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Intraoperative radiotherapy as an immediate adjuvant treatment of rectal cancer due to limited access to external-beam radiotherapy
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Abstract
Background
Neoadjuvant external-beam radiotherapy (EBRT) with concomitant chemotherapy is the current standard-of-care for locally-advanced rectal cancer. Intraoperative radiotherapy (IORT) is to date only recommended for pelvic recurrences or incompletely resectable tumors. We here report on patients with stage II/III rectal cancer that were treated with IORT in a regional Russian university center due to limited access to EBRT.
Methods
We retrospectively analyzed data from patients that were diagnosed with locally-advanced rectal cancer and underwent surgery from December 2012 to October 2016 at a regional oncological center in Russia (Krasnodar). During this period, access to EBRT was limited due to a temporary lack of a sufficient number of EBRT facilities. Patients unable to travel to a distant radiotherapy site received IORT alone, those that could travel received neoadjuvant external beam (chemo-) radiotherapy. Factors of interest were tumor stage, tumor differentiation, resection status, surgery type and neoadjuvant or adjuvant chemotherapy. We assessed local progression-free survival (L-PFS), PFS and overall survival (OS).
Results
A total of 172 patients were included in this analysis. Of those, 92 (53.5%) were treated with IORT alone (median dose: 15 Gy [8.4–17 Gy]) and 80 (46.5%) received both neoadjuvant EBRT (median dose: 50.4 Gy [40–50.4 Gy]) and IORT (median dose: 15 Gy [15–17 Gy]). The median age was 65 years [33–82]. The median follow-up was 23 months [0–63 months]. The incidence of toxicity was low in both groups with an overall complication rate of 5.4%. Local PFS at 4 years was comparable with 59.4% in the IORT group and 65.4% in the IORT/EBRT group (p = 0.70). Similarly, there was no difference in OS or PFS (p = 0.66, p = 0.51, respectively).
Conclusions
IORT is a valuable option for patients with locally-advanced rectal cancer in the absence of access to EBRT.
Springer Science and Business Media LLC
Title: Intraoperative radiotherapy as an immediate adjuvant treatment of rectal cancer due to limited access to external-beam radiotherapy
Description:
Abstract
Background
Neoadjuvant external-beam radiotherapy (EBRT) with concomitant chemotherapy is the current standard-of-care for locally-advanced rectal cancer.
Intraoperative radiotherapy (IORT) is to date only recommended for pelvic recurrences or incompletely resectable tumors.
We here report on patients with stage II/III rectal cancer that were treated with IORT in a regional Russian university center due to limited access to EBRT.
Methods
We retrospectively analyzed data from patients that were diagnosed with locally-advanced rectal cancer and underwent surgery from December 2012 to October 2016 at a regional oncological center in Russia (Krasnodar).
During this period, access to EBRT was limited due to a temporary lack of a sufficient number of EBRT facilities.
Patients unable to travel to a distant radiotherapy site received IORT alone, those that could travel received neoadjuvant external beam (chemo-) radiotherapy.
Factors of interest were tumor stage, tumor differentiation, resection status, surgery type and neoadjuvant or adjuvant chemotherapy.
We assessed local progression-free survival (L-PFS), PFS and overall survival (OS).
Results
A total of 172 patients were included in this analysis.
Of those, 92 (53.
5%) were treated with IORT alone (median dose: 15 Gy [8.
4–17 Gy]) and 80 (46.
5%) received both neoadjuvant EBRT (median dose: 50.
4 Gy [40–50.
4 Gy]) and IORT (median dose: 15 Gy [15–17 Gy]).
The median age was 65 years [33–82].
The median follow-up was 23 months [0–63 months].
The incidence of toxicity was low in both groups with an overall complication rate of 5.
4%.
Local PFS at 4 years was comparable with 59.
4% in the IORT group and 65.
4% in the IORT/EBRT group (p = 0.
70).
Similarly, there was no difference in OS or PFS (p = 0.
66, p = 0.
51, respectively).
Conclusions
IORT is a valuable option for patients with locally-advanced rectal cancer in the absence of access to EBRT.
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