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The Randomised Study of Preoperative Radiotherapy With Consolidating Chemotherapy for Unresectable Rectal Cancer

Primary Purpose

Rectal Cancer

Status
Unknown status
Phase
Phase 3
Locations
Poland
Study Type
Interventional
Intervention
Short course of radiotherapy
Radiochemotherapy
Sponsored by
Polish Colorectal Cancer Study Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Cancer focused on measuring Rectal cancer, Preoperative radiotherapy and consolidating chemotherapy

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with unresectable primary rectal cancer or with unresectable local recurrence without distant metastases.
  • WHO performance status ≤ 2.
  • Lower border of tumour ≤ 15 cm from anal verge.

Exclusion Criteria:

  • cardiac coronary arterial disease,
  • arrhythmias,
  • stroke even if they have occurred in the past and are controlled with medication

Sites / Locations

  • M. Sklodowska-Curie Memorial Cancer CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

25 Gy in 5 fractions of 5 Gy over 5 days. One week interval. Consolidating chemotherapy of 3 courses of FOLFOX4. Surgery 10-11 weeks from beginning of radiation and at least 4 weeks from the last dose of fluorouracil.

Conventionally fractionated chemoradiation with 50.4 Gy total dose in 28 fractions of 1.8 Gy over 5.5 weeks. Surgery 10-11 weeks from beginning of radiation and at least 4 weeks from the last dose of radiation.

Outcomes

Primary Outcome Measures

The rate of patients with R0 resection

Secondary Outcome Measures

Overall long-term survival
Progression-free long-term survival
The rate of local failures
The rate of distant metastases
The rate of early toxicity of neoadjuvant treatment according to the NCI CTCAE (version 3.0)
The rate of postoperative complications
The rate of late toxicity according to the RTOG/EORTC scale
The rate of complete pathological response

Full Information

First Posted
January 29, 2009
Last Updated
April 14, 2010
Sponsor
Polish Colorectal Cancer Study Group
Collaborators
Maria Sklodowska-Curie National Research Institute of Oncology, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Cracow, Poznan University of Medical Sciences, Medical University of Lublin
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1. Study Identification

Unique Protocol Identification Number
NCT00833131
Brief Title
The Randomised Study of Preoperative Radiotherapy With Consolidating Chemotherapy for Unresectable Rectal Cancer
Official Title
Short-course Preoperative Radiotherapy With Consolidating Chemotherapy vs. Preoperative Chemoradiation in Patients With Unresectable Rectal Cancer: Phase III Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2010
Overall Recruitment Status
Unknown status
Study Start Date
November 2008 (undefined)
Primary Completion Date
November 2012 (Anticipated)
Study Completion Date
November 2015 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Polish Colorectal Cancer Study Group
Collaborators
Maria Sklodowska-Curie National Research Institute of Oncology, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Cracow, Poznan University of Medical Sciences, Medical University of Lublin

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The addition of Oxaliplatin to conventionally fractionated chemoradiation (FULV or capecitabine) is considered as standard in unresectable rectal cancer by the panel of experts. The Investigators addressed the question whether short-course preoperative radiotherapy with consolidating chemotherapy of FOLFOX4 may increase the rate of R0 resection in patients with unresectable rectal cancer.
Detailed Description
Patients with unresectable primary rectal cancer or with unresectable local recurrence without distant metastases are randomly allocated to control or experimental arm. The preoperative treatment in the control arm is conventionally fractionated chemoradiation with 50.4 Gy total dose in 28 fractions of 1.8 Gy over 5.5 weeks simultaneously with 5-Fu, leucovorin and oxaliplatin. Experimental group receive 25 Gy in 5 fractions of 5 Gy over 5 days and after one week interval - consolidating chemotherapy of 3 courses of FOLFOX4. Surgery should be curried out 10-11 weeks from beginning of radiation and at least 4 weeks from the last dose of fluorouracil or radiation. The study hypothesis is that the short-course preoperative radiotherapy with consolidating chemotherapy produce at least 10% increase of the rate of R0 resection compared to preoperative chemoradiation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer
Keywords
Rectal cancer, Preoperative radiotherapy and consolidating chemotherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
540 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
25 Gy in 5 fractions of 5 Gy over 5 days. One week interval. Consolidating chemotherapy of 3 courses of FOLFOX4. Surgery 10-11 weeks from beginning of radiation and at least 4 weeks from the last dose of fluorouracil.
Arm Title
2
Arm Type
Active Comparator
Arm Description
Conventionally fractionated chemoradiation with 50.4 Gy total dose in 28 fractions of 1.8 Gy over 5.5 weeks. Surgery 10-11 weeks from beginning of radiation and at least 4 weeks from the last dose of radiation.
Intervention Type
Radiation
Intervention Name(s)
Short course of radiotherapy
Other Intervention Name(s)
short radiation, consolidating chemotherapy
Intervention Description
5 x 5 Gy and afer one week interval consolidating chemotherapy of 3 courses of FOLFOX4
Intervention Type
Radiation
Intervention Name(s)
Radiochemotherapy
Other Intervention Name(s)
chemoradiation
Intervention Description
28 x 1,8 Gy with simultaneous neoadjuvant chemotherapy: two courses of 5-Fu 325 mg/m2/day i.v. bolus and LV 20 mg/m2/day i.v.-bolus over 5 days given during 1-5 and 29-33 days of radiation. Oxaliplatin is given 50 mg/m2 once a week 5 times during 1, 8, 15, 22 and 29 days of radiation.
Primary Outcome Measure Information:
Title
The rate of patients with R0 resection
Time Frame
Surrogate endpoint available immediatly after surgery
Secondary Outcome Measure Information:
Title
Overall long-term survival
Time Frame
5 years
Title
Progression-free long-term survival
Time Frame
5 years
Title
The rate of local failures
Time Frame
5 years
Title
The rate of distant metastases
Time Frame
5 years
Title
The rate of early toxicity of neoadjuvant treatment according to the NCI CTCAE (version 3.0)
Time Frame
3 months
Title
The rate of postoperative complications
Time Frame
30 days
Title
The rate of late toxicity according to the RTOG/EORTC scale
Time Frame
5 years
Title
The rate of complete pathological response
Time Frame
Surrogate endpoint available immediatly after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with unresectable primary rectal cancer or with unresectable local recurrence without distant metastases. WHO performance status ≤ 2. Lower border of tumour ≤ 15 cm from anal verge. Exclusion Criteria: cardiac coronary arterial disease, arrhythmias, stroke even if they have occurred in the past and are controlled with medication
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wojciech Michalski, M. S.
Phone
+48226433909
Email
W.Michalski@coi.waw.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Krzysztof Bujko, Prof.
Organizational Affiliation
Roentgena 5, 02-781 Warsaw, Poland
Official's Role
Principal Investigator
Facility Information:
Facility Name
M. Sklodowska-Curie Memorial Cancer Centre
City
Warsaw
ZIP/Postal Code
02-781
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Krzysztof Bujko, Prof.
Phone
+48226439287
Email
bujko@coi.waw.pl
First Name & Middle Initial & Last Name & Degree
Krzysztof Bujko, Prof.

