Actively Recruiting
Salvage Systemic Therapy With or Without Stereotactic Ablative Radiotherapy for Recurrent Ovarian Cancer
Led by Yonsei University · Updated on 2023-11-24
270
Participants Needed
1
Research Sites
213 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Rationale Ovarian cancer is the 3rd most common gynecologic malignancy in Korea. The standard treatment is tumor debulking surgery with or without adjuvant chemotherapy. However, with a recurrence rate of 80%, the treatment results are the worst among gynecological cancers. The use of target and immune agents have demonstrated to improve survival. However, long-term maintenance of systemic therapy is often difficult because recurrent tumors do not respond uniformly to systemic therapy. In the 1980\~1990s, whole abdomen irradiation had been tried and faded out owing to many side effects with the introduction of taxane. Efforts have been made to find the role of salvage radiation therapy (RT) in recurrent ovarian cancer. Involved field radiotherapy (IFRT) emerged to cover the gross tumor plus regional microscopic disease in addition to salvage chemotherapy. It showed high local control, provided chemotherapy holiday in selected cases, but did not prevent out-field progression. Stereotactic ABlative Radiotherapy (SABR) is the latest treatment using an intensity modulated technique to increase the fractional dose, reduces the number of treatments, and destroys the tumor with high accuracy. SABR-COMET study, a representative clinical study, showed a significant increase in overall survival in solid cancers. Objectives The primary objective; to evaluate whether the addition of SABR to standard salvage treatment significantly improves 3-year overall survival (OS) in patients with recurrent ovarian cancer. The secondary objectives; * to check whether it significantly affects quality of life (Health-related QoL), patient-reported outcome (PRO) * to develop an deep learning-based predictive model for the treatment response of ovarian cancer subjects using radiomic and genomic analysis. Study design Arm 1; Standard salvage therapy Subjects will continue to receive current salvage treatment suitable for subjects at the discretion of their doctor, considering the location and size of recurrence, and the patient's comorbidities. Arm 2; Standard salvage therapy+ SABR Subjects receive SABR for lesions found in imaging studies. Before or After SABR, standard salvage treatment continues as planned at the discretion of the doctor. Stratification factors 1. The number of No ascites, Platinum-sensitive, Normal CA125 and ECOG0-1; 0\~3 vs. 4 2. Location of the lesion; Lymph node lesion vs. Non-lymph node lesion 3. PARP inhibitor; Used vs. Not used Randomization Arm 1 : Arm 2 = 1 : 2 Estimated Accrual : * The sample size 270 was calculated by setting the sample size to a Type I error rate (α) of 0.05 and Statistical Power of 80% using 2-Sided Equity and log-rank test. * Accurate time: 2 years, Follow-up: 3 years (total 5 years) * Alpha = 0.05, Power = 80% * 1 year drop-out: 5% per group * 3 year survival proportion: RT group 74.42%, No RT group 58% * Arm 1: Arm 2 = 1 : 2 ratio
CONDITIONS
Official Title
Salvage Systemic Therapy With or Without Stereotactic Ablative Radiotherapy for Recurrent Ovarian Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pathologically confirmed epithelial ovarian cancer
- Completed standard primary treatment including maximal debulking surgery and platinum-based chemotherapy
- Have 10 or fewer metastatic lesions (adjacent lesions count as one if treated together)
- Each metastatic lesion measures 5 cm or less in diameter
- Age 19 years or older
- Adequate bone marrow function within 60 days before enrollment (ANC ≥ 500/mm3, platelets ≥ 50,000/mm3, hemoglobin ≥ 8.0 g/dl)
- Zubrod performance status 0 to 2 within 60 days before enrollment
- Provided informed consent for research participation
You will not qualify if you...
- Brain metastasis
- Diffuse peritoneal carcinomatosis
- Malignant pleural effusion proven by fluid analysis
- Previous radiation therapy to metastases
- Metastatic lesions with unclear boundaries making targeting difficult
- Coexisting or prior invasive cancers (except thyroid cancer, cervical CIS, basal cell skin carcinoma, early gastric cancer) not disease-free for over 3 years
- Pregnancy
- Serious comorbidities including unstable angina or heart failure hospitalization within 6 months
- Myocardial infarction within 6 months
- Acute bacterial or fungal infections needing intravenous antibiotics at enrollment
- Severe respiratory disease exacerbation requiring hospitalization or hindering treatment
AI-Screening
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Trial Site Locations
Total: 1 location
1
Yonsei University Health System, Severance Hospital
Seoul, South Korea
Actively Recruiting
Research Team
Y
Yong Bae Kim
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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