Skip to content

A Phase Ⅱ Study of XELOX Chemotherapy With or Without Surgery of Primary Lesion for Colon Cancer Patients

A Randomized Phase Ⅱ Study of XELOX Chemotherapy With or Without Surgery of Primary Lesion for Colon Cancer Patients With Unresectable Metastatic Lesions

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02291744
Enrollment
130
Registered
2014-11-14
Start date
2014-10-31
Completion date
2017-10-31
Last updated
2015-11-11

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

Conditions

Metastatic Colon Cancer

Keywords

TFS (time to failure of strategy)

Brief summary

The primary endpoint is to evaluate the TFS (time to failure of strategy).

Detailed description

The primary endpoint is to evaluate the time to failure of strategy, that is the second progression time after induction therapy by the use of XELOX regimen, comparing XELOX regimen chemotherapy combined with or without surgical resection of the primary lesion from the time of randomization to maintenance therapy and reapplication of induction therapy, or time to the use of second line strategy (if no reapplication of induction therapy) or time to no further treatment.

Interventions

PROCEDUREresection of primary lesion

Oxaliplatin 130mg/m2 ivgtt d1 and capecitabine 1000mg/m2,bid,po,d1-d14,every three weeks for a cycle, and resection of primary lesion with metastatic colon cancer

DRUGXELOX

Oxaliplatin 130mg/m2 ivgtt d1 and capecitabine 1000mg/m2,bid,po,d1-d14,every three weeks for a cycle,

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. 18\ 75 ears old 2. Pathological diagnosis of colon cancer adenocarcinoma 3. No systemic chemotherapy for metastatic tumors 4. ECOG (Eastern Cooperative Oncology Group) 0-1 and expected survival period for 6 months or more 5. At least one measurable objective tumor lesions 6. ANC≥1.5\*109/L;PLT≥90\*109/L;HB≥90g/L;TBI≤1.5(UNL); ALT、AST≤2.5ULN;Cr≤1.0(ULN) screening within 7 days 7. Primary and metastatic tumors exist at the same time, and distant metastases are not resectable 8. Patients with voluntary participation, and sign the informed consent

Exclusion criteria

1. Operation intervention required for perforation, bleeding and obstruction of intestinal cavity 2. With uncontrollable large pleural or peritoneal effusion 3. Alcohol or drug addictions 4. Malignant tumour of the past five years with other organizations to source, but the full treatment of cervical carcinoma in situ and except skin basal cell carcinoma and squamous cell carcinomas 5. With brain metastasis 6. Multiple primary colorectal carcinoma 7. Pregnancy or breast-feeding women 8. There is an important organ failure or other serious diseases, including coronary artery disease, symptomatic cardiovascular disease or myocardial infarction within 12 months; serious neurological or psychiatric history; severe infection; actively disseminated vascula blood coagulation.

Design outcomes

Primary

MeasureTime frame
TFS time of failure of strategy (the second progression time after induction therapy, or time to the use of second line strategy (if no reapplication of induction therapy) or time to no further treatment)the second progression time after induction therapy, or time to the use of second line strategy (if no reapplication of induction therapy) or time to no further treatment. The average time is three years.

Countries

China

Contacts

Primary ContactWeijian Guo, doctor
mingzhuhuang0718@163.com13816066360

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026