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Phase II Study of Simvastatin for Relapsed/Refractory Myeloma

2017年12月27日 更新者:University of Louisville

Phase II Study of Simvastatin, Zoledronic Acid, Bortezomib, Bendamustine and Methylprednisolone for Relapsed/Refractory Myeloma

The purpose of this study test the hypothesis that the combination of simvastatin and zoledronic acid (for reversal of drug resistance), with bortezomib, high-dose methylprednisolone and bendamustine on a day 1,8 schedule (to reduce toxicity) will be an effective and well-tolerated treatment for relapsed and refractory multiple myeloma

調査の概要

詳細な説明

OBJECTIVES

Primary To estimate the overall response rate (ORR) (complete response (CR) + very good partial response (VGPR) + partial response (PR)) of patients with multiple myeloma who have relapsed or are refractory after bortezomib treatment and will now receive a combination therapy of simvastatin, zoledronic acid, bortezomib, bendamustine and methylprednisolone.

To evaluate safety and tolerability of studied therapy.

Secondary

  1. To estimate the progression-free Survival (PFS), time to progression (TTP), overall survival (OS) and duration of response (DOR).
  2. To describe toxicities (frequency and severity) during the treatment. 3 To estimate clinical benefit response (CBR) (ORR + minor response (MR)) and stable disease (SD).

4 Explore factors associated with ORR, PFS, OS, toxicity.

研究の種類

介入

段階

  • フェーズ2

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:

  • Patients must have a diagnosis of Multiple Myeloma (using the International Myeloma Working Group Guidelines)
  • Patients must have failed at least one prior treatment regimen containing bortezomib.

They may be refractory to primary therapy or relapsed and have measurable or assessable disease. (Refractory disease is defined as anything less than PR or progression within 60 days of completing therapy.)

  • Patients with Multiple Myeloma must have measurable active, progressive or symptomatic disease. Measurable disease may be paraprotein or free light chains in serum or urine, or the presence of bone marrow plasma cells.
  • Age- must be at least 18 years of age.
  • Prior therapies may include bendamustine, bortezomib, methylprednisolone, radiation, and autologous hematopoietic cell transplant.
  • Patients who have received therapy must be at least 4 weeks beyond prior chemotherapy (excluding corticosteroids).
  • If female patient with reproductive capacity: on effective means of birth control during the entire duration of the treatment.
  • Patients must have recovered from acute toxicities resulting from therapy administered prior to entering this study to grade 1 or less. Alopecia may not be resolved.
  • Ability to understand and willingness to sign a written informed consent document.
  • Life expectancy of greater than 8 weeks.
  • ECOG performance status 0, 1, or 2 (Karnofsky > 60%; see Appendix A).
  • Patients must have adequate bone marrow function as defined below:

absolute neutrophil count > 500/ul platelets > 30,000/ul

-Patients must have adequate liver function as defined below: total bilirubin < 2 times the upper limit of normal AST(SGOT), ALT(SGPT) < 3 x upper limit of normal

  • Patients must have adequate renal function as defined by a creatinine clearance > 40 mL/min (measured or estimated by the Cockcroft-Gault formula).
  • Patients must have no signs of significant rhabdomyolysis determined by CPK levels with a CK < 5 times the upper limit of normal.

Exclusion Criteria:

  • Patients who have not received any chemotherapy treatment for multiple myeloma prior to being enrolled in the study.
  • Patients who were receiving simvastatin (dose > 40 mg/day), or the equivalent dose of another statin) during last prior chemotherapy for multiple myeloma.
  • Patients who have had chemotherapy or radiotherapy within 4 weeks prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier.
  • Patients receiving any other investigational agent(s).
  • Active second malignancy in the last 5 years except for non-melanoma skin cancer or carcinoma-in-situ.
  • History of hypersensitivity reactions attributed to simvastatin, bortezomib, bendamustine or zoledronic acid.
  • Pregnant women are ineligible, as treatment involves unforeseeable risks to the embryo or fetus.
  • Patients receiving medications that may increase risk of rhabdomyolysis such as itraconazole, ketoconazole, erythromycin, cyclosporine, amiodarone, verapamil, niacin, HIV protease inhibitors.
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, myopathy, untreated hypothyroidism, hereditary myopathy in the family history, unstable angina pectoris, liver disease not due to multiple myeloma, cardiac arrhythmia that is symptomatic or not rate controlled, active connective tissue disease, active autoimmune disease, or psychiatric illness/social situations that would limit compliance with study requirements.

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:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Treatment with combination therapy
Treatment with combination therapy of Simvastatin, Zoledronic Acid, Bortezomib, Bendamustine, and Methylprednisolone.
  1. Simvastatin 80 mg PO daily starting day -2 through day 10.
  2. Zoledronic acid 4 mg IV over 15 minutes on day 1 and then monthly
  3. Bortezomib 1.3 mg/m2/day IV bolus on days 3,6 and 10.
  4. Bendamustine 100 mg/m2/day IV over 30 minute infusion on days 3 and 10.
  5. Methylprednisolone 1g/m2 IV over 30 minutes on days 1 and 8.
他の名前:
  • Simvastatin (ZOCOR)
  • メチルプレドニゾロン (メドロール)
  • Bortezomib (Voltarol, Diclofenac)
  • Bendamustine (Treanda)
  • Zoledronic acid (Zometa, Reclast, Zomera)

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
Response to treatment as defined by The International Myeloma Working Group response criteria for multiple myeloma.
時間枠:4 weeks after first dose of simvastatin

Response catergories (IMWG):

Complete Remission(CR), Very Good Partial Remission(VGPR), Partial Remission (PR), Minor Response (MR), Progressive Disease (PD), Stable Disease, Relapse,Refractory Disease, Overall Response.

4 weeks after first dose of simvastatin

二次結果の測定

結果測定
メジャーの説明
時間枠
Progression Free Survival (PFS)
時間枠:After 1 year of follow-up.
PFS is measured from date of study enrollment until the date of progressive disease is documented.
After 1 year of follow-up.
Incidence Rate of Toxicity
時間枠:End of study; monitoring during study.
Decriptive statistics will be provided regarding incidence rates of toxcity. Patients will be monitored for safety throughout the study.
End of study; monitoring during study.
Overall Survival (OS)
時間枠:After 1 year of follow-up
OS is measured from date of study enrollment until death.
After 1 year of follow-up

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。

スポンサー

捜査官

  • 主任研究者:Geoffrey Herzig, MD、James Graham Brown Cancer Center- University of Louisville

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

2011年4月1日

一次修了 (予想される)

2018年2月1日

研究の完了 (予想される)

2019年2月1日

試験登録日

最初に提出

2011年4月7日

QC基準を満たした最初の提出物

2011年4月8日

最初の投稿 (見積もり)

2011年4月11日

学習記録の更新

投稿された最後の更新 (実際)

2017年12月29日

QC基準を満たした最後の更新が送信されました

2017年12月27日

最終確認日

2017年12月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • BCC-HEM-10-001

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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