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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00460265
Other study ID # 20050251
Secondary ID
Status Completed
Phase Phase 3
First received April 12, 2007
Last updated February 3, 2014
Start date May 2007
Est. completion date May 2012

Study information

Verified date February 2014
Source Amgen
Contact n/a
Is FDA regulated No
Health authority Argentina: ANMAT (Administracion Nacional de Medicamentos Alimentos y Tecnologia Medica)Australia: Department of Health and Ageing Therapeutic Goods AdministrationAustralia: Human Research Ethics CommitteeAustria: Bundesamt für Sicherheit im GesundheitswesenBelgium: Federal Public Service (FPS) Health, Food Chain Safety and EnvironmentBrazil: ANVISA (Agência Nacional de Vigilância Sanitária)Bulgaria: Bulgarian Drug AgencyCanada: Health CanadaFrance: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)Germany: Paul_Ehrlich-Institut Bundesamt fur Sera und ImpfstoffeHong Kong: Department of HealthHungary: National Institute of PharmacyIndia: Central Drugs Standard Control OrganizationIreland: Irish Medicines BoardSpain: Agencia Española de Medicamentos y Productos SanitariosItaly: Ministry of HealthMexico: Ministry of HealthSweden: Medical Products AgencySwitzerland: Swissmedic (Swiss Agency for Therapeutic Products)Ukraine: Pharmacological Centre at the Ministry of Health of the Ukraine (Pharma Centre)United Kingdom: Medicines and Healthcare Products Regulatory AgencyUnited States: Food and Drug AdministrationUnited States: Institutional Review BoardMexico: SSA (Secretaria de Salud Publica)Peru: INS (Instituto Nacional de Salud)Poland: Drug InstitutPoland: Office for Registration of Medicinal Products, Medical Devices and Biocidal ProductsPortugal: Instituto Nacional da Farmácia e do Medicamento (INFARMED)Romania: Romanian National Drug AgencyRussia: Federal Service for Surveillance in the field of Healthcare and Social Development (a body of the Ministry of Health)Singapore: Health Science AuthoritySouth Korea: Korea Food & Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the treatment effect of Panitumumab in combination with chemotherapy versus chemotherapy alone as first line therapy for metastatic and/or recurrent squamous cell carcinoma of the head and neck.


Recruitment information / eligibility

Status Completed
Enrollment 658
Est. completion date May 2012
Est. primary completion date May 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Man or woman at least 18 years old.

- Histologically or cytologically confirmed metastatic and/or recurrent squamous cell carcinoma (or its variants) of the head and neck.

- Diagnosis of metastatic disease and/or recurrent disease following locoregional therapy and determined to be incurable by surgery or radiotherapy.

- Subjects who have received radiation as primary therapy are eligible if locoregional recurrence is in the field of radiation and has occurred =6 months after the completion of radiation therapy. Subjects whose locoregional recurrence is solely outside the field of radiation are eligible if the recurrence has occurred = 3 months after the completion of radiation therapy.

- Measurable and non-measurable disease.

- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

Exclusion Criteria:

- History or known presence of Central Nervous System (CNS) metastases.

- History of another primary cancer, except: curatively treated in situ cervical cancer, or curatively resected non-melanoma skin cancer, or other primary solid tumor curatively treated with no known active disease present and no treatment administered for = 2 years before randomization.

- Nasopharyngeal carcinoma.

- Prior systemic treatment for metastatic and/or recurrent SCCHN

- Prior cisplatin containing induction chemotherapy followed by cisplatin containing chemoradiotherapy

- Prior anti-EGFr (Epidermal growth factor receptor) antibody therapy or treatment with small molecule EGFr inhibitors

- Clinically significant cardiovascular disease (including myocardial infarction, unstable angina, symptomatic congestive heart failure, serious uncontrolled cardiac arrhythmia) less than or equal to 1 year prior to randomization. History of interstitial lung disease (eg, pneumonitis or pulmonary fibrosis) or evidence of interstitial lung disease on baseline chest computerized tomography (CT) scan.

- Symptomatic peripheral neuropathy grade = 2 based on the CTCAE v3.0

- Grade = 3 hearing loss based on the Common Terminology Criteria for Adverse Events (CTCAE) v3.0 Auditory/Ear (Hearing [without monitoring program])

Study Design

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


Related Conditions & MeSH terms


Intervention

Drug:
ARM 2
Subjects will receive Cisplatin plus 5FU
ARM 1
Subjects will receive Panitumumab plus cisplatin and 5FU

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Amgen

References & Publications (2)

Bach B, et al.SPECTRUM biomarkers HPV.Journal-004521;

Vermorken JB, Stöhlmacher-Williams J, Davidenko I, Licitra L, Winquist E, Villanueva C, Foa P, Rottey S, Skladowski K, Tahara M, Pai VR, Faivre S, Blajman CR, Forastiere AA, Stein BN, Oliner KS, Pan Z, Bach BA; SPECTRUM investigators. Cisplatin and fluorouracil with or without panitumumab in patients with recurrent or metastatic squamous-cell carcinoma of the head and neck (SPECTRUM): an open-label phase 3 randomised trial. Lancet Oncol. 2013 Jul;14(8):697-710. doi: 10.1016/S1470-2045(13)70181-5. Epub 2013 Jun 6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Survival Time from randomization to death Upto 56 months No
Secondary Overall Response Rate An objective tumor response of complete or partial response per modified Response Evaluation Criteria in Solid Tumors (RECIST) v1.0 that was confirmed no less than 28 days after the criteria for response were first met. Complete response = disappearance of all target lesions and partial response = =30% reduction in lesion size. Every 6 weeks until disease progression, up to 56 months No
Secondary Duration of Response Time from the first confirmed objective response of complete or partial response (that is subsequently confirmed at least 28 days later) to disease progression using a modified version of the RECIST v1.0 (see protocol Appendix H). Every 6 weeks until disease progression, up to 56 months No
Secondary Time to Progression Time from randomization date to date of disease progression using a modified version of the RECIST 1.0 (see protocol Appendix H) Every 6 weeks until disease progression, up to 56 months No
Secondary Time to Response Time from randomization date to the first confirmed objective response of complete or partial response (that is subsequently confirmed at least 28 days later) using a modified version of the RECIST v1.0. Every 6 weeks until disease progression, upto 56 months No
Secondary Progression Free Survival Time from randomization date to date of disease progression using a modified version of the RECIST v1.0 or death. Every 6 weeks until disease progression or deaths, upto 56 months No