A Phase II, Open-Label, Multicenter Trial of Cabazitaxel in Patients With Recurrent or Metastatic Head and Neck Cancer After Failure Of Cisplatin, Cetuximab and Taxanes

NCT ID: NCT01620242

Last Updated: 2021-03-02

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 31 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-04-30
• Study Completion Date: 2014-05-27

Brief Summary

This is a multi-center phase II study assessing whether cabazitaxel could be efficient for treatment of recurrent or metastatic head and neck cancer after failure of cisplatin, cetuximab and taxanes.

Detailed Description

Patients will be treated with intravenous cabazitaxel 25 mg/m2 every 3 weeks (D1=D22) for 6 cycles.

In absence of progression disease or unacceptable toxicity, the treatment could be continued until a maximum of 10 cycles.

Disease response will be assessed every 6 weeks (i.e. every 2 cycles) clinically and by CT-scan.

An interim analysis will be carried out after the inclusion of the first 10 eligible and assessable patients.

Conditions

Recurrent Head and Neck Cancer; Metastatic Head and Neck Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cabazitaxel

All patients are treated with Cabazitaxel.

Group Type: EXPERIMENTAL

Cabazitaxel

Intervention Type: DRUG

25 mg/m2 every 3 weeks by IV administration

Interventions

Cabazitaxel

25 mg/m2 every 3 weeks by IV administration

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Metastatic or recurrent Head and neck cancer

2. Progression after cisplatin, cetuximab and taxanes (drugs could have been administered alone or in combination) given for recurrent/metastatic disease

3. Age ≥ 18

4. ECOG performance status ≤ 2

5. At least one measurable lesion on CT-scan (as per RECIST criteria V1.1).

6. Life expectancy ≥ 3 months

7. Adequate hematologic function (neutrophils ≥ 1.5 x 109/L, platelets ≥ 100 x 109/L; Hb ≥ 9.0 g/dL), renal function (clearance creatinine using the CKD-EPI formula (Chronic Kidney Disease Epidemiology group) ≥ 60 mL/min) and hepatic function (serum bilirubin ≤ 1 ULN; AST and ALT ≤ 2.5 x ULN).

8. Potentially reproductive patients must agree to use an effective contraceptive method while on treatment, beginning 2 weeks before the first dose of investigational product and for 6 months after the final dose of investigational product.

9. Women of childbearing potential must have a negative serum beta-HCG pregnancy test within 14 days prior of enrolment and/or urine pregnancy test within 48 hours before the first administration of the study treatment.

10. Patients must be affiliated to a Social Security System.

11. Patient who have received the information sheet and signed the informed consent form.

12. Patients must be willing and able to comply with scheduled visits, treatment plan, laboratory tests and other study procedures

Exclusion Criteria

1. Active concurrent malignancy

2. Progression in the 3 months after the completion of treatment for localized disease

3. Patients with other concurrent severe and/or uncontrolled medical disease which could compromise participation in the study, such as :

• infection,
• cardiac disease such as uncontrolled hypertension, congestive cardiac failure, ventricular arrhythmias, active ischemic heart disease, myocardial infarction within one year, LVEF > grade 2,
• current active hepatic or biliary disease (with exception of subjects with Gilbert's syndrome, asymptomatic gallstones, liver metastasis or stable chronic liver disease per investigator assessment),
• renal disease,
• active GI tract ulceration, malabsorption syndrome, disease significantly affecting gastrointestinal function, or resection of the stomach or small bowel. Subjects with active, uncontrolled ulcerative colitis are also excluded,
• severely impaired lung function (spirometry and DLCO 70% or less of normal and O2 saturation of 88% or less at rest on room air).

4. Patients must have recovered of previous toxicity of chemotherapy and must not have toxicity grade > 1 ; grade ≥ 2 for neuropathy and grade ≥ 2 for cutaneous rash after cetuximab (in the CTCAE v4.0)

5. Hypersensitivity to cabazitaxel, to other taxanes, or to any excipients of the formulation including polysorbate 80

6. Pregnant women, women who are likely to become pregnant or are breast-feeding.

7. Patients with significantly altered mental status prohibiting the understanding of the study or with psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial.

8. Patients who received any other investigational drugs within the 14 days prior to the start of cabazitaxel.

9. Patients receiving radiation within 4 weeks prior to the first dose of study drug.

10. Patients already included in another therapeutic trial involving an experimental drug

11. Individual deprived of liberty or placed under the authority of a tutor.

12. Other primary tumors within the previous 3 years

13. Concomitant prohibited treatment. Concurrent or planned treatment with strong inhibitors or strong inducers of cytochrome P450 3A4/5. A one week wash-out period is necessary for patients who are already on these treatments.

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

Sponsors

UNICANCER

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Centre Oscar Lambret

Lille, , France

Centre Léon Berard

Lyon, , France

Centre Antoine Lacassagne

Nice, , France

Institut Curie

Paris, , France

Institut Gustave Roussy

Villejuif, , France

Countries

France

Other Identifiers

2011-004712-32

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

UC-0130/1106

Identifier Type: -

Identifier Source: org_study_id