A Phase II Study to Evaluate the Efficacy and Safety of Salvage Preoperative PD-1 Inhibitor Combined with Chemotherapy Neoadjuvant Therapy in Recurrent and Metastatic LPSCC/HPSCC

NCT ID: NCT06793761

Last Updated: 2025-01-27

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 260 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-02-01
• Study Completion Date: 2028-12-31

Brief Summary

A prospective, multicenter, randomized controlled phase II study; Patients who met the inclusion criteria were divided into groups according to whether they had received radical radiotherapy or postoperative radiotherapy in the past. Group A was the group that had not received radiotherapy in the past, and Group B was the group that had received radiotherapy. Group A was randomly given 3 cycles of pembrolizumab + chemotherapy (see P22 for detailed chemotherapy regimen) in the experimental group at a 1:1 ratio, followed by surgery. After surgery, the patients were stratified according to whether there were high-risk factors. The high-risk group received concurrent chemoradiotherapy + pembrolizumab maintenance therapy (up to 15 cycles), and the low-risk group received radiotherapy + pembrolizumab maintenance therapy (up to 15 cycles). The control group underwent direct surgery and received concurrent chemoradiotherapy or radiotherapy after surgery. The total dose of radiotherapy was (high-risk group: 60-66Gy, 2Gy/time; low-risk group: 44-50 Gy, 2Gy/time) adjuvant therapy, and the radiotherapy time was within 2 months after surgery. Group B was randomly given 3 cycles of pembrolizumab + chemotherapy in the experimental group at a ratio of 1:1, followed by surgery and maintenance therapy with pembrolizumab after surgery (up to 15 cycles). The control group was given surgery directly, and observation/re-radiotherapy or chemoradiotherapy was chosen by the doctor after surgery. The total dose of radiotherapy was (56-60Gy, 2Gy/time), and the radiotherapy time was within 2 months after surgery. The enrolled patients must be closely monitored for adverse reactions to chemotherapy, and the time, grade, treatment measures, and outcomes must be recorded. All patients received an examination after the end of neoadjuvant therapy, an examination after surgery, and an examination at the 9th week after the first radiotherapy, and then reviewed every 3 months for 1 year; after 1 year, they were reviewed once every 6 months for 3 years; the recurrence and survival data of the patients were recorded.

Conditions

Head and Neck Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm 1-Pembrolizumab group (no previous radiotherapy)

Patients who had not received RT previously received 3 cycles of pembrolizumab + cisplatin + nab-paclitaxel, followed by SOC treatment

Group Type: EXPERIMENTAL

Pembrolizumab

Intervention Type: DRUG

Pembrolizumab 200mg, IV, 3 cycles

Cisplatin

Intervention Type: DRUG

cisplatin 75mg/m2, IV, 3 cycles

Nab-paclitaxel

Intervention Type: DRUG

Nab-paclitaxel 260mg, IV, 3 cycles

Arm 2 - Control group (no previous radiotherapy)

Patients who had not received RT before received SOC treatment only

Group Type: NO_INTERVENTION

No interventions assigned to this group

Arm 3 - Pembrolizumab group (previously received radiotherapy)

Patients who had received RT before received 3 cycles of pembrolizumab + cisplatin + nab-paclitaxel, followed by SOC treatment

Group Type: EXPERIMENTAL

Pembrolizumab

Intervention Type: DRUG

Pembrolizumab 200mg, IV, 3 cycles

Cisplatin

Intervention Type: DRUG

cisplatin 75mg/m2, IV, 3 cycles

Nab-paclitaxel

Intervention Type: DRUG

Nab-paclitaxel 260mg, IV, 3 cycles

Arm 4 - Control group (previously received radiotherapy)

Patients who had received RT before received SOC treatment only

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Pembrolizumab

Pembrolizumab 200mg, IV, 3 cycles

Intervention Type: DRUG

Cisplatin

cisplatin 75mg/m2, IV, 3 cycles

Intervention Type: DRUG

Nab-paclitaxel

Nab-paclitaxel 260mg, IV, 3 cycles

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients with histologically and/or cytologically diagnosed squamous cell carcinoma of the larynx and hypopharynx
• Patients with recurrence of primary lesions or second primary lesions after definitive treatment
• At least 6 months from the end of the last platinum-containing treatment
• Cisplatin-tolerant
• Age ≥ 18 years
• ECOG 0-1
• Measurable disease as defined by RECIST v1.1
• Normal organ function
• Female and male participants of reproductive potential must agree to use appropriate contraception throughout the study and for 180 days after the last study treatment
• Male participants must not donate sperm throughout the study and for 180 days after the last study treatment

Exclusion Criteria

• T stage after relapse (rT) is T4b
• Presence of distant metastasis
• Received live vaccines within 30 days before enrollment
• Diagnosed with immunodeficiency or received systemic steroids or any other form of immunosuppressive therapy within 7 days before enrollment
• Have radiologically detectable (even if asymptomatic and/or previously treated) central nervous system metastases and/or carcinomatous meningitis;
• Have undergone surgery before starting the study or have not recovered adequately from toxicity or complications caused by the intervention;
• Have had allogeneic tissue/solid organ transplantation;
• Have severe hypersensitivity reactions (≥ grade 3) to PD-1 inhibitors and chemotherapy or any of its adjuvants, radiotherapy;
• Have active autoimmune disease and require systemic treatment in the past 2 years;
• Have a history of (non-infectious) pneumonia requiring steroid treatment;
• Have a history of human immunodeficiency virus (HIV) infection;
• Any medical history, treatment, or laboratory abnormality that could confound the study results, interfere with the participant's participation throughout the study, or be detrimental to the participant's best interests;
• A known history of psychiatric or substance abuse disorder

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Beijing Tongren Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

Xiaohong Chen

Role: CONTACT

trchxh@163.com

08658269106

Other Identifiers

TRENT-002

Identifier Type: -

Identifier Source: org_study_id