Diese Seite wurde automatisch übersetzt und die Genauigkeit der Übersetzung wird nicht garantiert. Bitte wende dich an die englische Version für einen Quelltext.

Arzoxifene or Tamoxifen in Preventing Breast Cancer in Premenopausal Women at High Risk for Breast Cancer

11. April 2011 aktualisiert von: The Cleveland Clinic

A Phase II Study of a Selective Estrogen Receptor Modulator (LY353381) vs. Tamoxifen vs. Placebo in Premenopausal Women With and Increased Risk for Breast Cancer

RATIONALE: Chemoprevention is the use of certain drugs to keep cancer from forming, growing, or coming back. Estrogen can cause the growth of breast cancer cells. Hormone therapy using arzoxifene or tamoxifen may prevent breast cancer by lowering the amount of estrogen the body makes. The use of arzoxifene or tamoxifen may keep breast cancer from forming in women at high risk for breast cancer.

PURPOSE: This randomized phase II trial is studying arzoxifene to see how well it works compared to tamoxifen or a placebo in preventing breast cancer in premenopausal women at high risk for breast cancer.

Studienübersicht

Detaillierte Beschreibung

OBJECTIVES:

  • Compare the effect of arzoxifene vs tamoxifen vs placebo on surrogate endpoints biomarkers, especially systemic insulin-like growth factor levels, in women at high risk for breast cancer.
  • Compare the toxic effects, biologic effects, clinical pharmacology, and pharmacodynamics of these drugs in these participants.
  • Determine the effect of these drugs on surrogate endpoint biomarkers in participants with BRCA1 and BRCA2 mutations.
  • Determine the feasibility of a chemoprevention study in participants with a strong family history of breast cancer.

OUTLINE: This is a randomized, placebo-controlled, double-blind study. Participants are randomized to 1 of 3 treatment arms.

  • Arm I: Participants receive oral tamoxifen once daily.
  • Arm II: Participants receive oral arzoxifene once daily.
  • Arm III: Participants receive an oral placebo once daily. In all arms, treatment continues for 6 months in the absence of disease progression or unacceptable toxicity. After the completion of 6 months of treatment, participants are offered the opportunity to continue treatment with their assigned study drug for an additional 6 months. Participants randomized to receive placebo are offered treatment with arzoxifene for an additional 6 months.

After completion of study treatment, participants are followed annually.

PROJECTED ACCRUAL: A total of 120 participants will be accrued for this study.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

3

Phase

  • Phase 2

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Weiblich

Beschreibung

DISEASE CHARACTERISTICS:

  • Estimated probability of carrying a BRCA1 or BRCA2 mutation ≥ 10% AND meets one of the following criteria:

    • Participants must have first-degree relatives (FDRs)* or second-degree relatives (SDRs)* (with an intervening male relative) with breast or ovarian cancer who satisfy one of the following criteria:

      • High-risk breast/ovarian cancer (non-Jewish families)

        • One FDR ≤ 40 years old** diagnosed with breast cancer
        • At least two FDRs or SDRs diagnosed with breast cancer at ≤ 50 years old OR had bilateral breast cancer
        • One FDR or one SDR diagnosed with breast cancer at ≤ 50 years old OR had bilateral breast cancer AND one FDR or SDR diagnosed with ovarian cancer
        • Three FDRs and/or SDRs diagnosed with breast or ovarian cancer (at least one in case of ovarian cancer)
        • Two FDRs and/or SDRs diagnosed with ovarian cancer
        • One male FDR or SDR diagnosed with breast cancer and one FDR or SDR (male or female) diagnosed with breast or ovarian cancer
      • Moderate-risk breast /ovarian cancer (non-Jewish families)

        • Two FDRs diagnosed with breast cancer with one ≤ 50 years old and/or both < 60 years old
        • One FDR and one SDR (mother or sister and maternal aunt or maternal grandmother) diagnosed with breast cancer if the sum of their ages is ≥ 118 years
        • One FDR and one SDR (mother or sister and paternal aunt or paternal grandmother) diagnosed with breast cancer if the sum of their ages is ≥ 78 years
        • Two SDRs (both maternal or both paternal) diagnosed with breast cancer if the sum of their ages is ≤ 98 years
        • One FDR with ovarian cancer
      • High-risk breast/ovarian cancer (Jewish families )

        • At least one FDR or SDR diagnosed with breast cancer at ≤ 50 years old
        • At least one FDR or SDR diagnosed with ovarian cancer
        • At least one FDR or SDR diagnosed with breast cancer at any age AND one FDR or SDR diagnosed with breast and/or ovarian cancer
        • At least one male FDR or SDR diagnosed with breast cancer NOTE: *FDRs are parents, siblings, and children of the participant; SDRs are aunts, uncles, grandparents, grandchildren, nieces, nephews, or half siblings of the participant

