Monitoring metabolic response using FDG PET-CT during targeted therapy for metastatic colorectal cancer

Autor: Lieveke Ameye, Raphaël Maréchal, Amélie Deleporte, Irina Vierasu, Erwin Woff, Thomas Guiot, Camilo Garcia, Alain Hendlisz, Thierry Delaunoit, Gauthier Demolin, Namur Gauthier, Renaud Lhommel, Patrick Flamen, Marc Van den Eynde, Stéphane Holbrechts
Přispěvatelé: UCL - SSS/IREC/MIRO - Pôle d'imagerie moléculaire, radiothérapie et oncologie, UCL - (SLuc) Service de médecine nucléaire, UCL - (SLuc) Unité d'oncologie médicale, UCL - (SLuc) Centre du cancer
Rok vydání: 2015
Předmět:
Oncology
Male
Colorectal cancer
medicine.medical_treatment
Phenylurea Compounds -- administration & dosage
030218 nuclear medicine & medical imaging
Targeted therapy
Tumoral heterogeneity
0302 clinical medicine
Positron Emission Tomography Computed Tomography
Antineoplastic Combined Chemotherapy Protocols
Radiopharmaceuticals -- pharmacokinetics
Molecular Targeted Therapy
Fluorodeoxyglucose F18 -- pharmacokinetics
Imagerie médicale
radiologie
tomographie

Metastatic colorectal cancer
Colorectal Neoplasms -- diagnostic imaging -- drug therapy -- secondary
General Medicine
Middle Aged
Sorafenib
Treatment Outcome
Drug Monitoring -- methods
Radiology Nuclear Medicine and imaging
030220 oncology & carcinogenesis
Fdg pet ct
Female
Original Article
Niacinamide -- administration & dosage -- analogs & derivatives
medicine.symptom
Drug Monitoring
Colorectal Neoplasms
medicine.drug
Adult
Niacinamide
medicine.medical_specialty
Sensitivity and Specificity
Capecitabine
Lesion
FDG PET-CT
03 medical and health sciences
Fluorodeoxyglucose F18
Internal medicine
medicine
Volume reduction
Humans
Molecular Targeted Therapy -- methods
Radiology
Nuclear Medicine and imaging

Aged
business.industry
Phenylurea Compounds
Reproducibility of Results
Positron Emission Tomography Computed Tomography -- methods
medicine.disease
Capecitabine -- administration & dosage
Discontinuation
Antineoplastic Combined Chemotherapy Protocols -- administration & dosage
Radiopharmaceuticals
business
Early metabolic response assessment
Zdroj: European Journal of Nuclear Medicine and Molecular Imaging
European Journal of Nuclear Medicine and Molecular Imaging, Vol. 43, p. 1792-1801 (2016)
European journal of nuclear medicine and molecular imaging, 43 (10
ISSN: 1619-7089
Popis: Introduction: The introduction of targeted drugs has had a significant impact on the approach to assessing tumour response. These drugs often induce a rapid cytostatic effect associated with a less pronounced and slower tumoural volume reduction, thereby impairing the correlation between the absence of tumour shrinkage and the patient’s unlikelihood of benefit. The aim of the study was to assess the predictive value of early metabolic response (mR) evaluation after one cycle, and its interlesional heterogeneity to a later metabolic and morphological response assessment performed after three cycles in metastatic colorectal cancer (mCRC) patients treated with combined sorafenib and capecitabine. Methods: This substudy was performed within the framework of a wider prospective multicenter study on the predictive value of early FDG PET-CT response assessment (SoMore study). A lesion-based response analysis was performed, including all measurable lesions identified on the baseline PET. On a per-patient basis, a descriptive 4-class response categorization was applied based upon the presence and proportion of non-responding lesions. For dichotomic response comparison, all patients with at least one resistant lesion were classified as non-responding. Results: On baseline FDG PET-CT, 124 measurable “target” lesions were identified in 38 patients. Early mR assessments showed 18 patients (47 %) without treatment resistant lesions and 12 patients (32 %) with interlesional response heterogeneity. The NPV and PPV of early mR were 85 % (35/41) and 84 % (70/83), respectively, on a per-lesion basis and 95 % (19/20) and 72 % (13/18), respectively, on a dichotomized per-patient basis. Conclusions: Early mR assessment performed after one cycle of sorafenib-capecitabine in mCRC is highly predictive of non-response at a standard response assessment time. The high NPV (95 %) of early mR could be useful as the basis for early treatment discontinuation or adaptation to spare patients from exposure to non-effective drugs.
SCOPUS: ar.j
info:eu-repo/semantics/published
Databáze: OpenAIRE