JNM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in JNM
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schöder, H.
Right arrow Articles by Larson, S. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schöder, H.
Right arrow Articles by Larson, S. M.
Journal of Nuclear Medicine Vol. 46 No. 8 1249-1251
© 2005 by Society of Nuclear Medicine


Invited Perspectives

CT in PET/CT: Essential Features of Interpretation

Heiko Schöder, MD, Henry W.D. Yeung, MD and Steven M. Larson, MD

Memorial Sloan-Kettering Cancer Center
New York, New York

Education is not something to prepare you for life; it is a continuous part of life.  Henry Ford

Since its clinical introduction in 2001, PET/CT has quickly made inroads and (where available) has become an essential tool for the work-up of patients with cancer. We now consider this imaging modality an indispensable component of our clinical practice and research endeavors. By many accounts, 80%–90% of all sales of PET scanners are now generated by combined PET/CT machines. How did this happen? Before PET/CT, PET alone, in particular with the radiotracer 18F-FDG, had already become a widely accepted imaging test for the assessment of many malignancies. Like other new imaging modalities (1–3), PET has a learning curve for interpretation; many normal variants and disease- and treatment-specific patterns of tracer uptake need to be recognized. Nevertheless, it is not uncommon to encounter problems in image interpretation that are related solely to the lack of anatomic information in the PET dataset. Combined PET/CT alleviates these shortcomings by improving the anatomic localization of PET findings and reducing the number of equivocal PET interpretations, often translating into improvements in patient management (4–11).

New techniques pose new challenges, and this is also true for the imaging sciences. Accordingly, with the clinical introduction of PET/CT, different philosophical and practical concepts emerged regarding the acquisition and interpretation of the combined study and the use of the CT data. The approach to reading the PET/CT studies was based primarily on the training of interpreting physicians and was influenced, to some degree, by institutional guidelines and reimbursement policies.

The CT portion of combined PET/CT provides not only anatomic information but also fast, reliable, and accurate attenuation correction of the PET emission data (12,13). Some characteristic artifacts, including those caused by highly concentrated oral or intravenous contrast material, as well as respiration, can also be introduced by this approach; however, these artifacts are easily recognized in most cases (14). Nevertheless, to avoid such pitfalls, some institutions have decided to acquire a low-dose CT scan for attenuation correction of PET data first, followed by PET emission images, followed by a full diagnostic CT scan with intravenous contrast material and breath holding. This approach is perhaps justified when both PET and diagnostic CT are requested by a referring physician and may be particularly useful when dual-phase or dynamic CT data are to be acquired. In this case, the diagnostic CT scan should be interpreted by a sufficiently trained physician, usually a diagnostic radiologist. It is conceivable that slight modifications in intravenous-contrast protocols (e.g., slower injection speed, greater time delay) will still provide a full diagnostic CT scan of good quality, without causing CT or PET/CT artifacts, thereby eliminating 1 step in this 3-step process (15). In that case, breath holding at mid expiration has been recommended (16) but may cause small lung nodules to be missed on CT. Many other institutions, including ours at this time, do not regularly acquire a full diagnostic CT scan as part of the PET/CT study. As a compromise and for dosimetry reasons, we obtain the CT scan as a low-dose scan (120–140 keV; 40–80 mAs) but administer 2% oral barium sulfate routinely. This approach further improves the anatomic localization of PET abnormalities without causing image artifacts. How about the interpretation of the CT data in this scenario? Should they be used for anatomic localization of PET abnormalities only, or should they be interpreted in their own right? It appears obvious that the CT scan cannot and should not be reduced to an expensive tool for correcting attenuation and finding anatomic landmarks alone. Even low-dose CT can provide important diagnostic information. Regardless of their professional background and training, PET/CT readers should therefore be able to recognize certain characteristic or important abnormalities on CT images. This thesis is addressed in an article by Osman et al. on pages 1352–1355 of this issue of The Journal of Nuclear Medicine (17). These authors report their findings on 250 patients undergoing combined PET/CT at Johns Hopkins University Medical Center. CT scans generated as part of the combined study were interpreted by a radiologist. Significant abnormalities on CT were noted in 7 of 250 patients (3%). This 3% prevalence is at the lower end of the 3%–10% range of important incidental abnormalities that have been reported for various CT screening or whole-body PET studies (1821). Significant CT abnormalities noted in the study of Osman et al. included 3 cases of masses or lesions suggestive of tumor, as well as aortic aneurysm, cirrhosis of the liver, and small lung nodules. Table 1 adds several other abnormalities that we consider important or sufficiently relevant to require reporting and some findings that may not affect the immediate management of the patient but should nevertheless be recognized. Many of these abnormalities we have indeed noted in our clinical practice. Some may have been known from previous imaging studies, whereas others may be new, and some may even be sufficiently advanced to require medical or surgical intervention. The article by Osman et al. does not address how many of their observed CT abnormalities were known before PET/CT (e.g., from another imaging study, either previous or concurrent). Nevertheless, knowledge of abnormalities before the PET/CT study would not necessarily relieve the reader of the responsibility of recording such findings. Although most PET/CT studies today are performed in addition to other imaging tests, such as full diagnostic CT, bone scanning, MRI, or ultrasound of certain body regions, it is conceivable that PET/CT will replace some of these tests in the future. It will then be even more important to provide a comprehensive interpretation of both datasets.


