Radiotherapy dose escalation for the non-operative management of patients with unresectable locally recurrent rectal cancer (STEP-UP): Study protocol for a multicentre, prospective, open-label feasibility study.
14 affiliations
- 1Department of Surgery, Catharina Hospital, Eindhoven, the Netherlands.
- 2GROW Research Institute for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.
- 3Department of Radiation Oncology, Catharina Hospital, Eindhoven, the Netherlands.
- 4Department of Clinical Epidemiology and Medical Technology Assessment (KEMTA), Maastricht University Medical Centre, Maastricht, the Netherlands.
- 5Department of Medical Oncology, Catharina Hospital, Eindhoven, the Netherlands.
- 6Department of Medical Oncology, Maastricht University Medical Centre, Maastricht, the Netherlands.
- 7Department of Medical Oncology, Rijnstate Hospital, Arnhem, the Netherlands.
- 8Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
- 9Department of Radiation Oncology, Erasmus Medical Centre, Rotterdam, the Netherlands.
- 10Department of Radiation Oncology, Radiotherapiegroep, Arnhem/Deventer, the Netherlands.
- 11Department of Radiation Oncology, Medisch Spectrum Twente, Enschede, the Netherlands.
- 12Department of Radiation Oncology, Maastro Clinic, Maastricht, the Netherlands.
- 13Department of Radiation Oncology, University Medical Centre Utrecht, Utrecht, the Netherlands.
- 14Department of Radiology, Catharina Hospital Eindhoven, the Netherlands.
Abstract
Background
Curative-intent management of locally recurrent rectal cancer (LRRC) generally comprises neoadjuvant therapy and surgery. In patients with unresectable LRRC, where surgical intervention is not feasible, management is limited to non-operative bimodality therapy with systemic therapy and radiotherapy. Evidence guiding the optimisation of non-operative management remains limited. In this context, the therapeutic goal is to achieve prolonged local control while minimising treatment-related adverse events and preserving quality of life. Radiotherapy dose escalation has been proposed as a potential strategy to achieve this balance. However, its feasibility and safety in the non-operative management of unresectable LRRC have not yet been established. As such, this study aims to evaluate the feasibility and safety of this radiotherapeutic approach, and to determine its impact on both symptom control and oncological outcomes.Methods
This prospective, multicentre, single-arm feasibility study will enrol 30 patients with unresectable or inoperable LRRC without distant metastases, or with (oligo)metastatic disease not requiring immediate systemic therapy. Previously irradiated patients will undergo reirradiation with stereotactic body radiotherapy (re-SBRT; 5 × 9 Gy) when feasible, or, alternatively hyperfractionated chemo-reirradiation (50.4 Gy in 1.2 Gy twice-daily fractions with concurrent capecitabine). Radiotherapy-naïve patients will receive chemoradiotherapy with a simultaneous integrated boost (25 × 2.6 Gy, EQD2Gyα/β=5Gy of 71 Gy with concurrent capecitabine). [1] The primary endpoint is treatment regimen feasibility, defined as grade ≥ 3 acute radiotherapy-related adverse events (CTCAE version 5.0) occurring in no more than seven patients (23%). Secondary endpoints include late adverse events, quality of life and symptom control, and 1- and 3-year progression-free survival, disease-free survival, and overall survival.Discussion
This protocol describes the STEP-UP study, which will determine the feasibility of radiotherapy dose escalation in unresectable LRRC. If feasible and safe, this approach could provide an effective treatment intensification strategy to improve local control and symptom burden in patients with unresectable LRRC, addressing a major unmet clinical need.Trial registration
ClinicalTrials.gov: NCT07721181Overview of Medical-Scientific Research in the Netherlands (OMON) Registry: NL-011150.International Clinical Trial Registry Platform (ICTRP): NL-OMON61161.
