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Trial of Paclitaxel/Bevacizumab +/- Everolimus for Patients With HER2-Negative Metastatic Breast Cancer

2014年12月11日 更新者:SCRI Development Innovations, LLC

A Randomized, Double-Blind, Placebo-Controlled Phase II Trial of Weekly Paclitaxel/Bevacizumab +/- Everolimus as First-Line Chemotherapy for Patients With HER2-Negative Metastatic Breast Cancer (MBC)

This randomized, double blind, placebo controlled trial will evaluate the impact of adding everolimus to the combination of weekly paclitaxel plus bevacizumab in the first-line treatment of women with HER2-negative metastatic breast cancer. Patients will be randomized (1:1) to receive either paclitaxel/bevacizumab/everolimus (Treatment Arm 1) or paclitaxel/ bevacizumab/placebo (Treatment Arm 2). Patients will be evaluated for response to treatment every 8 weeks; responding and/or stable patients will continue treatment, with re-evaluations every 8 weeks, until tumor progression or

intolerable toxicity occurs. Outcomes will be assessed for each treatment arm

separately. This trial is not intended to compare treatment arms primarily. Any such analyses are exploratory and will be conducted without adjustment for multiple hypothesis testing.

調査の概要

研究の種類

介入

入学 (実際)

113

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • California
      • LaVerne、California、アメリカ、91750
        • Wilshire Oncology Medical Group
    • Connecticut
      • Norwich、Connecticut、アメリカ、06360
        • Eastern Connecticut Hematology Oncology
    • Florida
      • Aventura、Florida、アメリカ、33180
        • Aventura Medical Center
      • Fort Myers、Florida、アメリカ、33901
        • Florida Cancer Specialists
    • Maine
      • Portland、Maine、アメリカ、04101
        • Mercy Hospital
    • Maryland
      • Bethesda、Maryland、アメリカ、20817
        • Center for Cancer and Blood Disorders
      • Bethesda、Maryland、アメリカ、20817
        • National Capital Clinical Research Associates
    • Ohio
      • Cincinnati、Ohio、アメリカ、45242
        • Oncology Hematology Care
      • Columbus、Ohio、アメリカ、43219
        • Mid Ohio Oncology/Hematology, Inc./ The Mark H. Zangmeister Center
    • South Carolina
      • Columbia、South Carolina、アメリカ、29210
        • South Carolina Oncology Associates, PA
    • Tennessee
      • Chattanooga、Tennessee、アメリカ、37404
        • Chattanooga Oncology Hematology Associates
      • Nashville、Tennessee、アメリカ、37023
        • Tennessee Oncology, PLLC
    • Texas
      • Dallas、Texas、アメリカ、75246
        • Texas Oncology
    • Virginia
      • Fairfax、Virginia、アメリカ、22031
        • Fairfax Northern Virginia Hem-Onc
      • Richmond、Virginia、アメリカ、23235
        • Virginia Cancer Institute

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  1. Female or male patients >=18 years of age.
  2. Histologically confirmed invasive breast cancer, locally unresectable or metastatic.
  3. No prior chemotherapy for MBC. Patients may have received adjuvant or

    neoadjuvant chemotherapy (including taxanes and/or bevacizumab) as long as

    treated was completed >12 months prior to relapse. Prior hormonal therapy in the

    adjuvant or metastatic setting will be permitted.

  4. Prior hormonal therapy in the adjuvant or metastatic setting is permitted. Estrogen receptor positive patients should be considered candidates for chemotherapy.
  5. HER2-negative breast cancer, defined as follows:

    • FISH-negative (FISH ratio <2.2), or
    • IHC 0-1+, or
    • IHC 2-3+ AND FISH-negative (FISH ratio <2.2).
  6. Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
  7. Adequate hematologic function, defined by:

    · Absolute neutrophil count (ANC) >1500/mm3

    • Platelet count >=100,000/mm3
    • Hemoglobin >9 g/dL
  8. Adequate liver function, defined by:

    · AST and ALT <=2.5 x the upper limit of normal (ULN) or <=5 x ULN in

    presence of liver metastases

    • Total bilirubin <=1.5 x ULN
  9. Adequate renal function, defined by:

    · Serum creatinine <=1.5 x ULN or calculated creatinine clearance of

    >=40 ml/min

  10. International normalized ratio (INR) <=1.5 or prothrombin time (PT)/partial

    thromboplastin time (PTT) within normal limits (WNL) of the institution (if patient is not on anti-coagulation therapy). Patients receiving anti-coagulation treatment with an agent such as warfarin or heparin are eligible if the INR is stable and within the therapeutic range prior to study treatment initiation.

