Intratumoral Application of L19IL2 in Patients With Malignant Melanoma
A Phase II Study of Intratumoral Application of L19IL2 in Patients With Stage III/IV Melanoma.
調査の概要
詳細な説明
Phase II, non-randomized, multicenter, prospective study designed to test the efficacy and safety of intratumorally administered L19IL2. L19IL2 binds with high affinity to the EDB domain of Fibronectin, a marker of angiogenesis which is strongly upregulated in malignant melanoma lesions. This binding leads to an increased residence time of the protein at the site of disease. The biologic effect of the IL2 moiety is identical to the one of free IL-2.
The study treatment is up to 20 MioIU L19IL2 per week in patients suffering from histopathologically-proven malignant melanoma with presence of injectable soft-tissue metastases either in clinical stage III or stage IV M1a without visceral metastases. The duration of treatment could be up to 20 weeks. After the end of study visit follow-up is performed every 6 weeks until 12 months from enrollment of each patient.
Tumor assessment will be performed within 2 weeks before start of treatment and at week 12 using immune-related response criteria and RECIST 1.1. To assure that patients do not develop visceral metastases under treatment, an additional tumor assessment will be performed already at week 6 after start of therapy. Assessments at week 24 and 36 will be performed according to RECIST vs. 1.1 criteria only.
Treatment emergent adverse events will be summarized by Common Toxicity Criteria (version 4.02, CTCAE) and worst grade for all treated patients. Laboratory values and change in vital signs will be summarized.
研究の種類
入学 (実際)
段階
- フェーズ2
連絡先と場所
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Histopathologically proven malignant melanoma.
- Presence of measurable and injectable soft tissue metastases either in clinical stage III or stage IV M1a.
- Males or females, age >/= 18 years.
- Either without, or after one line of prior systemic treatment for metastatic disease.
- ECOG performance status < 2.
- LDH < 2 x the upper limit of normal.
- Life expectancy of at least 12 weeks.
- Absolute neutrophil count > 1.5 x 10^9/L.
- Hemoglobin > 9.0 g/dL.
- Platelets > 100 x 10^9/L.
- Total bilirubin ≤ 30 µmol/L (or ≤ 2.0 mg/dl).
- ALT and AST ≤ 2.5 x the upper limit of normal (ULN) (5.0 x ULN for patients with hepatic involvement with tumor).
- Serum creatinine < 1.5 x ULN.
- All acute toxic effects (excluding alopecia) of any prior therapy must have resolved to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) (v4.02) Grade ≤ 1 unless otherwise specified above.
- Negative serum pregnancy test (for women of child-bearing potential only) at screening.
- If of childbearing potential, agreement to use adequate contraceptive methods (e.g., oral contraceptives, condoms, or other adequate barrier controls, intrauterine contraceptive devices, or sterilization) beginning at the screening visit and continuing until 3 months following last treatment with study drug.
- Able to provide written Informed Consent.
- Willingness and ability to comply with the scheduled visits, treatment plan, laboratory tests and other study procedures.
Exclusion Criteria:
- Primary ocular melanoma.
- Presence of visceral metastases at screening.
- Evidence of active brain metastases at screening.
- Previous or concurrent cancer that is distinct in primary site or histology from the cancer being evaluated in this study except cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors (TA, Tis & Ti) or any cancer curatively treated < 5 years prior to study entry.
- History of HIV infection or infectious hepatitis B or C.
- Presence of active infections (e.g. requiring antimicrobial therapy) or other severe concurrent disease, which, in the opinion of the investigator, would place the patient at undue risk or interfere with the study.
- History within the last year of acute or subacute coronary syndromes including myocardial infarction, unstable or severe stable angina pectoris.
- Inadequately controlled cardiac arrhythmias including atrial fibrillation.
- Heart insufficiency (> Grade II, New York Heart Association (NYHA) criteria).
- Uncontrolled hypertension.
- Ischemic peripheral vascular disease (Grade IIb-IV).
- Severe diabetic retinopathy.
- Active autoimmune disease.
- History of organ allograft or stem cell transplantation.
- Recovery from major trauma including surgery within 4 weeks prior to administration of study treatment.
- Known history of allergy to IL2, or other intravenously administered human proteins/peptides/antibodies.
- Breast feeding female.
- Anti-tumor therapy within 4 weeks of the administration of study treatment (except small surgery).
- Previous in vivo exposure to monoclonal antibodies for biological therapy in the 6 weeks before administration of study treatment.
- Planned administration of growth factors or immunomodulatory agents within 7 days before the administration of study treatment.
- Patients in need of systemic treatment for rapidly progressive systemic disease during study treatment and up to 2 weeks after injection of L19IL2.
- Patient requires, or is taking, corticosteroids or other immunosuppressant drugs on a long-term basis. Limited use of corticosteroids to treat or prevent acute hypersensitivity reactions is not considered an exclusion criterion.
- Any condition, that in the opinion of the investigator could hamper compliance with the study protocol.
研究計画
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:L19IL2
|
Patients will be treated with intratumoral injections of L19IL2 1-3 x weekly.
The maximum cumulative dose per week is 20 MioIU.
Treatment duration is up to 20 weeks.
|
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 |
時間枠 |
|---|---|
|
Rate of patients with complete response (CR) of L19IL2 treated Index/Non-Index lesions at week 12 .
時間枠:week 12
|
week 12
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
全生存期間 (OS)
時間枠:1年
|
1年
|
|
Safety of intratumoral administration of L19IL2
時間枠:1-29 days
|
1-29 days
|
|
Rate of patients with complete response (CR), partial response (PR) and stable disease (SD) of L19IL2 treated Index/Non-Index lesions at week 12.
時間枠:week 12
|
week 12
|
|
Duration of objective response and disease control of L19IL2 treated Index/Non-Index lesions
時間枠:week 6-46
|
week 6-46
|
|
Rate of patients with complete response (CR), partial response (PR) and stable disease (SD)of all metastases
時間枠:week 12
|
week 12
|
|
Objective response rate of all metastases
時間枠:week 24, week 36
|
week 24, week 36
|
|
Disease control rate of all metastases
時間枠:week 24, week 36
|
week 24, week 36
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- PH-L19IL2-03/09
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