Evaluate Efficacy of the Association Nimotuzumab(HR3) /Cisplatin-Vinorelbine on Patients With Cervical Carcinom

Cervical Cancer Clinical Trial

— CIMAHOPE  

Official title:

Multicenter Randomised Double-blind Study to Compare HR3 or Placebo in Combination With Cisplatin-navelbine for Patients With Cervical Carcinoma, Followed in Case of Progression by a Second Line.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03413579
• Other study ID #: CIMA-I3-05D143-01
• Status: Completed
• Phase: Phase 3
• Start date: November 2015
• Est. completion date: February 2021

Study information

• Verified date: March 2020
• Source: El Kendi Pharmaceuticals Manufacturing Company
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The objective of the present study is to estimate the overall survival of patients with cervical cancer after the administration of monoclonal antibody (mAb) Nimotuzumab (hR3) in combination with chemotherapy of first intention. Patients will be randomized in two parallel treatment groups. The first group will receive a dose of 200 mg of monoclonal antibody anti-hR3 (weekly during 18 weeks), combined with a chemotherapy (6 cycles, every 21 days of Cisplatin 70mg/m2, Vinorelbine 60 mg/m2 (Per Os) at D1 and D8 and then 80mg / m2. The second group will receive a placebo in combination with the same chemotherapy regimen as the first group. At the end of the first intention chemotherapy treatment, a dose of maintenance of Nimotuzumab will be administered at the dose of 200mg every 14 days until progression. A second chemotherapy in the second intention is proposed, this one is based on Carboplatin ( CBP) in an AUC (area under curve) of 6, and Paclitaxel (Txl) in 175 mg / m2 / BSA (body surface area ) in drip of 3 hours, every 3 weeks, concomitant with the administration of hR3, every 14 days, until a limit of toxicity or an ECOG (Eastern Cooperative Oncology Group) status superior to 3, appears.

Description:

The objective of the present study is to assess the overall survival of patients after administration of Nimotuzumab hR3 monoclonal antibodies (combined with a chemotherapy) in the treatment of patients with cervix epithelial tumors as first-line treatment. The patients included will be divided into two treatment groups. The first group receive a 200 mg dose of hR3 monoclonal antibody (weekly for 18 weeks), and chemotherapy (6 cycles, every 21 days: Cisplatin (CDDP) 70 mg / m2 on day 1, Vinorelbine 60 mg / m2 on day 1 and day 8) and then 80mg / m2. The second group receive a placebo in addition to the listed chemotherapy. After the first line , a 200mg dose of hR3 monoclonal antibodies will be given every 14 days until progress. A second -line chemotherapy is proposed, this is based on Carboplatin (CBP) at AUC of 6, and Paclitaxel (Txl) 175 mg / m2 / SC as 3 hour infusion, every 3 weeks, concomitant with the administration of hR3, every 14 days, until a toxicity limit or an ECOG status greater than 3 appears. The survival overall will be considered as the main variable of the response and survival without progression from the antitumor response, the toxicity assessment and the quality of life will be the secondary variables. In addition, the effects may arise during treatment will be identified, and tumor biopsy markers such as, EGF-R and HPV will be determined and those of p53, Ki67 and Bcl-2 by immunohistochemistry (IHC). It is expected to achieve a difference in survival between the treatment groups of 6.5 vs 10.5 months (0.278 vs 0.62) in favor of the group with mAb hR3.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 37
• Est. completion date: February 2021
• Est. primary completion date: March 2020
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Patients aged between 18 to 75, including both limits.
• Patients who give their written consent to participate to the study.
• Chemonaive patients with local cervical cancer and / or persistent or recurrent metastatic disease with measurable disease (RECIST criteria) by a physical examination (scanner or MRI). A confirmation by biopsy is necessary in case there is a single lesion less than 2 cm.
• Patients who had pelvic CT + radiotherapy may also be included in the study (concomitant chemotherapy as a radiotherapy stabilizer).
• Patients having a histopathological report: epidermoid carcinoma, adenocarcinoma, adenosquamous carcinoma and / or clear cells carcinoma.
• Patients with an ECOG score between 0-2
• Patients with a life expectancy greater than six months.
• Patients with Left Ventricular Ejection Fraction (LVEF) =50%, through Echocardiography.
• Patients with normal function of organs and bone marrow, defined by the following

parameters:

• Haemoglobin = 9 g / dL
• White Blood cell = 4000 /mm3
• Absolute neutrophil count= 1500 /mm3
• Platelet count= 100000 /mm3
• Total bilirubin up to 1.5 the upper limit of normal (ULN)
• Albumin = 2 g/dL (3,5 - 5,0 g /dl)
• Serum Glutamopyruvate Transférase (SGPT) and SErum Glutamooxaloacetate Transferase (SGTO) < or = 2.5 ULN
• Serum creatinine within the normal limits and the calculation of glomerular filtration according to Cockcroft formula = 60ml and according to MDRD formula for patients whose age is 70 years = 60ml . Glomerular filtration will be performed only on clinical discretion for patients suspected to have a kidney problem. (The normal laboratory values will be appropriate to the techniques and equipment used in the place where they are done).
• The determination or expression of EGF-R (epidermal growth factor receptor), p53, Ki67 and Bcl-2 by immuno-histochemistry in the primary tumor before treatment integrated in a paraffin block. The results are not an inclusion criterion, but will be evaluated as an indicator of prognostic response in the final assessment.

Exclusion Criteria:

• Pregnant or breastfeeding patients
• Patients with small cells and / or neuroendocrine cervical cancer.
• Patients receiving another onco-specific drug, for other clinical trial,
• Patients with a history of allergy attributed to chemical or biological compounds similar to the monoclonal antibody being evaluated or to chemotherapeutic agents.
• Patients having uncontrolled intercurrent diseases, including active infections, symptomatic congestive heart failure , unstable angina, cardiac arrhythmia, decompensated diabetes, uncontrolled hypertension and psychiatric disorders.
• Patients having a second tumor . Excepting for those receiving appropriate therapy for skin cancer (basal or squamous)
• Previous or concomitant malignancy with exception for non-melanoma skin carcinomas
• Patients having special conditions or circumstances that could significantly limit the complete follow up of the study

Related Conditions & MeSH terms

• Cervical Cancer
• Uterine Cervical Neoplasms

Intervention

Biological:
• Nimotuzumab ( h-R3)
Humanized monoclonal antibody

Other:
• Placebo

Locations

Country	Name	City	State
Algeria	Centre Pierre et Marie Curie (CPMC)	Algiers
Algeria	CAC Annaba	Annaba
Algeria	CAC Batna	Batna
Algeria	CHU Frantz Fanon	Blida
Algeria	CHU Sidi Belloua	Tizi Ouzou

Sponsors (1)

Lead Sponsor	Collaborator
El Kendi Pharmaceuticals Manufacturing Company

Country where clinical trial is conducted

Algeria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall survival in patients who received hR3 mAb treatment combined with Chemotherapy		Calculated from patient randomisation to death (36 months)
Secondary	Antitumor Response		up to 24months (every 3 months)
Secondary	Duration of response		from date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 60 months
Secondary	Time to progression		Time from randomization until objective tumor progression assessed up to 60 months
Secondary	Progression-free survival		Time from randomization until disease progression or death, assessed up to 60 months