Abstract

PurposeTo ascertain the dosimetric performance of a new delivery system (the Halcyon system, H) equipped with dual-layer stacked multi-leaf collimator (MLC) for risk-adapted targets in cervix uteri cancer patients compared to another ring-based system in clinical operation (Helical Tomotherapy, HT).MethodsTwenty patients were retrospectively included in a treatment planning study (10 with positive lymph nodes and 10 without). The dose prescription (45Gy to the primary tumour volume and a simultaneously integrated boost up to 55Gy for the positive patients) and the clinical planning objectives were defined consistently as recommended by an ongoing multicentric clinical trial. Halcyon plans were optimised for the volumetric modulated arc therapy. The plan comparison was performed employing the quantitative analysis of the dose-volume histograms.ResultsThe coverage of the primary and nodal target volumes was comparable for both techniques and both subsets of patients. The primary planning target volume (PTV) receiving at least 95% of the prescription isodose ranged from 97.2 ± 1.1% (node-negative) to 99.1 ± 1.2% (node-positive) for H and from 96.5 ± 1.9% (node-negative) to 98.3 ± 0.9% (node-positive) for HT. The uncertainty is expressed at one standard deviation from the cohort of patient per each group. For the nodal clinical target volumes, the dose received by 98% of the planning target volume ranged 55.5 ± 0.1 to 56.0 ± 0.8Gy for H and HT, respectively. The only significant and potentially relevant differences were observed for the bowels. In this case, V40Gy resulted 226.3 ± 35.9 and 186.9 ± 115.9 cm3 for the node-positive and node-negative patients respectively for Halcyon. The corresponding findings for HT were: 258.9 ± 60.5 and 224.9 ± 102.2 cm3. On the contrary, V15Gy resulted 1279.7 ± 296.5 and 1557.2 ± 359.9 cm3 for HT and H respectively for node-positive and 1010.8 ± 320.9 versus 1203.8 ± 332.8 cm3 for node-negative.ConclusionThis retrospective treatment planning study, based on the dose constraints derived from the Embrace II study protocol, suggested the essential equivalence between Halcyon based and Helical Tomotherapy based plans for the intensity-modulated rotational treatment of cervix uteri cancer. Different levels of sparing were observed for the bowels with H better protecting in the high-dose region and HT in the mid-low dose regions. The clinical impact of these differences should be further addressed.

Highlights

  • Primary chemoradiation and brachytherapy is the standard of care for patients with locally advanced cervical cancer

  • As the newer treatment algorithms envisage brachytherapy and nodal dose escalation, it’s imperative that doses to organs at risk that potentially receive a contribution from both external radiation and brachytherapy are minimised to the lowest possible level

  • Target definition and dose prescription A retrospective treatment planning study was performed on a cohort of 20 patients; 10 cases were selected with positive lymph nodes (N+) and 10 without positive nodes (N-) from the institutional trial database

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Summary

Introduction

Primary chemoradiation and brachytherapy is the standard of care for patients with locally advanced cervical cancer. External beam radiation therapy (EBRT), brachytherapy, and concomitant chemotherapy are the integral parts of this treatment. These are associated with clinically significant acute and late toxicity. While most of the late sequelae in organs at risk (rectum, sigmoid and bladder) may be attributed to brachytherapy, a significant proportion of gastrointestinal acute and late sequelae are a result of both low and high doses received by the bowel. In patients receiving extended field radiation due to para-aortic disease, higher incidence of gastrointestinal toxicity may be expected, and highly conformal radiation fields may help in reducing bowel dose. IGIMRT for EBRT is associated with a reduced incidence of gastrointestinal toxicity

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