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Clinical Investigations |
1 Department of Nuclear Medicine, Rambam Medical Center, Haifa, Israel
2 The B. Rappaport School of Medicine, Technion, Israel Institute of Technology, Haifa, Israel
3 Department of Diagnostic Imaging, Rambam Medical Center, Haifa, Israel
4 Department of Oncology, Rambam Medical Center, Haifa, Israel
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONREFERENCES |
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Key Words: PET • PET/CT • cancer recurrence • tumor markers
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONREFERENCES |
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Diagnosis of recurrent cancer by CT is based on the detection of a new abnormal mass or changes in the size of a known lesion caused by renewed cancer growth (4,5). Diagnosis of recurrent malignancy by PET using 18F-FDG is based on increased utilization of glucose by malignant cells. These 2 imaging modalities do not always yield congruent findings. As previously demonstrated, cancer relapse can be diagnosed by PET months and even years before it becomes evident on conventional, anatomic imaging modalities (5–7). However, diagnosis of early recurrent cancer-induced metabolic changes by PET is impaired by the lack of precise anatomic landmarks and by the presence of increased radiotracer uptake of physiologic or nonmalignant etiology associated with benign and treatment-related conditions and distorted anatomy after surgery (8,9).
PET/CT hybrid imaging, performed using a single device in a single diagnostic session, combines noninvasive structural and metabolic tumor assessment and, therefore, provides precise anatomic localization of areas of increased 18F-FDG uptake (10–12).
The objectives of the present study were to assess whether the fused metabolic and anatomic information provided by PET/CT has an incremental value in the diagnosis and localization of recurrence and in the subsequent clinical management of cancer patients with increasing concentrations of tumor serum markers and negative conventional imaging performed earlier.
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MATERIALS AND METHODS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONREFERENCES |
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Consecutive patients with matching inclusion criteria were included and no power analysis was performed. Five patients were excluded from further analysis because of lack of follow-up data after their PET/CT study. The final study population, therefore, included 36 patients: 19 women and 17 men with a mean age of 61 y (range, 32–84 y). The clinical characteristics of the study population are presented in Table 1. The last CT study was performed within a mean time of 52 d (range, 11–99 d) before the PET/CT study, without intervening therapeutic interventions. Additional investigations, such as physical examination, endoscopy, ultrasound, and bone scintigraphy, were also negative. The final diagnosis of the presence or absence of recurrent cancer was based on histologic findings obtained during surgery or biopsy, subsequent imaging, and clinical follow-up. Patients were considered to have no evidence of recurrent cancer if they showed a subsequent decrease in tumor marker levels or had a negative clinical and radiologic follow-up of at least 12 mo after their PET/CT examination.
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The PET/CT system is composed of a dedicated PET scanner with a full-ring bismuth germanate detector and a multislice CT (11,12). The protocol of the present study included an initial CT acquisition followed by the PET study. CT parameters used for acquisition included 140 kV, 80 mA, 4-slices helical, 0.5 s per rotation, and pitch of 6:1, with a slice thickness of 4.25 mm, equal to that of the PET. CT images were reconstructed onto a 512 x 512 matrix. PET was acquired by sequential fields of view, each covering 15 cm during an acquisition time of 5 min. PET acquisition was performed in 2-dimensional mode using a matrix of 128 x 128. PET data were reconstructed using ordered-subsets expectation maximization. Data obtained from the CT acquisition were used for low-noise attenuation correction of PET emission data and for fusion of attenuation-corrected PET images with the corresponding CT images.
After completion of PET acquisition, the reconstructed x-ray attenuation-corrected PET images, CT images, and fused images were available for review in axial, coronal, and sagittal planes, and in maximum-intensity-projection 3-dimensional cine mode, using the manufacturer’s review station (eNTEGRA; General Electric Medical Systems).
