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Neoadjuvant Chemotherapy for the Treatment of Resectable Locally Advanced Colon Cancer

A Randomized Controlled Clinical Trial to Investigate the Effect of Neoadjuvant Chemotherapy for the Treatment of Resectable Locally Advanced Colon Cancer

Status
UNKNOWN
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02882269
Enrollment
400
Registered
2016-08-29
Start date
2016-12-31
Completion date
2021-12-31
Last updated
2016-08-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colon Cancer

Keywords

locally advanced colon cancer, neoadjuvant chemotherapy

Brief summary

A randomized controlled clinical trial to compare the short and long outcomes of Neoadjuvant chemotherapy with postoperative chemotherapy in patients with resectable locally advanced colon cancer

Detailed description

For resectable locally advanced colon cancer, the preferred treatment is colectomy with en bloc removal of the regional lymph nodes followed by chemotherapy of about 6 months. However, surgery may postpone the administration of chemotherapy due to postoperative complications such as anastomosis leakage, abdominal infection, thus leads to a poor survival. Some scholars suggested that for patients with locally advanced colon cancer, chemotherapy given before surgery might shrink or downstage tumor, facilitate surgery and promote a better oncological outcome. Whether adjuvant chemotherapy benefits these patients with better outcome still remains controversial. In this study, eligible patients will be randomly allocated to receive either adjuvant chemotherapy or not. For patients receiving adjuvant chemotherapy, surgery will be performed 3-4 weeks later. Preoperative and postoperative chemotherapy will be given for a total of about 6 months. For patients receiving no preoperative chemotherapy, chemotherapy will be given for about 6 months postoperatively. The recommended chemotherapy regimes includes FOLFOX, CapeOX, FOLFIRI, Capecitabine monotherapy. Patients will be followed up every 3 months for 2 year, every 6 months for 3 years postoperatively.

Interventions

Locally advanced colon cancer patients will receive surgery first, followed by 6 months of chemotherapy. The recommended chemotherapy regimes includes FOLFOX, CapeOX, FOLFIRI, Capecitabine monotherapy.

DRUGNeoadjuvant chemotherapy

Neoadjuvant chemotherapy will be given to locally advanced colon cancer patients for 3-4 cycles. Surgery will be performed between 3 to 4 weeks subsequent to the last cycle of chemotherapy. After surgery, additional chemotherapy will be given. Preoperative and postoperative chemotherapy will be given for a total of 6 months. The recommended chemotherapy regimes includes FOLFOX, CapeOX, FOLFIRI, Capecitabine monotherapy.

Sponsors

The First Affiliated Hospital with Nanjing Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients suitable for curative surgery between 18 to 80 years old; * American Society of Anesthesiologists(ASA) grade I-III; * Pathological diagnosis of adenocarcinoma; * Tumor located between the cecum and sigmoid colon; * Enhanced CT scan of chest, abdominal and pelvic cavity: preoperative assessment of tumor stage is T3-T4 N0 or T any N+ (according to the National Comprehensive Cancer Network(NCCN) clinical practice guidelines in oncology: colon cancer version 2.2015);there is no distant metastasis; * Informed consent; * No preoperative chemoradiotherapy; * No history of familial adenomatous polyposis, ulcerative colitis or Crohn's disease.

Exclusion criteria

* Pregnant patient; * History of psychiatric disease; * Use of systemic steroids; * Simultaneous multiple primary colorectal cancer; * Preoperative imaging examination results show: 1. distant metastasis; 2. unable to perform R0 resection; * Postoperative pathology of T1-T2 N0; * History of any other malignant tumor in recent 5 years; * Patients need emergency operation: mechanic ileus, perforation.

Design outcomes

Primary

MeasureTime frame
disease-free survival3 years

Secondary

MeasureTime frameDescription
recurrence-free survival3 years
local recurrence rate3 years
length of postoperative hospital stay30 daysLength of postoperative hospital stay is defined as a duration between surgery and first discharge. An expected average is 10 days.
overall survival3 years
operative time1 day
number of lymph nodes retrieved1 day
early complication rate30 daysEarly complication is defined as a complication that occurred between the finish of the surgery and postoperative day 30. Complications includes anastomotic leakage, anastomotic bleeding, chyle leakage, wound infection, pulmonary embolism, myocardial infarction et al.The Clavien-Dindo Classification of Surgical Complications will be applied to access the degree of severity of postoperative complications.

Contacts

Primary ContactYueming Sun, PhD
jssym@vip.sina.com02568136026

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026