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Published online before print October 17, 2002, 10.1148/radiol.2253010886
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(Radiology 2002;225:759-765.)
© RSNA, 2002


Gastrointestinal Imaging

Local Staging of Pancreatic Carcinoma with Multi–Detector Row CT: Use of Curved Planar Reformations—Initial Experience1

Rupert W. Prokesch, MD, Lawrence C. Chow, MD, Christopher F. Beaulieu, MD, PhD, Matilde Nino-Murcia, MD, Robert E. Mindelzun, MD, Roland Bammer, PhD, Jing Huang, MS and R. Brooke Jeffrey, Jr, MD

1 From the Departments of Radiology, Lucas MRS Center (R.W.P., L.C.C., C.F.B., M.N.M., R.E.M., R.B., R.B.J.) and Statistics (J.H.), Stanford University, Calif; and Department of Radiology, Veterans Administration Palo Alto Health Care System, Calif (M.N.M.). Received May 4, 2001; revision requested June 22; final revision received May 8, 2002; accepted May 28. R.W.P. supported by a research grant from the Max Kade Foundation. Address correspondence to R.W.P., Department of Radiology, University of Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria (e-mail: rupert.prokesch@univie.ac.at).


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
PURPOSE: To evaluate the utility of curved planar reformations compared with standard transverse images in the assessment of pancreatic tumors.

MATERIALS AND METHODS: Forty-three patients suspected of having pancreatic tumors underwent contrast material–enhanced biphasic multi–detector row computed tomography (CT). Curved planar reformations were generated along the pancreatic duct, common bile duct, and major mesenteric vessels. Three blinded independent readers assessed the curved planar reformations and transverse images separately for the presence of tumor, resectability, and vascular involvement. The results were compared with those of a consensus panel who evaluated the curved planar reformations and transverse images together along with clinical data and surgical findings.

RESULTS: Of 43 patients, 20 had pancreatic malignancies as judged by the consensus panel and proven at biopsy and/or clinical follow-up. For tumor detection, transverse images and curved planar reformations had an average sensitivity of 95.0% and 98.4% (P > .05), respectively, and an average specificity of 90.9% and 91.3% (P > .05), respectively. For tumor resectability, transverse images and curved planar reformations had an average sensitivity of 85.7% and 71.4% (P > .05), respectively, and an average specificity of 85.2% and 84.3% (P > .05), respectively. Average interpretation time was 6.4 minutes with transverse images and 4.1 minutes with curved planar reformations.

CONCLUSION: Curved planar reformations are equivalent to transverse images in the detection of pancreatic tumors and determination of surgical resectability.

© RSNA, 2002

Index terms: Computed tomography (CT), multi–detector row, 770.12119 • Images, analysis • Pancreas, CT, 770.12112, 770.12115, 770.12117, 770.12119 • Pancreas, neoplasms, 770.32


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Despite the poor prognosis of pancreatic cancer, surgical resection represents the only potentially curative treatment. Laparotomy in such patients carries a substantial perioperative morbidity of 20%–30% and a mortality of up to 5% for Whipple resection (13). Therefore, careful patient selection based on accurate disease staging is of prime importance. Only 20% of patients with pancreatic cancer will have disease that is considered surgically resectable at the time of diagnosis (4). In patients with surgically resectable tumors, the 5-year survival rate is improved from less than 5% to about 20%. Computed tomography (CT) is the established method for diagnosing and staging pancreatic cancer, although approximately 25%–30% of patients who are deemed to have resectable disease at CT ultimately have unresectable lesions at surgery (57). Vascular involvement by the tumor and small liver and peritoneal and/or omental metastases constitute the majority of causes of unresectability not detected at preoperative CT (3,8).

