Dose-volume constraints for gastric and duodenal toxicity in pancreas moderately hypofractionated RT
MO-0220
Abstract
Dose-volume constraints for gastric and duodenal toxicity in pancreas moderately hypofractionated RT
Authors: SARA BROGGI1, Paolo Passoni2, Paolo Tiberio1, Alessandro Cicchetti3, Barbara Longobardi4, Najla Slim2, Michele Reni5, Antonella Del Vecchio1, Nadia Gisella Di Muzio2, Claudio Fiorino1
1San Raffaele Scientific Institute, Medical Physics, Milano, Italy; 2San Raffaele Scientific Institute, Radiotherapy, Milano, Italy; 3San Raffaele Scientific Institute, Medical Phyiscs, Milano, Italy; 4San Raffaele Scientific Institute, Medical Phyisics, Milano, Italy; 5San Raffaele Scientific Institute, Oncology, Milano, Italy
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Purpose or Objective
Hypofractionated radiotherapy (RT) of pancreatic adenocarcinoma is
challenging, due to the tolerance of adjacent normal tissues. Aim of the study
was to assess dose-volume histogram (DVH) related predictors of acute and late gastric
and duodenal toxicities for locally advanced pancreatic (LAP) patients.
Material and Methods
200 patients with histologically proven pancreatic
adenocarcinoma treated in the period 2004-2019 were considered. All patients
received induction chemotherapy (ChT) followed by concurrent chemoradiotherapy
(CRT). Delivered dose was 44.25 Gy in 15 fractions to pancreatic tumor and
lymphonodes radiologically involved. 28 pts received a simultaneous integrated
boost with doses in the range 48-55 Gy to a tumor sub-volume infiltrating the
vessels. RT was delivered with Helical Tomotherapy. Duodenum and stomach
absolute DVHs were collected and analyzed. Gastric/duodenal CTCAEv5 Grade ≥ 2 toxicities were considered. First, absolute DVHs of patients
with/without toxicities were compared through two-sided t-test; the DVH points
corresponding to the lowest p-values and the near Dmax value (D0.03
,dose received by 0.03 cc of OAR) were included and tested in univariate
and multivariate logistic regressions, testing the association between these
parameters and the risk of toxicity e. The best cut-off values discriminating
between patients with/without toxicity were also assessed through a ROC
analysis.
Results
Grade ≥ 2 toxicity occurred in 18 patients (6 acute and 12 late):
11 duodenal (ulcer, duodenitis) and 16 gastric (ulcer, stomatitis) toxicities
were reported. Both for stomach and duodenum, V44 and V15 were selected as the
most promising discriminating DVH parameters (figure 1). At univariate
analysis, duodenum V44 (p= 0.01; OR= 1.07) and D0.03 (p=0.03;
OR=1.2) were found the most predictive parameters for duodenal toxicity; V44
(p= 0.0033) was confirmed at multivariate analysis.
Regarding gastric toxicity, stomach D0.03 (p=
0.03; OR=1.20) was the only significant predictor.
The best duodenum V44 and D0.03 cut-off values were 9.1 cc and 46.7 Gy; for
both parameters a negative predictive value equal to 97% was found. Concerning stomach,
D0.03 > 45 Gy was the best cut-off value with a negative
predictive value of 94%.
The crude rates of
duodenal toxicity were 4/172 (2.3%) vs 5/23 (21.7%) if duodenum V44 < 9.1 cc
and ≥ 9.1 cc respectively. The crude rates of gastric toxicities were 9/144
(6.2%) and 7/56 (12.5%) if stomach D0.03 < 45 Gy and ≥ 45 Gy respectively.
Conclusion
In a large population of patients treated with hypofractionated
radiotherapy for LAP cancer, the risk of duodenal and gastric toxicities was
found to be related to the high dose region of duodenum and stomach DVH. The suggested
constraints (duodenum V44<9.1cc, D0.03 <46.7Gy; stomach D0.03
<45Gy) may help in planning optimization and in implementing future dose
escalation trials.