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Trial record 53 of 264 for:    Estrogen Resistance

CIrCuLAting Dna ESr1 Gene Mutations Analysis (CICLADES)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03318263
Recruitment Status : Recruiting
First Posted : October 23, 2017
Last Update Posted : February 6, 2019
Information provided by (Responsible Party):
Institut de Cancérologie de Lorraine

Brief Summary:

The estrogen-dependent nature of breast cancer was first reported in 1896 with the publication of George Beatson's observations on the regression of breast cancer following oophorectomy. Endocrine therapy, targeting ER either directly by selective estrogen receptor modulators (SERMs) and pure antagonists or indirectly by aromatase inhibitors (AIs) that block estrogen production, remains the mainstay of treatment of hormone-sensitive breast cancer in the adjuvant and metastatic settings.

Intrinsic (de novo) and acquired endocrine resistance constitutes an important clinical challenge in the treatment of breast cancer and multiple mechanisms are suspected to underlie the emergence of endocrine resistance.

The role of the estrogen receptor (ER), encoded by the ESR1 gene, in normal mammary gland development and the progression of breast cancer is well established. ESR1 mutations, occurring in 10 to 30% of ER-positive metastatic breast cancer resistant to AIs, lead to ligand-independent activation of the ER.

For patients treated with AIs, monitoring of circulating tumour DNA (ctDNA) for ESR1, PIK3CA and AKT1 mutations could permit early detection of resistance to AIs as recently reported during 2016 American Society of Clinical Oncology (ASCO) meeting.

Condition or disease Intervention/treatment Phase
Breast Cancer Diagnostic Test: next-generation sequencing (NGS) Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 146 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Monitoring of ESR1, PIK3CA and AKT ctDNA Mutations During Real-life Followup of Patients With Metastatic Breast Cancer Treated With Aromatase Inhibitors
Actual Study Start Date : December 7, 2017
Estimated Primary Completion Date : December 2019
Estimated Study Completion Date : June 2022

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer

Arm Intervention/treatment
experimental Diagnostic Test: next-generation sequencing (NGS)
ESR1, PI3KCA and AKT extensive exon sequencing will be performed using NGS (Miseq Illumina) at the Biopathology department, Institut de Cancérologie de Lorraine (ISO15189 certified lab). Samples taken at baseline (t0), at progression (tp) and 3 months before progression (tp-3) will be systematically analyzed. The intermediate samples will be stored and kept for additional studies. Follow up assessment will be performed according to prescriber's directions.

Primary Outcome Measures :
  1. incidence of ESR1 mutations [ Time Frame: 1 day ]

Secondary Outcome Measures :
  1. incidence of PIK3CA and AKT1 mutations [ Time Frame: 1 day ]
  2. prevalence of ESR1, PIK3CA and AKT1 mutations in patients with and without endocrine resistance at enrolment [ Time Frame: 1 day ]
  3. prevalence of ESR1, PIK3CA and AKT1 mutations in patients according to mono vs combo therapy. [ Time Frame: 1 day ]
  4. prevalence of mutations of other genes of interest included in the panel from the start of treatment to progression or end of follow-up [ Time Frame: 1 day ]
  5. ESR1, PIK3CA and AKT1 mutations predictor of progression free survival [ Time Frame: 1 day ]

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Female patient aged 18 and older
  2. Histologically confirmed estrogen-receptor-positive, HER2-negative breast cancer
  3. Proven metastatic (AJCC stage IV) or loco-regionally advanced (AJCC stage III) breast cancer, not amenable to surgery or radiation with curative intent.
  4. Indication to treat with first-line endocrine therapy for palliative care.

    • Patients already receiving first-line endocrine therapy can be enrolled up to 6 weeks after start of endocrine therapy.
    • Endocrine therapy can be prescribed in combination with a CDK4/6 inhibitor.
    • One prior regimen of chemotherapy for the treatment of advanced disease is allowed.
    • Prior (neo)adjuvant chemotherapy and/or (neo)adjuvant endocrine therapy is/are allowed; patients with recurrence while on adjuvant endocrine therapy can be enrolled.
  5. Patients who can benefit from an additional blood sample of 10ml. The total volume of each sample meets with the indications of the Order in force establishing the list of researches mentioned in 2 ° of Article L. 1121-1 of the Public Health Code.
  6. Informed consent explained to, understood by and signed by patient. Patient must be given a copy of informed consent.
  7. Patients affiliated to a social security scheme or benefit from a social regime

The prescription of medicinal product(s) is clearly separated from the decision to include the subject in this ISMRC.

Exclusion Criteria:

  1. Pregnant or breast-feeding woman.
  2. Patient who received any prior systemic hormonal therapy for advanced breast cancer; no more than one prior regimen of chemotherapy for the treatment of advanced disease is allowed.
  3. Chemotherapy in combination with endocrine therapy.
  4. Targeted therapy, except CDK 4/6 inhibitor, in combination with endocrine therapy.
  5. Planned surgery or radiation with curative intent.
  6. Other active malignancy.
  7. Any concurrent severe and/or uncontrolled medical condition(s) which could compromise participation in the study.
  8. Patient whose general state and / or conditions do not permit the collection of the additional blood sample.
  9. Patients under guardianship, under curatorship or deprived of liberty.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03318263

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Contact: MERLIN JEAN LOUIS 00 33 3 83 59 83 07
Contact: TOSTI PRISCILLIA, PhD 00 33 3 83 59 86 57

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Hôpital Claude Bernard Recruiting
Metz, France, 57070
Contact: GARDNER Miriam, MD         
CHR Metz-Thionville Recruiting
Metz, France, 57085
Contact: LONGO Rafaelle, MD         
Centre d'oncologie Gentilly Recruiting
Nancy, France
Contact: Célia BECUWE, MD         
Institut Jean Godinot Recruiting
Reims, France, 51100
Contact: SAVOYE Aude-Marie, MD         
Polyclinique de Courlancy Recruiting
Reims, France, 51100
Contact: PRULHIERE Karine, MD         
Centre Henri Becquerel Recruiting
Rouen, France, 76038
Contact: Florian CLATOT, MD         
Polyclinique de l'Orangerie Not yet recruiting
Strasbourg, France, 67000
Contact: ACHILLE Mihaela, MD         
Clinique Saint Anne Recruiting
Strasbourg, France, 67085
Contact: TAZI Youssef, MD         
CHU Strasbourg Recruiting
Strasbourg, France, 67091
Contact: BARHELEMY Philippe, MD         
Institut de cancérologie de Lorraine Recruiting
Vandœuvre-lès-Nancy, France, 54509
Sponsors and Collaborators
Institut de Cancérologie de Lorraine
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Principal Investigator: MASSARD VINCENT, MD Institut de Cancérologie de Lorraine

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Responsible Party: Institut de Cancérologie de Lorraine Identifier: NCT03318263     History of Changes
Other Study ID Numbers: 2017-A01767-46
First Posted: October 23, 2017    Key Record Dates
Last Update Posted: February 6, 2019
Last Verified: February 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Institut de Cancérologie de Lorraine:
Estrogen-receptor-positive breast cancer
aromatase inhibitor,
endocrine resistance
circulating tumor DNA
Additional relevant MeSH terms:
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Estrogen Antagonists
Breast Neoplasms
Neoplasms by Site
Breast Diseases
Skin Diseases
Aromatase Inhibitors
Steroid Synthesis Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Hormone Antagonists
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs