrosis within the submucosal lesion.
ce-2017-170f8.tif
Fig. 9.
Contrast enhanced harmonic endoscopic ultrasound images at 60 seconds after contrast administration- washout of the submucosal lesion.
ce-2017-170f9.tif
Table 1.
Descriptive Summary of Individual Studies
Study Aim of study Number of subjects Gender distribution Mean age (yr) Location of lesion Diameter of lesion Diagnostic modality Contrast agent Diagnostic test performance Complication
Kitano et al. (2008) [15], Japan Prelim study Human- 2 N/A N/A N/A N/A Imaging mode: extended pure harmonic detection mode Sonovue (2 mL) Visualization of 2 GIST with rich vasculature None
Mechanical index: 0.4
Frequency: 6 Hz
Kitano et al. (2008) [16], Germany and Japan Prelim study Animal (Dog)- 12 Humans- 2 (GIST- 1, pancreatic cancer- 1) N/A N/A N/A N/A Imaging mode: extended pure harmonic detection mode Definity Sonovue (2mL) Visualization of 1 GIST lesion with rich vasculature None
Mechanical index: 0.35-0.40
Frequency: 7.5 MHz
Zhao et al. (2016) [17], China - Grade malignant potential Human-18 1. Very Low grade and low grade- 1. Very Low-grade and low-grade-51.5±10.0 1. Gastric-18 1. Very Low-grade and low-grade-14.6±5.8 mm Imaging mode: extended pure harmonic detection mode Sonovue (59 mg/5 mL) Grade malignant potential: None
M- 6 2. Intermediate and high-grade-58.9±14.1 2. Intermediate and high-grade-33.4±10.6 mm Mechanical index: 0.25 Hyper-enhancement onCEH-EUS:
F- 4 Frequency: 4.7 MHz 1. Sensitivity- 75%
2. Intermediate and high grade- 2. Specificity-100%
M-5 3. PPV- 33%
F-3 4.NPV-100%
Ignee et al. (2017) [18], Romania, China and Germany - Differentiation of GIST from SMT Human- 57 N/A N/A 1. Gastric- 39 N/A Imaging mode: extended pure harmonic detection mode Sonovue (4.5 mL) Differentiation of GIST from SMT: None
2. Intestine- 17 hyper-enhancement on CEH-EUS:
3. Extra-intestinal- 1 1. Sensitivity- 98%
2. Specificity-100%
3. PPV-100%
4.NPV-93%
5. Accuracy- 98%
Kannengiesser et al. (2012) [19], Germany - Differentiation of GIST from SMT Human-17 M-9 69±12.0 N/A 1. GIST-25.4±18.6 mm Imaging mode: extended pure harmonic detection mode Sonovue (2 mL) Differentiation of GIST from SMT: 1. Bleeding-
F-8 2. Benign lesions-23.8±7.5 mm Hyper-enhanced lesion-100% accuracy a) Spontaneous-1
b) Secondary to biopsy- 5
Sakamoto et al. (2011) [20], Japan - Grade malignant potential Human-29 1. Low-grade- 1. Low grade-61.7 1. Low-grade-stomach- 11 duodenum- 2 1. Low-grade-2.9±2.1 cm (range, 1.1-5) Imaging mode: extended pure harmonic detection mode Sonazoid (15 μL/kg) Grade malignant potential: 1. Bleeding-a) Secondary to fine needle aspiration-1
- Differentiation of GIST from SMT M- 6 2. High grade-64.5 2. High-grade-stomach- 11 duodenum- 5
F-7 2. High-grade-3.2±2.5 cm (range, 2-12.1) Mechanical index: abnormal vessel visualization
2. High-grade- Frequency: 4.7 MHz
M- 6 1. Sensitivity- 100%
F-10 2. Specificity- 63%
3. Accuracy- 83%
Fukuta et al. (2005) [21], Japan - Histologic correlation of perfusion imaging Human- 0 M-4 64.7 1. Gastric- 8 N/A Imaging mode: contrast enhanced coded phase inversion harmonic US Levovist (2-5 g) Histologic correlation of perfusion imaging: None
