TRI-LARC: Pre-operative 3-DCRT vs IMRT for Locally Advanced Rectal Cancer
Study Details
Study Description
Brief Summary
The study aims to compare the incidence of acute grade 2 GI toxicity in the Control 3-D Conformal Radiotherapy compared to the Intensity Modulated Radiotherapy (IMRT) arm for locally advanced rectal cancer.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1/Phase 2 |
Detailed Description
Pre-operative radiotherapy (RT) or chemo-radiotherapy (CRT) is internationally accepted as standard practice in the management of locally advanced rectal cancer.
Multiple randomised trials have proved pre-operative CRT and RT, compared to surgery alone, reduce local recurrence, even prior to optimal surgery, and may improve survival for T3 circumferential resection margin (CRM) negative patients.
This study aims to determine if 3-DCRT or IMRT result in lower incidence of grade 2 GI toxicities.
Acute toxicities will be assessed weekly during radiotherapy, and at 2 and 4 week post treatment.
Late toxicities will be assessed at 3, 6, 9, 12, 18, 24 months post treatment, and annually to 10 years.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Experimental Arm 50.4 Gy / 28# external beam pelvic radiotherapy delivered using IMRT |
Radiation: IMRT
IMRT will be given to some patients to enable comparison of the acute grade 2 GI toxicities compared to those patients receiving their radiotherapy by 3-DCRT
|
| No Intervention: Control Arm 50.4 Gy / 28# external beam pelvic radiotherapy delivered using a 3-Dimensional (3-D) planned technique |
Outcome Measures
Primary Outcome Measures
- Reduction in incidence of grade 2 or higher GI toxicity [10 years]
To determine if there is a reduction in the incidence of grade 2 or higher acute GI toxicity in the IMRT arm, as compared to the Control / 3-D arm, graded by the NCI-CTCAE Version 4
Secondary Outcome Measures
- Compare incidence of acute grade > 2 GU toxicity [10 years]
To compare the incidence of acute grade > 2 GU toxicity in the IMRT arm, as compared to the Control / 3-D arm, graded by the NCI-CTCAE Version 4
- Evaluate incidence of late GI and GU toxicity [10 years]
To evaluate the incidence of late GI and GU toxicity graded by the NCI-CTCAE Version 4
- Rate of loco-regional control [10 years]
To estimate the rate of loco-regional control by assessing CT / MRI imaging / biopsy
- Assess quality of life [10 years]
To assess QoL according to the EORTC QLQ-C30 and EORTC QLQ-CR29
- Rate of disease free survival [10 years]
To estimate the rate of disease-free survival
- Estimate overall survival [10 years]
To estimate the overall survival rate
- Differences in the toxicity profile between the two types of neoadjuvant concomitant chemotherapy, graded by the NCI-CTCAE Version 4 [10 years]
To compare the differences in the toxicity profile between the two types of neoadjuvant concomitant chemotherapy, graded by the NCI-CTCAE Version 4
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Patients undergoing pre-operative pelvic chemo-radiotherapy for histologically confirmed rectal adenocarcinoma, with the following staging: cT3N0-2, cT4N0-2, cT(any)N1-2, cT(any)N(any) CRM at-risk [AJCC version V]
-
Staging / imaging of pelvis with MRI, and CT Thorax/Abdomen
-
No evidence of metastatic disease
-
ECOG Performance Status 0 - 2
-
Age > or equal to 18 years
-
Provision of written informed consent in line with ICH-GCP guidelines
Exclusion Criteria:
-
Previous radiotherapy to the pelvic region
-
Patients in whom induction chemotherapy has been delivered prior to chemo- radiotherapy
-
History of inflammatory bowel disease
-
Previous hip replacement
-
Previous bowel surgery (excluding procedures/operations which would not result in small bowel adhesions - at the discretion of the Principal Investigator)
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Patients with other syndromes/conditions associated with increased radiosensitivity
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Any other co-existing malignancies within the past 5 years other than non- melanoma skin cancer
-
Pregnancy or lactation at the time of proposed randomisation
-
Evidence of any other significant clinical disorder or laboratory finding that makes it undesirable for the patient to participate in the study or if it is felt by the research / medical team that the patient may not be able to comply with the protocol
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | St Luke's Radiation Oncology Network at Beaumont Hospital | Dublin | Ireland | 9 | |
| 2 | St Luke's Centre for Radiation Oncology at St James Hospital | Dublin | Ireland | ||
| 3 | St Luke's Centre for Radiation Oncology at St Lukes Hospital | Dublin | Ireland |
Sponsors and Collaborators
- Cancer Trials Ireland
Investigators
- Principal Investigator: Dr Brian O'Neill, MD, St Luke's Centre for Radiation Oncology
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CTRIAL-IE (ICORG) 12-38