Chemotherapy; Maternal, Affecting Fetus, Colorectal Neoplasms, Liver Neoplasms, Neoplasm Metastasis
Conditions
Keywords
Unresectable colorectal liver metastases, Pre-operation chemotherapy, Primary tumor resection, Survival
Brief summary
To evaluate the survival benefit of pre-operation chemotherapy of primary tumor tesection (PTR) compared upfront PTR for colorectal cancer (CRC) patients with an asymptomatic resectable primary tumor and synchronous unresectable liver-limited metastases with conversion therapy intent.
Detailed description
Fast recovery with fewer postoperative complications, prevention of potential tumor-related complications during chemotherapy, life quality improvement, and also can alleviate the tumor load of patients, are some advantages of PTR that may play a role in improving cancer-specific survival. However, it should be pointed out that nearly all the retrospective and prospective studies for the beneficial of PTR enrolled more multi-organ metastases mCRC patients, and with palliative treatment purpose. As for unresectable colorectal liver-limited metastases (CRLMs) with good Eastern Cooperative Oncology Group performance status (ECOG PS), the primary objective is to make metastases resectable by high-intensity conversion therapy and achieved a state of no-evidence of disease. PTR were preferred performed before enrollment in some related RCT studies, including the CELIM study, CAIRO and CAIRO2 studies. Pooled-analysis of our two RCT studies, PTR pre or post chemotherapy for these unresectable liver-limited metastases patients had less morbidities and no mortalities, but no RCTs have focused on survival benefit of pre-operation chemotherapy of PTR for unresectable CRLMs.
Interventions
DRUGchemotherapy ± targeted therapy
Chemotherapy regimen with either mFOLFOX6 plus cetuximab, bevacizumab or mFOLFOX6 alone were allocated, according the RAS genotype and patient affordability.
Sponsors
Second Affiliated Hospital, School of Medicine, Zhejiang University
Ruijin Hospital
Changhai Hospital
Fudan University
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
* age between 18 - 75 years old * colorectal adenocarcinoma pathologically * without any chemotherapy or radiotherapy * unresectable liver metastasis and without other metastasis * resectable colorectal cancer * suitable for chemotherapy * agreed by patients
Exclusion criteria
* age below 18 years old or greater than 75 years old * haven't pathological diagnosis of colorectal adenocarcinoma * with any chemotherapy or radiotherapy * resectable liver metastasis or without other metastasis * unresectable colorectal cancer * unsuitable for chemotherapy * not agreed by patients
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free survival | Up to 3 years | Time from randomization to the date of disease progression or to death of any cause |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall survival | Up to 3 years | Time from randomization to death from any cause or the date of the last follow-up |
| Tumor response | Up to 6 months | Response according to RECIST 1.1 |
| Secondary resection rate Second radical resectability | Up to 6 months | The rate of patients converted to resection for liver metastases |
| Surgical complications | 30 days after surgery | The proportion of patients with any complications occurred within 30 days after surgery |
| Toxicity of chemotherapy | Up to 6 months | Patients will be evaluated for Adverse Events at the start of each treatment cycle according to NCI CTC 3.0 criteria |
Countries
China
Outcome results
None listed