Evaluation of Symptom Benefit Rate of Trabectedin/PLD in Patients With Recurrent Ovarian Cancer

NCT ID: NCT03690739

Last Updated: 2022-02-24

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE3
• Total Enrollment: 9 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-08-09
• Study Completion Date: 2021-03-03

Brief Summary

This is an open-label, prospective, randomized, controlled, parallel group, multi-center phase III trial to evaluate the Symptom Benefit Rate of trabectedin/PLD in patients with recurrent ovarian cancer who achieve a stabilization of disease after 3 cycles of platinum-based reinduction therapy and with no clinical benefit.

Detailed Description

Approximately 330 patients will be randomized in a 1:1 ration to the treatments specified below:

Arm A - Platinum-based chemotherapy according to investigator's discretion Arm B - Pegylated liposomal doxorubicin 30 mg/m² + Trabectedin 1.1 mg/m² (q3w)

Conditions

Recurrent Ovarian Carcinoma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

platinum-based chemotherapy

According to the investigator's discretion

Group Type: ACTIVE_COMPARATOR

Carboplatin

Intervention Type: DRUG

Administration according to investigator's discretion

Gemcitabine

Intervention Type: DRUG

Administration according to investigator's discretion

Bevacizumab

Intervention Type: DRUG

Administration according to investigator's discretion

PLD

Intervention Type: DRUG

Administration according to investigator's discretion

Paclitaxel

Intervention Type: DRUG

Administration according to investigator's discretion

Cisplatin

Intervention Type: DRUG

Administration according to investigator's discretion

PLD + Trabectedin

PLD 30 mg/m² + Trabectedin 1.1 mg/m² q21

Group Type: ACTIVE_COMPARATOR

PLD

Intervention Type: DRUG

Administration 30 mg/m² q21

Trabectedin

Intervention Type: DRUG

Administration 1.1 mg/m² q21

Interventions

Carboplatin

Administration according to investigator's discretion

Intervention Type: DRUG

Gemcitabine

Administration according to investigator's discretion

Intervention Type: DRUG

Bevacizumab

Administration according to investigator's discretion

Intervention Type: DRUG

PLD

Administration according to investigator's discretion

Intervention Type: DRUG

Paclitaxel

Administration according to investigator's discretion

Intervention Type: DRUG

PLD

Administration 30 mg/m² q21

Intervention Type: DRUG

Trabectedin

Administration 1.1 mg/m² q21

Intervention Type: DRUG

Cisplatin

Administration according to investigator's discretion

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Females aged ≥ 18 years at time of signing informed consent form.

2. Histologically proven diagnosis of cancer of the ovary, the fallopian tube or primary peritoneal cancer.

3. Measurable or non-measurable disease (according RECIST v1.1) or CA-125 assessable disease (according GCIG criteria) or histologically proven diagnosis of relapse.

4. Platinum-treatment free interval (TFIp) > 6 months prior to cycle 1 day 1 of reinduction therapy.

5. Disease stabilization without remission or progression ac-cording to RECIST or GCIG criteria after three cycles of platinum-based chemotherapy for recurrent disease.

6. Symptomatic disease at time of baseline abdominal/GI symptom scale score >15 (EORTC QLQ-OV28)

7. Completion of EORTC QLQ-OV28 at Baseline within 7 days prior to treatment start.

8. Patients should have received previously a taxane derivative.

9. ECOG performance status ≤ 2.

10. Life expectancy of at least 12 weeks.

11. Adequate bone marrow, renal and hepatic function defined as:

• Absolute neutrophil count (ANC) ≥ 1.5 x 10^9/L
• Platelet count ≥ 100 x 10^9/L
• Hemoglobin ≥ 9.0 g/dL
• Serum creatinine ≤1.5 mg/dL (≤ 132.6 µmol/L) or creatinine clearance ≥ 60 mL/min
• Creatine phosphokinase (CPK) ≤ 2.5 x ULN
• Serum aspartate aminotransferase (AST, SGOT) or alanine aminotransferase (ALT, SGPT) ≤ 2.5 x ULN (≤ 5 x ULN in the presence of liver metastases)
• Alkaline phosphatase (ALP) ≤ 2.5 ULN
• Serum bilirubin ≤ ULN
• Albumin ≥ 25 g/l

12. Participation in an informed consent discussion with the appropriate trial-related health care representative, full understanding of the implications and constraints of the protocol, and provision of written informed consent prior to the commencement of the trial-related procedures.