CT criteria for unresectability have included metastatic disease, most commonly involving the liver or peritoneum, occlusion of a major peripancreatic vein by tumor, encasement of a major peripancreatic artery, and contiguous invasion of adjacent organs such as the stomach and colon. Helical CT has allowed further refinements in determining the unresectability of pancreatic tumors due to better evaluation of vessel encasement. Additional CT criteria that have been evaluated include the degree of circumferential vascular involvement by tumor (9), the tear drop sign of the superior mesenteric vein (10), and the presence of dilated small peripancreatic veins, which are best seen on thin-section helical CT scans (11,12). At our institution, we have implemented additional curved planar reformations generated from transverse CT data for the evaluation of pancreatic tumors with the belief that they provide an excellent overview of the pancreas along its longitudinal axis. The purpose of this study was to evaluate the utility of curved planar reformations compared with standard transverse images in the assessment of pancreatic tumors.


    MATERIALS AND METHODS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Patients
Between November 1998 and July 2000, all patients imaged at our hospital who were suspected of having pancreatic neoplasms were prospectively evaluated with multi–detector row CT. According to Stanford University guidelines, institutional review board approval was obtained for retrospective review of images on which the patient identity could be recognized. In addition, all patients undergoing CT imaging at our institution signed informed consent forms that their images may be used for research purposes. The presumptive diagnosis was based on clinical history, laboratory findings, and results of US and/or endoscopic retrograde cholangiopancreatography. The study group consisted of 26 women and 17 men (age range, 26–84 years; mean age, 59 years). Among these patients, 23 had final diagnoses other than pancreatic cancer. Final diagnoses were confirmed with surgery in 10 patients, biopsy in eight patients, autopsy in two patients, and clinical studies including history, laboratory data, and imaging findings in 23 patients.

CT Imaging
CT scans were obtained with a multi–detector row CT scanner (LightSpeed QX/i; GE Medical Systems, Milwaukee, Wis) according to a dual-phase pancreatic protocol. An initial unenhanced localizer scan was obtained during a 10–12-second breath hold with 10-mm collimation, a pitch of 6 (high-speed mode), low milliamperage (80 mA), and 120 kVp. Immediately before scanning, the patient was asked to ingest 900–1,000 mL of water as a negative intraluminal contrast agent. A helical scan was then obtained that extended from 2 cm above the origin of the celiac trunk to 3 cm below the caudal extent of the pancreas. A small field of view (25 cm) was used, which was centered over the superior mesenteric artery. After an 18- or 20-gauge catheter (Angiocath; Becton Dickinson, Sandy, Utah) was placed into an antecubital vein, 140 mL of nonionic contrast material with an iodine content of 300 mg/mL (iohexol [Omnipaque]; Nycomed-Amersham, Princeton, NJ) was injected at 4 mL/sec by using a power injector (Envision CT; Medrad, Indianola, Pa).

The scanning parameters were as follows: 120 kVp, 200–240 mA, 4 x 1.25-mm collimation, rotation time of 0.8 second, pitch of 6 (high-speed mode), and scanning delay of 40 seconds (pancreatic phase). A subsequent portal venous phase scan was obtained from the diaphragm to the symphysis pubis after a scanning delay of 70 seconds. Scanning parameters included 120 kVp, 200–240 mA, 4 x 5-mm collimation, rotation time of 0.8 second, and pitch of 6 (high-speed mode). The matrix size was 512 x 512 in both series. The images obtained during the pancreatic phase were reconstructed at 0.5-mm intervals. These data were then transferred to an independent workstation.

Curved Planar Reformations
Curved planar reformations allow single two-dimensional image display of structures, such as airways and blood vessels, that run through multiple oblique planes. By using thin collimation and fast scanning techniques (ie, multi–detector row CT), even the pancreatic and common bile ducts can be depicted in their entirety. To create these images, we used two workstations (Advantage Windows 3.1, GE Medical Systems, Milwaukee, Wis; and Vitrea 2.2, Vital Images, Minneapolis, Minn). Modern versions of three-dimensional software are capable of automatically extracting median centerlines of vessels and creating curved planar reformations. Because pancreatic and common bile ducts are small in comparison to major blood vessels, this method has not yet been optimized for their display. Therefore, at present, creation of these images is totally operator dependent.