View this table:
[in this window]
[in a new window]
 
TABLE 1 Categories of Potentially Important or Significant CT Findings in a PET/CT Study

 
In current practice, some groups have implemented PET/CT readout sessions jointly attended by body radiologists and nuclear medicine physicians. Although these provide a unique learning opportunity for both parties, this approach is clearly not sustainable in the long term unless both parties are rewarded for their time and effort. In recognition of this unique situation, the Society of Nuclear Medicine and the American College of Radiology have designed guidelines for minimum qualifications for radiologists and nuclear medicine physicians who want to interpret PET/CT studies on their own (22). These proposed training requirements serve as guidelines only, and certificates of competence will be issued at the local level through the credentialing process. Nevertheless, it is likely that hospital administrators and local insurance providers will require proof of expertise at some time in the future. As such, most nuclear medicine physicians who want to interpret PET/CT studies will require additional CT training. Although some may consider this a nuisance, there really is no other solution. Diagnostic radiology and nuclear medicine are imaging sciences in constant flux that have certain aspects in common but differ in many other respects. Limited training in CT or PET/CT interpretation will not qualify radiologists as nuclear medicine physicians or vice versa (although some might think so). It does, however, indicate a certain degree of merging between the 2 disciplines. This will become even more apparent when the number of combined anatomic and functional imaging studies increases, as is expected with the wider clinical introduction of SPECT/CT. Although this modality was originally designed to improve anatomic localization in nuclear medicine studies with highly specific tracers (e.g., antibody studies, metaiodobenzylguanidine), there is no reason why CT data should not be interpreted in their own right once available, regardless of whether the combined SPECT/CT is done for the assessment of coronary artery disease or the assessment of cancer.

Proper interpretation of a PET/CT scan requires considerably more time and effort than reading a standard PET scan. Unfortunately, this is not reflected in current administrative assessments, such as relative value units, or reimbursement policies. Nevertheless, PET/CT is a new imaging technique that is here to stay. Although some issues, including reimbursement, still need to be worked out, nuclear medicine physicians will have to embrace this new technique if they want to maintain professional expertise and competence. In particular, the additional CT training will require time, patience, and likely also financial resources. What do we gain? More work, yes, but also, we would hope, professional pride and satisfaction from providing better diagnoses (fewer equivocal PET and CT readings) and seeing them eventually translate into improved patient care.

FOOTNOTES

Received May 11, 2005; revision accepted May 12, 2005.

