Oxaliplatin, Leucovorin, and Fluorouracil Before and After Radiation Therapy and Surgery in Treating Patients With Rectal Cancer That Can Be Removed by Surgery

NCT ID: NCT01263171

Last Updated: 2016-09-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-04-30
• Study Completion Date: 2015-11-30

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as oxaliplatin, leucovorin, and fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving chemotherapy after surgery may kill any tumor cells that remain after surgery.

PURPOSE: This phase II trial is studying giving oxaliplatin, leucovorin, and fluorouracil together, before and after radiation therapy and surgery in treating patients with rectal cancer that can be removed by surgery.

Detailed Description

OBJECTIVES:

Primary

• To assess the feasibility of introducing 8 weeks of neoadjuvant oxaliplatin and fluorouracil followed by radiotherapy and immediate surgical resection in patients with resectable adenocarcinoma of the rectum.

Secondary

• Determine feasibility of achieving dose intensity for chemotherapy and radiotherapy in these patients.
• Determine the safety, in terms of NCI CTCAE version 4 toxicities, including postoperative complication rate (up to 30 days postoperatively), and late toxicity assessment at 1 year following surgery, in these patients.
• Determine how active is the neoadjuvant chemotherapy, in terms of down staging the rectal cancer, local recurrence-free, distant metastasis-free, and overall survival at 1 year following surgery in these patients.

Neoadjuvant therapy: Patients receive oxaliplatin and leucovorin (L-leucovorin or leucovorin calcium) IV over 2 hours on day 1 and fluorouracil IV over 46 hours on days 1-2. Treatment repeats every 2 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity.

Radiotherapy/Surgery: Beginning 1 week after completion of chemotherapy, patients undergo radiotherapy, followed by surgical resection of their primary tumor, within 7-14 days after completion of radiotherapy. Between 6-8 weeks following surgery, patients begin adjuvant therapy.

Adjuvant therapy: Patients receive oxaliplatin and leucovorin (L-leucovorin or leucovorin calcium) IV over 2 hours on day 1 and fluorouracil IV over 46 hours on days 1-2. Treatment repeats every 2 weeks for up to 8 courses in the absence of disease progression or unacceptable toxicity.

Blood and biopsy specimens are collected at baseline and periodically for translational research studies.

After completion of study therapy, patients are followed up periodically for 1 year.

Peer Reviewed and Funded or Endorsed by Cancer Research UK.

Conditions

Colorectal Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Neo-adjuvant chemotherapy

Neo-adjuvant chemotherapy prior to short course pre-operative radiotherapy followed by adjuvant chemotherapy.

Group Type: OTHER

Leucovorin

Intervention Type: DRUG

fluorouracil

Intervention Type: DRUG

leucovorin calcium

Intervention Type: DRUG

oxaliplatin

Intervention Type: DRUG

adjuvant therapy

Intervention Type: PROCEDURE

neoadjuvant therapy

Intervention Type: PROCEDURE

therapeutic conventional surgery

Intervention Type: PROCEDURE

radiation therapy

Intervention Type: RADIATION

Interventions

Leucovorin

Intervention Type: DRUG

fluorouracil

Intervention Type: DRUG

leucovorin calcium

Intervention Type: DRUG

oxaliplatin

Intervention Type: DRUG

adjuvant therapy

Intervention Type: PROCEDURE

neoadjuvant therapy

Intervention Type: PROCEDURE

therapeutic conventional surgery

Intervention Type: PROCEDURE

radiation therapy

Intervention Type: RADIATION

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histopathologically confirmed rectal adenocarcinoma meeting the following criteria:

• Inferior aspect of tumor is > 4 cm from anal verge on digital examination and pelvic MRI scan
• Superior aspect of tumor is not higher than the anterior aspect of the S1/S2 interspace on pelvic MRI scan
• Mesorectal fascia is not threatened or involved (tumor > 1 mm from mesorectal fascia)
• Primary tumor meets 1 of the following criteria:

• T3a-b (mesorectal primary tumor invasion seen ≤ 5 mm beyond muscularis propria) in the presence of 1 of the following:

• Extra-mural vascular invasion
• Mesorectal lymph node(s)/tumor deposit(s) with irregular border and mixed signal intensity
• Any T3c (primary tumor invasion seen > 5 mm beyond muscularis propria)-T4a (invasion of visceral peritoneum for tumors with a component above peritoneal reflection)
• Low tumors should not involve levator ani (> 1 mm gap between tumor and levator ani) or anal sphincters
• No evidence of distant metastases or stage T4b cancer with invasion into adjacent organs or structures
• Must have measurable disease at the baseline visit
• Impending rectal obstruction is permitted if relieved by a non-functioning ileostomy or colostomy
• No disease threatening mesorectal fascia (disease ≤ 1 mm from mesorectal fascia whether this is primary tumor, extra-mural vascular invasion, or tumor deposit with irregular border and mixed signal intensity)

PATIENT CHARACTERISTICS:

• ECOG performance status 0-1
• Hemoglobin ≥ 9 g/dL
• WBC ≥ 3 x 10^9/L
• Absolute neutrophil count ≥ 1.5 x10^9/L
• Platelet count ≥ 100 x10^9/L
• Total bilirubin ≤ 1.5 times upper limit of normal (ULN)
• Alkaline phosphatase ≤ 5 x ULN
• AST or ALT ≤ 2.5 x ULN
• Creatinine clearance ≥ 50 mL/min
• Magnesium and calcium normal
• Candidate for systemic therapy, in the opinion of the primary oncologist
• No known significant impairment of intestinal absorption (e.g., chronic diarrhea, inflammatory bowel disease)
• No evidence of established or acute ischemic heart disease (e.g., left bundle branch block, pathological q-waves, ST elevation, or ST-segment depression) and normal clinical cardiovascular assessment by ECG
• No enlarged pelvic sidewall lymph nodes
• No severe local bowel symptoms of tenesmus or irregularity or frequency of bowel habit precluding accurate assessment of diarrhea
• No pelvic sepsis
• No uncontrolled infection
• Not pregnant or nursing
• Fertile patients must use effective contraception during treatment and for 6 months after completion of treatment
• No other prior or current malignant disease that, in the judgement of the treating investigator, is likely to interfere with study treatment or assessment of response
• No clinically significant cardiovascular disease, including any of the following within the past year:

• Myocardial infarction
• Unstable angina
• Symptomatic congestive heart failure
• Serious uncontrolled cardiac arrhythmia
• No history of interstitial lung disease (e.g., pneumonitis or pulmonary fibrosis or evidence of interstitial lung disease)

PRIOR CONCURRENT THERAPY:

• No prior pelvic radiotherapy
• No metallic colon stent or rectal stent in situ
• More than 30 days since prior chemotherapy, radiotherapy, hormonal treatment, antibody therapy, immunotherapy, gene therapy, vaccine therapy, angiogenesis inhibitors, matrix metalloproteinase inhibitors, thalidomide, anti-VEGF/Flk-1 monoclonal antibodies, or other experimental drugs

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 120 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cancer Research UK

OTHER

Sponsor Role: collaborator

Cardiff University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Simon Gollins, MD

Role: PRINCIPAL_INVESTIGATOR

Glan Clwyd Hospital

Locations

Walsgrave Hospital

Coventry, England, United Kingdom

Leeds Cancer Centre at St. James's University Hospital

Leeds, England, United Kingdom

Christie Hospital

Manchester, England, United Kingdom

Rosemere Cancer Centre at Royal Preston Hospital

Preston, England, United Kingdom

Royal Marsden - Surrey

Sutton, England, United Kingdom

Velindre Cancer Center at Velindre Hospital

Cardiff, Wales, United Kingdom

Glan Clwyd Hospital

Rhyl, Denbighshire, Wales, United Kingdom

Countries

United Kingdom

Other Identifiers

WCTU-COPERNICUS

Identifier Type: OTHER

Identifier Source: secondary_id

2010-023083-40

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

C23134/A11537

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

CARDIFF-SPON830-10

Identifier Type: OTHER

Identifier Source: secondary_id

CDR0000691166

Identifier Type: -

Identifier Source: org_study_id