At our institution, full-time radiologic technologists who specialize in three-dimensional imaging and have been trained by radiologists routinely generate curved planar reformations and other three-dimensional reconstructions. These technologists are highly skilled and very efficient in this process, which truly is their area of expertise. In the event of complicated cases, a radiologist is always available for consultation. To generate these images, the operator must designate points on a two-dimensional image, following the course of the center of the pancreatic or the common bile duct. Lines through the volume connect these points, and the software extrapolates a two-dimensional image for display. The thickness of the curved plane is the voxel dimension perpendicular to the curved plane and depends on the orientation of the section on which it is drawn. The section thickness of the curved plane will never be larger than the effective section thickness or smaller than the transverse pixel dimensions. Two orthogonal curved planes are created through each structure, including a curved transverse, a curved sagittal, or a coronal reformation. The total time for obtaining the curved planar reformation is about 20 minutes. Because curved planar reformations are generated from two-dimensional images, creation of a three-dimensional volume is not necessary. Segmentation, or editing to mask out overlying structures, is also not required. This aids in the speed of creation of these images, making them practical in a clinical setting. Curved planar reformations were obtained of the pancreatic duct, the celiac artery, the hepatic artery, the splenic artery, the superior mesenteric artery, the portal vein, the superior mesenteric vein, and the splenic vein (Fig 1).



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Figure 1a. Curved planar reformations of normal pancreas and surrounding vasculature show (a) pancreatic duct (arrow), (b) celiac axis (white arrow) and hepatic artery (black arrow), (c) superior mesenteric artery (arrow), and (d) splenic (black arrow) and portal veins (open arrow).

 


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Figure 1b. Curved planar reformations of normal pancreas and surrounding vasculature show (a) pancreatic duct (arrow), (b) celiac axis (white arrow) and hepatic artery (black arrow), (c) superior mesenteric artery (arrow), and (d) splenic (black arrow) and portal veins (open arrow).

 


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Figure 1c. Curved planar reformations of normal pancreas and surrounding vasculature show (a) pancreatic duct (arrow), (b) celiac axis (white arrow) and hepatic artery (black arrow), (c) superior mesenteric artery (arrow), and (d) splenic (black arrow) and portal veins (open arrow).

 


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Figure 1d. Curved planar reformations of normal pancreas and surrounding vasculature show (a) pancreatic duct (arrow), (b) celiac axis (white arrow) and hepatic artery (black arrow), (c) superior mesenteric artery (arrow), and (d) splenic (black arrow) and portal veins (open arrow).

 
Image Analysis
Images were reviewed retrospectively by five experienced abdominal radiologists (R.B.J., C.F.B., L.C.C., M.N.M., R.E.M.). Three readers in the experimental group worked individually and interpreted image sets for all patients in two sessions. In the first session, they were presented with curved planar reformations alone; in the second session, with transverse images alone. In between these sessions, we required a minimum of 8 weeks to minimize case memory. Taken by itself, this phase of the study allowed only for the determination of the relative performance of each reader using curved planar reformations alone, compared with using transverse images alone. It did not allow for assessment of the results compared with "truth," which would ideally be obtained with surgical and/or pathologic analysis in all patients. Because only patients with potentially resectable disease undergo surgery, limiting our patient group to surgical patients would introduce a serious selection bias toward resectable disease. To overcome this limitation, we had two additional radiologists work as a consensus panel to set an independent standard based on imaging and clinical data combined.

The consensus readers were presented with both curved planar reformations and transverse images during the same session and were asked to consider the information from both display modes in reaching a final interpretation of the case. In addition, these readers were given clinical data that included patient findings at presentation, age, and biopsy or surgical findings. With this additional information, we assumed that the readers would arrive at the most accurate overall interpretation of the imaging data. By implementing the consensus group, we could compare the results of the individual experimental readers with this independent standard, thereby enabling a determination of overall reader accuracy on each of the display modes. The mean number of transverse images to read was 421 (range, 277–567), whereas curved planar reformation consisted of a set of 14 images (range, 11–16).

