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Study of Advanced Cancer Treatment on Head & Neck Cancer patients and Breast Cancer patients

Not Applicable
Conditions
Health Condition 1: null- Newly diagnosed, locally advanced Head & Neck Cancer and refractory / relapsed triple negative breast cancer patients
Registration Number
CTRI/2018/05/013727
Lead Sponsor
Tata Memorial Centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patients with locally advanced H&N Ca requiring neo-adjuvant therapy, aged 18-75 are eligible for the ACCEPT-H&N trial.

2.Patients from whom at least 100-200 mm3 non-necrotic tumor can be obtained by biopsy or surgery.

3.ECOG Performance Status of 0 â?? 1

Exclusion Criteria

1.Any other concurrent disease or illness, which in the judgment of the investigator

would make the subject inappropriate for entry into the study

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.To evaluate the predictive power of CANScriptTM by comparing CANScriptTM outcomes to clinical outcomes at the end of 2/3 cycles of chemotherapy in H&N cancer and TNBC patients.Timepoint: After completion of treatment
Secondary Outcome Measures
NameTimeMethod
1.To evaluate the predictive power of CANScriptTMby comparing CANScriptTM outcome to patientâ??s progression free survival and overall survival when followed for a period of 2 years from study enrollment to disease progression or death (whichever is earlier).Timepoint: After completion of treatment
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