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Clinical Trials/NCT01434147
NCT01434147
Completed
Phase 2

Preoperative Induction Chemotherapy in Combination With Bevacizumab Followed by Combined Chemoradiotherapy in Locally Advanced Rectal Cancer With High Risk of Recurrence- Phase II Pilot Study With Preoperative Administration of Capecitabine (Xeloda), Oxaliplatin and Bevacizumab (Avastin) Followed by Capecitabine (Xeloda) Plus Radiotherapy (RTx)

Austrian Breast & Colorectal Cancer Study Group7 sites in 1 country25 target enrollmentOctober 2011

Overview

Phase
Phase 2
Intervention
preoperative induction chemotherapy in combination with bevacizumab followed by combined radiochemotherapy with capecitabine
Conditions
Rectal Cancer
Sponsor
Austrian Breast & Colorectal Cancer Study Group
Enrollment
25
Locations
7
Primary Endpoint
termination of therapy
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Phase II pilot study of a preoperative induction chemotherapy in combination with Bevacizumab followed by combined radiochemotherapy for patients with locally advanced rectal carcinoma

Detailed Description

Induction chemotherapy combined with Radio chemotherapy: Therapy start: within 28 days after bioptical diagnosis capecitabine 1000 mg/m2 bid during 14 days (d1-d14) , oxaliplatin 130 mg/m2 and bevacizumab 7.5 mg/kg body weight d1; repetition day 22 and 43 (3 cycles) Combined Radiochemotherapy after 1 week of concluded 3rd cycle of induction chemotherapy: Radiotherapy: 5 x 5 days 1.8 Gy; cumulative dose 45 Gy Chemotherapy: capecitabine 825mg/m² bid, on each radiation day during the first 4 weeks of RCTx Surgery according to TME-criteria (total mesorectal excision) in compliance of an interruption of min. 14 days after RCTx

Registry
clinicaltrials.gov
Start Date
October 2011
End Date
August 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age 18-80 years
  • Histologic confirmation of rectal adenocarcinoma stage cT3 (≤ 5mm to the mesorectal fascia)/cT4( primary curative intention)NxM0
  • No former chemotherapy, no former radiotherapy of the pelvic, no former tumour resection of a rectal carcinoma
  • General condition WHO grade 0-2
  • Adequate bone marrow reserve ( leucocytes ≥3 000/μl, thrombocytes ≥100 000/μl)
  • Adequate renal function (creatinine ≤ 1,5 mg/dl, creatinine clearance \> 50ml/min (Cockcroft and Gault formula))
  • Adequate liver function (bilirubin ≤1,5x ULN, GOT and GPT ≤3,5xULN)
  • Exclusion of pregnancy for women with childbearing potential (negative pregnancy test urine or serum)
  • Female patients with childbearing potential and male patients that are not surgically sterile must be practicing a medically acceptable contraceptive regimen while on study treatment until 3 months after the end of the study (e.g. oral contraceptives, condom, intrauterine device)
  • Life expectancy of at least 3 months

Exclusion Criteria

  • Rectal carcinoma stage cT3 (\> 5mm from the mesorectal fascia) all stages \<cT3, M1
  • Other malignant tumours within the last 5 years except cervical carcinoma in situ and basal cell carcinoma of the skin
  • General contraindication or known hypersensitivity against Bevacizumab, Capecitabine and Oxaliplatin
  • Not malignant diseases for which treatment with radiotherapy, resection of the rectum and treatment with chemotherapy (Bevacizumab, Capecitabine) is contraindicated: uncontrolled hypertension (systolic \> 150 mmHG and/or diastolic \> 100 mmHG) or clinically significant (e.g. active) cardiovascular diseases: CVA (cardiovascular accident)/ apoplectic insult (≤ 6 months prior to registration), myocardial infarction (≤ 6 months prior to registration), unstable angina pectoris, CHF(congestive heart failure) with NYHA (New York heart Association) Grade II or higher, cardiac arrhythmia requiring therapy, hepatic diseases, significant neurologic or psychiatric disorders
  • Florid, serious infection at registration
  • Peripheral neuropathy (NCI CTCAE v 4.0 ≥ grade 1)
  • Juridically limited contractual capability, indication of neurological or psychiatric disease which constrains upon investigators opinion the patients capability to adhere to the study routines
  • Major surgical procedure within 28 days prior start of the study, open wounds
  • Significant traumatic injury, bone fracture, unhealed wounds
  • Patients with spinal cord compression or metastases in the central nervous system

Arms & Interventions

induction chemotherapy + radiochemotherapy

preoperative induction chemotherapy in combination with bevacizumab followed by combined radiochemotherapy with capecitabine induction chemotherapy: starts within 28 days after bioptical diagnosis. All patients are administered with capecitabine (Xeloda®) 1000 mg/m2 bid during 14 days (d1-d14), oxaliplatin 130 mg/m2 and bevacizumab (Avastin®) 7.5 mg/kg body weight on day 1; repetition days 22 and 43 (3 cycles) Combined radiochemotherapy: starts at the earliest one week after concluded third cycle of induction chemotherapy. Radiotherapy takes place on 5 x 5 days (dose: 1.8 Gy; cumulative dose: 45 Gy). For chemotherapy patients are administered with capecitabine (Xeloda®) 825mg/m² bid, on each radiation day during the first 4 weeks of radiochemotherapy.

Intervention: preoperative induction chemotherapy in combination with bevacizumab followed by combined radiochemotherapy with capecitabine

Outcomes

Primary Outcomes

termination of therapy

Time Frame: up to 17 weeks

before surgery (after conclusion of therapy phase)

occurence of toxicity

Time Frame: up to 18-19 weeks

until timepoint of discharge of patient

Secondary Outcomes

  • collection of response rate(up to week 18)
  • post-surgery morbidity(after 18-19 weeks)

Study Sites (7)

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