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Prediction of Response to Neoadjuvant Therapy in Rectal Cancer (PRENT-LARC)

Primary Purpose

Rectal Neoplasms

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
PET-CT Scan
Sponsored by
Colchester General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Rectal Neoplasms focused on measuring rectal cancer, neoadjuvant chemoradiotherapy, long course radiotherapy, response

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with biopsy-proven confirmed rectal cancer
  • MRI stage: T3/T4 and/or N1/N0.
  • No contraindication to MRI and PET-CT.

Exclusion Criteria:

  • Contraindication to MRI and/or PET-CT.
  • Inability to consent.
  • Severe claustrophobia.
  • Distant metastases.
  • Synchronous tumour.

Sites / Locations

  • Colchester General Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Long Course Radiotherapy

Arm Description

all patients diagnosed with rectal cancer, amenable for neoadjuvant chemoradiotherapy, who agree to participate in this study will undergo 2 PET-CT scans: at baseline and 9 weeks after commencing therapy.

Outcomes

Primary Outcome Measures

Accuracy of Texture analysis PET-CT
Sensitivity will be calculated from 2x2 contingency table.

Secondary Outcome Measures

Correlation between tumour response parameters to survival.
Correlation coefficient (r)
Accuracy of Texture analysis MRI
Sensitivity will be calculated from 2x2 contingency table.

Full Information

First Posted
April 23, 2015
Last Updated
May 8, 2015
Sponsor
Colchester General Hospital
Collaborators
Anglia Ruskin University
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1. Study Identification

Unique Protocol Identification Number
NCT02439086
Brief Title
Prediction of Response to Neoadjuvant Therapy in Rectal Cancer
Acronym
PRENT-LARC
Official Title
Prediction of Response to Neoadjuvant Chemoradiotherapy in Locally Advanced Rectal Cancer.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2015
Overall Recruitment Status
Unknown status
Study Start Date
September 2015 (undefined)
Primary Completion Date
September 2017 (Anticipated)
Study Completion Date
September 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Colchester General Hospital
Collaborators
Anglia Ruskin University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether 18F-FDG-PET-CT and texture analysis of MRI performed 9 weeks after Neoadjuvant Chemo-radiotherapy in patients with locally advanced rectal cancer has the ability to identify patients with Complete Response.
Detailed Description
In recent years, treatment with NCRT has revolutionised management of LARC. In addition to downstaging the tumour in 62% of cases, half of which decrease by more than 1 T stage; pathological complete response (pCR), with no viable tumour cells left in resected specimens, was demonstrated in up to 30% of patients. Only 3% of patients showed progressive disease. It has recently been shown that those with pathological complete response survive longer than those with partial response, with figures for 5-year disease free survival quoted between 83 and 91% for pCR; versus 65% for non pCR. Furthermore, it has been argued that those tumours which are sensitive to radiotherapy have a favourable biological tumour profile, with fewer propensities to recur or to metastasise than aggressive non-radiosensitive tumours. The key is to accurately be able to identify patients who exhibit complete response to radiotherapy, or to predict those who might show complete response. Positron Emission Tomography (18-F-FDG-PET-CT) as a tumour biomarker after radiotherapy has been shown to be able to predict patients who have responded to chemo radiotherapy, with a sensitivity of 79% and specificity of 88%. Texture Analysis (TA) assesses the aggressiveness of the tumour by assessing intra-tumoural heterogeneity. It has already been shown to be effective in assessing biological characteristics of solid tumours, including the oesophagus, breast, and liver. The aim of this study is to utilise these two novel molecular imaging techniques to identify rectal cancer patients who have responded completely from neoadjuvant chemo-radiotherapy. Parameters will be calculated as changes in measurable variables from baseline to post treatment scans. Pilot data The watch-and-wait approach could potentially reduce treatment-related toxicity in selected rectal cancer patients who have a clinical complete response (cCR) after chemoradiation. The "watch & wait" protocol has been adopted from studies performed in Brazil, United Kingdom, and the Netherlands. Studies indicate that accurate assessment of response to neoadjuvant therapy is the key to selecting patients who will benefit from the watch & wait approach. Therefore, determining the modality with highest accuracy and cost-effectiveness has been the holy grail of managing locally advanced rectal cancers. A study performed by our Chief Investigator on the efficiency and accuracy of 18-F-FDG-PET-CT has concluded that PET-CT has a proven role and is cost effective in monitoring therapy and in detecting recurrence in colorectal cancers; as this technology combines picomolar sensitivity with high-resolution CT imaging. It has therefore shown to be more sensitive than plain CT imaging in detecting recurrence and monitoring response to therapy. In other studies, the reported accuracy for PET-CT in determining responsiveness to NCRT was around 80%. Baseline PET-CT and subsequent PET-CT parameters, including SUV-based measurements, have been shown to be highly accurate in determining responses to NCRT. Texture Analysis is a biomarker technique that measures heterogeneity within solid tumours. Textural parameters (coefficient of variation [COV], skewness, and kurtosis) applied on PET-CT images has been shown to be able to predict response to NCRT, and to predict survival. A pilot study performed at our institution has indeed showed that textural parameters performed on pelvic MRI were associated with improved overall survival and disease- free survival. Study hypothesis PET-CT restaging done at 9 weeks rather than 6 weeks will be a more accurate predictor in assessing response to NCRT. Texture analysis of rectal MRI scans is a strong biomarker in assessing tumour response and identifying patients with Complete Response.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Neoplasms
Keywords
rectal cancer, neoadjuvant chemoradiotherapy, long course radiotherapy, response

