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Dose Escalation Using Hypoxia-adjusted Radiotherapy (DE-HyART)

Primary Purpose

Head and Neck Squamous Cell Carcinoma

Status
Recruiting
Phase
Phase 2
Locations
India
Study Type
Interventional
Intervention
DE-HyART
Standard Arm
Cisplatin injection
Standard fractionation (Radiation Oncology preference)
Sponsored by
Rajiv Gandhi Cancer Institute & Research Center, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Head and Neck Squamous Cell Carcinoma

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age: 18 - 70 years Willingness to sign informed consent (written/video documentation) Performance status: ECOG 0 - 2 Histology proved - squamous cell carcinoma Any grade, gender Tumour sites: Oral Cavity, Oropharynx, Hypopharynx and Larynx Sufficient bone marrow reserve within the last 14 days. Hb: > 10g/dl (corrected) TLC: > 4,000 per cumm Platelet: >1.5Lakh per cumm Liver functions and kidney functions within normal limits Nutritional and dental assessment before inclusion into the study Exclusion Criteria: HPV (p16) positive tumours Prior surgery and/or radiation therapy given for any HNC T1/T2 Glottis Metastatic disease or disease not amenable for definitive locoregional treatment. Medical co-morbidity hampering the administration of radiation and/or chemotherapy (cisplatin) Pregnancy or lactation

Sites / Locations

  • Rajiv Gandhi Cancer Institute and Research CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

Arm 3 - DE-HyART

Arm 2 - Hypoxic Comparator Arm

Arm 1 - Non-hypoxic arm

Arm Description

The radiation dose will be similar to 'arm 2'. In addition, the HSV identified on baseline FMISO scans will be contoured, and an isotropic margin of 5 mm will be given. This volume will be boosted in phase II to a total dose of 80 Gy. (Addition of 30 Gy in 3 Gy daily fraction added in phase II as a simultaneous integrated boost - SIB).

The prescribed radiotherapy dose will be 70 Gy in 2 Gy per fraction daily. The elective volume will be treated with 50 Gy in 2 Gy per fraction daily till the first 5 weeks. The entire treatment will be delivered in a phased mannered using sequential planning.

The patients will be treated with a standard of care where the treatment will not be controlled, and these patients will act as external control representing clinical practice. However, these patients will be discussed in the head and neck multispeciality clinic and follow the institutional approach. They will be subjected to treatment similar to 'arm 2' but are allowed protocol deviation as per treating radiation oncology discretion.

Outcomes

Primary Outcome Measures

Locoregional Control (LRC)
The duration of LRC was defined from the date of randomisation to the first histopathologically proven relapse of locoregional disease. If there is no proven recurrence, the LRC duration will be cut-off at the analysis point.

Secondary Outcome Measures

Overall Survival (OS)
The duration of OS was defined from the date of surgery to death from any cause. Therefore, if there is no death (for any reason), the OS duration will be cut-off at the analysis.

Full Information

First Posted
September 18, 2023
Last Updated
October 20, 2023
Sponsor
Rajiv Gandhi Cancer Institute & Research Center, India
Collaborators
Varian, a Siemens Healthineers Company
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1. Study Identification

Unique Protocol Identification Number
NCT06087614
Brief Title
Dose Escalation Using Hypoxia-adjusted Radiotherapy
Acronym
DE-HyART
Official Title
A Phase II Randomised Controlled Study Assessing the Role of Dose Escalation Using [18F] FMISO PET CT in Head and Neck Cancer: The DE-HyART (Dose Escalation Using Hypoxia-adjusted Radiotherapy) Protocol
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 2023 (Anticipated)
Primary Completion Date
April 2028 (Anticipated)
Study Completion Date
April 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rajiv Gandhi Cancer Institute & Research Center, India
Collaborators
Varian, a Siemens Healthineers Company

