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Colo-rectal CancerPhase 2NO-CUTNCT03565029

Total Neoadjuvant Treatment Without Surgery For Locally Advanced Rectal Cancer

A Phase 2 study testing XELOX and Radiotherapy in people with Colo-rectal Cancer, run by Niguarda Hospital at 1 site in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

NO-CUT is a one-stage phase II trial seeking to establish whether an oxaliplatin-based chemotherapy preceding standard neo-adjuvant fluoropyrimidines-based chemo radiotherapy, can safely spare demolitive surgical intervention in patients with operable rectal cancer, without increasing the risk of distant relapse. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Colo-rectal Cancer
What is being tested?
XELOX and Radiotherapy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
180 participants
Where
1 siteItaly
Study dates
1 Jun 2018to 20 Dec 2023
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Histologically confirmed diagnosis of adenocarcinoma of the medium/lower rectum
  • Patients must have Stage II (cT3-4 N0) or Stage III (cT1-4, N1-3) tumor
  • Locally advanced rectal cancer amenable to Total Mesorectal Excision (TME)/Abdominal-Perineal Amputation
  • No evidence of distant metastases by chest, abdomen, and pelvis contrast enhanced CT scan (TC-positron emission computed tomography (PET) Whole Body (WB) is acceptable alternative in patient allergic to iodate contrast medium)
  • No prior pelvic radiation therapy
  • No prior oncologic medical therapy or surgery for rectal cancer
Show all 13Show fewer
  • Age >18 years
  • No infections requiring systemic antibiotic treatment
  • Performance status 0-1 (ECOG Scale)
  • absolute neutrophil count (ANC) > 1.5 cell/mm3, Hb>8.0 g/ dL, Platelet Count (PLT)>150,000/mm3, total bilirubin < or equal or 1.5 x upper limit of normal, Aspartate Aminotransferase (AST) < or equal to three times upper limit of normal, Alanine Aminotransferase (ALT)< or equal to three times upper limit of normal; Serum creatinine level < or equal to 1.5 times the upper limit of normal
  • Patients must read, agree to, and sign a statement of Informed Consent prior to participation
  • Women with childbearing potential who are negative for pregnancy test (urine or blood) and who agree to use effective contraceptive methods
  • Male subjects must also agree to use effective contraception

Who cannot join

  • Recurrent rectal cancer
  • Patients with a history of any arterial thrombotic event within the past 6 months, including angina (stable or unstable), MI, or CVA
  • Intolerance or contraindication to Magnetic Resonance (MR) procedure
  • Patients with any other concurrent medical or psychiatric condition
  • Gastro-intestinal abnormalities, inability to take oral medication, any condition affecting absorption
  • Patients with a history of a prior malignancy within the past 5 years, except for adequately treated basal cell or squamous cell skin cancer, or in situ cervical cancer.
  • Patients with a history of thrombotic episodes, such as deep venous thrombosis, pulmonary embolus, Myocardial Infarction (MI) or cerebral vascular accident (CVA) occurring more than 6 months prior to enrollment may be considered for protocol participation, provided they are on stable doses of anticoagulant therapy. Patients who are anticoagulated for atrial fibrillation or other conditions may participate, provided they are on stable doses of anticoagulant therapy.
  • Patients receiving other anticancer or experimental therapy.

Trial locations and contacts

1 site in 1 country.

Italy1 site
  • ASST GOM Niguarda

    Milan, 20162

Other trials in Italy

About this study

Official title: Total Neoadjuvant Treatment Without Surgery For Locally Advanced Rectal Cancer: Prospective Clinical Trial To Assess Tumor Complete Response, Circulating Tumor Genetic And Epigenetic Biomarkers, And Stromal Transcriptome To Interpret Clinical Outcome

NO-CUT is a one-stage phase II trial seeking to establish whether an oxaliplatin-based chemotherapy preceding standard neo-adjuvant fluoropyrimidines-based chemo radiotherapy, can safely spare demolitive surgical intervention in patients with operable rectal cancer, without increasing the risk of distant relapse. The trial also has a translational component aimed at establishing whether selected genomic, epigenetic, and transcriptomic markers are predictive of tumor and patient outcome.

Read the detailed description

Colorectal cancer is the third most common cancer worldwide and the second leading cause of cancer death in Europe. Rectal cancer accounts for about 25-30% of all colorectal cancer diagnoses. Five-year survival rates depend on stage at diagnosis, about 92% for stage I, 87% for stage II A, 63% for stage II B, 89% for stage III A, 69% for stage III B, and for stage III C cancers the survival rate is about 53%; stage IV rectal cancers have a 5-year relative survival rate of about 11%. With the chemoradiation therapy (CRT), the resulting pathologic complete response (pCR) across all stages has been documented in up to 30% of patients. Most importantly, patients achieving pCR have lower rates of tumor recurrence, and improved survival, compared to those who do not achieve pCR. Moreover, data from the National Surgical Quality Improvement Project document a 35% risk of morbidity associated with both low anterior and abdominoperineal resection. Long-term morbidity includes bowel and bladder incontinence, sexual dysfunction, and complications associated with temporary and permanent stomas.

