Rucaparib MAintenance After Bevacizumab Maintenance Following Carboplatin Based First Line Chemotherapy in Ovarian Cancer Patients

Ovarian Cancer Clinical Trial

— MAMOC  

Official title:

Rucaparib MAintenance After Bevacizumab Maintenance Following Carboplatin Based First Line Chemotherapy in Ovarian Cancer Patients

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04227522
• Other study ID #: NOGGO ov42
• Status: Active, not recruiting
• Phase: Phase 3
• Start date: June 8, 2020
• Est. completion date: January 2025

Study information

• Verified date: April 2024
• Source: North Eastern German Society of Gynaecological Oncology
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

MAMOC is a multicenter, randomized, placebo controlled, double blind study including BRCA negative patients with histologically confirmed, advanced (FIGO stage IIIA, IIIB, IIIC, or IV of the 2014 FIGO classification) high grade serous or high grade endometrioid (based on local histopathological findings) ovarian cancer, fallopian tube cancer, primary peritoneal cancer and clear cell carcinoma of the ovary in first line therapy.

Description:

The main scope of this trial is to determine progression free survival in BRCA negative patients treated with Rucaparib as maintenance therapy vs. Placebo after receiving Bevacizumab for 12 to 15 months.

BRCA negative patients will be stratified according to time point of surgery (adjuvant vs. neoadjuvant), result of surgery (tumor free vs. not tumor free resection), study site and response (complete response (CR) vs. partial response (PR)/SD) and randomized 2:1 to receive either Rucaparib (Arm A) or Placebo (Arm B).

In both of the arms, tumor assessments (CT or MRI) are performed before randomization, and every 6 months thereafter.

During treatment, clinical visits (blood cell counts, detection of toxicity) occur every 4 weeks. Physical examinations will take place every 12 weeks. Safety will be monitored continuously by careful monitoring of all adverse events (AEs) and serious adverse events (SAEs).

About 30 sites in Germany will participate in this study to recruit 190 BRCA negative patientsin 24 months.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 190
• Est. completion date: January 2025
• Est. primary completion date: December 1, 2023
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Written informed consent and obtained from the subject prior to performing any protocol-related procedures, including screening evaluations.

2. Age = 18.

3. Patients with histologically confirmed, advanced (FIGO stage IIIA, IIIB, IIIC, or IV of the 2014 FIGO classification) high grade serous or high grade endometrioid (based on local histopathological findings) ovarian cancer, fallopian tube cancer, primary peritoneal cancer and clear cell carcinoma of the ovary in first line therapy.

4. Availability of archival tumor tissue for central next-generation sequencing (NGS) Analysis and no Detection BRCA mutation (BRCAnegative).

5. Treatment with Bevacizumab or respective biosimilar for 12 to 15 months, independent of dosage.

6. Patients who have completed first line platinum-taxane chemotherapy and at least stable disease after treatment with Bevacizumab before randomization.

7. Patients must be randomized at least 3 weeks and no more than 9 weeks after their last dose of Bevacizumab (last dose is the day of the last infusion) and all major toxicities from the previous chemotherapy must have resolved to CTCAE grade 1 or better (except alopecia and peripheral neuropathy).

8. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1

9. Patients must have normal organ and bone marrow function:

1. Hemoglobin = 10.0 g/dL independent of transfusion = 14 days prior to Screening hemoglobin assessment

2. Absolute neutrophil count (ANC) = 1.5 x 109 /L

3. Platelet count = 100 x 109 /L

4. Total bilirubin = 1.5 x institutional upper limit of normal (ULN); < 2 × ULN if hyperbilirubinemia is due to Gilbert's syndrome

5. Aspartate aminotransferase /Serum Glutamic Oxaloacetic Transaminase (ASAT/SGOT)) and Alanine aminotransferase /Serum Glutamic Pyruvate Transaminase (ALAT/SGPT)) =3 x ULN, unless liver metastases are present in which case they must be = 5 x ULN

6. Serum creatinine = 1.5 x institutional ULN and creatinine clearance > 30 mL/min

7. Patients not receiving anticoagulant medication who have an International Normalized Ratio (INR) =1.5 and an Activated ProThrombin Time (aPTT) =1.5 x ULN.

10. Postmenopausal or evidence of non-childbearing status for women of childbearing potential prior to the first dose of study treatment. Female patients of childbearing potential must have a negative serum pregnancy test result =3 days prior to administration of the first dose of rucaparib.

