Becotatug Vedotin Plus Pucotenlimab and Capecitabine Followed by Concurrent Chemoradiotherapy-Immunotherapy for Locally Advanced Squamous Cell Carcinoma of the Anal Canal
An Open-Label, Single-Arm, Phase Ⅱ Exploratory Clinical Study of Becotatug Vedotin Combined With Pucotenlimab and Capecitabine Followed by Concurrent Chemoradiotherapy Plus Immunotherapy for Locally Advanced Squamous Cell Carcinoma of the Anal Canal
調査の概要
状態
条件
詳細な説明
This is a single-arm, exploratory clinical study intended to enroll patients with EGFR-positive Locally Advanced Squamous Cell Carcinoma of the Anal Canal (T2-4N0-1M0). The study consists of two phases: a safety lead-in phase and an expansion phase. Six patients will be enrolled first with close monitoring for dose-limiting toxicities (DLTs). Further enrollment into the expansion phase will proceed only after safety is confirmed. The therapeutic regimen remains identical across both phases. The trial will be terminated if any DLT occurs during the safety lead-in phase. The observation period for the safety lead-in phase ends upon completion of 2 cycles of induction therapy.
After subjects provide written informed consent, eligible patients who meet the inclusion criteria following screening will receive induction therapy: Becotatug Bedotin (2.0 mg/kg intravenously on Day 1) combined with Pucotenlimab (200 mg intravenously on Day 1) and Capecitabine (1000 mg/m² orally twice daily). Treatment is administered every 3 weeks for a total of 2 cycles. All patients will undergo radiological assessment after completion of cycle 2 induction therapy. Patients without disease progression will subsequently enter the concurrent chemoradiotherapy-immunotherapy phase, receiving Capecitabine (825 mg/m² orally twice daily), Pucotenlimab (200 mg intravenously on Day 1), and mitomycin-C (10 mg/m² intravenously on Day 1 and Day 28), administered concurrently with definitive radiotherapy. In the maintenance phase, patients receive Pucotenlimab (200 mg) for a total duration of 1 year.
The primary endpoints of this study are the 40-week complete response (CR) rate and safety. Secondary endpoints include the objective response rate (ORR) and disease control rate (DCR) of induction therapy, event-free survival (EFS), overall survival (OS). Tumour response assessment will be performed according to RECIST version 1.1.
研究の種類
入学 (推定)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:Xin Wang
- 電話番号:+86 28 85423609
- メール:wangxin213@sina.com
研究連絡先のバックアップ
- 名前:Feng Wen
- 電話番号:+86 28 85422589
- メール:172571964@qq.com
研究場所
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-
Sichuan
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Chengdu、Sichuan、中国、610041
- West China Hospital
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コンタクト:
- Feng Wen
- 電話番号:+86 28 85422589
- メール:172571964@qq.com
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Aged between 18 and 75 years, male or female;
- Voluntarily signed the informed consent form and is willing to comply with protocol-specified requirements;
- Histologically confirmed locally advanced anal squamous cell carcinoma of cT2-4N0-1M0 stage;
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
- EGFR immunohistochemistry (IHC) score ≥1+ as assessed by pathological laboratory;
- At least one measurable target lesion according to RECIST version 1.1;
- Laboratory parameters meeting all of the following criteria:
(1) Bone marrow function: haemoglobin (Hb) ≥90 g/L; white blood cell count (WBC) ≥3.0×10⁹/L; absolute neutrophil count (ANC) ≥1.5×10⁹/L; platelet count ≥100×10⁹/L; (2)Renal function: serum creatinine (Cr) ≤1.5 × upper limit of normal (ULN), and endogenous creatinine clearance (Ccr) ≥55 mL/min; (3)Liver function: total bilirubin ≤1.5 × ULN; alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 × ULN; (4)Coagulation function: international normalized ratio of prothrombin time (PT-INR) ≤1.5 × ULN, and activated partial thromboplastin time (aPTT) within the normal reference range; 8. Left-ventricular ejection fraction (LVEF) ≥50%; 9. Female subjects of child-bearing potential agree to use contraception during the study and for 6 months after study completion; have a negative serum or urine pregnancy test within 7 days prior to enrolment, and are not breastfeeding. Male subjects agree to use contraception during the study and for 6 months after study completion; 10. No participation in other investigational-drug clinical trials within 4 weeks before enrolment; 11. The subject is capable of understanding and willing to adhere to protocol-required visits, treatment, laboratory tests and other study procedures.
Exclusion Criteria:
- Diagnosis of another malignancy within the past 5 years (excluding concurrent CIN2+ or cervical cancer; in-situ carcinomas and basal-cell carcinomas outside the pelvic region are permitted).