Since we were interested in only imaging features that determined local resectability, sites of extrapancreatic spread such as liver lesions, regional lymph node enlargement, and peritoneal implants were not considered. Transverse images and curved planar reformations derived from arterial phase data were analyzed for the presence of tumor, tumor size, and tumor conspicuity. The tumor conspicuity was rated by using a five-point scale based on visible tumor-pancreas attenuation difference, secondary signs such as mass effect and ductal obstruction, and extrapancreatic extension: 1 = isoattenuating, no mass effect, only secondary signs; 2 = isoattenuating, mass effect or moderate attenuation difference without mass effect; 3 = moderate attenuation difference, mass effect or clear attenuation difference without mass effect; 4 = clear attenuation difference, mass effect; and 5 = clear attenuation difference, mass effect, obvious extrapancreatic extension. The pancreatic duct was analyzed for normal caliber (<3 mm), diffuse dilatation, or focal dilatation. The common bile duct was assessed for normal caliber (<7 mm) or dilatation.

The amount of suspected circumferential vessel involvement was recorded for the celiac artery, hepatic artery, splenic artery, superior mesenteric artery, portal vein, superior mesenteric vein, and splenic vein. Circumferential involvement by the tumor was categorized as follows: category 1, less than one quarter circumference of vessel contiguous with tumor; category 2, between one quarter and one half of vessel circumference contiguous with tumor; category 3, more than one half and up to three quarters of vessel circumference contiguous with tumor; and category 4, more than three quarters of vessel circumference contiguous with tumor (9).

Criteria for unresectability were vascular involvement (more than 50% circumferential encasement and/or occlusion) and extrapancreatic extension (excluding the duodenum). The confidence level for tumor resectability was rated from 1 to 5 and was evaluated in each case. The interpretation time was assessed separately for each display modality. CT findings were compared with findings at surgery and with the final pathology report, when available.

Statistical Analysis
A McNemar test for paired data was used for each reader separately to compare the sensitivities and specificities of transverse images and curved planar reformations with regard to tumor detection, resectability, and vascular involvement. The level of significance was indicated by a P value of less than .05. Sensitivity, specificity, positive predictive value, and negative predictive value were calculated for each modality and each reader separately.

Interobserver agreement among the three readers reading transverse images and curved planar reformations was quantified by using {kappa} statistics. A {kappa} value of less than 0.20 was considered to indicate poor agreement; a {kappa} value of 0.20–0.39, fair agreement; a {kappa} value of 0.40–0.59, moderate agreement; a {kappa} value of 0.60–0.79, substantial agreement; and a {kappa} value of 0.80 or greater, excellent agreement.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
Among the patients, 23 had final diagnoses other than pancreatic cancer. These other diagnoses were a normal pancreas (n = 9), pancreatitis (n = 8), distal bile duct carcinoma (n = 3), duodenal carcinoma (n = 1), microcystic adenoma of the pancreas (n = 1), and intraductal papillary-mucinous tumor (n = 1). Twenty of the 43 patients were found to have pancreatic malignancies. The histologic findings in these patients were ductal adenocarcinoma (n = 16), adenosquamous carcinoma (n = 2), metastatic gastrinoma (n = 1), and primary endocrine cell tumor (n = 1).

Of the 43 patients, 20 were rated by the consensus panel as having positive findings for pancreatic cancer. The consensus readers considered seven tumors as resectable (Fig 2) and 13 as unresectable (Fig 3). Reader A rated 22 patients as having pancreatic cancer by using only curved planar reformations and 21 patients as having pancreatic cancer by using only transverse images. He rated 10 tumors as resectable and 12 as unresectable on curved planar reformations. On transverse images, he rated nine tumors as resectable and 13 as unresectable. Reader B rated 21 patients as having pancreatic cancer by using curved planar reformations and 25 patients as having pancreatic cancer by using only transverse images. He rated eight tumors as resectable and 13 as unresectable on curved planar reformations and 10 as resectable and 15 as unresectable on transverse images. Reader C rated 23 patients as having pancreatic cancer by using curved planar reformations and 20 patients as having pancreatic cancer by using only transverse images. Reader C considered 11 tumors resectable and 12 unresectable on curved planar reformations and 11 resectable and nine unresectable on transverse images.



