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Ovarian NeoplasmsNCT02687321

The Role of HE4 in the Follow-up of Advanced Ovarian, Fallopian Tube and Primary Peritoneal Cancer

An observational study of Ovarian Neoplasms, run by Brno University Hospital at 20 sites in 6 countries.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

To evaluate and to compare the effectiveness of CA-125 and HE4 serum levels in epithelial ovarian cancer (OC) in follow-up in terms of time to detection of elevation after the end of the first line treatment. Read more about this study

Who is it for?
Any age, women only
Conditions the study is for
Ovarian Neoplasms
What is being tested?
Determination of CA 125 and HE4, Computed tomography
Type of treatment
Injection or infusion
How many people
150 participants
Where
20 sitesin 6 countries
Study dates
Apr 2016to Jan 2020
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • Women only
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patient with histologically confirmed advanced epithelial ovarian, fallopian tube or primary peritoneal carcinoma with complete remission after first line treatment.

Who may be able to join

  • advanced ovarian cancer, stage FIGO III and IV
  • histology types: high-grade serous, low-grade serous, endometrioid, clear cell, undifferentiated
  • completed ovarian cancer surgery and platinum-based chemotherapy

Who cannot join

  • positivity of tumor markers CA 125 and HE4 during study enrollment
  • signs of cancer at computed tomography scan during study enrollment

Trial locations and contacts

20 sites in 6 countries.

Vit Weinberger, M.D., Ph.D. contact

+42053223 ext. 8306

vit.weinberger@gmail.com

20 sites in 6 countries

Czechia7 sites, 7 recruiting
  • Brno University Hospital

    Brno, 62500

    Vit Weinberger, M.D., Ph.D., +42053223 ext. 8306, vit.weinberger@gmail.com

    Jiri Presl, M.D., Ph.D., +420377105240, jiri.presl77@gmail.com

    Recruiting
  • Hospital Ceske Budejovice

    České Budějovice, 544256

    Petr Valha, M.D.

    Recruiting
  • Faculty Hospital in Hradec Králové

    Hradec Králové

    Iva Sedlakova, MD, Ph.D.

    Recruiting
  • Hospital Jihlava

    Jihlava

    Petra Herboltova, MD

    Recruiting
  • Faculty Hospital Pilsen

    Pilsen, 30100

    jiri Presl, M.D., Ph.D.

    Recruiting
  • General Hospital Prague

    Prague, 12000

    Filip Frühauf, M.D.

    Recruiting
  • Regional Hospital Pilsen

    Zlín, 585068

    Pavel Havelka, M.D., Ph.D.

    Recruiting

Other trials in Czechia

Poland6 sites, 6 recruiting
  • Swietokrzyskie Cancer Center

    Kielce, 25734

    Kamil Zalewski, M.D., Ph.D.

    Recruiting
  • Cancer Center, M.Sklodowska-Curie Memorial Institute

    Krakow

    Pavel Blecharz, Prof.

    Recruiting
  • Medical University of Lublin

    Lublin, 20093

    Krysztow Kulak, M.D.

    Recruiting
  • Pomeranian Medical University

    Szczecin

    Aleksandra Strojna, MD

    Recruiting
  • Medical University of Warsaw

    Warsaw, 02091

    Nadil Abdalla, M.D.

    Recruiting
  • Lower Silesian Cancer Center

    Wroclaw, 58413

    Marcin Jedryka, M.D., Ph.D.

    Recruiting

Other trials in Poland

Slovakia4 sites, 4 recruiting
  • Institute of Oncology, Bratislava

    Bratislava, 81250

    Ladislav Masak, M.D., Ph.D.

    Recruiting
  • National Institute of Oncology, Bratislava

    Bratislava, 83310

    Tibor Lengyel, M.D.

    Recruiting
  • University Hospital Bratislava

    Bratislava

    Mikulas Redecha, MD, Ph.D.

    Recruiting
  • FN Trencín

    Trenčín, 505820

    Peter Kascak, M.D., Ph.D.

    Recruiting

Other trials in Slovakia

Hungary1 site, 1 recruiting
  • University of Derecen

    Debrecen

    Robert Poka, Prof.

    Recruiting

Other trials in Hungary

Spain1 site, 1 recruiting
  • La Paz University Hospital. Madrid

    Madrid, 28046

    Ignacio Zapardiel, M.D., Ph.D.

    Recruiting

Other trials in Spain

Ukraine1 site, 1 recruiting
  • Lviv State Regional Oncological Center

    Lviv

    Oleh Tsolko, MD

    Recruiting

Other trials in Ukraine

About this study

Official title: The Role of HE4 in the Follow-up of Advanced Ovarian, Fallopian Tube and Primary Peritoneal Cancer: First Prospective Multicentre Observational Study

To evaluate and to compare the effectiveness of CA-125 and HE4 serum levels in epithelial ovarian cancer (OC) in follow-up in terms of time to detection of elevation after the end of the first line treatment. To evaluate the lead-time of the rise of marker levels before epithelial OC recurrence diagnosis by Computed tomography (CT) imaging method. To evaluate the appropriate HE4 cut-off value for follow-up of patients after the treatment of ovarian, Fallopian tube and primary peritoneal cancer.