- Pre-existing peripheral neuropathy ≥ Grade 2 (per CTCAE Version 5.0).
- Patients planning to undergo or having previously received organ or bone-marrow transplantation.
- Any major surgery within 4 weeks prior to the first study treatment (diagnostic biopsy excluded).
- Any anti-tumour therapy administered within 4 weeks prior to the first study treatment, including radiotherapy, chemotherapy, targeted therapy, immunotherapy, biologic therapy, etc.
- Presence of uncontrolled clinical cardiac signs or diseases.
- Active infection or fever (excluding confirmed tumour-related fever).
- History or evidence of interstitial lung disease or active non-infectious pneumonitis.
- Patients with other medical conditions rendering them ineligible for enrolment, such as immunodeficiency, active pulmonary tuberculosis, hepatitis B (enrolment is allowed if treated HBV-DNA <500 IU/mL with normal liver function; HPV-positive subjects are eligible; subjects with immunodeficiency with undetectable viral load and normal CD4-T-cell count may be enrolled), positive hepatitis-C virus testing, uncorrectable electrolyte disturbances, uncontrolled pericardial effusion, pleural effusion, and ascites.
- Known hypersensitivity to any study drug specified in this protocol.
- Pregnant or breastfeeding women.
- Subjects deemed ineligible for enrolment at the investigator's discretion.
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:Induction therapy → concurrent chemo-immunoradiotherapy → maintenance therapy
Patients first receive two cycles of induction therapy with Becotatug Bedotin plus Pucotenlimab and Capecitabine, followed by concurrent chemoradiotherapy-immunotherapy comprising mitomycin-C, capecitabine and pucotenlimab administered in parallel with definitive radiotherapy, and conclude with 1-year maintenance therapy using single-agent pucotenlimab.
|
Patients receive becotatug vedotin (2.0 mg/kg intravenously on Day 1) plus pucotenlimab (200 mg intravenously on Day 1) and capecitabine (1000 mg/m² orally twice daily) every 3 weeks for 2 consecutive cycles.
Following induction therapy, patients without disease progression receive capecitabine (825 mg/m² orally twice daily) combined with pucotenlimab (200 mg intravenously on Day 1) and mitomycin-C (10 mg/m² intravenously on Day 1 and Day 28), administered in parallel with definitive pelvic radiotherapy.
Radiotherapy doses were prescribed following NCCN, ESTRO and EORTC guideline recommendations.
After completion of concurrent chemoradiotherapy-immunotherapy, patients receive pucotenlimab (200 mg intravenously) every 3 weeks for up to 1 year as maintenance treatment.
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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 |
|---|---|---|
|
The Complete response (CR) rate at 40 weeks
時間枠:40 weeks after treatment
|
The CR rate at 40 weeks is defined as the number of patients who have no residual or metabolically active local tumour identified by digital rectal examination, colonoscopy with pathological assessment, and MRI, plus no distant metastasis confirmed by thoracic-abdominal CT at 40 weeks, divided by the total number of patients evaluable for CR status at 40 weeks.
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40 weeks after treatment
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Safety
時間枠:Up to 18 months
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Incidence and severity of adverse events, with severity determined according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) Version (v) 5.0, vital signs, and clinical laboratory test results in the Safety Analysis Set
|
Up to 18 months
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Event-free survival (EFS)
時間枠:From the first study-drug administration up to 3 years after the end of treatment.
|
The EFS is defined as the time from the first study-drug administration to the earliest occurrence of disease progression, recurrence, initiation of new therapy, or death.
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From the first study-drug administration up to 3 years after the end of treatment.
|
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Overall Survival(OS)
時間枠:From the first study-drug administration up to 3 years after the end of treatment.
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The OS is defined as the time from the first study-drug administration to death from any cause.
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From the first study-drug administration up to 3 years after the end of treatment.
|
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Objective Response Rate (ORR)
時間枠:At the end of Cycle 2 (each cycle is 21 days)
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The ORR is defined as the proportion of subjects achieving a complete response or partial response after completion of 2 cycles of induction therapy and prior to the initiation of concurrent chemoradiotherapy-immunotherapy.
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At the end of Cycle 2 (each cycle is 21 days)
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Disease Control Rate (DCR)
時間枠:At the end of Cycle 2 (each cycle is 21 days)
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The DCR is defined as the proportion of subjects achieving a complete response, partial response, or stable disease upon completion of induction therapy.
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At the end of Cycle 2 (each cycle is 21 days)
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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 (推定)
一次修了 (推定)
研究の完了 (推定)
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 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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
追加の関連 MeSH 用語
その他の研究ID番号
- BRIDGE
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
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