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BibTeX
@article{kerckhove2026radiotherapy,
title = {{Radiotherapy dose escalation for the non-operative management of patients with unresectable locally recurrent rectal cancer (STEP-UP): Study protocol for a multicentre, prospective, open-label feasibility study.}},
author = {F E C Vande Kerckhove and J L Beeftink and R H N Tijssen and J Zijlstra and A E Verrijssen and S M J van Kuijk and S G van Ravensteijn and I E G van Hellemond and T G A Calon and I M Werter and A M Couwenberg and C S E W Schuurhuizen and M D den Hartogh and E M Hendriksen and B Hupkens and J Buijsen and M Berbée and M P W Intven and J G Bloemen and J Nederend and J W A Burger and H M U Peulen},
journal = {Clinical and translational radiation oncology},
year = {2026},
month = oct,
doi = {10.1016/j.ctro.2026.101326},
url = {https://europepmc.org/article/MED/42927245},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - Radiotherapy dose escalation for the non-operative management of patients with unresectable locally recurrent rectal cancer (STEP-UP): Study protocol for a multicentre, prospective, open-label feasibility study.
AU - F E C Vande Kerckhove
AU - J L Beeftink
AU - R H N Tijssen
AU - J Zijlstra
AU - A E Verrijssen
AU - S M J van Kuijk
AU - S G van Ravensteijn
AU - I E G van Hellemond
AU - T G A Calon
AU - I M Werter
AU - A M Couwenberg
AU - C S E W Schuurhuizen
AU - M D den Hartogh
AU - E M Hendriksen
AU - B Hupkens
AU - J Buijsen
AU - M Berbée
AU - M P W Intven
AU - J G Bloemen
AU - J Nederend
AU - J W A Burger
AU - H M U Peulen
PY - 2026
DA - 2026/10/15
JO - Clinical and translational radiation oncology
DO - 10.1016/j.ctro.2026.101326
UR - https://europepmc.org/article/MED/42927245
AB - Background Curative-intent management of locally recurrent rectal cancer (LRRC) generally comprises neoadjuvant therapy and surgery. In patients with unresectable LRRC, where surgical intervention is not feasible, management is limited to non-operative bimodality therapy with systemic therapy and radiotherapy. Evidence guiding the optimisation of non-operative management remains limited. In this context, the therapeutic goal is to achieve prolonged local control while minimising treatment-related adverse events and preserving quality of life. Radiotherapy dose escalation has been proposed as a potential strategy to achieve this balance. However, its feasibility and safety in the non-operative management of unresectable LRRC have not yet been established. As such, this study aims to evaluate the feasibility and safety of this radiotherapeutic approach, and to determine its impact on both symptom control and oncological outcomes.Methods This prospective, multicentre, single-arm feasibility study will enrol 30 patients with unresectable or inoperable LRRC without distant metastases, or with (oligo)metastatic disease not requiring immediate systemic therapy. Previously irradiated patients will undergo reirradiation with stereotactic body radiotherapy (re-SBRT; 5 × 9 Gy) when feasible, or, alternatively hyperfractionated chemo-reirradiation (50.4 Gy in 1.2 Gy twice-daily fractions with concurrent capecitabine). Radiotherapy-naïve patients will receive chemoradiotherapy with a simultaneous integrated boost (25 × 2.6 Gy, EQD2Gyα/β=5Gy of 71 Gy with concurrent capecitabine). [1] The primary endpoint is treatment regimen feasibility, defined as grade ≥ 3 acute radiotherapy-related adverse events (CTCAE version 5.0) occurring in no more than seven patients (23%). Secondary endpoints include late adverse events, quality of life and symptom control, and 1- and 3-year progression-free survival, disease-free survival, and overall survival.Discussion This protocol describes the STEP-UP study, which will determine the feasibility of radiotherapy dose escalation in unresectable LRRC. If feasible and safe, this approach could provide an effective treatment intensification strategy to improve local control and symptom burden in patients with unresectable LRRC, addressing a major unmet clinical need.Trial registration ClinicalTrials.gov: NCT07721181Overview of Medical-Scientific Research in the Netherlands (OMON) Registry: NL-011150.International Clinical Trial Registry Platform (ICTRP): NL-OMON61161.
SN - 2405-6308
ER -