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Study of Physiological and High Dose Estradiol in the Treatment of Hormone Receptor Positive Metastatic Breast Cancer

29 janvier 2015 mis à jour par: Washington University School of Medicine

A Phase II Randomized Study of Physiological (6 mg Daily) and High Dose (30 mg Daily) Estradiol in the Treatment of Hormone Receptor Positive Metastatic Breast Cancer

This study aims to examine whether estradiol is an appropriate for future Phase 3 studies as second or third line endocrine treatment. In addition the protocol explores several approaches to enhance the safety of estrogen therapy, including the establishment of the efficacy of a lower dose than that currently recommended and through the early identification of non-responders to avoid drug exposure in patients who are unlikely to benefit to estrogen treatment.

Aperçu de l'étude

Statut

Complété

Les conditions

Intervention / Traitement

Description détaillée

The purpose of this study is to compare the effects of two doses (6 mg and 30 mg) of Estradiol, a type of estrogen. This and other forms of estrogen used at doses much higher than those used for postmenopausal hormone replacement therapy have been shown to cause tumor growth stabilization or shrinkage in patients with breast cancer.

Type d'étude

Interventionnel

Inscription (Réel)

66

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Illinois
      • Chicago, Illinois, États-Unis, 60637
        • University of Chicago
    • Missouri
      • St. Louis, Missouri, États-Unis, 63110
        • Washington University School of Medicine
    • New York
      • New York, New York, États-Unis, 10021
        • Memorial Sloan-Kettering Cancer Center
    • North Carolina
      • Chapel Hill, North Carolina, États-Unis, 27599
        • University of North Carolina Breast Clinic
      • Durham, North Carolina, États-Unis, 27710
        • Duke University Medical Center
    • Ohio
      • Cleveland, Ohio, États-Unis, 44106
        • Case Western University
      • Cleveland, Ohio, États-Unis, 44195
        • Cleveland Clinic, Lerner College of Medicine, Case Western Reserve University

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Femelle

La description

Inclusion Criteria:

  • Postmenopausal women with advanced hormone receptor positive (ER and or PgR) breast cancer, has received prior treatment with an aromatase inhibitor in the advanced disease setting, and experienced at least 24 weeks of progression free survival. As long as the patient experienced an aromatase inhibitor response as defined this way, she is still eligible even if she has received further lines of endocrine therapy, which may include other aromatase inhibitors or tamoxifen, even if these subsequent lines of treatment were unsuccessful (see below for permitted chemotherapy and trastuzumab therapy).

OR

  • Postmenopausal women with systemic or unresectable local relapse after taking at least two years of adjuvant aromatase inhibitor therapy.
  • Clinical diagnosis of postmenopausal status is defined as either:

    1. Age greater than 50 years and amenorrhea for 1 year
    2. Bilateral Surgical ovariectomy
    3. Serum FSH and estradiol level in the postmenopausal range before the initiation of AI therapy.
    4. If the patient was receiving an LHRH agonist to maintain a postmenopausal state during AI therapy this should be continued since recovery of menses would lead to uncontrolled estrogen exposure and pregnancy during estrogen therapy is contraindicated.
  • Tumor cell expression of ER and/or PgR can be ascertained on either the primary or the metastatic site. However when both types of tissue are available, the metastatic site should be used to determine eligibility. ER and/or PgR positive are defined as at least 10% of malignant cells with positive nuclear staining.
  • The patients may have received adjuvant and/or neoadjuvant chemotherapy.
  • Prior radiotherapy is permitted as long as it was planned before the start of the study medication and is completed within 3 weeks of trial medication starting.
  • Prior tamoxifen therapy is also permitted as adjuvant or advanced disease therapy.
  • Patients with ER+ HER2+ disease are eligible even of they have received trastuzumab in the past (and even if it was administered in combination with endocrine treatment) as long as they meet all other eligibility criteria. Trastuzumab therapy must be held during estradiol treatment.
  • Use of prior experimental agents alone or in combination with endocrine therapy is also permissible, but a wash out of one month is required if the immediate prior therapy involved a study medication that had not been subject to regulatory approval.
  • Prior adjuvant chemotherapy is permitted as well as one line of chemotherapy for advanced disease.
  • Patient must have at least one measurable lesion defined by RECIST criteria. To be considered measurable, a baseline lesion must have a minimum diameter to compensate for measurement error: 1 cm for soft tissue lesions, 1 cm for lung lesions including pleural lesions measured by CT scan, 1 cm for liver lesions measured by CT scan.
  • Patients with bone only disease can also be enrolled if they meet the following criteria:

    1. Four or more lesions more than one cm, measurable on CT scan bone windows.
    2. At least one tumor marker that is elevated to at least two times the upper limit of normal.
    3. All patients should have a baseline bone scan with X-ray evaluation of all hot spots, CT chest abdomen and pelvis (with bone windows), and tumor marker assessment. Also CT scan of the extremities should be done on suspicious areas seen on X-ray evaluation of all hot spots if these extremity lesions are to be followed for response.
  • The patient must have an ECOG performance status of 0-2
  • The patient should have a life expectancy of > 6 months.
  • The patient must have adequate hematologic function, defined as ANC >1000/mm3 and platelets > 75,000/mm3.
  • The patient must have adequate renal function, defined as serum creatinine less than or equal to 1.5 times the upper limit of normal.
  • The patient must have adequate liver function defined as serum bilirubin less than or equal to 1.5 times the upper limit of normal (three times the upper limit of normal for patients with hereditary benign hyperbilirubinaemia), transaminases (ALT, AST) less than or equal to 2.5 times the upper limit of normal in patients without liver metastasis or less than or equal to 5 times the upper limit of normal in patients with liver metastasis.
  • For patients with bone metastasis, treatment with i.v. bisphosphonates during the trial is mandatory because of the risk of hypercalcemia. Bisphosphonate therapy must be started before the patient begins protocol therapy.
  • Preexisting hypercalcemia should be treated and calcium normalized prior to study entry.
  • The patient must give written informed consent prior to initiation of any invasive study-related procedures that would otherwise not be performed, and must be able to comply with scheduled visits and evaluations.
  • Inclusion of Women and Minorities: Entry to this study is open to women of all racial and ethnic subgroups.
  • Patients with fasting blood glucose level ≤ 200 mg/dL. If greater, hyperglycemia must be treated before initiation of study investigations.

