MAintenance Therapy With Aromatase Inhibitor in Epithelial Ovarian Cancer (MATAO)

Last updated: June 26, 2023
Sponsor: Swiss GO Trial Group
Overall Status: Active - Recruiting

Phase

3

Condition

Digestive System Neoplasms

Peritoneal Cancer

Fallopian Tube Cancer

Treatment

Placebo

Letrozole 2.5mg

Clinical Study ID

NCT04111978
ENGOT-ov54/Swiss-GO-2/MATAO
2019-002264-27
Swiss-GO-2
ENGOT-ov54
  • Ages > 18
  • Female

Study Summary

The purpose of this study is to evaluate the efficacy of addition of letrozole to the standard maintenance therapy in subjects following a primary diagnosis of Estrogen-receptor (ER) positive high and low grade epithelial ovarian cancer (including fallopian tube and primary peritoneal cancer) and subsequent primary treatment surgery and chemotherapy. Half of the participants will receive to the standard maintenance treatment, letrozole, whilst the other half receives placebo.

The study's primary hypothesis is that the treatment with letrozole increases progression free survival in comparison to the maintenance standard treatment (superiority trial).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients must be ≥ 18 years of age
  • Willing and able to attend the visits and to understand all study-related procedures.
  • Primary, newly diagnosed FIGO Stage II to IV and histologically confirmed low or highgrade serous or endometrioid epithelial ovarian/fallopian tube/peritoneal cancer
  • (Interval-) debulking performed ECOG-Performance Status 0-2
  • Signed informed consents (ICF-1; ICF-2)
  • Paraffin-embedded tissue or paraffin-embedded cell block (from ascites) available
  • Positivity (≥ 1%) for ER expression (only determined by Histopathology Core Facilityof MATAO trial)
  • At least 4 cycles of platinum-based chemotherapy (neoadjuvant allowed)
  • Negative serum pregnancy test in women of childbearing potential who will get/havegotten a surgical resection or radiation sterilization, prior to the intervention inthe therapeutical maintenance setting.

Exclusion

Exclusion Criteria:

  • Progressive disease at the end of adjuvant treatment as defined in chapter 9.2.1 ofprotocol
  • Women of childbearing potential (not having undergone a surgical or radiationsterilization and not getting a surgical resection, prior to the intervention in thetherapeutical maintenance setting)
  • Pregnant or lactating women
  • Any other malignancy within the last 5 years which has impact on the prognosis of thepatient
  • < 4 cycles of chemotherapy in total
  • Contraindications to endocrine therapy
  • Inability or unwillingness to swallow tablets
  • Patients with a known intolerance to galactose, lactase deficiency andglucose-galactose malabsorption

Study Design

Total Participants: 540
Treatment Group(s): 2
Primary Treatment: Placebo
Phase: 3
Study Start date:
November 05, 2020
Estimated Completion Date:
October 01, 2030

Study Description

Femara (letrozole) is an extensively investigated, marketed aromatase inhibitor (AI) widely used as treatment in the maintenance phase of estrogen-receptor (ER) positive breast cancer, as it inhibit the synthesis of estrogens. Estrogen is a well known driver of cancer growth in ER-positive tumors and a high percentage of the epithelial ovarian cancers express ER as well. Of which low grade ovarian cancers demonstrates the highest level of expression, supporting our strategy of a sub-group analysis (LOGOS). Therefore, letrozole in this study be investigated prospectively and evaluated as maintenance therapy after standard surgical and chemotherapy treatment in comparison to placebo (which is the current standard maintenance treatment) in subjects with primary, ER-positive low or high grade serous or endometrioid epithelial ovarian cancer (including fallopian tube and primary peritoneal cancer) of FIGO Stage II-IV, whose cancer has not progressed by the end of the platinum-based chemotherapy.

The objectives are to evaluate the letrozole maintenance treatment compared to placebo in terms of

  • progression-free survival (PFS; primary endpoint)

  • overall survival (OS)

  • quality-adjusted progression free survival (QAPFS)

  • time to first subsequent treatment (TFST)

  • quality-adjusted time without symptoms of toxicity (Q-TWiST)

  • health related quality of life (QoL) assessed by EQ-5D-5L, FACT-ES and FACT-O questionnaires

Methods: 540 for this study eligible subjects are 1:1 allocated in this randomized, controlled, double-blinded, multi-centre study to either the test (letrozole) or control (placebo) group. The maximum maintenance treatment duration is 5 years or until symptoms of toxicity or progression of underlying disease.

Health and health-related quality of life will continuously be assessed at study entry and during routine recalls which are scheduled every 12 weeks for the first 2 years, followed by every 24 weeks for the next 3 years. Procedures performed to assess the participants' health are the same as are performed during the regular routine ovarian cancer follow-up visits: blood tests, physical as well as gynaecological examinations and may include imaging. In addition, the participants are asked to complete during the study quality of life (QoL) specific questionnaires and wear an activity tracker for one week just before the scheduled visits. These assessments will be used for the evaluation of letrozole's efficacy and burden in comparison to the standard maintenance treatment. Survival follow-up data after the mainentance treatment duration of 5 years (study end) are obtained for up to another 7 years.

