A Study of PEP503 With Radiotherapy in Combination With Concurrent Chemotherapy for Patients With Head and Neck Cancer

Phase 2TerminatedNCT02901483

PharmaEngine12 enrolled

Overview

It's a prospective, open-label, single arm, nonrandomized study of PEP503 in head and neck squamous cell carcinoma (HNSCC) patients. * Escalation portion (Phase 1b):A 3 + 3 dose escalation study design will be adopted in this phase to identify the recommended intratumor injection volumes of PEP503. * Expansion portion (Phase 2): Following confirmation of the recommended volumes, 18 additional patients will be enrolled at the recommended volume level to evaluate for safety and efficacy.

Primary Objectives: * Phase 1b (dose escalation portion): To assess the safety profile and determine the Dose Limiting Toxicity (DLT) and to define the recommended volumes (doses) of PEP503. * Phase 2 (expansion portion): To evaluate the anti-tumor activity in terms of the rate of locoregional control at one year and to evaluate the safety profile. Secondary Objectives: * Phase 1b: To characterize the body kinetic profile of PEP503. * Phase 2: Objective tumor response, progression free survival rate at 1 year and pathological response (pR). The target population is composed by patients who have pathologically confirmed squamous cell carcinoma of oral cavity with disease clinically staged as T4b who are not candidates for surgical resection or T3-4 who decline surgery or medical inoperable, or oropharynx, hypopharynx, or larynx with disease clinical staged as T3-4, without metastasis disease. ECOG performance status 0 or 1 and adequate bone marrow, renal, and hepatic function. Dose limiting toxicity (DLT) - The DLTs are related to PEP503, injection procedure, or concurrent chemo radiation therapy and occur in the DLT evaluation period. The DLT evaluation period starts from the intratumor injection of PEP503 to 4 weeks after the completion of radiation treatment. There are 6 levels (Level 1, Level 2, Level 3, Level 4, Level 3a and Level 5) in this phase 1b study. PEP503 will be given at the fixed concentration of 53.3g/L. The starting volume of PEP503 to be injected is 5% (Level 1) of the tumor volume confirmed by MRI.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Conditions

Head and Neck Squamous Cell Carcinoma

Interventions

PEP503DRUG

PEP503 will be administered by intratumoral route as slow injection

CisplatinDRUG

The concurrent chemoradiotherapy. Weekly cisplatin 40 mg/m2 or tri-weekly 100 mg/m2, depending on which dose level patients are in, with a minimum of accumulated 200 mg/m2 during the 7\~8 weeks' radiation period.

RadiotherapyRADIATION

Patients will receive 70-72 Gy, 2-2.12 Gy/fraction over 7\~8 weeks.

Eligibility

Sex: ALLMin age: 20 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Histologically or cytologically confirmed squamous cell carcinoma (SCC) of oral cavity, oropharynx, hypopharynx, or larynx * Locally advanced or recurrent disease of: Oral Cavity:T4b, N any, who are not candidates for surgical resection; or T3-4, N any, who decline surgery or medical inoperable; OR Oropharynx, hypopharynx, or larynx: T3-4, N any * No evidence of distant metastatic disease, as determined by a negative PET scan or CT scan * ECOG Performance Status 0 or 1 * Adequate function of bone marrow, kidney and liver: * White Blood Cell (WBC) ≥ 3.0 x 109/l * Absolute neutrophil count (ANC) ≥ 1.5 x 109/l * Platelet count ≥ 100 x 109/l * Hemoglobin ≥ 9.0 g/dL * Creatinine within normal range, for dose level with tri-weekly cisplatin, estimated GFR ≥ 60 mL/min/1.73m2 or CrCl ≥ mL/min is also required * AST ≤ 2.5 x ULN, ALT ≤ 2.5 x ULN and Alkaline phosphatase (ALP) ≤ 2.5 x ULN * Bilirubin ≤ 1.5 x ULN * 20 years of age or older * All female patients of childbearing potential must have negative urine pregnancy test within 7 days prior to study treatment with PEP503. Fertile patients must agree to use effective contraception during the study Exclusion Criteria: * Tumor ulceration combined with vascular risks * Prior radiotherapy to any area within the planned radiotherapy field * Uncontrolled intercurrent illness * Concurrent treatment with any other anticancer therapy * Participation in any investigational drug study within 4 weeks * Prior or concurrent non-head and neck malignancies, excluding adequately treated basal or squamous cell cancer of the skin, and in situ cervical cancer, and any other cancer from which the subject has been cancer free for 5 years * Patients unable to comply with scheduled visits and other study procedures. * Preexisting neuropathy ≥ Grade 2 (CTCAE) * Pre-existing hearing impairment \> Grade 2 (CTCAE) for patients receiving cisplatin 100 mg/m2 * History of allergic reaction to platinum product

Locations (1)

Keelung Chang Gung Memorial Hospital (Lovers Lake Branch)

Keelung, Taiwan

Outcomes

Primary Outcomes

Phase 1: Determination of the Recommended doses and the Dose Limiting Toxicities (DLT)

To determine the Recommended volumes and the Dose Limiting Toxicities (DLT) of PEP503 administered as intratumor injection, activated by CCRT

Time frame: 24 months

Phase 2: The rate of locoregional control at one year

To evaluate the rate of locoregional control at one year after PEP503 intratumor injection

Time frame: 24 months

Phase1 and 2: Evaluation of Safety profile of PEP503

Safety of PEP503, as intratumor injection schedule, activated by CCRT will be assessed in terms of incidence and severity of clinical and laboratory Adverse Events by NCI-CTCAE version 4.0

Time frame: 24 months

Secondary Outcomes

Phase 1: The body kinetic profile of PEP503

To characterize the body kinetics on Date of injection(DINJ) of PEP503 administered by intratumor injection before CCRT

Time frame: 24 months

Phase 2: Evaluation of objective tumor response as per Response Evaluation Criteria in Solid Tumors (RECIST)

To evaluate the objective tumor rate by using RECIST v1.1 after intratumor injection schedule, activated by CCRT

Time frame: 24 months

Phase 2: Pathological response (pR)

If patients receive tumor and/or neck lymph node dissection after treatment, to assess according to the evidence of viable tumor cell

Time frame: 24 months

Phase 2: Evalution of progression free survival rate at 1 year

Data from ClinicalTrials.gov

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