A Phase II Clinical Study to Evaluate the Efficacy and Safety of HLX07 Combination Therapy or Monotherapy in Patients With Advanced ESCC

NCT05221658 | Unknown Phase 2

• 1 other identifier: HLX07-ESCC201
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 17

Brief Summary

This study is conducted in patients with Locally advanced, unresectable, or metastatic esophageal squamous cell carcinoma (ESCC) or esophageal adenosquamous carcinoma. This study includes three arms: A, B1, and B2. Arm A will receive HLX07 combination therapy with HLX10 and Chemotherapy (Cisplatin+5-FU) as first line treatment. Arm B (Patients with EGFR expression H score ≥ 200) and Arm C (Patients with EGFR expression H score \< 200) will receive HLX07 monotherapy as third-line or above treatment. All of eligible patients will receive study drug treatment until loss of clinical benefit, unacceptable toxicity, death, withdrawal of informed consent (whichever occurs first, HLX10 treatment up to 2 years).

Conditions

ESCC or Esophageal Adenosquamous Carcinoma

Outcome Measures

Primary Outcomes (2)

• ORR

  Objective response rate by IRRC/INV assessment per RECIST

  up to 2 years

• PFS

  Progression-free survival by IRRC/INV assessment per RECIST

  from the first dose until firstly confirmed and recorded disease progression or death (whichever occurs earlier),assessed up to 2 years

Secondary Outcomes (2)

• OS

  from the date of first dose unitl the date of death from any cause，assessed up to 2 years

• DOR

  from the date when CR or PR (whichever recorded earlier) is firstly achieved until the date when disease progression or death is firstly recorded (whichever occurs earlier),assessed up to 2 years

Study Arms (3)

Arm A

EXPERIMENTAL

As first-line therapy

Drug: HLX07+HLX10+ Cisplatin+5-FU

Arm B1

EXPERIMENTAL

EGFR H score ≥ 200, as third-line or above therapy

Drug: HLX07

Arm B2

EXPERIMENTAL

EGFR H score \<200, as third-line or above therapy

Drug: HLX07

Interventions

HLX07+HLX10+ Cisplatin+5-FU DRUG

HLX07 1000mg + HLX10 200mg + Cisplatin 50 mg/m2 + 5-FU 2400mg/m2

Arm A

HLX07 DRUG

HLX07 1000mg iv Q2w

Arm B1; Arm B2

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Subjects who meet all of the following criteria are allowed to be enrolled into this study:
• Volunteer to participate in this clinical study; completely understand and know this study as well as sign the informed consent form (ICF); be willing to follow and be able to complete all study procedures;
• Age ≥ 18 years and ≤ 75 years when ICF is signed;
• Histopathologically or cytologically confirmed diagnosis of locally advanced, unresectable or metastatic esophageal squamous cell carcinoma (ESCC) or esophageal adenosquamous carcinoma.
• Subjects in Arm B1 and Arm B2 must provide eligible tumor tissue for EGFR expression level determination： Arm B1: Subjects with EGFR expression H score ≥ 200 confirmed by central laboratory immunohistochemistry (IHC) in tumor tissue.
• Arm B2: Subjects with EGFR expression H score \< 200 confirmed by central laboratory IHC.
• prior therapy: Arm A: Never received systemic anti-tumor drug therapy before. Exception: for patients who have received neoadjuvant/adjuvant treatment, the time from the last treatment to recurrence or progression can be screened for more than 6 months; Arms B1 and B2: Failed or intolerant to prior systemic anti-tumor therapy (at least 2 lines).
• According to the curative effect evaluation criteria in solid tumors (RECIST) v1.1, assessed by the investigator with at least one measurable lesions (such as esophageal cavity structure not as measurable lesions), measurable lesions should be not received radiotherapy, etc (lesions located in the usual radiation area, if confirm progress, can also be selected as the target lesion);
• Within 7 days before the first use of the study drug, ECOG: 0 \~ 1;
• Expected survival 12 weeks;
• The functions of the vital organs meet the following requirements (no blood transfusion, cytokine growth factor, or platelet raising drugs are allowed within 14 days before the first use of the study drugs); Absolute neutrophil count (ANC) ≥1.5×109/L platelet≥ 100×109/L; Hemoglobin≥ 90g/L; Serum albumin≥ 30g/L; Total bilirubin≤ 1.5 ULN, ALT, AST and/or ALP≤ 2.5 ULN;ALT and/or AST≤ 5 ULN in the presence of liver metastasis;If there is liver metastasis or bone metastasis ALP≤ 5 ULN; Serum creatinine ≤1.5 ULN or creatinine clearance \> 50 mL/min (Cockcroft-Gault formula); APTT, INR and PT ≤1.5 ULN;
• For fertile female subjects, the serum pregnancy test must be negative within 7 days before the first dose.
• With fertile women subjects, and the partner for childbearing age women of male subjects, needs during the therapy, and after the last use HLX10 / placebo at least 6 months and the last time to use at least 6 months after chemotherapy using an approved by the medical contraception (such as intrauterine device, the pill or condoms)

