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Study of Post-Op Adjuvant Concurrent Chemo-RT With or Without Nimotuzumab for Head & Neck Cancer

Primary Purpose

Carcinoma, Squamous Cell of Head and Neck

Status
Active
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Nimotuzumab
Placebo
Sponsored by
National Cancer Centre, Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carcinoma, Squamous Cell of Head and Neck focused on measuring Phase III Adjuvant Concurrent Chemo-RT +/- nimotuzumab

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age should be greater than or equal to the minimum age of consent in the applicable country
  • Histologically proven head and neck squamous cell cancer (excluding nasopharynx, salivary glands, paranasal sinuses and unknown primaries) on biopsy of the primary lesion or the neck mass.
  • Resectable stage III/IV according to the AJCC/UICC staging system with no evidence of distant metastasis.
  • Complete macroscopic resection.
  • Patients should have at least one of the following pathological features for inclusion: pT3 or pT4 and any nodal stage (N), except T3N0 of the larynx, with negative resection margins, or a tumor stage of 1 or 2 with a nodal stage of 2 or 3 and no distant metastasis (M0); patients with stage T1 or T2 and N0 or N1 who had unfavorable pathological findings (extranodal spread, positive resection margins, perineural involvement, or vascular tumor embolism) are also eligible, as are those with oral-cavity or oropharyngeal tumors with involved lymph nodes at level IV or V.
  • Performance status must be ECOG 0 or 1. Patients should be able to tolerate chemotherapy and radiotherapy.
  • Adequate bone marrow, renal and hepatic function:

    1. WBC>3000/mm3, platelets>100000/mm3
    2. Serum creatinine<upper limit of normal range as per institution and calculated creatinine clearance (according to the Cockcroft and Gault method) >50 ml/min.
    3. SAP, SGOT<2 x upper limit of normal range, bilirubin <1.5 x upper limit of normal range.
  • Written informed consent.

Exclusion Criteria:

  • Histology other than SCC or its subtype.
  • Patients with disease subsite deemed suitable for organ preservation approach, namely stage III/IV laryngeal or hypopharyngeal carcinoma with not more than low-volume T4 disease; low-volume T4 disease is defined as disease not eroding into cartilage or extending not more than 1 cm into the base of tongue.
  • Clinical or radiological evidence of distant metastasis.
  • Uncontrolled comorbidities such as diabetes mellitis, hypertension, cardiac disease.
  • Uncontrolled infection.
  • Uncontrolled hypercalcemia.
  • Prior history of cancer less than 5 years ago or a synchronous primary outside the head and neck area.
  • Prior treatment, head and neck radiotherapy, chemotherapy or surgery (excluding biopsy) or anti-EGFR therapy such as cetuximab/EGFR oral tyrosine kinase inhibitor.
  • Patients for whom compliance with follow-up is unlikely.

Sites / Locations

  • Flinders Medical Centre
  • Peter MacCallum Cancer Centre
  • National Institute of Oncology and Radiobiology
  • Alexandria University School of Medicine
  • National Cancer Institute, Cairo University
  • Apollo Hospital Bangalore
  • Narayana Hrudayalaya Hospital (Mazumdar Shaw Cancer Institute)
  • Amrita Institute of Medical Sciences
  • Tata Memorial Centre
  • Christian Medical College
  • Regional Cancer Center Trivandrum, India
  • Cipto Mangunkusumo General Hospital Indonesia
  • National Cancer Center Korea
  • INHA University Hospital
  • Samsung Medical Center
  • Severance Hospital, Yonsei University Health System
  • Pantai Medical Centre, Kuala Lumpur
  • Mahkota Medical Center
  • University of Santo Tomas Hospital
  • St. Luke's Medical Center
  • King Fahad Medical City
  • National Cancer Centre
  • The Oncology Centre
  • GVI Oncology
  • China Medical University Hospital
  • Taipei Med Univ Hosp [TMUH]
  • Taipei Veteran General Hospital
  • National Cancer Institute Bangkok (+Chulabhorn for RT)
  • Siriraj Hospital
  • Chiang Mai Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Nimotuzumab

Placebo

Arm Description

Comprising Adjuvant Cisplatin, Concurrent RT and Nimotuzumab

Comprising Adjuvant Cisplatin, Concurrent RT and Placebo

Outcomes

Primary Outcome Measures

To compare the disease-free survival between patients randomized to adjuvant nimotuzumab/cisplatin/RT with the control arm

Secondary Outcome Measures

To compare the overall survival between the two arms
To assess the Toxicity Profile between the 2 arms

Full Information

First Posted
August 11, 2009
Last Updated
April 4, 2022
Sponsor
National Cancer Centre, Singapore
Collaborators
National Medical Research Council (NMRC), Singapore, Innogene Kalbiotech Pte. Ltd
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1. Study Identification