- Grade malignant potential F-9 2. Duodenum- 3 Mechanical index: 0.6-0.8 Vessel density:
3. Jejunum-1 Frequency: 2-4 Hz 11.0 +/- 1.6/mm2poor versus 26.7 +/- 3.7/mm2 (p<0.0l)
4. Ileum-1 Grade malignant potential:
NPV-100%
PPV- 87.5%
Yamashita et al. (2015) [22], Japan - Histologic correlation of perfusion imaging Human-13 M- 6 68.2 1. Gastric-12 3.0 cm (range, 1.3-11) Imaging mode: extended pure harmonic detection mode Sonazoid (0.7 mL) Histologic correlation of perfusion imaging: None
- Grade malignant potential F-7 2. Duodenal-1 Mechanical index: 0.35 abnormal perfusion image correlation with histology and VEGF expression (p=0.005)
Frequency: 4.7 MHz Grade malignant potential:
NPV-100%
PPV- 83.3% (p=0.005)
Park et al. (2016) [23], Korea - Grade malignant potential Human- 35 M-18 56.9±11.9 1. Esophagus- 3 32.5±12.5 mm Imaging mode: extended pure harmonic detection mode Sonovue (2.4 mL) Grade malignant potential: None
- Differentiation of GIST from SMT GIST- 26 F-17 2. Gastric- 26 Mechanical index: 0.17 Sensitivity-18.2%
3. Duodenum- 3 Specificity- 73.3%
4. Rectum- 3 PPV- 33.3%
NPV- 55.0%
Accuracy- 42.9%
Differentiation of GIST from S.E.L.:
Sensitivity- 23.1%
Specificity-100%
PPV-100%
NPV- 55.0%
Accuracy- 50.0%

N/A, not available; GIST, gastrointestinal stromal tumor; CEH-EUS, contrast enhanced harmonic endoscopic ultrasound; PPV, positive predictive value; NPV, negative predictive value; SMT, submucosal tumor; VEGF, vascular endothelial growth factor; S.E.L, subepithelial lesion.

REFERENCES

1. Kim KM, Kang DW, Moon WS, et al. Gastrointestinal stromal tumors in Koreans: it’s incidence and the clinical, pathologic and immunohistochemical findings. J Korean Med Sci 2005;20:977-984.
crossref pmid pmc
2. Goettsch WG, Bos SD, Breekveldt-Postma N, Casparie M, Herings RM, Hogendoorn PC. Incidence of gastrointestinal stromal tumours is underestimated: results of a nation-wide study. Eur J Cancer 2005;41:2868-2872.
crossref pmid
3. Croom KF, Perry CM. Imatinib mesylate: in the treatment of gastrointestinal stromal tumours. Drugs 2003;63:513-522 discussion 523-524.
crossref pmid
4. Rammohan A, Sathyanesan J, Rajendran K, et al. A gist of gastrointestinal stromal tumors: a review. World J Gastrointest Oncol 2013;5:102-112.
crossref pmid pmc
5. Fletcher CD, Berman JJ, Corless C, et al. Diagnosis of gastrointestinal stromal tumors: a consensus approach. Int J Surg Pathol 2002;10:81-89.
crossref pmid
6. Chak A, Canto MI, Rösch T, et al. Endosonographic differentiation of benign and malignant stromal cell tumors. Gastrointest Endosc 1997;45:468-473.
crossref pmid
7. Kim GH, Kim KB, Lee SH, et al. Digital image analysis of endoscopic ultrasonography is helpful in diagnosing gastric mesenchymal tumors. BMC Gastroenterol 2014;14:7.
crossref pmid pmc pdf
8. Kim GH, Park DY, Kim S, et al. Is it possible to differentiate gastric GISTs from gastric leiomyomas by EUS? World J Gastroenterol 2009;15:3376-3381.