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Figure 2a. Images in 56-year-old woman with pancreatic adenocarcinoma deemed resectable at imaging and proved at surgery. (a, b) Transverse contrast-enhanced CT images show dilated middle to distal pancreatic duct (arrowheads) and low-attenuating mass (arrow) in the neck of pancreas, abutting splenic vein. (c) Curved planar reformation of pancreatic duct demonstrates relative dilatation of middle to distal portion resulting from mass (arrow). (d) Curved planar reformation of splenic vein (arrows), superior mesenteric vein (arrowheads), and portal vein (*) shows no involvement of these vessels.

 


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Figure 2b. Images in 56-year-old woman with pancreatic adenocarcinoma deemed resectable at imaging and proved at surgery. (a, b) Transverse contrast-enhanced CT images show dilated middle to distal pancreatic duct (arrowheads) and low-attenuating mass (arrow) in the neck of pancreas, abutting splenic vein. (c) Curved planar reformation of pancreatic duct demonstrates relative dilatation of middle to distal portion resulting from mass (arrow). (d) Curved planar reformation of splenic vein (arrows), superior mesenteric vein (arrowheads), and portal vein (*) shows no involvement of these vessels.

 


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Figure 2c. Images in 56-year-old woman with pancreatic adenocarcinoma deemed resectable at imaging and proved at surgery. (a, b) Transverse contrast-enhanced CT images show dilated middle to distal pancreatic duct (arrowheads) and low-attenuating mass (arrow) in the neck of pancreas, abutting splenic vein. (c) Curved planar reformation of pancreatic duct demonstrates relative dilatation of middle to distal portion resulting from mass (arrow). (d) Curved planar reformation of splenic vein (arrows), superior mesenteric vein (arrowheads), and portal vein (*) shows no involvement of these vessels.

 


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Figure 2d. Images in 56-year-old woman with pancreatic adenocarcinoma deemed resectable at imaging and proved at surgery. (a, b) Transverse contrast-enhanced CT images show dilated middle to distal pancreatic duct (arrowheads) and low-attenuating mass (arrow) in the neck of pancreas, abutting splenic vein. (c) Curved planar reformation of pancreatic duct demonstrates relative dilatation of middle to distal portion resulting from mass (arrow). (d) Curved planar reformation of splenic vein (arrows), superior mesenteric vein (arrowheads), and portal vein (*) shows no involvement of these vessels.

 


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Figure 3a. Images in 52-year-old woman with jaundice, abdominal pain, and weight loss due to unresectable pancreatic cancer. (a) Transverse contrast-enhanced CT image shows hypoattenuating mass in the head of the pancreas (*) abutting splenic vein (arrow). (b-d) Curved planar reformations (cpr) show mass adjacent to and deforming superior mesenteric vein (black arrows), inferior mesenteric vein (imv) (arrowheads), and splenic vein (white arrows).

 


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Figure 3b. Images in 52-year-old woman with jaundice, abdominal pain, and weight loss due to unresectable pancreatic cancer. (a) Transverse contrast-enhanced CT image shows hypoattenuating mass in the head of the pancreas (*) abutting splenic vein (arrow). (b-d) Curved planar reformations (cpr) show mass adjacent to and deforming superior mesenteric vein (black arrows), inferior mesenteric vein (imv) (arrowheads), and splenic vein (white arrows).

 


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Figure 3c. Images in 52-year-old woman with jaundice, abdominal pain, and weight loss due to unresectable pancreatic cancer. (a) Transverse contrast-enhanced CT image shows hypoattenuating mass in the head of the pancreas (*) abutting splenic vein (arrow). (b-d) Curved planar reformations (cpr) show mass adjacent to and deforming superior mesenteric vein (black arrows), inferior mesenteric vein (imv) (arrowheads), and splenic vein (white arrows).

