A Study to Evaluate a Chemotherapy Treatment Followed by Chemo and Radiotherapy in Patients With Rectal Cancer

NCT ID: NCT04009876

Last Updated: 2022-12-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-05-01
• Study Completion Date: 2022-10-21

Brief Summary

This is an exploratory, open-label, single arm, non-randomized, multicenter, phase II clinical trial to determine the efficacy and clinical complete response rate in patients with rectal cancer and tumor preoperative evaluation after NAC (Neoadjuvant Chemotherapy) with NALIRINOX (5-FU [fluorouracil)/LV [Leucovorin calcium] + oxaliplatin + nal-IRI [Liposomal Irinotecan]) and chemoradiotherapy.

Conditions

Locally Advanced Rectal Cancer (LARC)

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Chemotherapy + Surgery

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks) and surgical resection

Group Type: EXPERIMENTAL

nal-IRI

Intervention Type: DRUG

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks)

Surgical resection

Intervention Type: PROCEDURE

Surgical resection of the tumour

5-FU/LV

Intervention Type: DRUG

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks)

Oxaliplatin

Intervention Type: DRUG

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks)

Chemotherapy + Watch-and-wait

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks) and "watch-and-wait" surveillance protocol.

Group Type: EXPERIMENTAL

nal-IRI

Intervention Type: DRUG

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks)

Watch-and-wait

Intervention Type: OTHER

No surgery approach

5-FU/LV

Intervention Type: DRUG

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks)

Oxaliplatin

Intervention Type: DRUG

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks)

Interventions

nal-IRI

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks)

Intervention Type: DRUG

Surgical resection

Surgical resection of the tumour

Intervention Type: PROCEDURE

Watch-and-wait

No surgery approach

Intervention Type: OTHER

5-FU/LV

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks)

Intervention Type: DRUG

Oxaliplatin

Treatment with 5-FU/LV + Oxaliplatin + nal-IRI for 8 cycles followed by standard chemoradiation (5 weeks)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Male or females, aged ≥ 18 years.
• Agree to participate and sign voluntary written ICF (Informed Consent Form) before any study specific procedure.
• Patients with confirmed histopathological diagnosis of rectal cancer.
• Patients with locally advanced rectal cancer T3-T4N0M0 or TxN+M0 and selected T2N0M0 candidates to watch & wait program.
• Patients considered for neoadjuvant treatment according to usual clinical practice may also be potential candidates.
• ECOG (Eastern Cooperative Oncology Grou)vperformance status 0 or 1.
• Patients who can receive radiotherapy and chemotherapy.
• No prior or concurrent malignant disease unless in complete remission for more than three years, except for adequately treated in situ carcinoma of the cervix, basal or squamous skin cell carcinoma or in situ transitional bladder cell carcinoma.
• Women of childbearing potential (WOCBP) must have a negative serum pregnancy test before study entry. Both women and men must agree to use a highly effective contraceptive measure throughout the treatment period and for six months after discontinuation of treatment.
• Adequate hematologic function: hemoglobin ≥ 9g/dL; WBC (white blood cell count ) ≥ 4000/mm 3 ; neutrophils ≥ 1.5x10 9 /L; platelets ≥ 100x10 9 /L.
• Adequate hepatic function: total bilirubin ≤ 1.5xULN; ALT / AST (Alanine aminotransferase / Aspartate aminotransferase) ≤ 2.5xULN (Upper Limit of Normality) alkaline phosphatase ≤ 3xULN.
• Adequate renal function: creatinine ≤ 1xULN; creatinine clearance ≥ 60ml/min.
• No peripheral neuropathy (< Grade 2)
• No known history of dihydropyrimidine dehydrogenase deficiency (DPD)

Exclusion Criteria

• Patients with ECOG performance status ≥ 2.
• Stage I (T1N0M0) or stage IV (TxNxM1) AJCC (American Joint Committee on Cancer) rectal cancer.
• Any illness that the investigator considers will substantially increase the risk if the patient participates in the study.
• Pregnant or breast-feeding woman.
• Chronically active hepatitis B or C virus infection.
• Active uncontrolled infection.
• History, within last year, or presence of unstable angina, myocardial infarction, symptomatic congestive heart failure or asymptomatic left ventricular ejection fraction < 50% (assessed by multiple-gated acquisition scan or equivalent by ultrasound) or clinically significant valvular heart disease.
• Peripheral neuropathy (> Grade 1)
• Known history of dihydropyrimidine dehydrogenase deficiency (DPD)
• Known or suspected reactions to any component of the study medication (5-FU, leucovorin, irinotecan or oxaliplatin) or to components of similar chemical or biologic composition.
• Any phycological, familiar, sociological or geographical condition potentially hampering compliance with the study protocol or follow-up schedule.
• Concurrent participation in any other clinical trial likely to interfere with the therapeutic schedule.
• Patients that had received any previous treatment for their rectal cancer (surgery, chemotherapy or radiotherapy).

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Syntax for Science, S.L

INDUSTRY

Sponsor Role: collaborator

Fundación de investigación HM

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Antonio Cubillo, MD

Role: STUDY_DIRECTOR

Director

Locations

Hospital Universitario Puerta de Hierro Majadahonda

Majadahonda, Madrid, Spain

Hospital Universitario Madrid Sanchinarro

PAU de Sanchinarro, Madrid, Spain

Hospital General Universitario Gregorio Marañón

Madrid, , Spain

Hospital Universitario 12 de Octubre

Madrid, , Spain

Countries

Spain

Other Identifiers

HM-RE-2017-01

Identifier Type: -

Identifier Source: org_study_id