RECRUITING

Heated Intraperitoneal Chemotherapy Followed by Niraparib for Ovarian, Primary Peritoneal and Fallopian Tube Cancer

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Patients will be registered prior to, during or at the completion of neoadjuvant chemotherapy (Paclitaxel 175 mg/m2 IV over 3 hours and Carboplatin AUC 6 IV on Day 1 every 21 days for 3-4 cycles). Registered patients who progress during neoadjuvant chemotherapy will not be eligible for iCRS and will be removed from the study. Following completion of neoadjuvant chemotherapy, interval cytoreductive surgery (iCRS) will be performed in the usual fashion in both arms. Patients will be randomized at the time of iCRS (iCRS must achieve no gross residual disease or no disease \>1.0 cm in largest diameter) to receive HIPEC or no HIPEC. Patients randomized to HIPEC (Arm A) will receive a single dose of cisplatin (100mg/m2 IP over 90 minutes at 42 C) as HIPEC. After postoperative recovery patients will receive standard post-operative platinum-based combination chemotherapy. Patients randomized to surgery only (Arm B) will receive postoperative standard chemotherapy after recovery from surgery. Both groups will receive an additional 2-3 cycles of platinum-based combination chemotherapy per institutional standard (Paclitaxel 175 mg/m2 IV over 3 hours and Carboplatin AUC 6 IV on Day 1 every 21 days for 2-3 cycles) for a maximum total of 6 cycles of chemotherapy (neoadjuvant plus post-operative cycles) followed by niraparib individualized dosing until progression or 36 months (if no evidence of disease).

Official Title

GOG-3068: a Phase III Randomized Trial of Hyperthermic Intraperitoneal Chemotherapy (HIPEC) with Cisplatin Versus No HIPEC At the Time of Optimal Interval Cytoreductive Surgery Followed by Niraparib Maintenance in Patients with Newly Diagnosed Stage III and IV Ovarian, Primary Peritoneal, and Fallopian Tube Cancer (Heated Ovarian Treatment Trial)

Quick Facts

Study Start:2024-03-08
Study Completion:2034-08-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05659381