Connect with a study center

  • Krankenhaus der Barmherzigen Brüder Graz

    Graz, 8020
    Austria

    Active - Recruiting

  • Medizinische Universität Graz

    Graz, 8036
    Austria

    Active - Recruiting

  • Medizinische Universität Innsbruck

    Innsbruck, 6020
    Austria

    Active - Recruiting

  • Landeskrankenhaus Hochsteiermark Leoben

    Leoben, 8700
    Austria

    Site Not Available

  • Ordensklinikum Linz Barmherzige Schwestern

    Linz, 4010
    Austria

    Active - Recruiting

  • Universitätsklinikum Salzburg

    Salzburg, 5020
    Austria

    Site Not Available

  • Klinik Hietzing Wien

    Wien, 1130
    Austria

    Active - Recruiting

  • Medizinische Universität Wien

    Wien, 1090
    Austria

    Active - Recruiting

  • Charité - Universitätsmedizin Berlin Campus Virchow Klinikum

    Berlin, 13353
    Germany

    Active - Recruiting

  • Donauisar Klinikum

    Deggendorf, 94469
    Germany

    Active - Recruiting

  • Evangelisches Krankenhaus Düsseldorf

    Düsseldorf, 40217
    Germany

    Active - Recruiting

  • Evangelische Kliniken Essen Mitte GmbH

    Essen, 45136
    Germany

    Active - Recruiting

  • Klinikum Esslingen

    Esslingen, 73730
    Germany

    Active - Recruiting

  • University Hospital Freiburg

    Freiburg, 79106
    Germany

    Active - Recruiting

  • Gynäkologisch-Onkologische Gemeinschaftspraxis Dres. med. C.Uleer/J.Y.Pourfard

    Hildesheim, 31134
    Germany

    Active - Recruiting

  • Klinikum Konstanz

    Konstanz, 78464
    Germany

    Active - Recruiting

  • St. Elisabeth-Krankenhaus

    Köln, 50935
    Germany

    Active - Recruiting

  • University Hospital Münster

    Münster, 48149
    Germany

    Active - Recruiting

  • Studienzentrum Onkologie Ravensburg

    Ravensburg, 88212
    Germany

    Active - Recruiting

  • Leopoldina Krankenhaus der Stadt Schweinfurt

    Schweinfurt, 97422
    Germany

    Active - Recruiting

  • Helios Dr. Horst Schmidt Kliniken Wiesbaden

    Wiesbaden, 65199
    Germany

    Active - Recruiting

  • AMO Wolfsburg / AMO MVZ GmbH

    Wolfsburg, 38440
    Germany

    Active - Recruiting

  • Universitätsspital Basel

    Basel, Basel Stadt 4031
    Switzerland

    Active - Recruiting

  • Kantonsspital Aarau AG

    Aarau, Kanton Aargau 5001
    Switzerland

    Active - Recruiting

  • Oncology Institute of Southern Switzerland (IOSI)-Ente Ospedaliero Cantonale (EOC)

    Bellinzona, Ticino 6500
    Switzerland

    Active - Recruiting

  • Kantonsspital Baden AG

    Baden, 5404
    Switzerland

    Active - Recruiting

  • Basel Claraspital AG

    Basel, 4002
    Switzerland

    Active - Recruiting

  • Praxis im Frauenzentrum Lindenhofspital

    Bern, 3012
    Switzerland

    Active - Recruiting

  • Universitätsklinik für Medizinische Onkologie, Inselspital

    Bern, 3010
    Switzerland

    Active - Recruiting

  • Kantonspital Graubünden (KSGR),

    Chur, 7000
    Switzerland

    Active - Recruiting

  • Kantonsspital Frauenfeld

    Frauenfeld, 8501
    Switzerland

    Active - Recruiting

  • Hôpitaux Universitaires de Genève

    Geneva, 1205
    Switzerland

    Active - Recruiting

  • Frauenklinik Spital Grabs

    Grabs, 9472
    Switzerland

    Active - Recruiting

  • Universitätsspital Waadt/ CHUV

    Lausanne, 1011
    Switzerland

    Active - Recruiting

  • Kantonsspital Baselland

    Liestal, 4410
    Switzerland

    Active - Recruiting

  • Luzerner Kantonsspital

    Luzern, 6000
    Switzerland

    Active - Recruiting

  • Tumorzentrum Hirslanden Klinik St. Anna

    Luzern, 6006
    Switzerland

    Active - Recruiting

  • Kantonsspital Münsterlingen

    Münsterlingen, 8596
    Switzerland

    Active - Recruiting

  • Kantonsspital St. Gallen

    Saint Gallen, 9007
    Switzerland

    Active - Recruiting

  • Kantonsspital Winterthur

    Winterthur, 8401
    Switzerland

    Active - Recruiting

  • Klinik für Onkologie und Hämatologie Hirslanden Zürich AG

    Zürich, 8032
    Switzerland

    Active - Recruiting

  • Stadtspital Triemli

    Zürich, 8063
    Switzerland

    Active - Recruiting

  • Unispital Zürich

    Zürich, 8091
    Switzerland

    Active - Recruiting

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