Study Interpretation
Two experienced nuclear medicine physicians who were aware of each patient’s clinical history initially interpreted together the stand-alone 18F-FDG PET images with the previously performed high-resolution, contrast-enhanced CT studies available for side-by-side visual comparison and with the knowledge that these studies had been initially reported as negative for the presence of cancer. The presence and localization of any area of increased 18F-FDG uptake was recorded, and each lesion was characterized as benign, malignant, or equivocal. A focus of increased 18F-FDG uptake was defined as benign when related to physiologic biodistribution of 18F-FDG or to a known nonmalignant process. A focal abnormal 18F-FDG activity, of higher intensity than that of surrounding tissues—not related to the physiologic or benign 18F-FDG uptake—was defined as malignant. Any area of increased 18F-FDG uptake that could not be clearly characterized was defined as equivocal.
Two experienced radiologists, who were aware of each patient’s history and clinical data but unaware of current 18F-FDG PET results, reviewed the previously performed diagnostic CT and the CT component of the PET/CT study. The presence of lesions, previously undiagnosed and only retrospectively detected on the contrast-enhanced, high-resolution CT, or new abnormalities, seen only on the CT component of the PET/CT study, were recorded.
A combined team, including 2 nuclear medicine physicians and 2 radiologists, interpreted the fused PET/CT images in subsequent reading sessions with knowledge of the results of the PET and CT studies. Fused PET/CT data were prospectively recorded using the same criteria as for PET, including characterization and localization of all suspected sites. Disagreements concerning final interpretation were resolved by a majority opinion.
Data Analysis
PET evaluated with side-by-side comparison with previously performed high-resolution, contrast-enhanced CT, and further PET/CT studies, were analyzed and compared for each suspected site and for each patient.
For the site-based analysis, a true-positive (TP) lesion was defined as malignant or equivocal on PET or PET/CT with subsequent confirmed tumor involvement. A FP site was defined as malignant or equivocal on PET or PET/CT with no further evidence of disease. A true-negative (TN) site was defined as benign or physiologic on PET or PET/CT with no further evidence of disease. A false-negative (FN) site was defined as benign or physiologic on PET or PET/CT showing subsequent evidence of malignancy. Differences in lesion definition between PET and fused PET/CT images were documented for each suspected site. The additional value of PET/CT was defined as new information regarding the classification and localization of foci of 18F-FDG uptake, provided by fused images and not previously available from separate PET with side-by-side CT evaluation.
For the patient-based analysis, a patient was defined as TP on the PET or PET/CT study when it showed at least one lesion with further confirmed malignancy. A FP study showed at least one lesion defined as malignant with no evidence of active cancer on further evaluation. A TN study showed only sites defined as benign, or no abnormal findings, and the patient had no further evidence of active cancer. A negative study in a patient who had further evidence of active disease was defined as FN. Studies with no abnormal 18F-FDG foci detected on PET (and therefore on PET/CT as well) were included, as TN or FN, only in the patient-based analysis. Differences in patient categorization between PET and fused PET/CT data for diagnosis of recurrence were documented. The additional value of PET/CT was defined as new information regarding the diagnosis of recurrence, provided by fused images and not previously available from separate PET with side-by-side CT evaluation.
The impact of fused PET/CT images on the management of patients was evaluated, based on information regarding further clinical decisions obtained from patient files and interviews of the treating physicians or patients. Referral of patients for previously unplanned therapeutic modalities based on PET/CT results was recorded.
The sensitivity, specificity, and accuracy were calculated for both the site-based and the patient-based analysis. In addition, the positive predictive value (PPV) and negative predictive value (NPV) were calculated for the site-based analysis. The differences in site- and patient-based analysis of performance indices between PET and PET/CT were compared using the McNemar test for paired proportions. The differences in treatment decisions prompted by PET and those induced by PET/CT were assessed by 
2 analysis of contingency tables. A P value < 0.05 was considered as statistically significant.