NOTE: **Age is approximated to the earliest age possible (e.g., a relative diagnosed in their 40's should be considered 40)

  • Patterns of cancer cases must all be on the maternal or paternal side of the family
  • Participants not meeting any of the above FDR or SDR criteria may provide medical documentation stating that they, a FDR, or a SDR carry BRCA1 or BRCA2 mutations

    • Participants with a prior history of breast cancer are eligible provided they have a remaining breast that has not been irradiated, all therapy for breast cancer was completed more than 2 years ago, and they are premenopausal
    • No ovarian cyst during screening
    • No more than 12 months since prior Pap smear with normal cytological results OR human papilloma virus negative if atypical squamous cells of uncertain significance (ASCUS) present
  • No higher degrees of atypia beyond ASCUS on Pap smear

    • No known history of osteoporosis (bone mineral density > 1.5 standard deviations below young adult norms)
    • Hormone receptor status
  • Not specified

PATIENT CHARACTERISTICS:

Menopausal status

  • Premenopausal, as defined by 1 of the following:

    • Last menstrual period < 6 months ago
    • Less than 45 years old AND underwent partial hysterectomy OR follicle-stimulating hormone within institutional pre-menopausal range within the past 3 months

Sex

  • Female

Performance status

  • ECOG 0-1

Life expectancy

  • More than 2 years

Hematopoietic

  • WBC ≥ 3,000/mm^3
  • Platelet count ≥ 125,000/mm^3
  • Hemoglobin ≥ 10 g/dL

Hepatic

  • Bilirubin ≤ 1.5 mg/dL
  • AST < 2 times upper limit of normal (ULN)
  • Albumin ≥ 3.0 g/dL
  • PT/PTT ≤ 1.25 times ULN

Renal

  • Creatinine ≤ 1.5 mg/dL OR
  • Creatinine clearance ≥ 60 mL/min

Cardiovascular

  • No history of deep venous thrombosis

Pulmonary

  • No history of pulmonary embolism

Other

  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile participants must use effective barrier-method contraception during and for 3 months after completion of study treatment
  • No other malignancy within the past 2 years except curatively treated basal cell or squamous cell skin cancer or cervical cancer ≤ stage I
  • No known addiction
  • Not undergoing treatment for an illicit drug addiction
  • Willing and able to undergo required study procedures (e.g., research-related breast biopsies)

PRIOR CONCURRENT THERAPY:

Chemotherapy

  • More than 2 years since prior chemotherapy

Endocrine Therapy

  • At least 3 months since prior oral contraceptives or intramuscular progestational agent
  • At least 3 months since prior luteinizing-hormone releasing hormone (LHRH) agonists or antagonists if agent was administered daily or monthly
  • At least 6 months since prior LHRH agonists or antagonists if agent was administered every 3 months
  • At least 6 months since prior antiestrogens (e.g., tamoxifen, toremifene, and raloxifene)
  • No concurrent progestational or contraceptive agents

Radiotherapy

  • See Disease Characteristics
  • More than 2 years since prior radiotherapy

Surgery

  • No prior prophylactic bilateral mastectomy

Other

  • No concurrent cholestyramine
  • No concurrent routine warfarin, bromocriptine, or phenobarbital
  • No other concurrent investigational agents

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Verhütung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Doppelt

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Arm I
Participants receive oral tamoxifen once daily for 6 months in the absence of disease progression or unacceptable toxicity. After the completion of 6 months of treatment, participants are offered the opportunity to continue treatment for an additional 6 months.
Mündlich gegeben
Experimental: Arm II
Participants receive oral arzoxifene once daily for 6 months in the absence of disease progression or unacceptable toxicity. After the completion of 6 months of treatment, participants are offered the opportunity to continue treatment for an additional 6 months.
Given orally
Placebo-Komparator: Arm III
Participants receive an oral placebo once daily once daily for 6 months in the absence of disease progression or unacceptable toxicity. After the completion of 6 months of treatment, participants are offered treatment with arzoxifene for an additional 6 months.
Given orally
Mündlich gegeben

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Ki67 in breast tissue of enrolled patients
The primary endpoint was changed in Ki67 in breast tissue of enrolled patients

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Toxizität

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Januar 2002

Primärer Abschluss (Tatsächlich)

1. April 2005

Studienabschluss (Tatsächlich)

1. April 2005

Studienanmeldedaten

Zuerst eingereicht

11. November 2005

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

11. November 2005

Zuerst gepostet (Schätzen)

15. November 2005

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

13. April 2011

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

11. April 2011

Zuletzt verifiziert

1. April 2011

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

Abonnieren