The SHAPERS study is a multicentre, open-label, randomised, pragmatic clinical trial, comparing standard-of-care neoadjuvant treatment options for older (i.e., ≥70 years) subjects with high-risk stage II and stage III rectal cancer.
The SHAPERS study is a multicentre, open-label, randomised, pragmatic clinical trial, comparing standard-of-care neoadjuvant treatment options for older (i.e., ≥70 years) subjects with high-risk stage II and stage III rectal cancer. Subjects meeting all eligibility criteria will be randomised in a 1:1 ratio to either the conventional arm or the TNT arm (The study design is shown in figure 3.1 and 3.2). Conventional arm consists of: * SCRT (5 fractions of 5 Gy), followed by * Surgery (according to the principles of TME) or watch \& wait, followed by * Optional adjuvant chemotherapy OR * LCCRT (25-28 fractions of 1.8-2.0 Gy each +/- a boost to the primary tumour and involved lymph nodes, for a total of 50-56 Gy of radiation combined with either continuous infusion fluorouracil or capecitabine) followed by * Surgery (according to the principles of TME) or watch \& wait, followed by * Optional adjuvant chemotherapy TNT arm Different treatment regimens can be used in the TNT arm including Rapido, Rapido light, OPRA INCT-CRT or OPRA CRT-CNCT. The regimen to use will be decided by the investigator and will need to be declared before randomisation. No switch between regimens is allowed during the study treatment period. The Rapido regimen consists of: * SCRT (5 fractions of 5 Gy), followed by * Up to 18 weeks of oxaliplatin based chemotherapy (mFOLFOX6 or CAPOX), followed by * Surgery (according to the principle of TME) or "watch \& wait". The Rapido light regimen consists of: * SCRT (5 fractions of 5 Gy), followed by * Up to 12 weeks of oxaliplatin based chemotherapy (mFOLFOX6 or CAPOX), followed by * Surgery (according to the principle of TME) or "watch \& wait". The OPRA with induction chemotherapy (INCT-CRT) regimen, consists of: * Up to 16 weeks of oxaliplatin-based chemotherapy (mFOLFOX6 or CAPOX), followed by * CRT (25-28 fractions of 1.8-2.0 Gy each +/- a boost to the primary tumour and involved lymph nodes, for a total of 50-56 Gy of radiation combined with either continuous infusion fluorouracil or capecitabine) followed by * Surgery (according to the principle of TME) or "watch \& wait" The OPRA with consolidation chemotherapy (CRT-CNCT) regimen consists of: * CRT (25-28 fractions of 1.8-2.0 Gy each +/- a boost to the primary tumour and involved lymph nodes, for a total of 50-56 Gy of radiation combined with either continuous infusion fluorouracil or capecitabine) followed by * Up to 16 weeks of oxaliplatin-based chemotherapy (mFOLFOX6 or CAPOX), followed by * Surgery (according to the principle of TME) or "watch \& wait".
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Enrollment
230
Patients will receive 5 daily fractions of radiotherapy. Each fraction will consist of 5 Gy for a total dose of 25 Gy.
The choice of the adjuvant chemotherapy is to the investigator's discretion.
Surgery must be performed according to the principles of total mesorectal excision. A "watch \& wait" approach is allowed for those subjects who have clinical complete response according to the local assessment.
ZAS Antwerpen
Antwerp, Antwerpen, Belgium
RECRUITINGUZA Antwerpen
Overall survival
Overall survival (OS) will be calculated from randomisation to death from any cause.
Time frame: At 3 years after randomisation
Progression-free survival
Progression-free survival (PFS) will be calculated from randomisation to any of the following events: unresectable tumour due to local tumour progression, R2 resection of the primary tumour, loco-regional recurrence after an R0/R1 resection, distant metastases, or death from any cause.
Time frame: At 3 years after randomisation
Any grade peripheral sensory neuropathy
Any grade peripheral sensory neuropathy as assessed by the investigator according to the NCI-CTCAE v5.0 will be analysed.
Time frame: At 3 years after randomisation
Grade ≥3 toxicities during treatment
Grade ≥3 toxicities during treatment (i.e., from the 1st day of treatment until the EOT visit) as assessed by the investigator according to the NCI-CTCAE v5.0 will be analysed.
Time frame: At 3 years after randomisation
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
The choice of the TNT is left to the investigator's discretion. If RAPIDO: * SCRT (5 fractions of 5 Gy), followed by * Up to 18 weeks of oxaliplatin based chemotherapy (mFOLFOX6 or CAPOX) If RAPIDO light: * SCRT (5 fractions of 5 Gy), followed by * Up to 12 weeks of oxaliplatin based chemotherapy (mFOLFOX6 or CAPOX) If OPRA with induction chemotherapy: * Up to 16 weeks of oxaliplatin-based chemotherapy (mFOLFOX6 or CAPOX), followed by * CRT (25-28 fractions of 1.8-2.0 Gy each +/- a boost to the primary tumour and involved lymph nodes, for a total of 50-56 Gy of radiation combined with either continuous infusion fluorouracil or capecitabine) If OPRA with consolidation chemotherapy: * CRT (25-28 fractions of 1.8-2.0 Gy each +/- a boost to the primary tumour and involved lymph nodes, for a total of 50-56 Gy of radiation combined with either continuous infusion fluorouracil or capecitabine) followed by * Up to 16 weeks of oxaliplatin-based chemotherapy (mFOLFOX6 or CAPOX)
Patients will receive 25-28 fractions of 1.8-2.0 Gy each +/- a boost to the primary tumour and involved lymph nodes, for a total of 50-56 Gy of radiation combined with either continuous infusion fluorouracil or capecitabine
Edegem, Antwerpen, Belgium
AZ Turnhout
Turnhout, Antwerpen, Belgium
RECRUITINGInstitut Jules Bordet
Anderlecht, Brussels Capital, Belgium
RECRUITINGChirec Delta
Auderghem, Brussels Capital, Belgium
RECRUITINGCHU Saint-Pierre
Brussels, Brussels Capital, Belgium
RECRUITINGCHU Brugmann
Brussels, Brussels Capital, Belgium
RECRUITINGUZ Gent
Ghent, East Flanders, Belgium
RECRUITINGAZ Nikolaas
Sint-Niklaas, East Flanders, Belgium
RECRUITINGHôpital de Jolimont
Haine-Saint-Paul, Hainaut, Belgium
RECRUITING...and 9 more locations