Phase II trial of docetaxel/pembrolizumab in head and neck squamous cell carcinoma

JRCT ID: jRCTs011210068

Registered date:01/02/2022

Basic Information

• Recruitment status: Recruiting
• Health condition(s) or Problem(s) studied: head and neck squamous cell carcinoma
• Date of first enrollment: 06/07/2022
• Target sample size: 27
• Study type: Interventional
• Intervention(s): Patients with head and neck squamous cell carcinoma receive docetaxel and pembrolizumab every 3 weeks.

Outcome(s)

• Primary Outcome: overall response rate (ORR)
• Secondary Outcome: overall survival (OS), progression-free survival (PFS), duration of response (DoR), toxicity and tolerability

Key inclusion & exclusion criteria

• Age minimum: >= 20age old
• Age maximum: Not applicable
• Gender: Both

Include criteria

1)Have histologically or cytologically-confirmed R/M HNSCC that is considered incurable by local therapies.
Subjects should not have had prior systemic therapy administered in the recurrent or metastatic setting. Systemic therapy which was completed more than 6 months prior to signing consent if given as part of multimodal treatment for locally advanced disease is allowed.
The eligible primary tumor locations are oropharynx, oral cavty,hypopharynx, and larynx.
Subjects may not have a primary tumor site of nasopharynx (any histology).
2)Be willing and able to provide written informed consent for the trial.
3)Have results from testing of PD-L1 status.
4)Be >=20 years of age on day of signing informed consent.
5)Have measurable disease based on RECIST 1.1. Lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions.
6)Have a performance status of 0 or 1 on the ECOG Performance Scale.
7)Have adequate organ function.
8)Have results from testing of HPV status for oropharyngeal cancer.
9)Female subjects of childbearing potential should have a negative blood pregnancy test within 72 hours prior to receiving the first dose of study medication.
10)Female subjects of childbearing potential should be willing to use 2 methods of birth control or be surgically sterile or abstain from heterosexual activity for the course of the study through 180 days after the last dose of study medication.
11)Male subjects should agree to use an adequate method of contraception starting with the first dose of study therapy through 180 days after the last dose of study therapy.

Exclude criteria

1)Has disease that is suitable for local therapy administered with curative intent.
2)Has a life expectancy of less than 3 months and/or has rapidly progressing disease in the opinion of the treating investigator.
3)Has received prior systemic anti-cancer therapy including radiation therapy, other non-systemic therapy or investigational agents within 4 weeks prior to the first dose of trial treatment.
4)Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy, or used an investigational device, any of which occurred within 4 weeks of the first dose of treatment.
5)Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy (using prednisolone >= 10mg per day) or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment.
6)Has a diagnosed and/or treated additional malignancy within 2 years prior to randomization with the exception of curatively treated basal cell carcinoma of the skin, squamous cell carcinoma of the skin, curatively resected esophageal cancer, curatively resected in situ cervical cancer, and curatively resected in situ cancer.
7)Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
8)Active autoimmune disease that has required systemic treatment in past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs).
9) Has a history of (non-infectious) pneumonitis that required steroids or current pneumonitis. Pneumonitis include active radiation pneumonitis.
10)Has an active infection requiring systemic therapy.
11)Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-CTLA-4 agent.
12) Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies). Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA is detected).
13) Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
14) Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
15) Is pregnant or breastfeeding or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 180 days after the last dose of trial treatment.
16)Has had an allogeneic tissue/solid organ transplant.
17)Has received a live vaccine within 30 days of planned start of study therapy.

Related Information

• Primary Sponsor: Shimizu Yasushi
• Source(s) of Monetary Support: MSD Co., Ltd