You may not qualify if:

• Subjects who meet any of the following criteria are not allowed to be enrolled in this study:
• A history of gastrointestinal perforation and/or fistula within 6 months prior to the first administration;
• Obvious invasion of tumor into adjacent organs (aorta or trachea) of esophageal lesions leads to high risk of bleeding or fistula;3. Subjects after endotracheal stent implantation;
• Uncontrollable pleural effusion, pericardial effusion or ascites requiring repeated drainage;
• Previous allergies to monoclonal antibody, HLX10, 5-fu, cisplatin and other platinum drugs;
• Have received any of the following treatments:
• A.Prior systemic anti-EGFR monoclonal antibody therapy Previous treatment with anti-pd-1 or anti-pd-L1 antibodies （Arm A）; B. Have received any research drugs within 4 weeks before the first use of the study drugs; C. Be enrolled in another clinical study at the same time, unless it is an observational (non-interventional) clinical study or a follow-up interventional clinical study; D. Receive the final anticancer treatment within 4 weeks before the first use of the study drug;Palliative radiotherapy for bone metastases was allowed and was completed 2 weeks before the first dose.Radiotherapy covering more than 30% of the bone marrow area is not allowed within 28 days before the first dose.
• E. Subjects who require systemic treatment with corticosteroids (\> 10 mg/ day prednisone therapeutic dose) or other immunosuppressive agents within 14 days prior to the first use of the study drug;In the absence of active autoimmune disease, inhalation or topical use of steroids is permitted, and the therapeutic dose of prednisone 10mg/ day is allowed.
• F. Those who have received the anti-tumor vaccine or the live vaccine within 4 weeks before the first dose of the study drug; G. Have undergone major surgery within 28 days prior to the first use of the study drug. Major surgery in this study is defined as requiring at least 3 weeks of postoperative recovery time before being able to receive the surgery treated in this study.Tumor puncture or lymph node biopsy were allowed.

Sponsors & Collaborators

• Shanghai Henlius Biotech: lead

Study Sites (17)

Cancer Hospital Chinese Academic of Medical Sciences

Beijing, Beijing Municipality, China

RECRUITING

Fujian Cancer Hospital

Fuzhou, Fujian, China

NOT YET RECRUITING

The First Affiliated Hospital of Xiamen University

Xiamen, Fujian, China

NOT YET RECRUITING

Cancer Hospital Chinese Academic of Medical Sciences, Shenzhen Center

Shenzhen, Guangdong, China

NOT YET RECRUITING

Anyang Cancer Hospital

Anyang, Hebei, China

NOT YET RECRUITING

Xingtai People's Hospital

Xingtai, Hebei, China

NOT YET RECRUITING

Henan Cancer Hospital & Affiliated Cancer Hospital of Zhengzhou University

Zhenzhou, Henan, China

NOT YET RECRUITING

Hunan Cancer Hospitla

Changsha, Hunan, China

NOT YET RECRUITING

Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, Nanjing Medical University Affiliated Cancer Hospital

Nanjing, Jiangsu, China

NOT YET RECRUITING

Jiangsu People Hospital & The First Affiliated with Nanjing Medical University

Nanjing, Jiangsu, China

NOT YET RECRUITING

Xuzhou Center Hospital

Xuzhou, Jiangsu, China

NOT YET RECRUITING

Shandong Cancer Hospital

Jinan, Shandong, China

NOT YET RECRUITING

Affiliated Hospital of Jining Medical University

Jining, Shandong, China

NOT YET RECRUITING

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, China

NOT YET RECRUITING

Shanxi Cancer Hospital

Taiyuan, Shanxi, China

NOT YET RECRUITING

Sichuan Cancer Hospital

Chengdu, Sichuan, China

NOT YET RECRUITING

Yunnan Cancer Hospital & The Third Affiliated Hospital of Kunming Medical University & Yunnan Cancer Center

Kunming, Yunnan, China

NOT YET RECRUITING

Related Publications (1)

• Liu Y, Wang Y, Zhu Y, Wu T, Liu Z, Zhou J, Yuan Y, Yang M, Liu B, Tan Z, Zhuang W, Chen J, Li N, Wang Y, Hu X, Wang L, Yu H, Wang Q, Zhu J, Huang J. HLX07 alone or combined with serplulimab, cisplatin and 5-fluorouracil for advanced esophageal squamous cell carcinoma: A phase 2 study. Cancer Commun (Lond). 2024 Dec;44(12):1431-1443. doi: 10.1002/cac2.12621. Epub 2024 Oct 24.

  PMID: 39446605 DERIVED

MeSH Terms

Interventions

HLX07

Central Study Contacts

Jing Huang

CONTACT

(010)87788102; huangjingwg@163.com

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 22, 2022
• First Posted: February 3, 2022
• Study Start: August 25, 2022
• Primary Completion: June 30, 2024
• Study Completion: August 30, 2025
• Last Updated: August 29, 2022

Record last verified: 2022-08

Locations

CN (17)