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Role of Neo-adjuvant Chemotherapy in Tongue Preservation in Locally Advanced Squamous Cell Carcinoma of Oral Tongue

Primary Purpose

Tongue Neoplasms, Squamous Cell Carcinoma, Anterior Tongue Squamous Cell Carcinoma

Status
Unknown status
Phase
Phase 2
Locations
India
Study Type
Interventional
Intervention
Docetaxel
Cisplatin
5FU
Radiotherapy
Glossectomy
Sponsored by
HealthCare Global Enterprise Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tongue Neoplasms focused on measuring Neoadjuvant Chemotherapy, Tongue Malignancy, Squamous Cell Carcinoma

Eligibility Criteria

1 Year - 99 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients of newly diagnosed squamous cell carcinoma (well/ moderately/ poorly differentiated) of oral tongue (anterior two third) presenting to Health Care Global Enterprises Ltd between January 2016 to March 2017 will be included in the study.
  • Stage III and stage IV (T3, 4 N0-3, M 0) and selected cases of T2 with advanced nodal status will also be included in the study.

Exclusion Criteria:

  • Patients having recurrence/ residual disease of oral tongue.
  • Patients who have received alternative treatments before being evaluated for NACT
  • Patient who are not fit for NACT
  • Patient not able to give consent

Sites / Locations

  • HealthCare Global Enterprises LtdRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Neoadjuvant Arm

Arm Description

Study Subjects, eligible for NACT would undergo a pretreatment workup with Evaluation Under Anesthesia for tumor Mapping and tissue biopsy along with a PET-CT scan. They would undergo 3 cycles of NACT (weekly thrice) with injection Docetaxel, Cisplatin and 5-FU after which reassessment with PET-CT and EUA +/- biopsy would be done. Those achieving CR would undergo adjuvant CTRT while subjects with PR in PET-CT scan will be reclassified based on the biopsy report. If biopsy is negative for malignancy, they will undergo adjuvant CTRT but would undergo surgery if in the PR group. Subjects with SD or PD would undergo surgery. PET-CT and EUA +/- HPE analyses would be repeated on follow-up after 3 months of treatment completion.

Outcomes

Primary Outcome Measures

Tongue Preservation Rate
A ratio of the number of study subjects who have achieved a complete response and do not require surgery, after 3 cycles of NaCT to the total number of subjects recruited to the study.

Secondary Outcome Measures

Overall Survival
Overall Survival Rate (Date of diagnosis to date of death or last follow-up) in different sub-cohorts of the study
Progression Free Survival
Progression Free Survival Rate (Primary treatment end date to date of progression or last follow-up) in difference sub-cohorts of the study
Sensitivity and Specificity of PET-CT
Ability of PETCT (along with HPE and EUA) to detect response rates in study subjects undergoing NACT for Ca Tongue

