18 april 2009: Bron: 1: Clin Cancer Res. 2009 Apr 15;15(8):2856-2863. Epub 2009 Apr 7.Click here to read

Al na 1 chemokuur kan een Petscan bepalen of chemo werkt bij agressieve vormen van weke delen sarcoma. Dit blijkt uit een eerste studie waarbij de suikeropname van kankercellen een voorspellende factor bleek voor het al of niet effectief zijn van de chemokuur. Wanneer er sprake was van meer dan 35% reductie in de suikeropname bleek de chemokuur 100% effectief. tegenover 65% in de groep die minder dan 35% reductie in suikeropname van de kankercel had. Het lijkt een kleine studie maar dit wordt door onderzoekers gezien als een belangrijke uitkomst.  

 

FDG-PET/CT Imaging Predicts Histopathologic Treatment Responses after the Initial Cycle of Neoadjuvant Chemotherapy in High-Grade Soft-Tissue Sarcomas.

Authors' Affiliations: Ahmanson Biological Imaging Division, Department of Molecular and Medical Pharmacology; Divisions of Medical Oncology and Orthopedic Oncology; Departments of Pathology, Biostatistics, and Radiology; and Division of Surgical Oncology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, California and Abteilung Nuklearmedizin, University of Freiburg, Freiburg, Germany.

PURPOSE: In patients with soft-tissue sarcoma (STS), the early assessment of treatment responses is important. Using positron emission tomography/computed tomography (PET/CT) with [(18)F]fluorodeoxyglucose (FDG), we determined whether changes in tumor FDG uptake predict histopathologic treatment responses in high-grade STS after the initial cycle of neoadjuvant chemotherapy.

EXPERIMENTAL DESIGN: From February 2006 to March 2008, 50 patients with resectable high-grade STS scheduled for neoadjuvant therapy and subsequent tumor resection were enrolled prospectively. FDG-PET/CT before (baseline), after the first cycle (early follow-up), and after completion of neoadjuvant therapy (late follow-up) was done. Tumor FDG uptake and changes were measured by standardized uptake values. Histopathologic examination of the resected specimen provided an assessment of treatment response. Patients with >/=95% pathologic necrosis were classified as treatment responders. FDG-PET/CT results were compared with histopathologic findings.

RESULTS: At early follow-up, FDG uptake decreased significantly more in 8 (16%) responders than in the 42 (84%) nonresponders (-55% versus -23%; P = 0.002). All responders and 14 of 42 nonresponders had a >/=35% reduction in standardized uptake value between baseline and early follow-up. Using a >/=35% reduction in FDG uptake as early metabolic response threshold resulted in a sensitivity and specificity of FDG-PET for histopathologic response of 100% and 67%, respectively. Applying a higher threshold at late follow-up improved specificity but not sensitivity. CT had no value at response prediction.

CONCLUSION: A 35% reduction in tumor FDG uptake at early follow-up is a sensitive predictor of histopathologic tumor response. Early treatment decisions such as discontinuation of chemotherapy in nonresponding patients could be based on FDG-PET criteria.

PMID: 19351756 [PubMed - as supplied by publisher]

 


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