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Neo-adjuvant Chemoradiation With Oxaliplatin/5-FU in Rectal Cancer

Phase 2
Completed
Conditions
Colorectal Cancer
Interventions
Procedure: mesorectal excision
Registration Number
NCT00831181
Lead Sponsor
Beth Israel Medical Center
Brief Summary

RATIONALE: 5FU based neoadjuvant chemoradiation (nCRT) is the standard of care for Stage II/III rectal cancer. Pathologic complete response (pCR) and downstaging have been associated with improved outcomes. The addition of oxaliplatin (OXA) to neoadjuvant therapy may reduce distant disease recurrence. Adjuvant treatment with OXA for rectal cancer has been motivated by benefits demonstrated in stage III colon cancer.

Objective: To determine the feasibility, toxicity, and efficacy of preoperative OXA/5FU and RT followed by total mesorectal excision (TME) and adjuvant

PURPOSE: This phase II trial is studying the side effects and how well giving neo-adjuvant combination chemotherapy with radiation works in treating patients undergoing surgery for rectal cancer.

Detailed Description

OBJECTIVES:

Primary

* To assess the complete pathologic response rate in patients with rectal cancer treated with radiation, modified neoadjuvant FOLFOX 6 chemotherapy followed by total mesorectal excision and adjuvant modified FOLFOX 6 chemotherapy.

Secondary

* To observe the overall pathologic response rate in these patients.

* To correlate pathologic staging with preoperative ultrasound and pelvic MRI staging.

* To assess toxic side effects of these regimens in these patients.

* To assess patterns of disease relapse, disease-free survival outcomes, and overall survival outcomes of these patients.

OUTLINE:

Patients with stage II/III rectal cancer were treated with OXA 60mg/m2 weekly continuous infusion 5FU of 225 mg/m2/d d1-5 with pelvic RT of 1.8Gy/d for 28 doses. Adjuvant therapy consisted of 6 cycles of biweekly FOLFOX6.

Surgery: Patients undergo total mesorectal excision by anterior resection or an abdominal perineal resection within 4 weeks after completion of neoadjuvant therapy.

Adjuvant therapy: Within 4 weeks after surgery, patients receive modified FOLFOX 6 chemotherapy comprising oxaliplatin and leucovorin calcium IV over 2 hours on day 1 and continuous fluorouracil IV over 46 hours on days 1-2. Treatment repeats every 14 days for 6 courses in the absence of disease progression or unacceptable toxicity.

Patients complete quality of life assessment questionnaires at baseline and at each follow-up visit.

After completion of study treatment, patients are followed every 3 months for 2 years, every 6 months for 3 years, and annually thereafter.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
27
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Preoperative Chemoradiationmesorectal excisionPreoperative Chemoradiation with oxaliplatin/5-FU followed by mesorectal excision and 5-FU / leucovorin (FOLFOX 6)
Preoperative ChemoradiationOxaliplatinPreoperative Chemoradiation with oxaliplatin/5-FU followed by mesorectal excision and 5-FU / leucovorin (FOLFOX 6)
Preoperative ChemoradiationleucovorinPreoperative Chemoradiation with oxaliplatin/5-FU followed by mesorectal excision and 5-FU / leucovorin (FOLFOX 6)
Preoperative Chemoradiation5-FUPreoperative Chemoradiation with oxaliplatin/5-FU followed by mesorectal excision and 5-FU / leucovorin (FOLFOX 6)
Primary Outcome Measures
NameTimeMethod
Pathologic Response and Complete ResponseTotal mesorectal excision (TME) participants were evaluated at the time of surgical resection, an average of 3.5 months

Pathologic Response and Complete Response to preoperative therapy will be determined at the time of surgical resection. All grossly visible areas of ulceration and/or induration with be measured and submitted for histological evaluation.

The unit of measure is the tumor response rate to preoperative chemoradiation.

Pathologic complete response (pCR) is defined as no evidence of invasive tumor cells on pathologic examination of the primary rectal cancer.

Tumor regression grade (TRG) will be quantitated into five grades:

TRG 1 (complete regression) -absence of residual cancer and fibrosis extending from the site of original tumor through the layers of the rectal wall.

TRG 2 characterized by the presence of rare residual cancer cells scattered through the fibrosis.

TRG 3 characterized by an increase in the number of residual cancer cells, but fibrosis still predominant.

TRG 4 -residual cancer outgrowing fibrosis. TRG 5 characterized by absence of regressive changes.

Secondary Outcome Measures
NameTimeMethod
Disease-free Survivalmedian 22 months follow-up
Treatment ToxicityWeekly during chemoradiation treatment (3 months). Bi-weekly during adjuvant FOLFOX therapy (3.5 months).

Toxicity was assessed weekly during neoadjuvant chemotherapy and radiation therapy, bi-weekly during adjuvant FOLFOX therapy.

Complete Resectability RatesTotal mesorectal excision (TME) participants were evaluated at the time of surgical resection, 3 months after beginning of chemoradiation treatment.

Complete resectability rates assessed by circumferential margin.

Local Regional Controlmedian follow-up 22 months post-TME

subjects were followed for median of 22 months post-surgery

Overall Survivalmedian follow-up 22 months
Patterns of Disease Failure, Including Local Recurrence and Distant Metastasis Assessed by CT Scanmedian follow-up 22 months
Number of Participants With Comparison of Preoperative Stage With Post-treatment Pathologic StageTotal mesorectal excision (TME) participants were evaluated at the time of surgical resection, 3 months after beginning of chemoradiation treatment.

Thin-section high resolution pelvic MRI was used to image the tumor prior to chemoradiation and repeated prior to surgery, and then compared to post-treatment pathological stage.

Trial Locations

Locations (2)

St. Luke's-Roosevelt Hospital Center - Roosevelt Division

🇺🇸

New York, New York, United States

Beth Israel Medical Center - Philipps Ambulatory Care Center

🇺🇸

New York, New York, United States

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