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Outcomes Assessor
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Long Course Radiotherapy
Arm Type
Experimental
Arm Description
all patients diagnosed with rectal cancer, amenable for neoadjuvant chemoradiotherapy, who agree to participate in this study will undergo 2 PET-CT scans: at baseline and 9 weeks after commencing therapy.
Intervention Type
Device
Intervention Name(s)
PET-CT Scan
Intervention Description
patients will have 2 PET CT scans: one before radiotherapy, and one 9 weeks after.
Primary Outcome Measure Information:
Title
Accuracy of Texture analysis PET-CT
Description
Sensitivity will be calculated from 2x2 contingency table.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Correlation between tumour response parameters to survival.
Description
Correlation coefficient (r)
Time Frame
6 months
Title
Accuracy of Texture analysis MRI
Description
Sensitivity will be calculated from 2x2 contingency table.
Time Frame
6 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with biopsy-proven confirmed rectal cancer MRI stage: T3/T4 and/or N1/N0. No contraindication to MRI and PET-CT. Exclusion Criteria: Contraindication to MRI and/or PET-CT. Inability to consent. Severe claustrophobia. Distant metastases. Synchronous tumour.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Medhat S Alaker, MCh, MD(Res)
Phone
+447746147851
Email
medhat.alaker@nhs.net
First Name & Middle Initial & Last Name or Official Title & Degree
Tan Arulampalam, MD
Phone
01206742456
Email
laptan1@yahoo.org.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tan Arulampalam, MD
Organizational Affiliation
ICENI Centre director
Official's Role
Principal Investigator
Facility Information:
Facility Name
Colchester General Hospital
City
Colchester
ZIP/Postal Code
CO4 5JL
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
11167864
Citation
Arulampalam TH, Costa DC, Loizidou M, Visvikis D, Ell PJ, Taylor I. Positron emission tomography and colorectal cancer. Br J Surg. 2001 Feb;88(2):176-89. doi: 10.1046/j.1365-2168.2001.01657.x.
Results Reference
background
PubMed Identifier
24752672
Citation
Bundschuh RA, Dinges J, Neumann L, Seyfried M, Zsoter N, Papp L, Rosenberg R, Becker K, Astner ST, Henninger M, Herrmann K, Ziegler SI, Schwaiger M, Essler M. Textural Parameters of Tumor Heterogeneity in (1)(8)F-FDG PET/CT for Therapy Response Assessment and Prognosis in Patients with Locally Advanced Rectal Cancer. J Nucl Med. 2014 Jun;55(6):891-7. doi: 10.2967/jnumed.113.127340. Epub 2014 Apr 21.
Results Reference
background
Citation
HABR-GAMA, A., PEREZ, R., LYNN, P., SãO JULIãO, G. and GAMA RODRIGUES, J., 2012. Selective non-operative management of distal rectal cancer: The Watch & Wait Protocol. In: R. SCHIESSEL and P. METZGER, eds, Springer Vienna, pp. 43-53.
Results Reference
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PubMed Identifier
15383798
Citation
Habr-Gama A, Perez RO, Nadalin W, Sabbaga J, Ribeiro U Jr, Silva e Sousa AH Jr, Campos FG, Kiss DR, Gama-Rodrigues J. Operative versus nonoperative treatment for stage 0 distal rectal cancer following chemoradiation therapy: long-term results. Ann Surg. 2004 Oct;240(4):711-7; discussion 717-8. doi: 10.1097/01.sla.0000141194.27992.32.
Results Reference
background
PubMed Identifier
20692872
Citation
Maas M, Nelemans PJ, Valentini V, Das P, Rodel C, Kuo LJ, Calvo FA, Garcia-Aguilar J, Glynne-Jones R, Haustermans K, Mohiuddin M, Pucciarelli S, Small W Jr, Suarez J, Theodoropoulos G, Biondo S, Beets-Tan RG, Beets GL. Long-term outcome in patients with a pathological complete response after chemoradiation for rectal cancer: a pooled analysis of individual patient data. Lancet Oncol. 2010 Sep;11(9):835-44. doi: 10.1016/S1470-2045(10)70172-8. Epub 2010 Aug 6.
Results Reference
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PubMed Identifier
24877151
Citation
Niccoli-Asabella A, Altini C, De Luca R, Fanelli M, Rubini D, Caliandro C, Montemurro S, Rubini G. Prospective analysis of 18F-FDG PET/CT predictive value in patients with low rectal cancer treated with neoadjuvant chemoradiotherapy and conservative surgery. Biomed Res Int. 2014;2014:952843. doi: 10.1155/2014/952843. Epub 2014 May 4.
Results Reference
background
PubMed Identifier
30451764
Citation
Aker M, Ganeshan B, Afaq A, Wan S, Groves AM, Arulampalam T. Magnetic Resonance Texture Analysis in Identifying Complete Pathological Response to Neoadjuvant Treatment in Locally Advanced Rectal Cancer. Dis Colon Rectum. 2019 Feb;62(2):163-170. doi: 10.1097/DCR.0000000000001224.
Results Reference
derived

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Prediction of Response to Neoadjuvant Therapy in Rectal Cancer

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