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NCT04838496Active, not recruitingPhase 2

Induction chemotherapy for locally advanced rectal cancer.

Neo-adjuvant FOLFOXIRI and chemoradiotherapy for high risk (“ugly”) locally advanced rectal cancer.

Source: EU CTIS (euclinicaltrials.eu) · Last updated 25 Mar 2024

Brief summary (registry, in English)

The primary objective of this study is to evaluate if the addition of induction chemotherapy with FOLFOXIRI leads to a higher pathological complete response (pCR) rate and clinical complete response (cCR) rate at 1 year in patients with hr-LARC compared to the currently available literature regarding hr-LARC patients treated with (chemo)radiotherapy alone or followed by consolidation chemotherapy.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
128 (estimated)
First submitted
6 Mar 2024
Start date
21 Jul 2021
Lead sponsor
Catharina Ziekenhuis Stichting
NCT number
NCT04838496
EU CT number
2023-509758-74-00
EudraCT number
2020-003134-20

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 128
  • 20 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Evidence of metastatic disease at time of inclusion or within six months prior to inclusion except for patients with enlarged iliac or inguinal lymph nodes and aspecific lung nodules
  • Any chemotherapy within the past 6 months
  • Previous radiotherapy in the pelvic area precluding chemoradiotherapy with a dose of 50-50.4 Gy
  • Any contraindication to undergo surgery, as determined by the surgeon and/or anaesthesiologist
  • Concurrent malignancies that interfere with the planned study treatment or the prognosis of the resected tumour

Other illness

  • Any contraindication for the planned systemic therapy (e.g. severe allergy, pregnancy, kidney dysfunction and thrombocytopenia), as determined by the medical oncologist
  • Any contraindication for the planned chemoradiotherapy (e.g. severe allergy to the chemotherapy agent or no possibility to receive radiotherapy), as determined by the medical oncologist and/or radiation oncologist

Other

  • Homozygous DPD deficiency

Who the study is looking for

  • 18 years or older
  • WHO performance score 0-1
  • Fit for (modified dose) triple chemotherapy (FOLFOXIRI)
  • Histopathologically confirmed rectal cancer
  • Lower border of the tumour located on or below the sigmoidal take-off as established on MRI of the pelvis
  • Confirmed high-risk locally advanced rectal cancer, at high risk of treatment failure, meeting one of the following imaging based criteria: *Tumour invasion of the mesorectal fascia (MRF+); *The presence of grade 4 extramural venous invasion (mrEMVI); *The presence of tumour deposits (TD); *The presence of bilateral extramesorectal lymph nodes with a short-axis size ≥ 7mm (LLN) or extensive LLN involving pelvic side wall structures, at high risk of an incomplete resection
  • Resectable disease as determined on magnetic resonance imaging (MRI) or deemed resectable disease after neo-adjuvant treatment (Expected gross incomplete resection with overt tumour remaining in the patient after resection, tumour invasion in the neuroforamina, encasement of the sciatic nerve and invasion of the cortex from S2 and upwards are considered not resectable)
  • Written informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (20)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Amsterdam UMC
Coordinator of this site? Confirm its status
AmsterdamNetherlandsActive, not recruiting
Netherlands Cancer Institute
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AmsterdamNetherlandsActive, not recruiting
Radiotherapiegroep
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ArnhemNetherlandsActive, not recruiting
Rijnstate Ziekenhuis Stichting
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ArnhemNetherlandsActive, not recruiting
Deventer Ziekenhuis
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DeventerNetherlandsActive, not recruiting
Catharina Ziekenhuis Stichting
Coordinator of this site? Confirm its status
EindhovenNetherlandsActive, not recruiting
Stichting St. Anna Zorggroep
Coordinator of this site? Confirm its status
GeldropNetherlandsActive, not recruiting
Elkerliek ziekenhuis
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HelmondNetherlandsActive, not recruiting
Radiotherapeutisch Instituut Friesland
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LeeuwardenNetherlandsActive, not recruiting
Medisch Centrum Leeuwarden B.V.
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LeeuwardenNetherlandsActive, not recruiting
Leids Universitair Medisch Centrum (LUMC)
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LeidenNetherlandsActive, not recruiting
Medical Center Haaglanden
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LeidschendamNetherlandsActive, not recruiting
Maastricht University Medical Center
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MaastrichtNetherlandsActive, not recruiting
Maastro Clinic
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MaastrichtNetherlandsActive, not recruiting
Radboud Universitair Medisch Centrum (Radboudumc)
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NijmegenNetherlandsActive, not recruiting
Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)
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RotterdamNetherlandsActive, not recruiting
Universitair Medisch Centrum Utrecht
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UtrechtNetherlandsActive, not recruiting
Maxima Medisch Centrum
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VeldhovenNetherlandsActive, not recruiting
St. Jans Gasthuis
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WeertNetherlandsActive, not recruiting
Isala Klinieken Stichting
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ZwolleNetherlandsActive, not recruiting

This page is information, not medical advice. Discuss any trial with your doctor.