 


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Figure 3d. Images in 52-year-old woman with jaundice, abdominal pain, and weight loss due to unresectable pancreatic cancer. (a) Transverse contrast-enhanced CT image shows hypoattenuating mass in the head of the pancreas (*) abutting splenic vein (arrow). (b-d) Curved planar reformations (cpr) show mass adjacent to and deforming superior mesenteric vein (black arrows), inferior mesenteric vein (imv) (arrowheads), and splenic vein (white arrows).

 
The average sensitivity for tumor detection (Table 1) on transverse images was 95.0% and that on curved planar reformations was 98.4%. The average specificity was 90.9% on transverse images and 91.3% on curved planar reformations. For resectability (Table 2), the average sensitivity was 85.7% on transverse images and 71.4% on curved planar reformations. The average specificity was 85.2% on transverse images and 84.3% on curved planar reformations.


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TABLE 1. Tumor Detection

 

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TABLE 2. Tumor Resectability

 
The average sensitivity for vascular involvement (Table 3) was 77.3% by reading transverse images and 78.1% by reading curved planar reformations. Average specificity was 96.7% by reading transverse images and 96.0% by reading curved planar reformations. The McNemar test revealed no significantly different sensitivities or specificities between transverse images and curved planar reformations in regard to tumor detection, resectability, and vascular involvement (P > .05).


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TABLE 3. Vascular Involvement

 
The {kappa} values for tumor resectability were 0.67 and 0.64 for transverse images and curved planar reformations, respectively. For tumor detection, the {kappa} values were 0.70 for transverse images and 0.65 for curved planar reformations. {kappa} values for vessel involvement were 0.68 for transverse images and 0.66 for curved planar reformations. Generally, {kappa} values ranging from 0.60 to 0.79 indicate substantial consistency.

The average examination interpretation time for readers A-C was 6.4 minutes ± 2.17 for transverse images and 4.1 minutes ± 1.55 for curved planar reformations. The average examination interpretation time for the consensus panel was 13.5 minutes ± 4.38. By using a five-point scale, the average confidence level for tumor resectability was 4.3 ± 0.10 with transverse images and 4.2 ± 0.5 with curved planar reformations for readers A-C. In the consensus group, the average confidence level for tumor resectability was 4.8 ± 0.57.

Analysis of tumor size and the diameter of the common bile and pancreatic ducts revealed no difference between transverse images and curved planar reformations.


    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
While evaluation of pancreatic tumors may be performed with a variety of imaging modalities, including ultrasonography and magnetic resonance (MR) imaging, the most important advances in pancreatic imaging have come as a result of improvements in CT. The effectiveness of CT and MR imaging in the diagnosis and staging of carcinoma is well established. Positive predictive values for surgical unresectability have been excellent, ranging from 89% to 95% (58). Among patients with tumors judged potentially resectable on the basis of CT criteria, however, surgical results show that 60%–91% of the tumors are truly resectable. The other patients have local tumor extension, lymph node metastases, or small peritoneal, omental, or hepatic metastases not identified at preoperative CT (6,7,9,1316).

One of the most common causes of unresectability not detected with CT is vascular involvement by tumor. The sensitivity of helical CT for vascular invasion is reported to be between 60% and 89% (13,14). In patients with pancreatic head tumors, staging of circumferential vessel involvement by tumor as shown with CT has proved to be a useful tool in predicting surgical resectability (9). Because survival may be increased only in patients in whom complete surgical resection with negative margins is possible, the aim of our study was to determine if curved planar reformations are a useful tool in the evaluation of pancreatic tumor resectability. Recent advances in multi–detector row CT technology have allowed the acquisition of near isotropic volumetric datasets. Postprocessing of these data with various three-dimensional reconstruction techniques such as curved planar reformation, volume rendering, and maximum intensity projection permits excellent display of anatomic information in multiple formats, which are likely to be more easily interpreted by referring physicians and surgeons (17,18).

Our data suggest that interpretation of curved planar reformations and transverse images results in no significant difference in detection of pancreatic tumors or determination of their resectability. While the data suggest that curved planar reformations are significantly equivalent to transverse images in the detection of pancreatic tumors and determination of vascular involvement of these tumors, it is important to point out that they do not represent a replacement for the transverse images. The interpreter of these images must realize that the curved planar reformation is only 1 pixel thick and does not represent the organ in its entirety. Additionally, there are many structures and portions of the anatomy that are not included on the curved planar reformations, and incidental findings in other organs would be easily overlooked if the curved planar reformation is evaluated in isolation. Thus, correlation with source images is imperative.