Due to the observation of the absence of residual tumor in the pathological specimens of a significant proportion of patients treated with CRT for local or locally advanced rectal cancer, in the early-2000s, two clinical issues arose: firstly, if pCR could be predicted after CRT with clinical, radiological, or endoscopic restaging assessment thus defining clinical complete response (cCR); and secondly if patients with cCR should necessarily undergo radical surgery to achieve cure at the cost of morbidity, mortality, and functional consequences associated with radical rectal surgery. Consequently, an increasing number of reports suggested that non-operative management (NOM), consisting of close surveillance of patients with cCR, could be an acceptable alternative to rectal surgery (proctectomy). Led by small prospective series published since the late 90's by Habr-Gama and colleagues, several small international series have reported similar oncologic outcomes in cCR patients followed by close active surveillance (the so-called watch-and-wait (W\&W) or NOM approach) compared to those treated with radical surgery.

Between 2011 and 2013 a NOM approach was carried out in 31 patients achieving cCR out of 259 (12%). In their analysis, a further 98 patients, selected from a United Kingdom regional registry, similarly managed from 2005 to 2015, were added to the NOM group (129 patients). Overall Survival and Disease Free Survival rates resulted at least comparable to that of patients treated with standard surgery following neo-adjuvant CRT.

On the other hand, these small single institution pilot studies have been conducted enrolling small cohorts of patients with less than 500 patients having been evaluated worldwide. A high variability in stage at diagnoses, local recurrence rate, distant recurrence rate (0-60% and 0-17%, respectively) and type and outcome of salvage therapy (0 to 100%) have been reported and no reliable data on long term outcomes are available. Based on these limitations, the NOM of rectal cancer deserves consideration within purposely designed clinical trials.

Being tested
XELOX, Radiotherapy
Keywords
rectal cancer, neoadjuvant, non operative management
Medical subject headings
Colonic Neoplasms, Rectal Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • XELOXDrug

    Capecitabine and Oxaliplatin (4x cycles)

  • RadiotherapyRadiation

    Pelvic radiotherapy

Study groups in NCT03565029
Study groupRoleWhat they receive
Medium/low locally advanced rectal cancerExperimentalPatients with Stage II (cT3-4 N0) or Stage III (cT1-4, N1-3) locally advanced rectal cancer amenable to Total Mesorectal Excision (TME)/Abdominal-Perineal Amputation
Receives: Drug: XELOX; Radiation: Radiotherapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Distant Relapse-Free Survival (DRFS)

    Disease free survival rate

    Measured: 2.5 years

Secondary outcomes (5)
  1. Clinical complete response rate

    Clinical complete response rate

    Measured: 2 months

  2. Local recurrence and organ preservation rate

    Local recurrence and organ preservation rate

    Measured: 6 months

  3. Colostomy-free survival

    Colostomy-free survival

    Measured: 6 months

  4. Overall survival

    Overall survival

    Measured: 2.5 years

  5. Patient reported outcomes

    European Organization for Research and Treatment of Cancer [EORTC] Quality of Life Questionnaire-C30 and its colorectal cancer specific module Quality of Life Questionnaire-38)

    Measured: 2.5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Jun 2018
  2. Study start1 Jun 2018
  3. Primary completion31 Oct 2022
  4. Study completion20 Dec 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
one-stage phase II trial seeking to establish whether an oxaliplatin-based chemotherapy preceding standard neo-adjuvant fluoropyrimidines-based chemo radiotherapy, can safely spare demolitive surgical intervention in patients with operable rectal cancer, without increasing the risk of distant relapse. The trial also has a translational component aimed at establishing whether selected genomic, epigenetic, and transcriptomic markers are predictive of tumor and patient outcome.
Masking
None (open label)
Enrolment
180 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03565029
Sponsor's protocol ID
2017-003671-60
Other IDs
2017
Acronym
NO-CUT
Status last verified
Dec 2024
First submitted
8 Jun 2018
Last updated
27 Dec 2024
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Weekly Scientific Board Commission meetings

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing XELOX and Radiotherapy in people with Colo-rectal Cancer, run by Niguarda Hospital at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 13 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Dec 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Distant Relapse-Free Survival (DRFS) (time frame: 2.5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Dec 2024.

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