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Patients must have a pathologic diagnosis of high grade serous or endometrioid epithelial ovarian, fallopian tube, or primary peritoneal carcinoma, stage III or IV documented on CT scan/MRI, must be recommended to undergo neoadjuvant chemotherapy (3-4 cycles allowed) and are considered candidates for interval cytoreductive surgery (iCRS) as determined by the enrolling investigator.
  2. 2. Patients with stage IV disease must have complete response of extra-abdominal disease on preoperative imaging (e.g. pleural effusion, mediastinal, inguinal, supraclavicular lymphadenopathy, or other extra-abdominal metastases).
  3. 3. Patient must have no gross residual disease or no disease \>1.0 cm in largest diameter following iCRS and prior to randomization.
  4. 4. Patients must have Myriad myChoice HRD test results available prior to registration.
  5. 5. Patient must have adequate bone marrow and organ function:
  6. 6. Patients must have a GOG performance status of 0 or 1.
  7. 7. Patient must be age \> 18.
  8. 8. Patients must have a life expectancy \> 3 months.
  9. 9. Patients of childbearing potential must have a negative serum pregnancy test within 2 weeks prior to iCRS and must be practicing an effective form of contraception (with failure rate \<1% per year) during the study period and for 6 months following the last dose of niraparib. Patients of childbearing potential must consent to pregnancy testing prior to receiving niraparib and monthly thereafter for the duration of the study.
  10. 10. Patients must have normal blood pressure (BP) or adequately treated and controlled hypertension based on local standard of care (systolic BP \< 140 mmHg and diastolic \< 90 mmHg)
  11. 11. Patients receiving corticosteroids may continue as long as their dose is stable for at least 4 weeks prior to randomization.
  12. 12. Patients must agree to not donate blood during the study or for 90 days after the last dose of study treatment.
  13. 13. Patients with known human immunodeficiency virus (HIV) are allowed if they meet all of the following criteria:
  14. 1. Cluster of differentiation 4 ≥350/µL and viral load \<400 copies/mL
  15. 2. No history of acquired immunodeficiency syndrome-defining opportunistic infections within 12 months prior to randomization
  16. 3. No history of HIV associated malignancy for the past 5 years
  17. 4. Concurrent antiretroviral therapy as per the most current National Institutes of Health (NIH) Guidelines for the Use of Antiretroviral Agents in Adults and Adolescents Living with HIV started \>4 weeks prior to randomization.
  18. 1. Patients with low-grade serous, clear cell, mucinous, non-epithelial ovarian cancers and borderline tumors.
  19. 2. Patients who have received prior treatment for ovarian cancer other than the first 3-4 cycles of platinum based neoadjuvant chemotherapy.
  20. 3. Patients not eligible for iCRS based on evidence of progression of disease during neoadjuvant chemotherapy (documented on CT scan/MRI required within 28 days of iCRS).
  21. 4. Patients not eligible to iCRS based on medical co-morbidites as per enrolling investigator.
  22. 5. Patients with stage IV disease without complete response of extra-abdominal disease on preoperative imaging (e.g., pleural effusion, mediastinal, inguinal, supraclavicular lymphadenopathy, or other extra-abdominal metastases) who are not deemed resectable with iCRS.
  23. 6. Patients with a history of Myelodysplastic Syndrome or Acute Myeloid Leukemia.
  24. 7. Patients who are pregnant or lactating.
  25. 8. Patients with a hypersensitivity or allergy to paclitaxel, docetaxel, carboplatin, cisplatin, or niraparib.
  26. 9. Patients with a severe infection requiring IV antibiotics within 2 weeks of planned randomization.
  27. 10. Patients with other uncontrolled, inter-current medical conditions.
  28. 11. Patient with metastatic disease to the central nervous system.
  29. 12. Patient with uncontrolled insulin dependent diabetes (HbA1c greater than or equal to 6%) or pre-existing renal condition.
  30. 13. Patients with pre-existing hearing loss.
  31. 14. Patients with Prior Reversible Encephalopathy Syndrome (PRES).
  32. 15. Patients with current active liver or biliary disease (with the exception of Gilbert's syndrome or asymptomatic gallstones, liver metastases or otherwise stable chronic liver disease per investigator assessment). Severe hepatic impairment patients should be excluded.
  33. 16. Patients with any clinically significant gastrointestinal (GI) abnormalities that may alter absorption such as malabsorption syndrome or major resection of the stomach and/or bowels.
  34. 17. Patients with clinically significant cardiovascular disease (e.g., significant cardiac conduction abnormalities, uncontrolled hypertension, myocardial infarction, uncontrolled cardiac arrhythmia or unstable angina \<6 months prior to randomization, New York Heart Association Grade 2 or greater congestive heart failure, serious cardiac arrhythmia requiring medication, Grade 2 or greater peripheral vascular disease, and history of cerebrovascular accident within 6 months).
  35. 18. Patients with an increased bleeding risk due to concurrent conditions (e.g., major injuries or major surgery within the past 28 days prior to study randomization and/or history of hemorrhagic stroke, transient ischemic attack, subarachnoid hemorrhage, or clinically significant hemorrhage within the past 3 months).
  36. 19. Patients with known active hepatitis B (e.g., hepatitis B surface antigen reactive) are excluded unless their HBV is stably controlled on nucleos(t)ide analogs (e.g. entecavir or tenofovir) which will be continued for the duration of the study. A patient who is HCV Ab positive but HCV RNA negative due to prior treatment or natural resolution should be eligible.
  37. 20. Patient has had investigational therapy administered within 4 weeks or within a time interval less than at least 5 half-lives of the investigational agent, whichever is longer, prior to study randomization.
  38. 21. Patient has received a live vaccine within 30 days of study randomization. COVID19 vaccines that do not contain live viruses are allowed at any time during study treatment.
  39. 22. Patient has a diagnosis, detection, or treatment of another type of cancer ≤ 2 years prior to randomization (except basal or squamous cell carcinoma of the skin and cervical cancer in situ that has been definitively treated)
  40. 23. Patients who have had radiotherapy encompassing \> 20% of the bone marrow within 2 weeks of randomization; or any radiation therapy within 1 week prior to randomization.
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Jennifer Klein, MEd
CONTACT
6784310300
jklein@gog.org

Principal Investigator

Oliver Zivanovic, MD
STUDY_CHAIR
GOG Foundation

Study Locations (Sites)