13. Geographically accessibility for treatment and follow-up.

14. For women of childbearing potential (WOCBP): agreement to remain abstinent (refrain from heterosexual inter-course) or use a contraceptive method with a failure rate of < 1 per-centage per year during the treatment period and for at least six months after administration of the last dose of chemo-therapy. A woman is considered to be of childbearing po-tential if she is postmenarcheal, has not reached a post-menopausal state (≥ 12 continuous months of amenorrhea with no identified cause other than menopause), and has not undergone surgical sterilization (removal of ovaries, fal-lopian tubes, and/or uterus). Examples of contraceptive methods with a failure rate of < 1 percentage per year in-clude but are not limited to bilateral tubal ligation and/or oc-clusion, male sterilization, and intrauterine devices, and nor-mal and low dose combined oral pill plus male condom or Cerazette (desogestrel) plus male condom. Cerazette is currently the only highly efficacious progesterone based pill. The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation meth-ods) and withdrawal are not acceptable methods of contra-ception.

Exclusion Criteria

1. Ovarian tumors of low malignant potential (e.g. borderline tumors).

2. Non-epithelial ovarian or mixed epithelial/non epithelial tumors (e.g. mixed Müllerian tumors).

3. Patients with an objective response in terms of a partial or complete remission or alternatively progressive disease ac-cording to RECIST or GCIG criteria after three cycles of platinum-based reinduction chemotherapy.

4. Patients who have received previous radiotherapy for ovarian cancer.

5. History of congestive heart failure (NYHA classification > 2, even if medically con-trolled).

6. History of myocardial infarction within the last six months (documented or by electrocardiogram).

7. History of atrial or ventricular arrhythmias.

8. Impaired liver function, hyperbilirubinemia, Serum creatinine >1.5 mg/dL or > 132.6 μmol/L or creatinine clearance < 60 mL/min, left ventricular ejection fraction < 45 %.

9. Severe active or uncontrolled infection.

10. Concurrent severe medical problems unrelated to malignancy, which would significantly limit full compliance with the trial or expose the patient to extreme risk or decreased life expectancy.

11. Patients with known hypersensitivity to the active substance or their compounds related to trabectedin or PLD and patients with known hypersensitivity to one of active substances or one of their compounds used in platinum-based chemotherapy as described in the Summaries of Medicinal Products.

12. Patients with potential risks according to contraindication, warnings or interactions of the used chemotherapeutic agents as stated in the SmPCs are not eligible for participation in this trial.

13. Patients with contraindication regarding CT or MRI (only in case of contrast allergy) are excluded.

14. Women of childbearing potential (WOCBP) not using highly effective contraceptive methods.

15. Pregnancy or breast-feeding.

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

AGO Research GmbH

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Felix Hilpert, MD, PhD

Role: STUDY_CHAIR

Mammazentrum am Krankenhaus Jerusalem, Hamburg

Locations

Klinikum Aschaffenburg-Alzenau

Aschaffenburg, Bavaria, Germany

Hochtaunus-Kliniken

Bad Homburg, , Germany

Sozialstiftung Bamberg

Bamberg, , Germany

Evangelisches Krankenhaus Bergisch Gladbach

Bergisch Gladbach, , Germany

Charité - Universitätsmedizin Berlin

Berlin, , Germany

Universitätsfrauenklinik Bonn

Bonn, , Germany

Schwerpunktpraxis für Onkologie / Hämatologie

Bottrop, , Germany

Frauenärzte Casparistraße

Braunschweig, , Germany

Universitätsklinikum Carl Gustav Carus

Dresden, , Germany

Evang. Kliniken Essen-Mitte

Essen, , Germany

Agaplesion Markus Krankenhaus

Frankfurt, , Germany

Universitätsmedizin Greifswald

Greifswald, , Germany

Mammazentrum Hamburg am Krankenhaus Jerusalem

Hamburg, , Germany

Klinikum Itzehoe

Itzehoe, , Germany

ViDia Christliche Kliniken Karlsruhe

Karlsruhe, , Germany

Klinikum Ludwigsburg

Ludwigsburg, , Germany

Klinikum Magdeburg

Magdeburg, , Germany

Katholisches Klinikum Mainz

Mainz, , Germany

Universitätsfrauenklinik Mannheim

Mannheim, , Germany

Klinikum Memmingen

Memmingen, , Germany

Klinikum rechts der Isar

München, , Germany

Kliniken des Landkreises Neumarkt

Neumarkt, , Germany

Universitätsklinik für Innere Medizin, Onkologie und Hämatologie

Oldenburg, , Germany

Klinikum Ernst von Bergmann

Potsdam, , Germany

Agaplesion Diakonieklinikum Rotenburg

Rotenburg (Wümme), , Germany

Thüringen Kliniken "Georgius Agricola"

Saalfeld, , Germany

g.Sund Gyn. Kompetenzzentrum

Stralsund, , Germany

Kreiskrankenhaus "Johann Kentmann"

Torgau, , Germany

Helios Dr. Horst Schmidt Kliniken

Wiesbaden, , Germany

Countries

Germany

Other Identifiers

AGO-OVAR 2.32

Identifier Type: -

Identifier Source: org_study_id