There were several limitations of this study. One possible bias involves the degree of familiarity that readers have with transverse images when compared with curved planar reformations. Readers are experienced in the interpretation of transverse images, have a systematic approach to reading such images, and are well versed in the distinction between normal and abnormal images. In contrast, curved planar reformations are a new addition to our protocol, with which readers have had substantially less experience. Additionally, curved planar reformation creates images in an arbitrary plane, which can be disorienting. While the structure of interest is exquisitely displayed, the neighboring anatomy becomes distorted. For these reasons, it would be expected for there to be a learning curve associated with the interpretation of the curved planar reformation. Unfortunately, this type of bias was unavoidable.

Ideally, the study protocol would have included evaluation of the curved planar reformations and transverse images together, as well as in isolation, by the blinded readers in comparison to the results of consensus panel. Unfortunately, this would have introduced additional memory bias, which could have skewed interpretation of the images. Additionally, because the order of the presentation of curved planar reformations and transverse images was not randomized, an order bias may have been introduced. Furthermore, a true pathologic standard was not available in all cases, and thus, a consensus panel that had access to all available clinical information was substituted.

While not an uncommon tumor, the small overall numbers of pancreatic malignancies seen in our institution resulted in a relatively small population size for our study. With only 20 cases, differences in the interpretation of presence or absence of tumor and resectability in just a few cases resulted in larger differences in individual reader’s sensitivity and specificity. The small sample size could also have resulted in a limitation of statistical power, preventing demonstration of a significant difference in detection of pancreatic tumors or determination of their resectability with the two display methods.

The most important clinical utility of curved planar reformations is most likely their ability to provide an excellent and quickly comprehensible overview of pertinent anatomy and structures for referring clinicians. This type of information can be of great use to surgeons in preoperative planning. With current multi–detector row CT technology and protocols, biphasic pancreatic studies easily produce hundreds of transverse images. While it remains necessary for the radiologist to evaluate each of the transverse images, the curved planar reformation provides a much more time-efficient and intuitive method of display for referring physicians interested in reviewing the pertinent findings. Finally, since our aim was to focus on tumor resectability, we did not perform a dedicated comparison of the performance of curved planar reformations versus transverse images in patients without tumors. It would be of interest in later studies to determine the value of curved planar reformation in nonmalignant pancreatic disorders.

In summary, in this cohort of patients, we were unable to detect a significant difference between curved planar reformations and transverse images for the detection and local staging of pancreatic carcinoma.


    FOOTNOTES
 
Author contributions: Guarantors of integrity of entire study, R.B.J., C.F.B., R.W.P.; study concepts, C.F.B., R.W.P.; study design, R.B.J., L.C.C., R.W.P.; literature research, R.B., R.W.P.; clinical studies, R.B.J., R.E.M., M.N.M.; data acquisition and analysis/interpretation, R.E.M., L.C.C., M.N.M., R.B.J., C.F.B.; statistical analysis, R.B., J.H.; manuscript preparation, R.W.P., L.C.C., R.B.; manuscript definition of intellectual content, R.B.J., C.F.B., R.W.P.; manuscript editing, R.W.P., L.C.C., J.H.; manuscript revision/review, R.B.J., C.F.B., R.B., R.E.M., J.H.; manuscript final version approval, R.B.J., L.C.C., R.B., C.F.B.


