Changes in functional imaging parameters following induction chemotherapy have important implications for individualised patient-based treatment regimens for advanced head and neck cancer

Ceri Powell, M Schmidt, M Borri, Dow-Mu Koh, Mike Partridge, Angela Riddell, Gary Cook, SA Bhide, Chris Nutting, Kevin Harrington, Kate Newbold

Research output: Contribution to journalArticlepeer-review

35 Citations (Scopus)

Abstract

Background
When induction chemotherapy (IC) is used prior to chemoradiotherapy (CRT) in head and neck cancer (HNC), functional imaging (FI) may inform adaptation of treatment plans with the aim of optimising outcomes. Understanding the impact of IC on FI parameters is, therefore, essential.

Purpose
To prospectively evaluate the feasibility of acquiring serial FI (18F-FDG-PET, diffusion-weighted (DW) and dynamic contrast-enhanced (DCE) MRI) and its role in defining individualised treatment regimens following IC in HNC.

Methods and materials
Ten patients with stage III and IV HNC underwent conventional (CT and MRI) and functional (DW, DCE-MRI and 18F-FDG-PET/CT) imaging at baseline and following two cycles of IC prior to definitive CRT.

Results
One patient withdrew due to claustrophobia. Seven out of nine patients had a complete metabolic response to IC on 18F-FDG-PET imaging. DCE-MRI showed a significant fall in transfer constant (Ktrans) (0.209 vs 0.129 min−1P < 0.01) and integrated area under gadolinium curve at 60 s (IAUGC6O) (18.4 vs 11.9 mmol/min, P < 0.01) and DW-MRI a rise in ADC (0.89 vs 1.06 × 10−3 mm2/s, P < 0.01) following IC.

Conclusions
Acquiring FI sequences is feasible in HNC. There are marked changes in FI parameters following IC which may guide adaptation of individualised treatment regimens.
Original languageEnglish
Article numberN/A
Pages (from-to)112-117
Number of pages6
JournalRadiotherapy and Oncology
Volume106
Issue number1
DOIs
Publication statusPublished - 1 Jan 2013

Fingerprint

Dive into the research topics of 'Changes in functional imaging parameters following induction chemotherapy have important implications for individualised patient-based treatment regimens for advanced head and neck cancer'. Together they form a unique fingerprint.

Cite this