Unique Protocol Identification Number
NCT00957086
Brief Title
Study of Post-Op Adjuvant Concurrent Chemo-RT With or Without Nimotuzumab for Head & Neck Cancer
Official Title
Phase III, Double-Blind, Placebo-Controlled Study of Post-Operative Adjuvant Concurrent Chemo-Radiotherapy With or Without Nimotuzumab for Stage III/IV Head & Neck Squamous Cell Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
August 13, 2009 (Actual)
Primary Completion Date
January 1, 2024 (Anticipated)
Study Completion Date
January 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Cancer Centre, Singapore
Collaborators
National Medical Research Council (NMRC), Singapore, Innogene Kalbiotech Pte. Ltd

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the study is to improve the loco-regional control rate and overall survival of locally advanced head and neck squamous carcinoma (HNSCC). The investigators hypothesize that the addition of nimotuzumab (a recombinant humanized murine immune antibody that blocks both epidermal growth factor (EGF) and transforming growth factor (TGF)) to the current gold standard of concurrent chemoradiotherapy (CCRT) (7)(8), an adjuvant setting in patients after resection of their locally advanced HNSCC will confer therapeutic advantage.
Detailed Description
The aim of the study is to improve the loco-regional control rate and overall survival of locally advanced head and neck squamous carcinoma (HNSCC). We hypothesize that the addition of nimotuzumab (a recombinant humanized murine immune antibody that blocks both epidermal growth factor (EGF) and transforming growth factor (TGF)) to the current gold standard of concurrent chemoradiotherapy (CCRT) (7)(8), an adjuvant setting in patients after resection of their locally advanced HNSCC will confer therapeutic advantage. We have designed a phase III randomized study that includes a placebo arm. We assume a 10% increase in 2 year disease free survival (from 60% to 70%). To achieve statistical significance at 90% power, we calculate the need for 355 patients per arm, assuming also a 10% dropout rate. We aim to accomplish this study with the involvement of a multidisciplinary team of surgical, radiation and medical oncologists actively involved in the management of HNSCC coming from multiple institutions and spanning at least 12 different countries. For quality assurance we will have the involvement of Singapore Clinical Research Institute who will lead the data coordination and ensure fidelity of data collected and statistical analysis; the European Society of Therapeutic Radiation Oncology (EQUAL-ESTRO) for radiation dose and fields and an international independent panel of medical oncologist, radiation oncologist and biostatistician for the Data Monitoring Committee (DMC). This committee will monitor significant events and advise on continuation or termination of trial. Concurrent with the randomized trial, we will be collecting bio specimens including blood, tumour and saliva, pre-treatment and on completion of surgical resections. We hypothesize that there are important biomarkers including clusters of genes, cancer stem cells that will predict prognosis and treatment response. The analyses performed will be very powerful because of the large sample size, the specimens are collected prospectively and because the statistical analyses will be multivariate, incorporating not only treatment but biological and staging data.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma, Squamous Cell of Head and Neck
Keywords
Phase III Adjuvant Concurrent Chemo-RT +/- nimotuzumab