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 MATERIALS AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 

  1. Warshaw AL, Fernandez-Del-Castillo C. Pancreatic carcinoma. N Engl J Med 1992; 326:455-465.[Medline]
  2. Fuhrman GM, Charnsangavej C, Abbruzzese JL, et al. Thin-section contrast-enhanced computed tomography accurately predicts the resectability of malignant pancreatic neoplasms. Am J Surg 1994; 167:104-113.[CrossRef][Medline]
  3. Warshaw AL, Gu Z, Wittenberg J, Waltman AC. Preoperative staging and assessment of resectability of pancreatic cancer. Arch Surg 1990; 125:230-233.[Abstract]
  4. American Cancer Society. Cancer facts and figures 1998 Atlanta, Ga: American Cancer Society, 1998.
  5. Freeny PC, Marks WM, Ryan JA, Traverso LW. Pancreatic ductal adenocarcinoma: diagnosis and staging with dynamic CT. Radiology 1988; 166:125-133.[Abstract/Free Full Text]
  6. Freeny PC, Traverso LW, Ryan JA. Diagnosis and staging of pancreatic adenocarcinoma with dynamic computed tomography. Am J Surg 1993; 165:600-606.[CrossRef][Medline]
  7. Megibow AJ, Zhou XH, Rotterdam H, et al. Pancreatic adenocarcinoma: CT versus MR imaging in the evaluation of resectability—report of the Radiology Diagnostic Oncology Group. Radiology 1995; 195:327-332.[Abstract/Free Full Text]
  8. Bluemke DA, Cameron JL, Hruban RH, et al. Potentially resectable pancreatic adenocarcinoma: spiral CT assessment with surgical and pathologic correlation. Radiology 1995; 197:381-385.[Abstract/Free Full Text]
  9. O’Malley ME, Boland GW, Wood BJ, Fernandez-Del-Castillo C, Warshaw AL, Mueller PR. Adenocarcinoma of the head of the pancreas: determination of surgical unresectability with thin section pancreatic-phase CT. AJR Am J Roentgenol 1999; 173:1513-1518.[Abstract]
  10. Hough TJ, Raptopoulos V, Siewert B, Matthews JB. Teardrop superior mesenteric vein: CT sign for unresectable carcinoma of the pancreas. AJR Am J Roentgenol 1999; 173:1509-1512.[Abstract]
  11. Hommeryer SC, Freeney PC, Crabo LG. Carcinoma of the head of the pancreas: evaluation of the pancreaticoduodenal veins with dynamic CT—potential for improved accuracy in staging. Radiology 1995; 196:133-238.
  12. Vedantham S, Lu DSK, Reber HA, Kadell B. Small peripancreatic veins: improved assessment in pancreatic cancer patients using thin-section pancreatic phase helical CT. AJR Am J Roentgenol 1998; 170:377-383.[Abstract/Free Full Text]
  13. Zeman RK, Cooper C, Zeiberg AS, et al. TNM staging of pancreatic carcinoma using helical CT. AJR Am J Roentgenol 1997; 169:459-464.[Abstract/Free Full Text]
  14. Diehl SJ, Lehmann KJ, Sadick M, Lachmann R, Georgi M. Pancreatic cancer: value of dual-phase helical CT in assessing resectability. Radiology 1998; 206:373-378.[Abstract/Free Full Text]
  15. Lu DSK, Vedantham S, Krasny RM, Kadell B, Berger WL, Reber HA. Two-phase helical CT for pancreatic tumors: pancreatic versus hepatic phase enhancement of tumor, pancreas, and vascular structures. Radiology 1996; 199:697-701.[Abstract/Free Full Text]
  16. Lu DSK, Reber HA, Krasny RM, Kadell BM, Sayre J. Local staging of pancreatic cancer: criteria for unresectability of major vessels as revealed by pancreatic-phase, thin-section helical CT. AJR Am J Roentgenol 1997; 168:1439-1443.[Abstract/Free Full Text]
  17. Nino-Murcia M, Jeffrey RB, Jr, Beaulieu CF, Li KCP, Rubin GD. Multidetector CT of the pancreas and bile duct system: value of curved planar reformations. AJR Am J Roentgenol 2001; 176:689-693.[Free Full Text]
  18. Fishman EK, Horton KM, Urban BA. Multidetector CT angiography in the evaluation of pancreatic carcinoma: preliminary observations. J Comput Assist Tomogr 2000; 24:849-853.[CrossRef][Medline]



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