Read the detailed description

Ovarian cancer (OC) is the second most common gynaecologic cancer and the leading cause of death from gynaecologic malignancy among women in industrialized countries. The global incidence in both developed and developing countries can be estimated as 165,000 new cases per year. A heavy difference in prognosis exists between the early-stage disease FIGO I-II (International Federation of Gynaecology and Obstetrics and the advanced stages (FIGO III-IV). Unfortunately, at present, we do not have an effective screening strategy for this malignancy; most (70-80%) of the cases are diagnosed as advanced-stage disease, and this explains the high mortality rate. These aggressive features of the OC encouraged in recent years a big effort in order to find new strategies for early diagnosis of OC. These studies focused dominant on new markers and diagnostic algorithms among new markers. HE4 is one of the most promising. It is a protein initially identified in the epithelium of the distal epididymis and may be involved in sperm maturation. Despite its wide distribution, it is overexpressed only in pathological tissue, and it has demonstrated good sensitivity and specificity in detecting OC, overcoming the traditional role of CA-125. Despite an aggressive upfront treatment strategy (surgery plus chemotherapy), leading to clinical remission in more than 80% of patients, the relapse-free survival varies from 95.8% (for early FIGO stages) to 33.6% (for advanced stages) at 2 years. At present, periodical evaluation of CA-125 combined with physical examination is the recommended strategy for OC follow-up, typically every 3 to 4 months in the first 2 years after primary treatment and then every 6 months until the fifth year. Five years' overall survival rate, however, is 49.7% (ranging from 83%-89% in stage I OC to 18% in stage IV). New markers should be tested in the follow-up of patients with OC to improve the surveillance program performance: the challenge is to try to anticipate the diagnosis of OC recurrence and to translate this early diagnosis of relapse in a survival improvement. Few studies only are available to date about HE4 use in follow up of ovarian cancer. All of these studies analyzed a small number of women (8-73). HE4 was shown as an earlier indicator of recurrence of OC with respect to CA-125, with a lead-time of 5 to 8 months. Only 1 prospective controlled study has been published. In this study the sensitivity and specificity of HE4, alone or in association with other markers (CA-125, CA-72-4), seems to be higher in the diagnosis of the OC relapse with respect to CA-125 alone. The other side of the question is whether the patient is advantaged by an earlier detection of the recurrent disease, in terms of overall survival, disease-free survival, and quality of life. Early detection and treatment of cancer in general or its recurrence are usually associated with better outcomes for patient, this being the rationale behind screening programs and follow-up strategies. In OC follow-up, periodical CA-125 evaluation can detect recurrence of cancer about 5 months before clinical signs or symptoms. At the same time, we have to remind, that treatments of relapsing OC are rarely curative and have heavy adverse effects, and elevation of CA-125 is often cause of anxiety in patients undergoing follow-up. The main study, that tried to clarify the role of CA-125 in OC follow-up was MRC OV05/EORTC (European Organisation for Research and Treatment of Cancer) 55955 trial a randomized study comparing early versus delayed treatment in women with relapsed OC. Patients in the delayed treatment group were treated only at clinical or symptomatic relapse. Women assigned to early treatment started chemotherapy 4.8 months earlier than those allocated to the delayed treatment. With a median follow-up of 56.9 months, there was no evidence of a difference in overall survival between the 2 groups. In particular, the results provided no evidence of an improved overall survival or a better quality of life in the early treatment group. The authors' explanation for these findings was that the lead-time between CA-125 rise and the clinical recurrence could be too short for chemotherapy to give a beneficial effect. At present, periodical evaluation of CA-125 combined with physical examination is the recommended strategy for OC follow-up, typically every 3 to 4 months in the first 2 years after primary treatment and then every 6 months until the fifth year. Five years' overall survival rate, however, is 49.7% (ranging from 83%-89% in stage I OC to 18% in stage IV).

Being tested
Determination of CA 125 and HE4, Computed tomography
Medical subject headings
Ovarian Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Determination of CA 125 and HE4, Computed tomographyOther

    Blood sample collection to determinate tumor marker found in blood elevated by the presence of cancer recurrence.In case of one or both of tumor markers are elevated, computed tomography examination with intravenous contrast agent of chest and abdomen is performed to detect the recurrence of the disease.

Study groups in NCT02687321
Study groupRoleWhat they receive
Advanced ovarian cancer patientsPatient with histologically confirmed advanced (FIGO III and IV) epithelial ovarian, fallopian tube or primary peritoneal carcinoma with complete remission after first line treatment are included into the study. The patient is regularly followed up every 3-4 months, blood sample collection is performed to determinate tumor marker found in blood, elevated by the presence of cancer recurrence. In case of one or both of tumor markers are elevated, computed tomography examination with intravenous contrast agent of chest and abdomen is performed to detect the recurrence of the disease.
Receives: Other: Determination of CA 125 and HE4, Computed tomography

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Serum levels of tumor marker CA-125

    kU/l

    Measured: two years after study enrollment

  2. Serum levels of tumor marker HE4

    pmol/l

    Measured: two years after study enrollment

Secondary outcomes (1)
  1. Ovarian cancer recurrence diagnosed by computed tomography scan

    Measured: two years after study enrollment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Feb 2016 (estimated)
  2. Study startApr 2016
  3. Primary completionJan 2020 (estimated)
  4. Study completionJan 2020 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
150 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02687321
Sponsor's protocol ID
HE4
Status last verified
Jul 2018
First submitted
17 Feb 2016
Last updated
26 Jul 2018
Results posted
No
Data monitoring committee
Yes
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Ovarian Neoplasms, run by Brno University Hospital at 20 sites in 6 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 26 Jul 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 20 sites in Czechia, Poland, Slovakia, Hungary, Spain and 1 more country. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Vit Weinberger, M.D., Ph.D. (+42053223 ext. 8306, vit.weinberger@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Serum levels of tumor marker CA-125 (time frame: two years after study enrollment). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Jul 2018.

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