Patients are considered to be of childbearing potential unless 1 of the following applies:

1. Considered to be permanently sterile. Permanent sterilization includes hysterectomy, bilateral salpingectomy, and/or bilateral oophorectomy; or

2. Is postmenopausal, defined as no menses for at least 12 months without an alternative medical cause. A high follicle-stimulating hormone (FSH) level consistently in the postmenopausal range (30 milli International Units/milliliter (mIU/mL) or higher) may be used to confirm a postmenopausal state in women not using hormonal contraception or hormonal replacement therapy; however, in the absence of 12 months of amenorrhea, a single FSH measurement is insufficient to confirm a postmenopausal state.

Female patients of reproductive potential must practice highly effective methods (failure rate < 1% per year) of contraception with their partners, if of reproductive potential, during treatment and for 6 months following the last dose of rucaparib or longer if requested by local authorities. Highly effective contraception includes: Ongoing use of progesterone only injectable or implantable contraceptives; Placement of an intrauterine device (IUD) or intrauterine system (IUS); Bilateral tubal occlusion; Sexual abstinence as defined as complete or true abstinence, acceptable only when it is the usual and preferred lifestyle of the patient; periodic abstinence (eg, calendar, symptothermal, post-ovulation methods) is not acceptable; or Sterilization of the male partner, with appropriate post-vasectomy documentation of absence of sperm in ejaculate.

Exclusion Criteria:

1. Non-epithelial origin of the ovary, the fallopian tube or the peritoneum (i.e. germ cell tumors) and Ovarian tumors of low malignant potential (e.g. borderline tumors), or low grade serous ovarian cancer, or low grade endometrioid ovarian cancer, or mucinous carcinoma.

2. Patients with myelodysplastic syndrome/acute myeloid leukemia history.

3. Patients receiving radiotherapy within 6 weeks prior to study treatment.

4. Major surgery within 4 weeks of starting study treatment and patients must have recovered from any effects of any major surgery.

5. Previous allogeneic bone marrow transplant.

6. Use of any other PARP-inhibitor in first line therapy.

7. Administration of other simultaneous chemotherapy drugs, any other anti-cancer therapy or anti-neoplastic hormonal therapy, or simultaneous radiotherapy during the trial treatment period (hormonal replacement therapy is permitted as are steroidal antiemetics).

8. Clinically significant (e.g. active) cardiovascular disease.

9. Previous Cerebro-Vascular Accident (CVA), Transient Ischemic Attack (TIA) or Sub-Arachnoids Hemorrhage (SAH) within 6 months prior to randomization.

10. History or evidence of hemorrhagic disorders within 6 months prior to randomization.

11. Evidence of bleeding diathesis or significant coagulopathy (in the absence of coagulation).

12. History or evidence for brain metastases or spinal cord compression.

13. History or evidence upon neurological examination of central nervous system (CNS) disease, unless adequately treated with standard medical therapy (e.g. uncontrolled seizures).

14. Significant traumatic injury during 4 weeks prior to randomization.

15. Non-healing wound, active ulcer or bone fracture. Patients with granulating incisions healing by secondary intention with no evidence of facial dehiscence or infection are eligible but require 3 weekly wound examinations.

16. Current, clinically relevant bowel obstruction, including sub-occlusive disease, related to underlying disease.

17. Evidence of any other disease, metabolic dysfunction, physical examination finding or laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or puts the patient at high risk for treatment related complications.

18. Pregnant or lactating women, women of child-bearing potential who do not agree to the usage of highly effective contraception methods (see inclusion criteria).

19. Participation in another clinical study with an investigational product immediately prior to randomization.

20. Patients unable to swallow orally administered medication and patients with gastrointestinal disorders likely to interfere with absorption of the study medication.

21. Patients with a known hypersensitivity to Rucaparib or any of the recipients of the product.

22. Known human immunodeficiency virus (HIV) or acquired immunodeficiency Syndrome (AIDS)-related illness, or history of chronic hepatitis B or C.

23. Other active malignancy requiring treatment.

24. Patient who might be dependent on the sponsor, Clinical Research Organization (CRO), site or the investigator.

25. Patient who has been incarcerated or involuntarily institutionalized by court order or by the authorities § 40 Abs. 1 S. 3 Nr. 4 Arzneimittelgesetz (AMG).

