PMID- 24997081 OWN - NLM STAT- MEDLINE DCOM- 20140919 LR - 20181202 IS - 1790-5427 (Print) IS - 1790-5427 (Linking) VI - 17 IP - 2 DP - 2014 May-Aug TI - Can 3'-deoxy-3'-(18)F-fluorothymidine or 2'-deoxy-2'-(18)F-fluoro-d-glucose PET/CT better assess response after 3-weeks treatment by epidermal growth factor receptor kinase inhibitor, in non-small lung cancer patients? Preliminary results. PG - 90-6 LID - 10.1967/s002449910136 [doi] AB - The objectives of this study was to study the diagnostic efficacy of 3'-deoxy-3'-fluorine-18-fluorothymidine ((18)F-FLT) and of 2'-deoxy-2'-(18)F-fluoro-d-glucose ((18)F-FDG) positron emission tomography/computed tomography (PET/CT) for response evaluation following three weeks treatment by epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) in non small cell lung cancer (NSCLC) patients. Fifteen patients of advanced stage (IIIB-IV) NSCLC planned for oral 1st or 2nd/3rd line EGFR-TKI treatment were enrolled in the study. Baseline, prior to treatment, and follow-up after three weeks, (18)F-FLT and (18)F-FDG PET/CT imaging was performed in all patients. The standard uptake lean body mass (SULpeak) and total lesion glycolysis (TLG) values of the hottest lesions were calculated in all patients using semi-quantitative analysis. Statistical analysis on PET semi-quantitative data was used to evaluate the overall survival (OS) and progression free survival (PFS). The patients were either classified as responders or non-responders or at a steady state according to the PET response criteria in solid tumors (PERCIST). The receiver operating characteristic curve (ROC) analysis was done on the (18)F-FDG PET/CT clinical responders, to derive the cut-off values on the corresponding data sets between responders and non responders. Results showed that in responders (18)F-FDG SULpeak values better predicted OS and PFS values when compared to (18)F-FLT SULpeak values and also were a better predictor of OS as compared to the TLG values. In responders, the ROC analysis carried out on (18)F-FLT PET/CT imaging data in responders indicated a decrease of >/=22% in SULpeak and a decrease of >/=0.7 in absolute values. Three (3/15) patients developed resistance to EGFR-TKI treatment at 3 months of follow-up. In conclusion, in both responders and in non responders, patients with NSCLC treated for 3 weeks by EGFR-TKI, both OS and PFS were better predicted by (18)F -FDG SULpeak than by (18)F -FLT SULpeak. Although, the difference was only borderline, yet, (18)F -FDG SULpeak was a better predictor of OS compared to TLG values. However, to validate these findings, studies need to be carried in a larger number of patients. FAU - Bhoil, Amit AU - Bhoil A AD - Department of Nuclear Medicine and PET, PGIMER, Chandigarh-160012, India. drbsingh5144@yahoo.com. FAU - Singh, Baljinder AU - Singh B FAU - Singh, Navneet AU - Singh N FAU - Kashyap, Raghava AU - Kashyap R FAU - Watts, Ankit AU - Watts A FAU - Sarika, Sharma AU - Sarika S FAU - Mittal, Bhagwant Rai AU - Mittal BR LA - eng PT - Clinical Trial PT - Comparative Study PT - Journal Article DEP - 20140705 PL - Greece TA - Hell J Nucl Med JT - Hellenic journal of nuclear medicine JID - 101257471 RN - 0 (Antineoplastic Agents) RN - 0 (Dideoxynucleosides) RN - 0 (Protein Kinase Inhibitors) RN - 0Z5B2CJX4D (Fluorodeoxyglucose F18) RN - EC 2.7.10.1 (ErbB Receptors) RN - PG53R0DWDQ (alovudine) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Antineoplastic Agents/pharmacology/therapeutic use MH - Carcinoma, Non-Small-Cell Lung/*diagnosis/diagnostic imaging/drug therapy MH - *Dideoxynucleosides MH - Disease-Free Survival MH - ErbB Receptors/*antagonists & inhibitors MH - Female MH - *Fluorodeoxyglucose F18 MH - Humans MH - Lung Neoplasms/*diagnosis/diagnostic imaging/drug therapy MH - Male MH - Middle Aged MH - Multimodal Imaging MH - *Positron-Emission Tomography MH - Protein Kinase Inhibitors/pharmacology/therapeutic use MH - Time Factors MH - *Tomography, X-Ray Computed MH - Treatment Outcome EDAT- 2014/07/06 06:00 MHDA- 2014/09/23 06:00 CRDT- 2014/07/06 06:00 PHST- 2014/04/01 00:00 [received] PHST- 2014/06/23 00:00 [accepted] PHST- 2014/07/06 06:00 [entrez] PHST- 2014/07/06 06:00 [pubmed] PHST- 2014/09/23 06:00 [medline] AID - s002449910136 [pii] AID - 10.1967/s002449910136 [doi] PST - ppublish SO - Hell J Nucl Med. 2014 May-Aug;17(2):90-6. doi: 10.1967/s002449910136. Epub 2014 Jul 5.