Chemotherapy Response Evaluation in Metastatic Colorectal Cancer with FDG PET/CT and CT Scans
Background: [18F]-fluorodeoxyglucose with positron-emission tomography (PET) and computed tomography (CT) scans were used to assess morphological and metabolic tumour response after chemotherapy in metastatic colorectal cancer. Patients and Methods: Twenty-five patients were evaluated after 4 course...
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Published in | Anticancer research Vol. 29; no. 7; pp. 2563 - 2568 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Attiki
International Institute of Anticancer Research
01.07.2009
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Subjects | |
Online Access | Get full text |
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Summary: | Background: [18F]-fluorodeoxyglucose with positron-emission tomography (PET) and computed tomography (CT) scans were used
to assess morphological and metabolic tumour response after chemotherapy in metastatic colorectal cancer. Patients and Methods:
Twenty-five patients were evaluated after 4 courses of chemotherapy (±target therapy), and among them 20 patients after 2
courses. Response Evaluation Criteria In Solid Tumors (RECIST) and European Organisazion for Research and Treatment of Cancer
(EORTC) criteria were used to evaluate CT and PET respectively. Results: Discrepancies between the two procedures were noted
after 4 courses of chemotherapy in patient-based analysis. Two morphologically complete responses (CR) were correlated with
metabolic response. Seven morphological partial responses (PR) were evaluated as 3 metabolic PR, 2 CR and 1 progressive disease
(PD). Seventeen cases of morphologically stable disease (SD) were evaluated as 3 metabolic CR, 13 PR and 1 PD. These discrepancies
were confirmed in lesion-based analysis. Perfect concordance was noted between metabolic responses obtained after 2 and 4
cycles. Conclusion: Morphological and metabolic imaging does not permit concordant therapeutic assessment in metastatic colorectal
cancer. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0250-7005 1791-7530 |