City of Hope
Duarte, California, 91010
United States
Hoag Memorial Hospital Presbyterian
Newport Beach, California, 92663
United States
Stanford Ambulatory Surgery Center Lane Operating Room
Palo Alto, California, 94034
United States
Stanford Women's Cancer Center
Palo Alto, California, 94304
United States
Stanford Hospital
Palo Alto, California, 94305
United States
University of Colorado Hospital - Anshutz Cancer Pavilion
Aurora, Colorado, 80045
United States
Smilow Cancer Hospital at Yale- New Haven
New Haven, Connecticut, 06511
United States
Yale University School of Medicine
New Haven, Connecticut, 06520
United States
Sylvester Comprehensive Cancer Center - The Lennar Foundation Medical Center
Coral Gables, Florida, 33146
United States
University of Miami Hospital and Clinics - Deerfield Beach
Deerfield Beach, Florida, 33442
United States
University of Miami Hospital and Clinics
Miami, Florida, 33136
United States
Miami Cancer Institute
Miami, Florida, 33176
United States
Sylvester Comprehensive Cancer Center - Plantation
Plantation, Florida, 33324
United States
University of Kansas Hospital
Kansas City, Kansas, 66160
United States
University of Kansas Medical Center MOB
Kansas City, Kansas, 66160
United States
University of Kansas Cancer Center Overland Park
Overland Park, Kansas, 66210
United States
University of Kansas Indian Creek Breast Surgery
Overland Park, Kansas, 66211
United States
University of Kansas Cancer Center Westwood
Westwood, Kansas, 66205
United States
University of Kansas Clinical Research Center
Westwood, Kansas, 66205
United States
University of Kentucky Medical Center
Lexington, Kentucky, 40536
United States
University Medical Center New Orleans
New Orleans, Louisiana, 70112
United States
University of Kansas Cancer Center
Kansas City, Missouri, 64116
United States
University of Kansas Cancer Center North
Kansas City, Missouri, 64154
United States
University of Kansas Cancer Center Lee's Summit
Lee's Summit, Missouri, 64064
United States
Holy Name Medical Center
Teaneck, New Jersey, 07666
United States
University of New Mexico Comprehensive Cancer Center
Albuquerque, New Mexico, 87102
United States
Duke Cancer Center
Durham, North Carolina, 27710
United States
Duke Women's Cancer Care Raleigh
Raleigh, North Carolina, 27607
United States
UH Geauga Medical Center
Chardon, Ohio, 44024
United States
TriHealth Cancer Institute - Good Samaritan Hospital
Cincinnati, Ohio, 45220
United States
TriHealth Cancer Institute- Thomas Comprehensive Care Center
Cincinnati, Ohio, 45242
United States
University Hospitals Cleveland Medical Center
Cleveland, Ohio, 44106
United States
Cleveland Clinic
Cleveland, Ohio, 44195
United States
SCC at Lake University
Mentor, Ohio, 44060
United States
UH Minoff Health Center at Chagrin Highlands
Orange Village, Ohio, 44122
United States
St. John Medical Center
Westlake, Ohio, 44145
United States
Jefferson Abington Hospital
Abington, Pennsylvania, 19001
United States
Jefferson Hospital
Jefferson Hills, Pennsylvania, 15025
United States
Forbes Hospital
Monroeville, Pennsylvania, 15146
United States
West Penn Hospital
Pittsburgh, Pennsylvania, 15224
United States
Wexford Hospital
Wexford, Pennsylvania, 15090
United States
Asplundh Cancer Pavilion
Willow Grove, Pennsylvania, 19090
United States
Lankenau Medical Center/Mainline Medical Center
Wynnewood, Pennsylvania, 19096
United States
Medical University of South Carolina (Hollings Cancer Center)
Charleston, South Carolina, 29425
United States
Texas Oncology - Central South
Austin, Texas, 78758
United States
Baylor College of Medicine Medical Center
Houston, Texas, 77030
United States
O'Quinn Medical Tower at McNair Campus
Houston, Texas, 77054
United States

Collaborators and Investigators

Sponsor: GOG Foundation

  • Oliver Zivanovic, MD, STUDY_CHAIR, GOG Foundation

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-03-08
Study Completion Date2034-08-01

Study Record Updates

Study Start Date2024-03-08
Study Completion Date2034-08-01

Terms related to this study

Keywords Provided by Researchers

  • HIPEC

Additional Relevant MeSH Terms

  • Stage III Ovarian Cancer
  • Stage IV Ovarian Cancer
  • Stage III Primary Peritoneal Cancer
  • Stage IV Primary Peritoneal Cancer
  • Stage III Fallopian Tube Cancer
  • Stage IV Fallopian Tube Cancer