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A Phase II Study of Axitinib in Metastatic Non-clear Cell Renal Cell Carcinoma Patients Previously Treated With Temsirolimus

2020年12月4日 更新者:Se-Hoon Lee、Seoul National University Hospital
  • 1. There is no standard treatment option for non-clear cell renal cell carcinoma (RCC).
  • 2. Patients with non-clear cell RCC is strongly assumed to have benefit from anti-VEGF treatment.
  • 3. There is no trial of axitinib for non-clear cell RCC.
  • 4. Axitinib is expected to show more potent efficacy over sorafenib or sunitinib in renal cell carcinoma.

調査の概要

詳細な説明

  1. Renal Cell Carcinoma Renal cell carcinoma is a malignant tumor occurring most frequently of primary malignant tumors in kidney.1 According to Korea Central Cancer Registry (KCCR) data, renal cancer affects 4.4 out of 100,000 males and 2.1 out of 100,000 females. About 30% of renal cancer patients accompany remote metastasis at the time of diagnosis and renal cancer even recurs in about 40% of the patients who underwent surgery for radical treatment of renal cancer as a local disease.1 New treatment strategies against renal cell carcinoma have been developed, but they have not obtained satisfactory therapeutic outcomes. Thus, constant clinical studies are necessary to improve therapeutic efficacy.
  2. Treatment of Metastatic Renal Cell Carcinoma The treatment for metastatic renal cell carcinoma has been improved a lot for the recent few years, which is, however, limited to clear cell renal cell carcinoma. The drugs showing antitumor activity against clear cell renal cell carcinoma include axitinib, sunitinib, sorafenib, bevacizumab, temsirolimus, and everolimus.

    Of them, axitinib, sunitinib, sorafenib, bevacizumab, etc. are neovascularization inhibitors which inhibit vascular endothelial growth factor (VEGF) and its receptor (VEGFR). As a first-line treatment, sunitinib prolongs progression-free survival (PFS) compared to interferon-alpha, being recognized as a first-line standard therapy. Sorafenib, a second-line treatment, shows significant prolongation of PFS against clear cell renal cell carcinoma compared to the placebo control group, establishing itself as a second-line drug. Concomitantly administered with interferon-alpha, bevacizumab shows significant prolongation of PFS compared to the single use of interferon-alpha, establishing itself as another first-line therapy. Temsirolimus, an mammalian target of rapamycin (mTOR) inhibitor, extended survival time in a clinical study of both clear and non-clear cell renal cell carcinoma. However, this clinical study was limited to patients with renal cell carcinoma having bad prognostic factors. This renal cell carcinoma with bad prognostic factors only accounts for 10-20% of entire metastatic renal cell carcinoma. Everolimus, an another mTOR inhibitor, showed a significant prolongation of PFS in the placebo-controlled phase III clinical study of patients with clear cell renal cell carcinoma in whom sunitinib therapy failed, establishing itself as a second-line therapy in case the first-line standard sunitinib therapy fails.

  3. Treatment of Metastatic Non-clear Cell Renal Cell Carcinoma (nccRCC) In fact, VEGF antagonists are shown to have some efficacy also in nccRCC. Sunitinib was effective against nccRCC. A worldwide expanded access trial of sunitinib has been undertaken. A subgroup analysis of patients with non-clear-cell histology was performed and 276 patients (11.8%) with non-clear-cell histology were identified, although distinction between different subtypes was not made. A response rate of 5.4%, clinical benefit (defined as response and stable disease was more than 3 months) of 47% and median PFS of 6.7 months was seen in this subgroup. This result compared with an overall response rate for the entire patient group of 9.3%, clinical benefit of 52.3%, and median PFS of 8.9 months. The investigators concluded that sunitinib was active in the non-clear-cell subgroup; however, these data need to be interpreted with caution because of the nonrandomization of patients in the expanded access trial and the lack of pathology verification. Also, recently, phase 2 trial of sunitinib in non-clear cell renal cell carcinoma showed remarkable efficacy with response rate of 36% and median PFS of 6.4 months. The study enrolled non-clear cell RCC patients who did not receive previous anti-angiogenic treatment.

    Sorafenib also showed some efficacy in nccRCC, though not so efficacious. The Advanced Renal Cell Carcinoma Sorafenib Expanded Access Program allowed patients in the United States and Canada with metastatic RCC to receive treatment with sorafenib prior to its regulatory approval. This non-randomized, open-label program treated 158 subjects with papillary RCC of a total of 1891 evaluable subjects (81% clear cell, 8% non-clear, and 11% unclassified histology). Of the 107 evaluable subjects with papillary RCC, 90 (84%) had a measurable response to treatment with 3 partial responders and 87 with stable disease for at least 8 weeks, while 17 (16%) subjects demonstrated early progression on treatment. The side effect profile for sorafenib was similar across histologic subtypes, and the authors concluded that sorafenib has some activity in papillary tumors.

