Reactivating NK Cells in Treating Refractory Head and Neck Cancer

Head and Neck Squamous Cell Carcinoma Clinical Trial

— NKEXPHNC  

Official title:

Phase I/II Study of Expanded, Activated Autologous Natural Killer Cell Infusions With Cetuximab for Patients With EGFR-Positive Nasopharyngeal Carcinoma or Head and Neck Squamous Cell Carcinoma

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02507154
• Other study ID #: NK0906
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: July 2015
• Est. completion date: August 2019

Study information

• Verified date: August 2018
• Source: National University Hospital, Singapore
• Contact: Chwee Ming Lim, MBBS
• Phone: 6772 2631
• Email: chwee_ming_lim[@]nuhs.edu.sg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study aims to determine the safety and efficacy of expanded activated autologous NK cells administered after cetuximab in patients with EGFR-positive nasopharyngeal carcinoma or head and neck squamous cell carcinoma.

Description:

Natural killer (NK) cells are cytotoxic lymphocytes of the innate immune system that are responsible for direct and indirect cytolytic killing of virally-transformed and/or cancer cells. Harnessing NK cells in cancer immunotherapy therefore, provides a direct cytotoxic effect on cancer cells which further stimulates further downstream adaptive anti-tumor immune responses against the cancer. In order to effect a more targeted killing of these tumor cells, using a monoclonal antibody (mAb) to direct these NK cells to the target site is feasible, provided a specific tumor antigen can be identified. In nasopharyngeal Carcinoma (NPC) and head and neck squamous cell carcinoma (HNSCC) where epidermal growth factor receptor (EGFR) is ubiquitously expressed, combining NK cell therapy with cetuximab (a chimeric mouse/human anti-EGFR monoclonal antibody) to direct these NK cells against these EGFR tumor targets is possible. In this study, we seek to enhance the antitumor activity of cetuximab to treat EGFR-positive head and neck cancers by combing infusion of activated expanded autologous NK cells with cetuximab. Patients selected for this trial are those with refractory NPC and HNSCC where no feasible therapeutic options are available. This is a lead-in phase I followed by a phase II study. The phase I study will enroll 9 patients and will test the feasibility and safety of this combination strategy and determine the tolerated dose of NK cell infusion (1x1^06/kg or 1x10^7/kg NK cells) in adult EGFR positive NPC and HNSCC patients. For the first 3 patients, each new patient will only be enrolled at least 3 weeks after treatment of the preceding patient to allow sufficient time to monitor toxicities. Initial phase of treatment consists of 7 weeks of cetuximab monotherapy. At week 8, clinical evaluation will be done to determine patients who are suitable to continue this study with NK cell therapy, based on the severity of toxicities encountered. Eligible patients will undergo apheresis (Day -10) to harvest NK cells. The collected NK cells will be expanded and activated in the laboratory. During cycle 1, cetuximab will be given on day 1 with subcutaneous IL-2 (three times per week for 2 weeks); followed by expanded NK cells on day 2. The purpose of IL-2 is to sustain activity of these NK cells in-vivo. Cetuximab will be administered weekly for additional 2 weeks following the NK cell infusion during cycle 1. For cycle 2 and 3, cetuximab monotherapy will be administered every 21 days. Clinical evaluation will be performed upon completion of cycle 3. Patients with stable disease or with partial response will be allowed to continue with a second NK infusion dose as per cycle 1, followed by additional 2 more cycles of cetuximab monotherapy (every 21 days).

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 31
• Est. completion date: August 2019
• Est. primary completion date: August 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria

1. Age >21

2. Histologically confirmed diagnosis of EGFR-positive nasopharyngeal carcinoma or EGFR positive HNSCC (based on >80% immunohistochemistry of biopsy of recurrent tumor Ventana (Roche) clone 3C6

3. Recurrent cancer that is not surgically salvageable

4. Metastatic disease (after one course of palliative chemotherapy has been completed)

5. Presence of measurable tumor by RECIST 1.1 criteria

6. At least two weeks since receipt of any biological therapy, chemotherapy, and/or radiation

7. Adequate organ function

8. Haemoglobin = 9g/dL ANC = 1500/µL Platelet count = 100,000/µL Creatinine clearance =60ml/minute Total bilirubin = 1.5 x upper limit normal (ULN) AST = 5 x upper limit normal ALT = 2 x upper limit normal INR and PTT <1.5 x upper limit normal (ULN)

9. ECOG performance status of 0-2

10. Life expectancy of at least 60 days

11. Localized radiotherapy for palliative pain management is permissible

12. Written consent to participate on study

13. Physiological dose of steroid replacement is permissible

Exclusion Criteria

1. Treatment within the last 30 days with any investigational drug

2. Hypersensitivity to cetuximab or any excipients of the NK cell product

3. Concurrent administration of any other tumor therapy, including cytotoxic chemotherapy, hormonal therapy, and immunotherapy

4. Major surgery within 28 days of study drug administration

5. Radiotherapy to the target lesions during study or within 3 weeks prior to study treatment.

6. Autologous bone marrow transplant

7. Active infection that in the opinion of the investigator would compromise the patient's ability to tolerate therapy

8. Lactating or pregnant

9. Unwilling to use adequate barrier contraception measures during study period.

10. Second primary malignancy that is clinically detectable at the time of consideration for study enrolment

11. Receipt of immunosuppressives or steroids (=1mg/kg) during time period of 3 days prior to expanded NK cell infusion to 30 days after infusion (i.e. day -3 to day +30).

12. Symptomatic brain metastases

13. Electrocardiogram with clinically significant findings.

14. Serious concomitant disorders that would compromise the safety of the patient or compromise the patient's ability to complete the study, at the discretion of the investigator; serious cardiac illness or medical conditions including but not limited to:

• Patients with dyspnea at rest.

• History of documented congestive heart failure

• High risk uncontrolled arrhythmias

• Angina pectoris requiring a medicinal product

• Clinically significant valvular disease

• Poorly controlled hypertension

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Squamous Cell
• Head and Neck Neoplasms
• Head and Neck Squamous Cell Carcinoma
• Nasopharyngeal Cancer
• Nasopharyngeal Neoplasms

Intervention

Drug:
• Cetuximab + NK cells

Locations

Country	Name	City	State
Singapore	National University Hospital	Singapore

Sponsors (1)

Lead Sponsor	Collaborator
National University Hospital, Singapore

Country where clinical trial is conducted

Singapore, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety as measured by clinical examination including hematology, renal and liver function tests, adverse events and any significant biochemical abnormalities or toxicities	During cycle 1 (21 days) and for at least 21 days following a second NK cell infusion if administered, patients will be reviewed twice a week. Clinical examination including hematology, renal and liver function tests will be performed. Any adverse events (using NCI CTC grading) and concomitant medications notation will be recorded. Any significant biochemical abnormalities or toxicities will be monitored till resolution of these findings or 30 days after patient withdraws from this study, whichever occurs later.; During cycles with cetuximab monotherapy, patients with be reviewed once every cycle (21 days).	12- 18 weeks
Primary	Objective tumor response	In this study, treatment response will be determined using RECIST 1.1 criteria, after two and four cycles of therapy. The endpoints of the study are objective tumor response including overall response rate (ORR), partial response (PR), duration of complete response (DCR) and duration of partial response (DPR). Complete response is defined by complete resolution of target lesion while partial response is defined by reduction of the target lesion by at least 20% from its baseline. Duration of tumor response will be censored at the date of the last follow-up visit for tumor responders who are still alive and who have not progressed.	Up to 24 months