Literature DB >> 28674853

FDG-PET/CT for response evaluation of invasive bladder cancer following neoadjuvant chemotherapy.

E E Fransen van de Putte1, E Vegt2, L S Mertens3, A Bruining4, K Hendricksen3, M S van der Heijden5, S Horenblas3, B W G van Rhijn3.   

Abstract

PURPOSE: We investigated the accuracy of FDG-PET/CT response identification following neoadjuvant or induction chemotherapy (NAIC) for invasive bladder cancer (BC) as to better select patients for radical cystectomy (RC).
METHODS: Between 2010 and 2014, 37 cT1-4N1-3 BC patients received a FDG-PET/CT before and after NAIC followed by RC. Metabolic lymph node (LN) response was evaluated according to EORTC recommendations. Additionally, primary tumor response was evaluated for 23 patients by means of delayed pelvic imaging after forced diuresis. Gold standard was response on pathologic analysis of RC specimens. Response was defined as partial response (pPR, any pathologic downstaging) or complete response (pCR, <ypT1N0). Cancer-specific survival (CSS) was correlated with pCR and metabolic CR.
RESULTS: Twenty-four cN+ patients achieved LN pCR. FDG-PET/CT identified pCR with 67% sensitivity and 46% specificity. Primary tumor response was evaluable for 17/23 patients, of whom 12 were responders. Tumor downstaging (pPR or pCR) was identified with 83% sensitivity and 80% specificity. Tumor pCR was detected with 70% sensitivity and 71% specificity. pCR of overall disease (primary tumor and LNs, n = 17) was detected with 67% sensitivity and 75% specificity. CSS was positively associated with pathologic CR (HR 0.16, p = 0.027), but not with metabolic CR (HR 0.560, p = 0.612).
CONCLUSION: FDG-PET/CT can accurately distinguish primary tumor downstaging from non-response, which suggests that response monitoring (in cN0 patients) might be used to adjust neoadjuvant treatment. pCR identification is less accurate, especially for LN metastases, which suggests that FDG-PET/CT cannot be used to select patients for RC.

Entities:  

Keywords:  Chemotherapy; Fluorodeoxyglucose F18; Metabolic response; Positron emission tomography; Urinary bladder neoplasms

Mesh:

Substances:

Year:  2017        PMID: 28674853     DOI: 10.1007/s11255-017-1637-4

Source DB:  PubMed          Journal:  Int Urol Nephrol        ISSN: 0301-1623            Impact factor:   2.370


  21 in total

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3.  Clinical value of fluorine-18 2-fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography in bladder cancer.

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4.  Response to induction chemotherapy and surgery in non-organ confined bladder cancer: a single institution experience.

Authors:  R P Meijer; J A Nieuwenhuijzen; W Meinhardt; A Bex; H G van der Poel; B W van Rhijn; J M Kerst; A M Bergman; E van Werkhoven; S Horenblas
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5.  11C-acetate PET/CT in bladder urothelial carcinoma: intraindividual comparison with 11C-choline.

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6.  Prognostic value of lymph-node dissection in patients undergoing radical cystectomy following previous oncological treatment for bladder cancer.

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7.  Measurement of clinical and subclinical tumour response using [18F]-fluorodeoxyglucose and positron emission tomography: review and 1999 EORTC recommendations. European Organization for Research and Treatment of Cancer (EORTC) PET Study Group.

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Review 5.  Management of Localized Muscle-Invasive Bladder Cancer from a Multidisciplinary Perspective: Current Position of the Spanish Oncology Genitourinary (SOGUG) Working Group.

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