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RESULTS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONREFERENCES |
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Site-Based Performance of PET and PET/CT for Diagnosis of Recurrence
PET interpreted with side-by-side evaluation of CT defined 94 of the 111 sites of increased 18F-FDG uptake as malignant or equivocal (18 equivocal) and 17 as benign. On the basis of PET, there were 80 TP sites, 14 TN, 14 FP, and 3 FN sites, for a sensitivity, specificity, and accuracy of 96%, 50%, and 85%, respectively, and a PPV and NPV of 85% and 82%, respectively. PET/CT analysis defined 86 sites as malignant and 25 as benign. On the basis of PET/CT, there were 83 TP sites, 25 TN, 3 FP, and no FN lesions, for a sensitivity, specificity, and accuracy of 100%, 89%, and 97%, respectively, and a PPV and NPV of 97% and 100%. PET/CT yielded a statistically significant increase in specificity (P < 0.005) and accuracy (P < 0.001) as compared with PET.
PET/CT changed the classification of 11 sites considered as malignant on PET from FP to TN, including 18F-FDG uptake in vascular calcifications, in inflammatory changes due to the presence of a stent or surgical scar, and physiologic tracer activity in the gastrointestinal tract. PET/CT changed the definition of 3 areas of increased 18F-FDG uptake from FN to TP. These sites, considered as representing physiologic bowel uptake by PET, were precisely characterized as liver metastasis, mesenteric lymph node involvement, and a local colon recurrence.
Three 18F-FDG-avid lesions were FP on both PET and PET/CT. Two of these sites were histologically assessed, including 1 site of benign neurofibromatosis in the thigh and 1 retrocaval anthracotic lymph node. The third site was a single 18F-FDG-avid cervical lymph node in a patient with lung cancer who showed no evidence of malignancy for a follow-up of 21 mo, with a further decreased level of serum tumor markers, and was therefore considered to represent only nonspecific inflammatory changes.
Thirty-two of the 85 malignant lesions (38%) were retrospectively identified on the previously performed diagnostic CT. This included 16 lymph node metastases, 8 liver metastases, and 1 soft-tissue mass in the chest wall, with diameters ranging between 8 and 20 mm, and 7 bone metastases. New structural abnormalities were observed on the CT component of the hybrid imaging study in 30 sites (35%).
The site-based comparative performance of PET and PET/CT is summarized in Table 2.
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Tumor marker serum levels decreased during follow-up in 4 of the 6 patients with no further evidence of disease. None of the 6 patients showed any suggestive lesions on imaging studies performed during the follow-up period.
PET/CT changed the classification of 1 site considered as malignant on PET from FP to TN. This patient had a single abdominal focus of increased 18F-FDG uptake considered as suspicious by PET and precisely defined by PET/CT as physiologic bowel activity. The patient showed no evidence of disease for a follow-up of 15 mo (Fig. 1).
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The patient-based comparative performance of PET and PET/CT is summarized in Table 3.
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Surgery with curative intent was performed in 9 patients with solitary malignant lesions. Eight of these 9 patients were referred for surgery based on the PET/CT diagnosis and precise localization of single tumor foci, including 3 lymph node metastases, 3 local recurrences of colon cancer (Fig. 2), 1 liver metastasis, and 1 second primary gastric cancer. Additional investigations guided by PET/CT findings (colonoscopy or gastroscopy) were performed in 2 of these 8 patients before the tumor resection.
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Radiation treatment was administered to 4 patients. One patient with a single bone metastasis received local-field radiotherapy, and 131I treatment was administered to a second patient with metastatic thyroid cancer. PET/CT findings induced changes in the localization and size of radiation fields in 2 patients, including 1 patient with a single bone metastasis and a second patient with a single soft-tissue metastasis, precisely localized by PET/CT. There was a statistically significant difference (P < 0.01) between the number of patients referred to a different treatment modality based on PET and PET/CT (Table 4).
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONREFERENCES |
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CT is the primary tool of investigation for suspected recurrence due to its widespread availability and relatively low cost. However, the CT size-based criteria for malignancy may be inaccurate estimates of tumor involvement (5,15,16). Up to 50% of patients considered suitable candidates for curative surgery by CT are found to have unresectable, disseminated disease during surgery (4,16). CT is also challenging for differentiating a recurrent tumor from treatment-induced morphologic changes (17,18).
Exploratory laparotomy has a high detection rate for abdominal recurrences (4,19). However, detection of unforeseen neoplastic spread during surgery results in a high percentage of nonresectable tumors. In addition, about 5%–11% of explorations are negative for the presence of active cancer, in spite of elevated levels of serum markers (20).
