Published October 1, 2015 | Version v1
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18F-FDG PET imaging of breast cancer: evaluation of the metabolic behaviour of the different breast cancer subtypes and prediction of the tumor response to neoadjuvant chemotherapy

Description

Positron Emission Tomography (PET) with 18Fluoro-deoxyglucose (18F-FDG) is the reference imaging examination for in-vivo quantification of the glucidic metabolism of tumour cells. It allows for the monitoring of tumour metabolic changes during chemotherapy. Breast cancer comprises several distinct genomic entities with different biological characteristics and clinical behaviours, leading to different tailored treatments. The aim of this doctoral thesis was to evaluate the relationship between the different biological entities of breast cancer and the tumour metabolic behaviour during neoadjuvant chemotherapy. We have also retrieved, among the various metabolic parameters on PET images, the most reliable ones to predict, as early as after the first neoadjuvant cycle, the final tumour histologic response and patient's outcome. We have also evaluated early changes in tumour blood flow, using a tumour first-pass model derived from a dynamic 18F-FDG-PET acquisition. The first article presented in this thesis has underlined the strong correlation between breast cancer subtypes, and the tumour metabolic behaviour during chemotherapy. The following three articles have demonstrated that tumour metabolic changes after the first neoadjuvant cycle can predict the final histologic complete response at the end of the treatment, both in triple-negative and HER2 positive tumours. Concerning the luminal/HER2 subtype, the early metabolic response mainly predicts patient's outcome. These results should lead, in the near future, to PET-guided neoadjuvant strategies, in order to adapt the neoadjuvant treatment in poor-responding women. Such a strategy should lead to enhanced personalized medicine. (author)

Abstract (French)

La Tomographie par Emission de Positons (TEP) au 18Fluoro-desoxyglucose (18F-FDG) est l'imagerie de reference pour la quantification in vivo du metabolisme glucidique des cellules tumorales. Elle permet, entre autre, de suivre les modifications du metabolisme tumoral en cours de chimiotherapie. Le cancer du sein regroupe differentes entites genomiques dont les comportements clinico-biologiques et la prise en charge therapeutique divergent. L'objectif de cette these etait d'etudier le lien entre ces diverses entites biologiques du cancer du sein et le comportement metabolique tumoral en cours de chimiotherapie neoadjuvante. Nous avons egalement extrait, parmi les differents parametres metaboliques tumoraux des images TEP, les criteres les plus robustes pour predire des la fin des la premiere cure de chimiotherapie neoadjuvante la reponse histologique finale et la survie des patientes. Nous avons egalement applique un modele de mesure de la perfusion tumorale, derivee d'une acquisition dynamique du premier passage arteriel et tumoral du 18F-FDG. Le premier article de cette these souligne l'impact majeur du phenotype tumoral sur le comportement metabolique en cours de chimiotherapie de la tumeur primitive mammaire. Les trois articles suivants montrent que, pour les tumeurs triple-negatives et HER2 positives, les modifications metaboliques tumorales observees par la TEP au 18F-FDG predisent la reponse histologique complete a l'issue du traitement. Concernant le phenotype tumoral luminal/HER2 negatif, la reponse metabolique apporte surtout une information pronostique. L'imagerie TEP au 18F-FDG pourrait permettre dans un avenir proche de guider les choix therapeutiques du clinicien, en proposant une alternative therapeutique aux patientes non-repondeuses identifiees des la premiere cure de chimiotherapie neoadjuvante. (auteur)

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Additional details

Additional titles

Original title (French)
Imagerie TEP au 18F-FDG du cancer du sein: etude du comportement metabolique des differents phenotypes tumoraux et prediction de la reponse tumorale a la chimiotherapie neoadjuvante

Publishing Information

Imprint Pagination
233 p.
Report number
FRNC-TH--15805

Optional Information

Notes
355 refs.; Available from the INIS Liaison Officer for France, see the INIS website for current contact and E-mail addresses