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
710 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Nimotuzumab
Arm Type
Active Comparator
Arm Description
Comprising Adjuvant Cisplatin, Concurrent RT and Nimotuzumab
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Comprising Adjuvant Cisplatin, Concurrent RT and Placebo
Intervention Type
Drug
Intervention Name(s)
Nimotuzumab
Intervention Description
Administered by intravenous infusion at 200 mg absolute per dose, diluted in 250 ml of sodium chloride over 30 minutes. 8 weekly doses of study drug will be given, beginning on first week of radiotherapy.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Administered by intravenous infusion at 200 mg absolute per dose, diluted in 250 ml of sodium chloride over 30 minutes. 8 weekly doses of study drug will be given, beginning on first week of radiotherapy.
Primary Outcome Measure Information:
Title
To compare the disease-free survival between patients randomized to adjuvant nimotuzumab/cisplatin/RT with the control arm
Time Frame
5 years
Secondary Outcome Measure Information:
Title
To compare the overall survival between the two arms
Time Frame
5 years
Title
To assess the Toxicity Profile between the 2 arms
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age should be greater than or equal to the minimum age of consent in the applicable country Histologically proven head and neck squamous cell cancer (excluding nasopharynx, salivary glands, paranasal sinuses and unknown primaries) on biopsy of the primary lesion or the neck mass. Resectable stage III/IV according to the AJCC/UICC staging system with no evidence of distant metastasis. Complete macroscopic resection. Patients should have at least one of the following pathological features for inclusion: pT3 or pT4 and any nodal stage (N), except T3N0 of the larynx, with negative resection margins, or a tumor stage of 1 or 2 with a nodal stage of 2 or 3 and no distant metastasis (M0); patients with stage T1 or T2 and N0 or N1 who had unfavorable pathological findings (extranodal spread, positive resection margins, perineural involvement, or vascular tumor embolism) are also eligible, as are those with oral-cavity or oropharyngeal tumors with involved lymph nodes at level IV or V. Performance status must be ECOG 0 or 1. Patients should be able to tolerate chemotherapy and radiotherapy. Adequate bone marrow, renal and hepatic function: WBC>3000/mm3, platelets>100000/mm3 Serum creatinine<upper limit of normal range as per institution and calculated creatinine clearance (according to the Cockcroft and Gault method) >50 ml/min. SAP, SGOT<2 x upper limit of normal range, bilirubin <1.5 x upper limit of normal range. Written informed consent. Exclusion Criteria: Histology other than SCC or its subtype. Patients with disease subsite deemed suitable for organ preservation approach, namely stage III/IV laryngeal or hypopharyngeal carcinoma with not more than low-volume T4 disease; low-volume T4 disease is defined as disease not eroding into cartilage or extending not more than 1 cm into the base of tongue. Clinical or radiological evidence of distant metastasis. Uncontrolled comorbidities such as diabetes mellitis, hypertension, cardiac disease. Uncontrolled infection. Uncontrolled hypercalcemia. Prior history of cancer less than 5 years ago or a synchronous primary outside the head and neck area. Prior treatment, head and neck radiotherapy, chemotherapy or surgery (excluding biopsy) or anti-EGFR therapy such as cetuximab/EGFR oral tyrosine kinase inhibitor. Patients for whom compliance with follow-up is unlikely.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
K C Soo, Prof
Organizational Affiliation
National Cancer Centre
Official's Role
Study Chair
Facility Information:
Facility Name
Flinders Medical Centre
City
Bedford Park
Country
Australia
Facility Name
Peter MacCallum Cancer Centre
City
Melbourne
ZIP/Postal Code
VIC 3002
Country
Australia
Facility Name
National Institute of Oncology and Radiobiology
City
Vedado
Country
Cuba
Facility Name
Alexandria University School of Medicine
City
Alexandria
Country
Egypt
Facility Name
National Cancer Institute, Cairo University
City
Cairo
Country
Egypt
Facility Name
Apollo Hospital Bangalore
City
Bangalore
Country
India
Facility Name
Narayana Hrudayalaya Hospital (Mazumdar Shaw Cancer Institute)
City
Bangalore
Country
India
Facility Name
Amrita Institute of Medical Sciences
City
Kerala
Country
India
Facility Name
Tata Memorial Centre
City
Mumbai
Country
India
Facility Name
Christian Medical College
City
Tamil Nadu
Country
India
Facility Name
Regional Cancer Center Trivandrum, India
City
Trivandrum
Country
India
Facility Name
Cipto Mangunkusumo General Hospital Indonesia
City
Jakarta
Country
Indonesia
Facility Name
National Cancer Center Korea
City
Gyeonggi-do
Country
Korea, Republic of
Facility Name
INHA University Hospital
City
Incheon
Country
Korea, Republic of
Facility Name
Samsung Medical Center
City
Seoul
Country
Korea, Republic of
Facility Name
Severance Hospital, Yonsei University Health System
City
Seoul
Country
Korea, Republic of
Facility Name
Pantai Medical Centre, Kuala Lumpur
City
Kuala Lumpur
Country
Malaysia
Facility Name
Mahkota Medical Center
City
Melaka
Country
Malaysia
Facility Name
University of Santo Tomas Hospital
City
Manila
Country
Philippines
Facility Name
St. Luke's Medical Center
City
Quezon City
Country
Philippines
Facility Name
King Fahad Medical City
City
Riyadh
Country
Saudi Arabia
Facility Name
National Cancer Centre
City
Singapore
Country
Singapore
Facility Name
The Oncology Centre
City
Durban
Country
South Africa
Facility Name
GVI Oncology
City
Panorama
Country
South Africa
Facility Name
China Medical University Hospital
City
Taichung
Country
Taiwan
Facility Name
Taipei Med Univ Hosp [TMUH]
City
Taipei
Country
Taiwan
Facility Name
Taipei Veteran General Hospital
City
Taipei
Country
Taiwan
Facility Name
National Cancer Institute Bangkok (+Chulabhorn for RT)
City
Bangkok
Country
Thailand
Facility Name
Siriraj Hospital
City
Bangkok
Country
Thailand
Facility Name
Chiang Mai Hospital
City
Chiang Mai
Country
Thailand

12. IPD Sharing Statement

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Study of Post-Op Adjuvant Concurrent Chemo-RT With or Without Nimotuzumab for Head & Neck Cancer

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