Full Information

First Posted
September 29, 2016
Last Updated
December 2, 2016
Sponsor
HealthCare Global Enterprise Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT02985255
Brief Title
Role of Neo-adjuvant Chemotherapy in Tongue Preservation in Locally Advanced Squamous Cell Carcinoma of Oral Tongue
Official Title
Role of Neo-adjuvant Chemotherapy in Organ Preservation in Locally Advanced Squamous Cell Carcinoma of Oral Tongue
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Unknown status
Study Start Date
April 2016 (undefined)
Primary Completion Date
June 2017 (Anticipated)
Study Completion Date
June 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
HealthCare Global Enterprise Ltd.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients enrolled for the study, who are eligible for NACT, will undergo a pre-treatment workup comprising of Evaluation Under Anesthesia (EUA) for tumor Mapping and tissue biopsy along with a PET-CT scan. Subsequently, they would undergo 3 cycles of NACT (weekly thrice) with DCF. They would be reassessed with PET-CT and EUA +/- biopsy after the end of the third cycle. Those who are achieving CR would undergo adjuvant CTRT. Subjects who have a PR in the PET-CT scan will be re-classified based on the biopsy report. If they remain in the PR group they will undergo surgery but if the biopsy in is negative for malignancy, they will undergo adjuvant CTRT. Those subjects with SD or PD would undergo surgery. Subsequently, further radiation and/ or chemotherapy will be decided based on the final histopathology (of the surgical specimen) reports. PET-CT and EUA +/- HPE analyses would be repeated on follow-up after 3 months of treatment completion.
Detailed Description
Patients enrolled for the study, who are eligible for Neoadjuvant chemotherapy, will undergo a pre-treatment workup comprising of Evaluation Under Anesthesia (EUA) for tumor Mapping and tissue biopsy along with a PET-CT scan. Subsequently, they would undergo 3 cycles of Neoadjuvant chemotherapy (weekly thrice) with injection Docetaxel, Cisplatin, and 5-FU. They would be reassessed with PET-CT and EUA +/- biopsy after the end of the third cycle. Those who are achieving a Complete Response (CR) would undergo adjuvant chemo-radiotherapy. Subjects who have a partial response (PR) in the PET-CT scan will be re-classified based on the biopsy report. If they remain in the PR group they will undergo surgery. If the biopsy in these patients is negative for malignancy, they will undergo adjuvant chemoradiotherapy. Those subjects with stable disease (SD) or progressive disease (PD) would undergo surgery. Subsequently, further radiation and/ or chemotherapy will be decided based on the final histopathology (of the surgical specimen) reports. PET-CT and EUA +/- HPE analyses would be repeated on follow-up after 3 months of treatment completion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tongue Neoplasms, Squamous Cell Carcinoma, Anterior Tongue Squamous Cell Carcinoma
Keywords
Neoadjuvant Chemotherapy, Tongue Malignancy, Squamous Cell Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Neoadjuvant Arm
Arm Type
Experimental
Arm Description
Study Subjects, eligible for NACT would undergo a pretreatment workup with Evaluation Under Anesthesia for tumor Mapping and tissue biopsy along with a PET-CT scan. They would undergo 3 cycles of NACT (weekly thrice) with injection Docetaxel, Cisplatin and 5-FU after which reassessment with PET-CT and EUA +/- biopsy would be done. Those achieving CR would undergo adjuvant CTRT while subjects with PR in PET-CT scan will be reclassified based on the biopsy report. If biopsy is negative for malignancy, they will undergo adjuvant CTRT but would undergo surgery if in the PR group. Subjects with SD or PD would undergo surgery. PET-CT and EUA +/- HPE analyses would be repeated on follow-up after 3 months of treatment completion.
Intervention Type
Drug
Intervention Name(s)
Docetaxel
Intervention Description
Neoadjuvant Arm
Intervention Type
Drug
Intervention Name(s)
Cisplatin
Intervention Description
Neoadjuvant Arm
Intervention Type
Drug
Intervention Name(s)
5FU
Intervention Description
Neoadjuvant Arm
Intervention Type
Radiation
Intervention Name(s)
Radiotherapy
Intervention Description
Neoadjuvant Arm
Intervention Type
Procedure
Intervention Name(s)
Glossectomy
Intervention Description
Neoadjuvant Arm
Primary Outcome Measure Information:
Title
Tongue Preservation Rate
Description
A ratio of the number of study subjects who have achieved a complete response and do not require surgery, after 3 cycles of NaCT to the total number of subjects recruited to the study.
Time Frame
At Response evaluation post 3rd CT Cycle (approximately 7 months post recruitment)
Secondary Outcome Measure Information:
Title
Overall Survival
Description
Overall Survival Rate (Date of diagnosis to date of death or last follow-up) in different sub-cohorts of the study
Time Frame
2 years post treatment completion
Title
Progression Free Survival
Description
Progression Free Survival Rate (Primary treatment end date to date of progression or last follow-up) in difference sub-cohorts of the study
Time Frame
2 years post treatment completion
Title
Sensitivity and Specificity of PET-CT
Description
Ability of PETCT (along with HPE and EUA) to detect response rates in study subjects undergoing NACT for Ca Tongue
Time Frame
At Baseline and after 12-15 weeks (post 3 cycles of NaCT (Typically 3 weeks))