Exclusion Criteria:

  • Patients with CNS involvement with metastatic breast cancer or life threatening lymphangitic or large volume lung or liver disease that threatens organ function.
  • Patients with history of deep venous thrombosis, pulmonary embolism, stroke, acute myocardial infarction, congestive cardiac failure, untreated hypertension.
  • Ischemic changes on a baseline EKG or other evidence of ischemic heart disease.
  • Undiagnosed abnormal genital bleeding
  • Untreated cholelithiasis
  • Fasting serum triglycerides greater than 400. Patients should be treated and triglycerides controlled prior to study entry.
  • Treatment with fulvestrant within 12 months of study initiation (fulvestrant has been shown to antagonize estradiol induced apoptosis in preclinical models (5).
  • The patient's only qualifying lesion (s) have been previously irradiated or are scheduled for irradiation following study entry.
  • Severe or uncontrolled concomitant disease from other causes.
  • EGOG Performance status 3 or 4.
  • The patient has previous malignancies other than breast cancer except a) adequately treated in situ carcinoma of the cervix, b) localized basal or squamous cell carcinoma of the skin c) any previous malignancy treated with curative intent with a recurrence risk of less than 30%.
  • The patient is unable to understand the informed consent or is unlikely to be compliant with the protocol.
  • More than one line of palliative chemotherapy for advanced disease.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur actif: Arm 1 (6 mg estradiol)
6 mg of estradiol daily (2 mg tid).
Comparateur actif: Arm 2 (30 mg estradiol)
30 mg of estradiol. (10 mg tid)

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Clinical Benefit Rate (CR Plus PR Plus SD)
Délai: 24 weeks after start of treatment

Complete response (CR) + partial response (PR) + stable disease (SD) using RECIST 1.0

CR = disappearance of all target lesions

PR = at least a 30% decrease in the sum of the longest diameter of target lesions taking as reference the baseline sum longest diameter

SD = neither sufficient shrinkage to quality for PR nor sufficient increase to qualify for progressive disease

SD is defined as lack of disease progression by 24 weeks.

24 weeks after start of treatment

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Progression-free Survival (PFS)
Délai: Up to 48 weeks

Defined as the time from treatment initiation to disease progression or death.

Time of last observation for patients remaining in the study and the time at which dose reductions, study drug termination, and withdrawal of consent occurred were treated as censored data.

Indicated as number of participants who had not progressed at 12 weeks, 24 weeks, 36 weeks, and 48 weeks.

Progression per RECIST 1.0 = at least a 20% increase in the sum of the longest diameter of target lesions taking as references the smallest sum longest diameter recorded since the treatment started or the appearance of one or more new lesions.

Up to 48 weeks
Quality of Life
Délai: Baseline and Day 28

Surveyed using a 6 item estrogen adverse effect questionnaire (headaches, bloating, breast tenderness, retention of fluid, nausea, and vomiting).

Used a 5-point scale ranging from 0 (not at all) to 4 (very much).

The scores from the 6 estrogen adverse effect items were summed to produce a single score, ranging from 0-24, with higher scores indicating higher adverse effects.

Baseline and Day 28
Quality of Life (FACT-B Mean Score)
Délai: Day 28

Surveyed using the multidimensional Functional Assessment of Cancer Therapy-Breast (FACT-B) questionnaire

The FACT-B (version 4) questionnaire consists of 36 items with five-point scale, ranging from 0-4, where a total score ranges from 0-144 and higher scores indicate better QoL. The total FACT-B score is the sum of scores for five subscales including: physical well-being (7 items), social/family well-being (7 items), emotional well-being (6 items), functional well-being (7 items), and specific breast cancer concerns (9 items).

Day 28
Frequency of Response to Re-treatment With the Same Aromatase Inhibitor That Immediately Preceded Treatment With Estradiol on Protocol.
Délai: 12 weeks post-treatment termination
Best overall response
12 weeks post-treatment termination
Frequency of Response to Re-treatment With Estradiol for Patients Who Have a Secondary Response to an Aromatase Inhibitor After the First Response to Estradiol.
Délai: Every 3 months
Every 3 months
Overall Survival (OS)
Délai: Until patient death
Until patient death

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Matthew Ellis, M.D., Ph.D., Washington University School of Medicine

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 août 2004

Achèvement primaire (Réel)

1 mars 2011

Achèvement de l'étude (Réel)

1 août 2014

Dates d'inscription aux études

Première soumission

8 mai 2006

Première soumission répondant aux critères de contrôle qualité

8 mai 2006

Première publication (Estimation)

10 mai 2006

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

16 février 2015

Dernière mise à jour soumise répondant aux critères de contrôle qualité

29 janvier 2015

Dernière vérification

1 janvier 2015

Plus d'information

Termes liés à cette étude

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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