Nimotuzumab Plus Docetaxel in Chemotherapy-Refractory/Resistant Patients With Advanced Non-Small-Cell Lung Cancer

Advanced Non-Small Cell Lung Cancer Clinical Trial

Official title:

Phase II Study of Nimotuzumab Plus Docetaxel in Chemotherapy-refractory/Resistant Patients With Advanced Non-small-cell Lung Cancer

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00983047
• Other study ID #: BT-IST-NSCLC-010
• Status: Terminated
• Phase: Phase 2
• First received: September 21, 2009
• Last updated: August 25, 2015
• Start date: August 2009
• Est. completion date: August 2015

Study information

• Verified date: August 2015
• Source: Biotech Pharmaceutical Co., Ltd.
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Food and Drug AdministrationChina: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

Nimotuzumab is a humanized monoclonal anti-body targeting the epidermal growth factor receptor (EGFR). Clinical trials are ongoing globally to evaluate nimotuzumab in different indications. Nimotuzumab has demonstrated a unique clinical profile, where anti-tumor activity was observed in absence of severe skin, renal, gastrointestinal mucosa toxicities commonly associated with EGFR-targeting antibodies. Nimotuzumab has been granted approval for use in squamous cell carcinoma of head and neck (SCCHN), glioma and nasopharyngeal cancer in many countries. The investigators compared docetaxel plus nimotuzumab with docetaxel alone in chemotherapy-refractory/resistant patients with advanced EGFR-positive non-small-cell lung cancer to assess the efficacy and safety.

Description:

Nimotuzumab and Docetaxel will be administered to the patient until disease progression or unacceptable toxicity had occurred.Docetaxel was administered every 3 weeks 75mg/m2; Nimotuzumab treatment at 200mg per week,at least 12 weeks.The patients'hematology and biochemistry examination will be monitored weekly, a physical exam and assessment of the tumor will be performed and every 6 weeks. The patients will be followed up every 3 months to evaluate the survival.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 30
• Est. completion date: August 2015
• Est. primary completion date: August 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Histological/cytological confirmed Non-small cell lung cancer

2. EGFR expression is positive (Immunohistochemistry)

3. Locally advanced or advanced NSCLC patients(Stage IIIb \ IV)

4. Patients must have had progressive disease after only one prior chemotherapy regimen.This regimen must have been platinum-based.(For the patients who received new adjuvant chemotherapy or adjuvant chemotherapy, only disease free survival within 9 months will be eligible to enrollment).

5. The last dose of chemotherapy must be finished at least 3 weeks before the study, the acute toxicity of chemotherapy must be recovery.

6. The patients previously received radiotherapy could be recruited. (bone marrow influenced by radiotherapy should be less than 25% of the total quantity of general bone marrow ,and the patients didn't receive the whole pelvis radiation, last radiotherapy must be finished at least 4 weeks before the enrollment. )

7. Patients with at least one tumor lesion that can accurately be measured by magnetic resonance imaging, or computed tomography in at least one dimension with longest diameter to be recorded as = 20 mm using conventional techniques or = 10 mm with spiral CT.

8. ECOG performance status 0-2.

9. Life expectancy = 12 weeks.

10. Adequate organic function must be according with the following:

• Barrow: Absolute neutrophil count = 1.5×109/L, platelet count = 100×109/L, Haemoglobin = 90g/L;

• Liver function: BIL = 1.5 x ULN, ALP, AST and ALT= 3x ULN or = 5 ULN (Liver metastasis);

• Renal function: Ccr = 45ml/min;

11. No history of clinically significant or uncontrolled cardiac disease, normal electrocardiogram(ECG).

12. Use of an effective contraceptive method for patients of both genders during study and after the end of 3 months, female subjects must be non breast feeding period and serum or urine pregnancy test should be negative.

13. Signed informed consent and submit to the organization of research

Exclusion Criteria:

1. Brain metastasis and with symptom

2. Previously treatment regimen including:Docetaxel, anti EGFR monoclonal antibody,anti-angiogenesis targeted medicine,small molecule tyrosine kinase inhibitor(TKIs)

3. Receiving other anti-cancer medicine treatment during the study

4. Uncontrolled pleural effusion?seroperitoneum?pericardial effusion

5. Serious illness or other malignancies diagnosed within the past five years.

6. Patients with any serious active infection

7. The second primary malignant tumor

8. Serious accompanying disease would influenced the study (such as cardiac disease,Diabetes mellitus etc)

9. Contraindication of hormone therapy

10. Previous definable peripheral neuropathy and with symptom

11. Do not sign informed consent form

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Advanced Non-Small Cell Lung Cancer
• Carcinoma, Non-Small-Cell Lung
• Lung Neoplasms

Intervention

Drug:
• Nimotuzumab and Docetaxel
The chemotherapy treatment:Docetaxel was administered every 3 weeks 75 mg/m2, efficacy will be evaluated after two cycles,the chemotherapy will be administered continually 2 cycles if the response is CR\PR\SD. No more than 4 cycles chemotherapy was given. Nimotuzumab treatment: Dose of 200 mg intravenous infusion per week was continued after the end of chemotherapy until disease progression or unacceptable toxicity.

Locations

Country	Name	City	State
China	Peking University School of Oncology, Beijing Institute for Cancer Research, Beijing Cancer Hospital	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Biotech Pharmaceutical Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Median Survival Time		12 months	No
Secondary	Disease control rate		12 months	No
Secondary	Time to progression		12 months	No
Secondary	Safety of the Nimotuzumab and docetaxel (NCI CTC3.0)		12 months	Yes
Secondary	Quality of life before and after the treatment (QLQ-C30)		12 months	No
Secondary	Analysis EGFR expression, EGFR mutation and amplification, K-ras mutation in the tumor tissues		12 months	No