Related Conditions & MeSH terms

• Carcinoma, Ovarian Epithelial
• Clear Cell Carcinoma
• Fallopian Tube Cancer
• Fallopian Tube Neoplasms
• Ovarian Cancer
• Ovarian Neoplasms
• Primary Peritoneal Cancer

Intervention

Drug:
• Rucaparib
A starting dose of 600 mg Rucaparib is taken twice daily orally by the patients as maintenance after previous maintenance therapy (Bevacizumab) for a period of 12 to 15 months.
• Placebos
Placebo is taken daily orally by the patients as maintenance after previous maintenance therapy (Bevacizumab) for a period of 12 to 15 months.

Locations

Country	Name	City	State
Germany	Universitätsklinikum Aachen	Aachen
Germany	ANregiomed Frauenklinik Ansbach	Ansbach
Germany	Charité - Universitätsmedizin Berlin, Campus Virchow Klinikum	Berlin
Germany	Helios Klinikum Berlin-Buch	Berlin
Germany	Universitätsklinikum Bonn	Bonn
Germany	Städtisches Klinikum Dessau	Dessau
Germany	Universitätsklinikum Carl Gustav Carus	Dresden
Germany	Kliniken Essen Mitte	Essen
Germany	Universitätsklinikum Hamburg-Eppendorf	Hamburg
Germany	ViDia Christliche Kliniken Karlsruhe Vincentius-Diakonissen-Kliniken g AG	Karlsruhe
Germany	Städtisches Krankenhaus Kiel	Kiel
Germany	ZAGO-Zentrum für ambulante gynäkologische Onkologie	Krefeld
Germany	Universitätsklinikum Mannheim	Mannheim
Germany	LMU Klinikum Großhadern	München
Germany	Universitätsklinikum Münster	Münster
Germany	CaritasKlinikum Saarbrücken	Saarbrücken
Germany	Helios Dr. Horst Schmidt Kliniken Wiesbaden	Wiesbaden

Sponsors (3)

Lead Sponsor	Collaborator
North Eastern German Society of Gynaecological Oncology	Clovis Oncology, Inc., Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression free survival (PFS)	time from randomization until disease progression or death	48 months
Secondary	Progression free survival 2 (PFS2)	time from randomization to second progression or death	48 months
Secondary	Quality of Life (QoL) 1	Patients are asked to answer the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire Core 30 (QLQ-C30). Responses of questions 1-28 are based on a 4-point scale (1=not at all; 4=Very much), with a higher score indicating a high degree of symptomatology and must therefore be assessed negatively. Responses of questions 29 and 30 are based on a 7-point scale (1=Very poor; 7=Excellent), with a higher score indicating a better global health status.	48 months
Secondary	Quality of Life 2	Patients are asked to answer the EORTC QoL Questionnaire-Ovarian Cancer (QLQ-OV28). Responses are based on a 4-point scale (1=Not at all; 4=Very much), with a lower score indicating better symptoms.	48 months
Secondary	Quality of Life/ Global health status 3	Patients are asked to answer the short version of the SF-36 Health Survey (SF-12). The questionnaire contains a total of 12 questions with different response options. For questions 1, 8 and 12 there are 5 (1=excellent, 5=bad), for question 2-3 there are 3 (1=yes, very restricted, 3=no, not restricted at all) and for questions 9-11 there are 6 response options (1= always, 6 = never). Questions 4-7 can be answered with "Yes" or "No".	48 months
Secondary	Quality of Life 4	Patients are asked to answer the questionnaire Fatigue Symptom Inventory (FSI). Responses are based on a 10 point grading scale (0=not at all tired/ exhausted; 10=completely tired/ exhausted), with a lower score indicating a lower symptomatology of fatigue.	48 months
Secondary	Quality of Life 5	Patients are asked to answer the Everyday Memory Questionnaire. Responses are based on a 5-point scale (1=occasionally; 5=very often), with a lower score indicating a better performance on memory associated Everyday activities.	48 months
Secondary	Quality of Life 6	Patients are asked to answer a custom form of the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events developed by the National Cancer Institute (NCI PRO-CTCAE™) Version 1.0. The frequency and strength of symptoms is queried. There are 5 possible answers: "not at all", "a little", "moderate", "quite", "very".	48 months
Secondary	Determination of time to next medical intervention	(e.g. bowel obstruction, Ascites puncture)	48 months
Secondary	Time to next subsequent therapy	e.g. chemotherapy	48 months
Secondary	Number of participants with treatment-related adverse events and/or serious adverse events as assessed by CTCAE v4.03	AEs/SAEs	48 months
Secondary	Overall survival (OS)	defined as time from Randomization to death by any cause	72 months