    On the other hand, in randomized phase 3 trial of single-agent Axitinib in 723 renal cell carcinoma patients who progressed despite first-line therapy containing sunitinib, bevacizumab plus interferon-alpha, temsirolimus or cytokines, the median PFS duration was significantly longer with axitinib than with sorafenib in the entire population (6.7 months versus 4.7 months, respectively: p less than 0.0001).

  4. Rationale In short,

    1. There is no standard treatment option for non-clear cell RCC.
    2. Patients with non-clear cell RCC is strongly assumed to have benefit from anti-VEGF treatment.
    3. There is no trial of axitinib for non-clear cell RCC.
    4. Axitinib is expected to show more potent efficacy over sorafenib or sunitinib in renal cell carcinoma.

Based on above, this clinical study is designed to examine efficacy and adverse events of axitinib for non-clear cell renal cell carcinoma.

研究の種類

介入

入学 (実際)

41

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

      • Seoul、大韓民国、110744
        • Seou National University Hospital

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:

  • Histologically or cytologically confirmation of RCC without a clear cell histologic component, e.g., papillary type, chromophobe type, medullary type or unclassified)
  • Patients with stage IV or recurrent disease not amenable to surgery, radiotherapy, or combined modality therapy with curative intent
  • Previous treatment with temsirolimus
  • Measurable disease according to RECIST criteria
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  • Age 18 years or older
  • Adequate cardiac function
  • Adequate bone marrow, hepatic, and renal function
  • Hematology:

Neutrophil same or more than 1.5 x 10^9/L Platelet same or more than 75 x 10^9/L Hemoglobin same or more than 9 g/dL -Liver function tests: Total bilirubin same or less than 1.5 x upper limit normal (xULN) aspartate aminotransferase(AST), alanine aminotransferase (ALT) same or less than 2.5 xULN Alkaline phosphatase same or less than 2.5 xULN

-Renal function tests: Creatinine clearance same or more than 30 mL/min

  • Life expectancy more than 3 months
  • Signed and dated informed consent of document indicating that the patient (or legally acceptable representative) has been informed of all pertinent aspects of the trial prior to enrollment

Exclusion Criteria:

  • Clear cell type RCC
  • Composed of mostly sarcomatoid carcinoma
  • Collecting duct type RCC
  • Diagnosis of any serious secondary malignancy within the last 2 years, except for adequately treated basal cell or squamous cell carcinoma of skin, or in situ carcinoma of cervix uteri
  • Hypertension that cannot be controlled by medications (blood pressure 150/90 mmHg despite optimal medical therapy)
  • Pregnancy or breast feeding
  • Other severe acute or chronic medical or psychiatric condition
  • Prior treatment on sunitinib, sorafenib, pazopanib or bevacizumab
  • Uncontrolled central nerve system (CNS) metastasis (brain and/or leptomeningeal metastasis)
  • Patients who require concomitant treatment with potent cytochrome P 3A4 ( CYP3A4) inducers and inhibitors

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:Axitinib
This is a single arm study. Axitinib arm is the only arm who receive axitinib.
Axitinib 5mg twice will be orally administered daily with one cycle of 4 weeks. The package of axitinib must be opened right before the administration due to its photosensitivity.

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
時間枠:Followed up during study drug administration till disease progression, unacceptable toxicitiy, or 1 year
PFS is a time from study enrollment to documented disease progression or death from any cause
Followed up during study drug administration till disease progression, unacceptable toxicitiy, or 1 year

二次結果の測定

結果測定
メジャーの説明
時間枠
Response Rate
時間枠:Every 8 weeks till disease progression, unacceptable toxicity or 1 year
Tumor response according to Response Evaluation Criteria for Solid Tumor (RECIST) criteria version 1.1
Every 8 weeks till disease progression, unacceptable toxicity or 1 year
Disease control rate (DCR)
時間枠:Every 8 weeks till disease progression, unacceptable toxicity or 1 year
Disease control (complete remission + partial remission + stable disease) rate according to RECIST criteria version 1.1
Every 8 weeks till disease progression, unacceptable toxicity or 1 year
Overall survival
時間枠:Every 8 weeks till disease progression, unacceptable toxicity or 1 year
Duration from study enrollment to death from any cause
Every 8 weeks till disease progression, unacceptable toxicity or 1 year
Number of patients who experience adverse events related to drug and serious adverse events
時間枠:Every 4 weeks till disease progression, unacceptable toxicity or 1 year
Every 4 weeks till disease progression, unacceptable toxicity or 1 year

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

  • 主任研究者:Se-Hoon Lee, MD, PhD、Seoul National University Hospital

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

便利なリンク

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

2013年2月1日

一次修了 (実際)

2015年6月1日

研究の完了 (実際)

2016年12月1日

試験登録日

最初に提出

2013年2月20日

QC基準を満たした最初の提出物

2013年2月21日

最初の投稿 (見積もり)

2013年2月25日

学習記録の更新

投稿された最後の更新 (実際)

2020年12月8日

QC基準を満たした最後の更新が送信されました

2020年12月4日

最終確認日

2020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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