crossref pmid pmc
9. Desser TS, Jeffrey RB. Tissue harmonic imaging techniques: physical principles and clinical applications. Semin Ultrasound CT MR 2001;22:1-10.
crossref pmid
10. Kollmann C. New sonographic techniques for harmonic imaging--underlying physical principles. Eur J Radiol 2007;64:164-172.
crossref pmid
11. Sanchez MV, Varadarajulu S, Napoleon B. EUS contrast agents: what is available, how do they work, and are they effective? Gastrointest Endosc 2009;69(2 Suppl):S71-S77.
crossref pmid
12. Săftoiu A, Dietrich CF, Vilmann P. Contrast-enhanced harmonic endoscopic ultrasound. Endoscopy 2012;44:612-617.
crossref pmid pdf
13. Wilson SR, Greenbaum LD, Goldberg BB. Contrast-enhanced ultrasound: what is the evidence and what are the obstacles? AJR Am J Roentgenol 2009;193:55-60.
crossref pmid
14. Unnikrishnan S, Klibanov AL. Microbubbles as ultrasound contrast agents for molecular imaging: preparation and application. AJR Am J Roentgenol 2012;199:292-299.
crossref pmid
15. Kitano M, Sakamoto H, Matsui U, et al. A novel perfusion imaging technique of the pancreas: contrast-enhanced harmonic EUS (with video). Gastrointest Endosc 2008;67:141-150.
crossref pmid
16. Kitano M, Kudo M, Sakamoto H, et al. Preliminary study of contrast-enhanced harmonic endosonography with second-generation contrast agents. J Med Ultrason (2001) 2008;35:11-18.
crossref pmid
17. Zhao Y, Qian L, Li P, Zhang S. The diagnostic value of endoscopic ultrasonography and contrast-enhanced harmonic endoscopic ultrasonography in gastrointestinal stromal tumors. Endosc Ultrasound 2016;5:111-117.
crossref pmid pmc
18. Ignee A, Jenssen C, Hocke M, et al. Contrast-enhanced (endoscopic) ultrasound and endoscopic ultrasound elastography in gastrointestinal stromal tumors. Endosc Ultrasound 2017;6:55-60.
crossref pmid pmc
19. Kannengiesser K, Mahlke R, Petersen F, et al. Contrast-enhanced harmonic endoscopic ultrasound is able to discriminate benign submucosal lesions from gastrointestinal stromal tumors. Scand J Gastroenterol 2012;47:1515-1520.
crossref pmid
20. Sakamoto H, Kitano M, Matsui S, et al. Estimation of malignant potential of GI stromal tumors by contrast-enhanced harmonic EUS (with videos). Gastrointest Endosc 2011;73:227-237.
crossref pmid
21. Fukuta N, Kitano M, Maekawa K, Chikugo T, Kudo M. Estimation of the malignant potential of gastrointestinal stromal tumors: the value of contrast-enhanced coded phase-inversion harmonics US. J Gastroenterol 2005;40:247-255.
crossref pmid
22. Yamashita Y, Kato J, Ueda K, et al. Contrast-enhanced endoscopic ultrasonography can predict a higher malignant potential of gastrointestinal stromal tumors by visualizing large newly formed vessels. J Clin Ultrasound 2015;43:89-97.
crossref pmid
23. Park HY, Jeon SW, Lee HS, et al. Can contrast-enhanced harmonic endosonography predict malignancy risk in gastrointestinal subepithelial tumors? Endosc Ultrasound 2016;5:384-389.
crossref pmid pmc
Editorial Office
Korean Society of Gastrointestinal Endoscopy
#817, 156 Yanghwa-ro(LG Palace, Donggyo-dong), Mapo-gu, Seoul, 04050, Korea
TEL: +82-2-335-1552   FAX: +82-2-335-2690    E-mail: ksge@gie.or.kr
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Copyright © Korean Society of Gastrointestinal Endoscopy. All rights reserved.