For correspondence or reprints contact: Heiko Schöder, MD, Department of Radiology/Nuclear Medicine, Memorial Sloan-Kettering Cancer Center, 1275 York Ave., New York, NY 10021.

E-mail: schoderh{at}mskcc.org

REFERENCES

  1. Caldwell DP, Pulfer KA, Jaggi GR, Knuteson HL, Fine JP, Pozniak MA. Aortic aneurysm volume calculation: effect of operator experience. Abdom Imaging. February 1, 2005 [Epub ahead of print].
  2. Taylor SA, Halligan S, Burling D, et al. CT colonography: effect of experience and training on reader performance. Eur Radiol. 2004;14:1025.– 1033.[Medline]
  3. Mullerad M, Hricak H, Wang L, Chen HN, Kattan MW, Scardino PT. Prostate cancer: detection of extracapsular extension by genitourinary and general body radiologists at MR imaging. Radiology. 2004;232:140–146.[Abstract/Free Full Text]
  4. Lardinois D, Weder W, Hany TF, et al. Staging of non-small-cell lung cancer with integrated positron-emission tomography and computed tomography. N Engl J Med. 2003;348:2500–2507.[Abstract/Free Full Text]
  5. Antoch G, Saoudi N, Kuehl H, et al. Accuracy of whole-body dual-modality fluorine-18–2-fluoro-2-deoxy-D-glucose positron emission tomography and computed tomography (FDG-PET/CT) for tumor staging in solid tumors: comparison with CT and PET. J Clin Oncol. 2004;22:4357–4368.[Abstract/Free Full Text]
  6. Schoder H, Yeung HW, Gonen M, Kraus D, Larson SM. Head and neck cancer: clinical usefulness and accuracy of PET/CT image fusion. Radiology. 2004;231:65–72.[Abstract/Free Full Text]
  7. Bar-Shalom R, Yefremov N, Guralnik L, et al. Clinical performance of PET/CT in evaluation of cancer: additional value for diagnostic imaging and patient management. J Nucl Med. 2003;44:1200–1209.[Abstract/Free Full Text]
  8. Israel O, Mor M, Guralnik L, et al. Is 18F-FDG PET/CT useful for imaging and management of patients with suspected occult recurrence of cancer? J Nucl Med. 2004;45:2045–2051.[Abstract/Free Full Text]
  9. Yeung H, Schöder H, Smith A, Gonen M, Larson SM. Clinical value of combined positron emission tomography/computed tomography imaging in the interpretation of 2-deoxy-2-[F-18]fluoro-D-glucose positron emission tomography studies in cancer patients. Mol Imaging Biol. 2005;7:229–235.[Medline]
  10. Hany TF, Steinert HC, Goerres GW, Buck A, von Schulthess GK. PET diagnostic accuracy: improvement with in-line PET-CT system: initial results. Radiology. 2002;225:575–581.[Abstract/Free Full Text]
  11. Cohade C, Osman M, Leal J, Wahl RL. Direct comparison of (18)F-FDG PET and PET/CT in patients with colorectal carcinoma. J Nucl Med. 2003;44:1797–1803.[Abstract/Free Full Text]
  12. Nakamoto Y, Osman M, Cohade C, et al. PET/CT: comparison of quantitative tracer uptake between germanium and CT transmission attenuation-corrected images. J Nucl Med. 2002;43:1137–1143.[Abstract/Free Full Text]
  13. Kamel E, Hany TF, Burger C, et al. CT vs 68Ge attenuation correction in a combined PET/CT system: evaluation of the effect of lowering the CT tube current. Eur J Nucl Med Mol Imaging. 2002;29:346–350.[Medline]
  14. Schoder H, Erdi YE, Larson SM, Yeung HW. PET/CT: a new imaging technology in nuclear medicine. Eur J Nucl Med Mol Imaging. 2003;30:1419–1437.[Medline]
  15. Beyer T, Antoch G, Bockisch A, Stattaus J. Optimized intravenous contrast administration for diagnostic whole-body 18F-FDG PET/CT. J Nucl Med. 2005;46:429–435.[Abstract/Free Full Text]
  16. Goerres GW, Burger C, Kamel E, et al. Respiration-induced attenuation artifact at PET/CT: technical considerations. Radiology. 2003;226:906.– 910.[Abstract/Free Full Text]
  17. Osman MM, Cohade C, Fishman EK, Wahl RL. Clinically significant incidental findings on the unenhanced-CT portion of PET/CT studies: frequency in 250 patients. J Nucl Med. 2005;46:1352–1355.[Abstract/Free Full Text]
  18. Agress H Jr, Cooper BZ. Detection of clinically unexpected malignant and premalignant tumors with whole-body FDG PET: histopathologic comparison. Radiology. 2004;230:417–422.[Abstract/Free Full Text]
  19. Xiong T, Richardson M, Woodroffe R, Halligan S, Morton D, Lilford RJ. Incidental lesions found on CT colonography: their nature and frequency. Br J Radiol. 2005;78:22–29.[Abstract/Free Full Text]
  20. Pickhardt PJ, Choi JR, Hwang I, et al. Computed tomographic virtual colonoscopy to screen for colorectal neoplasia in asymptomatic adults. N Engl J Med. 2003;349:2191–2200.[Abstract/Free Full Text]
  21. Gluecker TM, Johnson CD, Wilson LA, et al. Extracolonic findings at CT colonography: evaluation of prevalence and cost in a screening population. Gastroenterology. 2003;124:911–916.[Medline]
  22. Coleman RE, Delbeke D, Guiberteau MJ, et al. Concurrent PET/CT with an integrated imaging system: intersociety dialogue from the joint working group of the American College of Radiology, the Society of Nuclear Medicine, and the Society of Computed Body Tomography and Magnetic Resonance. J Nucl Med. 2005;46:1225–1239.[Abstract/Free Full Text]