The alternative strategy of relying only on the clinical observation of patients with increasing concentrations of tumor markers may miss the opportunity to resect limited disease (15). Surgeons, therefore, have emphasized the need for better preoperative identification of this subgroup of patients, who will derive the highest benefit from surgery (21).
18F-FDG PET is a whole-body screening technique that may detect metabolic abnormalities preceding structural changes (11,22,23). PET detected occult recurrent colorectal cancer in up to 67% of patients with elevated carcinoembryonic antigen levels and had a good per-patient performance for diagnosis of recurrent tumors (23–25). This was also confirmed by the high TP rate in the present, more heterogeneous patient population. However, lesion-based performance of PET is less encouraging (26). Sites of recurrent tumor, such as pelvic metastases and diffuse peritoneal involvement, may be missed or falsely reported as physiologic or equivocal FDG uptake (5,24,25). PET, therefore, offers only a partial solution for the diagnostic and therapeutic dilemma of elevated levels of tumor markers and may induce the need for additional confirmatory diagnostic procedures.
PET/CT has been advocated as the tool of the future for the diagnosis of recurrent cancer (19,23,26). Hybrid imaging can precisely localize and improve the characterization of foci of increased 18F-FDG uptake. In the present study population, the availability of simultaneous anatomic CT mapping by PET/CT precisely defined 18 equivocal sites (16%) of increased 18F-FDG uptake as malignant or benign (Figs. 1 and 2). The anatomic location provided by fused images guided subsequent tissue diagnosis and therapeutic procedures in the setting of a small recurrent tumor load (Fig. 2). Although PET alone allowed for the correct diagnosis of recurrence in the majority of patients (83%), the statistically significant improved performance of hybrid imaging for evaluating individual lesions indicates that PET/CT has an impact on the subsequent management of cancer patients, beyond the diagnosis of recurrence. The precise PET/CT localization and definition of suspicious 18F-FDG foci led to a better assessment of the extent of recurrent disease, with subsequent treatment planned on the basis of the unique information provided by hybrid imaging in one third of the total study population.
The clinical contribution of PET/CT is indicated mainly by the number of patients referred for resection with curative intent. Surgery was performed in 8 patients following PET/CT results, in addition to 1 patient who may have been referred to surgery based only on PET results. Six of these 8 patients were referred for surgery based solely on the results of hybrid imaging, sparing further unnecessary diagnostic procedures.
When PET, a highly sensitive test, indicates the presence of widespread disease, the precise localization of each malignant site is, as a rule, less clinically relevant. Of the present study population, 13 patients were referred for chemotherapy based on PET alone. Administration of chemotherapy to 2 additional patients was enabled by PET/CT-based precise definition of equivocal foci of 18F-FDG uptake as additional malignant lesions and diagnosis of multifocal recurrence.
In the present study radiation therapy planning was modified in 2 patients after the use of PET/CT. The potentially important role of hybrid imaging in this clinical setting cannot be fully appreciated from this small patient sample.
In some of the evaluated patients, the relatively long time interval between the previous CT reported as negative and the current PET/CT study as well as the patient sample with different primary malignancies and a preponderance toward colorectal tumors are limitations of the present study. Including tumors with low metabolic rates, such as prostate cancer, may also induce biases in the study results. The benefit of improved selection criteria and the potential value of a positive PET study at baseline need to be assessed. Further studies with long-term follow-up in large homogeneous patient cohorts with single histologic tumor types need to follow. These studies will have to clarify whether PET/CT should be used, in the future, as the first step in the evaluation of patients with suspected occult recurrent cancer.
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CONCLUSION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONREFERENCES |
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ACKNOWLEDGMENTS |
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FOOTNOTES |
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For correspondence or reprints contact: Ora Israel, MD, Department of Nuclear Medicine, Rambam Medical Center, Haifa 35254, Israel.
E-mail: o_israel{at}rambam.health.gov.il
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONCONCLUSIONREFERENCES |
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