  11. Adequate lipid profile: total cholesterol <=300 mg/dL OR <=7.75 mmol/L and fasting triglyceride 2.5 x ULN. Note: In case one or both of these thresholds are exceeded,the patient can only be included after initiation of appropriate lipid lowering medication.
  12. Patients with proteinuria at screening as demonstrated by either:

    · Urine protein creatinine (UPC) ration >1.0 at screening

    or

    • Urine dipstick for proteinuria >=2+ (patients discovered to have

    >=2+ proteinuria on dipstick urinalysis at baseline should undergo a 24 hour

    urine collection and must demonstrate <1 g of protein in 24 hours to be

    eligible).

  13. Measurable disease by RECIST criteria.
  14. Life expectancy >=12 weeks.
  15. Ability to swallow oral medications.
  16. Adequate cardiac function, defined by baseline left ventricular ejection fraction (LVEF) value >= normal per institutional guidelines by MUGA scan or

    echocardiogram (ECHO).

  17. Adequate recovery from recent surgery.

    • Major surgical procedure >28 days from study entry
    • Minor surgical procedure >7 days from study entry (Portacath placement

    excepted - patients can start treatment <7 days after portacath placement.)

  18. Patients with previous history of invasive cancers (including breast cancer) are eligible if definitive treatment was completed more than 5 years prior to initiating current study treatment, and there is no evidence of recurrent disease.
  19. Patient must be accessible for treatment and follow-up.
  20. All patients must be able to understand the investigational nature of the study and give written informed consent prior to study entry.

    -

Exclusion Criteria:

  1. Patients with active brain metastases or meningeal metastases. Patients who have had brain metastases resected, or have received brain radiation therapy >4 weeks prior to study entry are eligible, if they meet all of the following criteria: 1) residual symptoms < grade 2, 2) no dexamethasone requirement, and 3) follow-up MRI shows regression of lesions after treatment and no new lesions appearing.
  2. Previous treatment with an m-TOR inhibitor (sirolimus, temsirolimus, everolimus) or anti-angiogenesis agent unless:

    • in the adjuvant setting, and
    • >=12 months prior to recurrence.
  3. Previous radiotherapy for metastatic disease completed <2 weeks prior to study treatment initiation.
  4. Patients who are current receiving systemic cancer therapy or have received

    previous systemic therapy within 4 weeks of the start of study drug (e.g.

    chemotherapy, antibody therapy, targeted agents).

  5. Women who are pregnant or lactating. All patients with reproductive potential must agree to use effective contraception from time of study entry until at least 3 months after the last administration of study drug.
  6. Uncontrolled hypertension defined as systolic blood pressure >150 mmHg or

    diastolic pressure >100 mmHg, despite optimal medical management.

  7. Concurrent use of CYP3A4 inhibitors and inducers from 72 hours prior to initiation of study treatment until the end of treatment with everolimus.
  8. Cardiac disease, including: congestive heart failure (CHF) > Class II per New York Heart Association (NYHA) classification; unstable angina (anginal symptoms at rest) or new-onset angina (i.e., began within the last 3 months), or myocardial infarction within the past 6 months; symptomatic CHF, unstable angina pectoris, or cardiac ventricular arrhythmias requiring anti-arrhythmic therapy.
  9. History of stroke or transient ischemic attack within 6 months prior to first

    bevacizumab dose.

  10. Patients with any non-healing wound, ulcer, or long-bone fracture.
  11. Patients with clinical history of hemoptysis or hematemesis.
  12. Patients with any history of a bleeding diathesis or coagulopathy.
  13. Patients with a PEG or G tube cannot be enrolled into this trial.
  14. History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to beginning bevacizumab.
  15. Patients with an impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of everolimus (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection).
  16. Patients who have any severe and/or uncontrolled medical conditions or other

    conditions that could affect their participation such as:

    • severe impaired lung functions as defined as spirometry and DLCO that is 50% of the normal predicted value and/or 02 saturation that is 88% or less at rest on room air
    • uncontrolled diabetes as defined by fasting serum glucose >1.5 x ULN.
  17. History of any other disease, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates use of an investigational drug, or that might affect interpretation of the results of this study, or render the subject at high risk for treatment complications.
  18. History of hypersensitivity to Cremophor EL (polyoxyethylated castor oil) or a drug formulated in Cremophor EL, such as paclitaxel.
  19. Patients may not receive any other investigational or anti-cancer treatments while participating in this study.
  20. Patients receiving chronic, systemic treatment with corticosteroids or another immunosuppressive agent. Topical or inhaled corticosteroids are allowed.
  21. Patients should not receive immunization with attenuated live vaccines within one week of study entry or during study period.
  22. Concurrent severe, uncontrolled infection or intercurrent illness including, but not limited to, ongoing or active infection, or psychiatric illness/social situations that would limit compliance with study requirements.
  23. Patients with a known hypersensitivity to RAD001 (everolimus) or other rapamycins (sirolimus, temsirolimus) or its excipients.
  24. Patients with a known HIV seropositivity.

    -

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:トリプル

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ:paclitaxel/bevacizumab/everolimus
Systemic Therapy
Everolimus 10mg PO daily continuously for all 28 days of a cycle
他の名前:
  • アフィニター
  • RAD001
  • 全身療法
Bevacizumab 10mg/kg IV Days 1 and 15 of 28 day cycle
他の名前:
  • アバスチン
  • 全身療法
Paclitaxel 90mg/m2 1-hour IV infusion Days 1, 8 and 15 of 28 day cycle. Patients will receive standard pre-medication before each paclitaxel treatment to prevent a hypersensitivity reaction.
他の名前:
  • タキソール
  • 全身療法
Bevacizumab 10mg/kg IV days 1 and 15 of 28 day cycle
他の名前:
  • アバスチン
  • 全身療法
プラセボコンパレーター:paclitaxel/bevacizumab/placebo
Systemic Therapy
Bevacizumab 10mg/kg IV Days 1 and 15 of 28 day cycle
他の名前:
  • アバスチン
  • 全身療法
Paclitaxel 90mg/m2 1-hour IV infusion Days 1, 8 and 15 of 28 day cycle. Patients will receive standard pre-medication before each paclitaxel treatment to prevent a hypersensitivity reaction.
他の名前:
  • タキソール
  • 全身療法
Bevacizumab 10mg/kg IV days 1 and 15 of 28 day cycle
他の名前:
  • アバスチン
  • 全身療法
Placebo PO daily continuously for all 28 days of a cycle
他の名前:
  • 全身療法

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Progression-Free Survival (PFS)
時間枠:every 8 weeks until progressive disease, expected average of 18 months
Progression-free survival will be measured from Day 1 of study drug administration to disease progression defined by Response Evaluation Criteria in Solid Tumors Criteria (RECIST v1.1) as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions
every 8 weeks until progressive disease, expected average of 18 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Number of Patients With Treatment-related Adverse Events (AEs) as a Measure of Safety and Tolerability
時間枠:every 4 weeks until intolerable toxicity occurs
Assessments will be made based on the analysis of reported incidence of treatment-emergent AEs
every 4 weeks until intolerable toxicity occurs
Overall Response Rate (ORR)
時間枠:every 8 weeks until treatment discontinuation, expected average of 18 months
The number of patients with observed complete response [CR] or partial response [PR]. Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR
every 8 weeks until treatment discontinuation, expected average of 18 months
Duration of Response (DOR)
時間枠:every 8 weeks until treatment discontinuation, expected average 6 months
Defined as time between date of objective response and date of response to disease progression or death, as defined by RECIST v1.1 criteria. Objective response is defined as either complete response [CR] or partial response [PR]. Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions
every 8 weeks until treatment discontinuation, expected average 6 months
Overall Survival (OS)
時間枠:every 8 weeks until treatment discontinuation, expected average 6 months
Assessed from Day 1 of study drug administration to date of death due to any cause.
every 8 weeks until treatment discontinuation, expected average 6 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

協力者

捜査官

  • スタディチェア:Denise A. Yardley, M.D.、SCRI Development Innovations, LLC

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2009年7月1日

一次修了 (実際)

2014年6月1日

研究の完了 (実際)

2014年7月1日

試験登録日

最初に提出

2009年6月4日

QC基準を満たした最初の提出物

2009年6月4日

最初の投稿 (見積もり)

2009年6月8日

学習記録の更新

投稿された最後の更新 (見積もり)

2014年12月22日

QC基準を満たした最後の更新が送信されました

2014年12月11日

最終確認日

2014年12月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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