Related articles in JNM:

THIS MONTH IN JNM

JNM 2005 46: 8a-9a. [Full Text]  



This article has been cited by other articles:


Home page
JNMHome page
J. Tian, X. Yang, L. Yu, P. Chen, J. Xin, L. Ma, H. Feng, Y. Tan, Z. Zhao, and W. Wu
A Multicenter Clinical Trial on the Diagnostic Value of Dual-Tracer PET/CT in Pulmonary Lesions Using 3'-Deoxy-3'-18F-Fluorothymidine and 18F-FDG
J. Nucl. Med., February 1, 2008; 49(2): 186 - 194.
[Abstract] [Full Text] [PDF]


Home page
RadiologyHome page
K. Strobel, R. Dummer, D. B. Husarik, M. Perez Lago, T. F. Hany, and H. C. Steinert
High-Risk Melanoma: Accuracy of FDG PET/CT with Added CT Morphologic Information for Detection of Metastases
Radiology, August 1, 2007; 244(2): 566 - 574.
[Abstract] [Full Text] [PDF]


Home page
Br. J. Radiol.Home page
A C Pfannenberg, P Aschoff, K Brechtel, M Muller, M Klein, R Bares, C D Claussen, and S M Eschmann
Value of contrast-enhanced multiphase CT in combined PET/CT protocols for oncological imaging
Br. J. Radiol., June 1, 2007; 80(954): 437 - 445.
[Abstract] [Full Text] [PDF]


Home page
JNMHome page
U. Metser, E. Miller, H. Lerman, G. Lievshitz, S. Avital, and E. Even-Sapir
18F-FDG PET/CT in the Evaluation of Adrenal Masses
J. Nucl. Med., January 1, 2006; 47(1): 32 - 37.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Related articles in JNM
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Schöder, H.
Right arrow Articles by Larson, S. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schöder, H.
Right arrow Articles by Larson, S. M.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
JOURNAL OF NUCLEAR MEDICINE TECHNOLOGY THE JOURNAL OF NUCLEAR MEDICINE