Rectal Cancer
Conditions
Keywords
rectum, colorectal, cancer, adenocarcinoma, anti-EGFR, monoclonal antibodies, neoadjuvant therapy, preoperative radiotherapy
Brief summary
The purpose of this study is to investigate the activity of panitumumab in combination with standard preoperative radiotherapy in locally advanced rectal cancer, followed by complete surgery and adjuvant chemotherapy. The main hypothesis of the study is that the association of EGFR-targeting agent and radiation therapy could be as effective or even improve the rate of pathological complete tumoral response with fewer toxicities in comparison to the standard of care using chemoradiation therapy.
Detailed description
Anti-EGFR monoclonal antibodies have radiosensitizing properties. In particular, cetuximab in combination with curative-intent radiotherapy has been reported to increase median overall survival over radiation therapy alone in locally advanced head and neck carcinoma. Similar benefit in rectal cancer is expected. However, preliminary studies revealed that the combination of chemoradiation and cetuximab did not seem to improve the pathological tumor response. However, in the past studies, the selection of patients' population was not optimal since KRAS mutational status was not considered during recruitments. Therefore, new trials to investigate EGFR-targeting therapies in combination with radiotherapy in wild-type KRAS patients are required. Adjuvant chemotherapy has also shown to decrease the risk of local relapse in patients who did not receive chemotherapy during radiotherapy. In our study, since there will be no chemotherapy given during the preoperative setting, the administration of adjuvant chemotherapy postoperatively is highly recommended.
Interventions
DRUGpanitumumab
intravenous infusion of panitumumab, 6 mg per kg body weight, once every 14 days for a total of 42 days
Sponsors
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* ECOG Performance Status 0-1 * Histologically proven adenocarcinoma of the rectum, T3-T4 and/or N+ M0 * Wild-type KRAS * No prior pelvic irradiation * Normal bone marrow, hepatic, renal, cardiac functions * No secondary malignancy * No other active, uncontrolled disease * Signed informed consent
Exclusion criteria
* KRAS mutation * Established or suspected metastasis * Prior pelvic irradiation * Previous exposure to EGFR-targeting therapies * Patients under any other investigational agent(s) * Concurrent systemic immune therapy, chemotherapy, hormone therapy * Drug and/or alcohol abuse * Grade 3 to 4 allergic reaction to any of the components of the treatment * History or presence of interstitial lung disease * Active, uncontrolled cardiovascular disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pathological Complete Response (pCR) | 11 weeks |
Secondary
| Measure | Time frame |
|---|---|
| Safety, pathologic R0 resection, negative Circumferential Resection Margin, pathologic downstaging, tumor regression grade, quality of mesorectal excision, rate of sphincter-preservation, Disease-Free Survival, local control rate, translational research | 24 months |
Countries
Belgium
Outcome results
None listed