12. IPD Sharing Statement

Citations:
PubMed Identifier
18207596
Citation
Bujko K, Kolodziejczyk M. The 5 x 5 Gy with delayed surgery in non-resectable rectal cancer: a new treatment option. Radiother Oncol. 2008 Jun;87(3):311-3. doi: 10.1016/j.radonc.2007.12.020. Epub 2008 Jan 18. No abstract available.
Results Reference
background
PubMed Identifier
31192355
Citation
Cisel B, Pietrzak L, Michalski W, Wyrwicz L, Rutkowski A, Kosakowska E, Cencelewicz A, Spalek M, Polkowski W, Jankiewicz M, Stylinski R, Bebenek M, Kapturkiewicz B, Maciejczyk A, Sadowski J, Zygulska J, Zegarski W, Jankowski M, Las-Jankowska M, Toczko Z, Zelazowska-Omiotek U, Kepka L, Socha J, Wasilewska-Tesluk E, Markiewicz W, Kladny J, Majewski A, Kapuscinski W, Suwinski R, Bujko K; Polish Colorectal Study Group. Long-course preoperative chemoradiation versus 5 x 5 Gy and consolidation chemotherapy for clinical T4 and fixed clinical T3 rectal cancer: long-term results of the randomized Polish II study. Ann Oncol. 2019 Aug 1;30(8):1298-1303. doi: 10.1093/annonc/mdz186.
Results Reference
derived
PubMed Identifier
26884592
Citation
Bujko K, Wyrwicz L, Rutkowski A, Malinowska M, Pietrzak L, Krynski J, Michalski W, Oledzki J, Kusnierz J, Zajac L, Bednarczyk M, Szczepkowski M, Tarnowski W, Kosakowska E, Zwolinski J, Winiarek M, Wisniowska K, Partycki M, Beczkowska K, Polkowski W, Stylinski R, Wierzbicki R, Bury P, Jankiewicz M, Paprota K, Lewicka M, Cisel B, Skorzewska M, Mielko J, Bebenek M, Maciejczyk A, Kapturkiewicz B, Dybko A, Hajac L, Wojnar A, Lesniak T, Zygulska J, Jantner D, Chudyba E, Zegarski W, Las-Jankowska M, Jankowski M, Kolodziejski L, Radkowski A, Zelazowska-Omiotek U, Czeremszynska B, Kepka L, Kolb-Sielecki J, Toczko Z, Fedorowicz Z, Dziki A, Danek A, Nawrocki G, Sopylo R, Markiewicz W, Kedzierawski P, Wydmanski J; Polish Colorectal Study Group. Long-course oxaliplatin-based preoperative chemoradiation versus 5 x 5 Gy and consolidation chemotherapy for cT4 or fixed cT3 rectal cancer: results of a randomized phase III study. Ann Oncol. 2016 May;27(5):834-42. doi: 10.1093/annonc/mdw062. Epub 2016 Feb 15.
Results Reference
derived

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The Randomised Study of Preoperative Radiotherapy With Consolidating Chemotherapy for Unresectable Rectal Cancer

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