Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

Sunday
May 08
16:55 - 17:55
Mini-Oral Theatre 2
16: RTT treatment planning, OAR & target definitions
Barbara Barbosa, Portugal;
Marjolein van Os, The Netherlands
2580
Mini-Oral
RTT
Partial irradiation in cervical cancer MRgRT: a dosimetric evaluation
Claudio Votta, Italy
MO-0650

Abstract

Partial irradiation in cervical cancer MRgRT: a dosimetric evaluation
Authors:

Claudio Votta1, Luca Boldrini1, Giuditta Chiloiro1, Angela Romano1, Elisa Bonelli1, Rosa Autorino1, Marco Bianchi1, Maura Campitelli1, Elena Galofaro1, Alessia Nardangeli1, Matteo Nardini1, Lorenzo Placidi1, Maria Antonietta Gambacorta1, Vincenzo Valentini1

1Fondazione Policlinico Universitario A. Gemelli IRCCS, Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Rome, Italy

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Purpose or Objective

Although survival rates for patients with locally advanced cervical cancer (LACC) are improving, local relapse and toxicity still remain major concerns. Despite the current consensus contouring guidelines for intensity modulated radiotherapy (IMRT) for cervical cancer (CC) suggests to include the whole uterus in the clinical target volume (CTV), there is no unequivocal evidence supporting this indication. Pathological analyses of surgical resection specimens suggest that a 10 mm uterine margin around the primary tumour (GTV) would cover all microscopic disease extension more than adequately.  Magnetic resonance imaging (MRI) is considered the elective imaging modality for identifying GTV in CC. In this context, the recent development of hybrid MRI-radiotherapy systems (MRgRT) may represent a significant step-forward in the clinical management of CC, ensuring the most reliable target identification ever.

Material and Methods

Patients with LACC undergoing chemoradiotherapy (CRT) were retrospectively selected. Each patient received 45 Gy delivered in 25 daily fractions using the MRIdian system (ViewRay, Mountain View, California, US). Each patient's original plan (OP) was used as planning reference.

A new treatment plan (PI) was obtained by considering the CTV as GTV plus an expansion of  1,2cm within uterus and up to 2 cm caudally in the vagina plus pelvic elective nodes and parametria (Figure 1).

Dose-volume histogram (DVH) was analyzed to determine the difference in dose values. PTV V95%, V45 for bowel bag, V10 for body and  Dmax, Dmean for different OARs (bowel bag, bowel loops, bladder, rectum, femoral heads) were extracted from DVHs for plan comparison. 


Results

21 patients were finally enrolled for the study. OP and PI plans achieved comparable target dose coverage (Average V95% = -0,07±0,9).

PI plans delivered a lower Dmean to the all OARs considered (figure2). Dmean difference was higher for bowel bag (Average ∆Dmean = -1,07Gy±0,8), for bowel loops (Average ∆Dmean = -1,36Gy±0,99) and bladder (Average ∆Dmean = -1,31Gy±0,93).

Average Dmax was better in PI,  however,  Dmax variation was less than 1Gy for all OARs.

Doses to bowel bag was reduced using PI (Average ∆ V45= -6,94cc±5,72).

Moreover, low-dose spillage was less in the PI compared to OP (Average ∆ V10Body= -230,23cc±221,25).

Conclusion

The dosimetric comparison carried out in this study suggests that MRgRT for partial irradiation of the uterine cervix is feasible and linked to dose reduction to all OARs. The observed dosimetric advantages could reduce toxicity rates and be advantageous especially in young patients.

However, the real clinical impact of this approach must be investigated prospectively.