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients of newly diagnosed squamous cell carcinoma (well/ moderately/ poorly differentiated) of oral tongue (anterior two third) presenting to Health Care Global Enterprises Ltd between January 2016 to March 2017 will be included in the study. Stage III and stage IV (T3, 4 N0-3, M 0) and selected cases of T2 with advanced nodal status will also be included in the study. Exclusion Criteria: Patients having recurrence/ residual disease of oral tongue. Patients who have received alternative treatments before being evaluated for NACT Patient who are not fit for NACT Patient not able to give consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vishal US Rao, MS
Phone
00919739774949
Email
drvishalrao@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Sataksi Chatterjee, MS
Phone
00918971966903
Email
sataksis2007@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vishal US Rao, MS
Organizational Affiliation
Dept of Head & Neck Surgery, HealthCare Global Enterprises Ltd.
Official's Role
Principal Investigator
Facility Information:
Facility Name
HealthCare Global Enterprises Ltd
City
Bangalore
State/Province
Karnataka
ZIP/Postal Code
560027
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vishal US Rao, MS
Phone
00919739774949
Email
drvishalrao@yahoo.com
First Name & Middle Initial & Last Name & Degree
Sataksi Chatterjee, MS
Phone
00918971966903
Email
sataksis2007@gmail.com
First Name & Middle Initial & Last Name & Degree
Shekhar Patil, DM
First Name & Middle Initial & Last Name & Degree
Radheshyam Naik, DM
First Name & Middle Initial & Last Name & Degree
Vijay Agarwal, Phd
First Name & Middle Initial & Last Name & Degree
Ajai BS Kumar, MS
First Name & Middle Initial & Last Name & Degree
Kumara Swamy, MD
First Name & Middle Initial & Last Name & Degree
Vikram Maiya, MD
First Name & Middle Initial & Last Name & Degree
Ravi Nayar, MS
First Name & Middle Initial & Last Name & Degree
Sataksi Chaterjee, MS
First Name & Middle Initial & Last Name & Degree
Raghavendra M Rao, PhD
First Name & Middle Initial & Last Name & Degree
Amritanshu Ram, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19107949
Citation
Barringer DA, Hutcheson KA, Sturgis EM, Kies MS, Lewin JS. Effect of induction chemotherapy on speech and swallowing function in patients with oral tongue cancer. Head Neck. 2009 May;31(5):611-7. doi: 10.1002/hed.20989.
Results Reference
background
PubMed Identifier
22009800
Citation
Kies MS, Boatright DH, Li G, Blumenschein G, El-Naggar AK, Brandon Gunn G, Lewin JS, Steinhaus GD, Sturgis EM. Phase II trial of induction chemotherapy followed by surgery for squamous cell carcinoma of the oral tongue in young adults. Head Neck. 2012 Sep;34(9):1255-62. doi: 10.1002/hed.21906. Epub 2011 Oct 19.
Results Reference
background
PubMed Identifier
19446902
Citation
Pignon JP, le Maitre A, Maillard E, Bourhis J; MACH-NC Collaborative Group. Meta-analysis of chemotherapy in head and neck cancer (MACH-NC): an update on 93 randomised trials and 17,346 patients. Radiother Oncol. 2009 Jul;92(1):4-14. doi: 10.1016/j.radonc.2009.04.014. Epub 2009 May 14.
Results Reference
background
PubMed Identifier
23835714
Citation
Blanchard P, Bourhis J, Lacas B, Posner MR, Vermorken JB, Cruz Hernandez JJ, Bourredjem A, Calais G, Paccagnella A, Hitt R, Pignon JP; Meta-Analysis of Chemotherapy in Head and Neck Cancer, Induction Project, Collaborative Group. Taxane-cisplatin-fluorouracil as induction chemotherapy in locally advanced head and neck cancers: an individual patient data meta-analysis of the meta-analysis of chemotherapy in head and neck cancer group. J Clin Oncol. 2013 Aug 10;31(23):2854-60. doi: 10.1200/JCO.2012.47.7802. Epub 2013 Jul 8.
Results Reference
background
PubMed Identifier
23182993
Citation
Forastiere AA, Zhang Q, Weber RS, Maor MH, Goepfert H, Pajak TF, Morrison W, Glisson B, Trotti A, Ridge JA, Thorstad W, Wagner H, Ensley JF, Cooper JS. Long-term results of RTOG 91-11: a comparison of three nonsurgical treatment strategies to preserve the larynx in patients with locally advanced larynx cancer. J Clin Oncol. 2013 Mar 1;31(7):845-52. doi: 10.1200/JCO.2012.43.6097. Epub 2012 Nov 26.
Results Reference
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Role of Neo-adjuvant Chemotherapy in Tongue Preservation in Locally Advanced Squamous Cell Carcinoma of Oral Tongue

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