Randomized Trial of Standard Dose Versus High Dose of Radiotherapy in Rectal Preservation With Chemo-radiotherapy to Patients With Early Low and Mid Rectal Cancer: The Watchful Waiting 3 Trial (WW3)

Status: Recruiting
Location: See all (5) locations...
Intervention Type: Drug, Radiation
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

In recent years, an increasing number of retrospective and prospective observational studies have indicated that a subset of rectal cancer patients may avoid surgery if they can achieve a complete response to chemoradiotherapy. Prospective trials, including the previous Danish Watchful Waiting trials (NCT00952926, NCT02438839) in early rectal cancer have demonstrated high levels of organ preservation with dose-escalation, but it is unclear whether this was primarily due to tumor stage or dose level. The aim of the present study is to investigate if a higher dose of radiotherapy is superior compared to a standard dose in patients with early rectal cancer undergoing chemoradiotherapy with curative intent.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Histopathologically verified adenocarcinoma of the rectum

• MDT conference finds patient a candidate for rectal resection

• Clinical tumor category cT1-3

• MRI findings

‣ Maximal cross-sectional size of 4.5 cm (axial plane relative to the rectum)

⁃ Lowest edge of tumor located at or below the peritoneal reflection on MRI

• Performance status 0-2

• Age ≥ 18 years

• Eligible for radiotherapy and capecitabine according to investigator, including

‣ Adequate function of bone marrow (neutrophils ≥ 1.5 x 10\^9/l and thrombocytes ≥ 100 x 10\^9/l)

⁃ Adequate function of liver (ALAT \< 2.5 x upper limit of normal, bilirubin \< 2.5 x upper limit of normal)

⁃ Adequate kidney function (Serum creatinine \< 1.5 x upper limit of normal or measured GFR \> 30 ml/min)

• Fertile women must present a negative pregnancy test and use secure contraceptives during and three months after treatment

• Written and orally informed consent

Locations
Other Locations
Denmark
Aalborg University Hospital
RECRUITING
Aalborg
Copenhagen University Hospital, Righshospitalet and Bispebjerg Hospital
RECRUITING
Copenhagen
Zealand University Hospital, Næstved
NOT_YET_RECRUITING
Næstved
Zealand University Hospital, Roskilde
NOT_YET_RECRUITING
Roskilde
Department of Oncology, Vejle Hospital
RECRUITING
Vejle
Contact Information
Primary
Lars H Jensen, MD, PhD
lars.henrik.jensen@rsyd.dk
+45 7940 6802
Time Frame
Start Date: 2020-01-20
Estimated Completion Date: 2028-12
Participants
Target number of participants: 111
Treatments
Active_comparator: A: Standard chemoradiotherapy
50.4 Gy to the tumor and elective volume. The dose is given in 28 fractions on weekdays concomitantly with capecitabine 825 mg/m2 twice daily on weekdays.
Experimental: B: High-dose radiotherapy
62 Gy to the clinical tumor volume and 50.4 Gy to the elective volume. The dose is given in 28 fractions on weekdays concomitantly with capecitabine 825 mg/m2 twice daily on weekdays
Related Therapeutic Areas
Sponsors
Leads: Vejle Hospital

This content was sourced from clinicaltrials.gov