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

11 aprile 2011 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

3

Fase

  • Fase 2

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Femmina

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Prevenzione
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Dato oralmente
Sperimentale: 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
Comparatore placebo: 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
Dato oralmente

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Ki67 in breast tissue of enrolled patients
The primary endpoint was changed in Ki67 in breast tissue of enrolled patients

Misure di risultato secondarie

Misura del risultato
Tossicità

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 gennaio 2002

Completamento primario (Effettivo)

1 aprile 2005

Completamento dello studio (Effettivo)

1 aprile 2005

Date di iscrizione allo studio

Primo inviato

11 novembre 2005

Primo inviato che soddisfa i criteri di controllo qualità

11 novembre 2005

Primo Inserito (Stima)

15 novembre 2005

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

13 aprile 2011

Ultimo aggiornamento inviato che soddisfa i criteri QC

11 aprile 2011

Ultimo verificato

1 aprile 2011

Maggiori informazioni

Termini relativi a questo studio

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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