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
DE-HyART is a phase II clinical trial aimed at understanding the effects of escalating radiation doses to hypoxic sub-volumes inherent to squamous cell head and neck cancer. The study is aimed at assessing locoregional control, feasibility, and acceptable toxicity with such a strategy.
Detailed Description
DE-HyART is a randomized, non-blinded study that assesses the effects of combining IMRT (using SIB-Sequential planning) with dose-escalation to hypoxic sub-volume delineated using [18-F] FMISO. The treatment protocol will also include concurrent chemotherapy with cisplatin at standard uniform dosing. Patients with HNSCC whose cancer is determined to originate from the oral cavity, oropharynx, larynx, and hypopharynx will be selected. The included patients will be subjected to [18F] FMISO scan, labeled as baseline FMISO. Depending upon the result of the baseline FMISO, the patient will be either hypoxic or anoxic. Patients exhibiting no hypoxia in their tumor will be labeled as Arm 1 and act as an external cohort. Patients with hypoxia will be randomized (1:1) into two arms - Arms 2 and 3. Both arms will be subjected to chemoradiation by IMRT and concurrent chemotherapy with cisplatin at 40mg/m2. In Arm 3, the trial arm will receive an additional 10 Gy @ 2 Gy per fraction in phase II (total 80 Gy) to the HSV + 5mm isotropic margin. One twenty-four patients will recruited in a 1:1 fashion between Arm 3 and Arm 2. The primary endpoint will be locoregional control and its possible increase in control.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Squamous Cell Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
124 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm 3 - DE-HyART
Arm Type
Experimental
Arm Description
The radiation dose will be similar to 'arm 2'. In addition, the HSV identified on baseline FMISO scans will be contoured, and an isotropic margin of 5 mm will be given. This volume will be boosted in phase II to a total dose of 80 Gy. (Addition of 30 Gy in 3 Gy daily fraction added in phase II as a simultaneous integrated boost - SIB).
Arm Title
Arm 2 - Hypoxic Comparator Arm
Arm Type
Active Comparator
Arm Description
The prescribed radiotherapy dose will be 70 Gy in 2 Gy per fraction daily. The elective volume will be treated with 50 Gy in 2 Gy per fraction daily till the first 5 weeks. The entire treatment will be delivered in a phased mannered using sequential planning.
Arm Title
Arm 1 - Non-hypoxic arm
Arm Type
Placebo Comparator
Arm Description
The patients will be treated with a standard of care where the treatment will not be controlled, and these patients will act as external control representing clinical practice. However, these patients will be discussed in the head and neck multispeciality clinic and follow the institutional approach. They will be subjected to treatment similar to 'arm 2' but are allowed protocol deviation as per treating radiation oncology discretion.
Intervention Type
Radiation
Intervention Name(s)
DE-HyART
Other Intervention Name(s)
Dose escalated radiotherapy, Hypoxic sub volume, FMISO
Intervention Description
The HSV delineation will be done for patients in arm 3 using baseline FMISO. The HSV will be contoured and adjusted according to the second FMISO scan done between the 4th - the 5th week of radiation treatment. A planning CT will also be repeated at the time for adjusting the HSV to account for temporal changes. The Biological Target Volume thus generated after adequate margins will be prescribed 30 Gy in 10 fractions over and above the standard fractination.
Intervention Type
Radiation
Intervention Name(s)
Standard Arm
Other Intervention Name(s)
Standard Sequential fractionation without dose escalation
Intervention Description
The prescribed radiotherapy dose will be 70 Gy in 2 Gy per fraction daily. The elective volume will be treated with 50 Gy in 2 Gy per fraction daily till the first 5 weeks. The entire treatment will be delivered in a phased mannered using sequential planning.
Intervention Type
Drug
Intervention Name(s)
Cisplatin injection
Intervention Description
Concurrent chemotherapy, weekly Inj Cisplatin 40mg/m2. This will be given if clinically indicated
Intervention Type
Radiation
Intervention Name(s)
Standard fractionation (Radiation Oncology preference)
Intervention Description
Standard institutional practice is detailed before starting the patient. Doses 66-70 Gy over 6-7 weeks
Primary Outcome Measure Information:
Title
Locoregional Control (LRC)
Description
The duration of LRC was defined from the date of randomisation to the first histopathologically proven relapse of locoregional disease. If there is no proven recurrence, the LRC duration will be cut-off at the analysis point.
Time Frame
Disease recurrence locally or analysis cut-off point. The analysis cut off pint is 24 months
Secondary Outcome Measure Information:
Title
Overall Survival (OS)
Description
The duration of OS was defined from the date of surgery to death from any cause. Therefore, if there is no death (for any reason), the OS duration will be cut-off at the analysis.
Time Frame
Death during following up or analysis cut-off point. The analysis cut off pint is 24 months
Other Pre-specified Outcome Measures:
Title
Acute toxicity
Description
The acute toxicity will be measured by Common Terminology Criteria for Adverse Events (CTCAE) v5.0
Time Frame
Till 6 months of finishing radiotherapy
Title
Late toxicity assessment
Description
Measuring scale: (RTOG/European Organisation for the Research and Treatment of Cancer late toxicity criteria)
Time Frame
At 1 year and 2 year follow-up
Title
Patient-reported outcome
Description
EORTC QLQ-C30 and QLQ-H and N35
Time Frame
During treatment, at 3 month and 6 month interval of completion of radiotherapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 18 - 70 years Willingness to sign informed consent (written/video documentation) Performance status: ECOG 0 - 2 Histology proved - squamous cell carcinoma Any grade, gender Tumour sites: Oral Cavity, Oropharynx, Hypopharynx and Larynx Sufficient bone marrow reserve within the last 14 days. Hb: > 10g/dl (corrected) TLC: > 4,000 per cumm Platelet: >1.5Lakh per cumm Liver functions and kidney functions within normal limits Nutritional and dental assessment before inclusion into the study Exclusion Criteria: HPV (p16) positive tumours Prior surgery and/or radiation therapy given for any HNC T1/T2 Glottis Metastatic disease or disease not amenable for definitive locoregional treatment. Medical co-morbidity hampering the administration of radiation and/or chemotherapy (cisplatin) Pregnancy or lactation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Munish Gairola, MD,DNB Radiation Oncology
Organizational Affiliation
Rajiv Gandhi Cancer Institute and Research Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rajiv Gandhi Cancer Institute and Research Centre
City
Delhi
ZIP/Postal Code
110085
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sarthak Tandon, DNB Radiation Oncology
Phone
(+91)11-47022009
Email
drsarthaktandon@yahoo.in
First Name & Middle Initial & Last Name & Degree
Munish Gairola, MD, DNB Radiation Oncology
First Name & Middle Initial & Last Name & Degree
Sarthak Tandon, DNB Radiation Oncology

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
data privacy issues with the country laws before any commitment
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Dose Escalation Using Hypoxia-adjusted Radiotherapy

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