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A Fast-Track care program to quickly diagnose and treat patients with anaplastic thyroid cancer.

Prospective Pilot Study of ATC-RETS: An Anaplastic Thyroid Carcinoma Rapid Evaluation & Treatment Service - ATC-RETS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/01/100798
Enrollment
20
Registered
2026-01-09
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C73- Malignant neoplasm of thyroid gland

Interventions

Intervention1: Nil: Nil Intervention2: Care Pathway: A structured navigator-assisted rapid care pathway for patients with suspected or confirmed anaplastic thyroid carcinoma involving expedited diagno

Sponsors

Tata Memorial Centre Research Administration Council
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age Greater than or equal to 18 years. 2. New patient with suspected ATC (cytology and biopsy highly suspicious) or histologically confirmed ATC. 3. Presents to HBCHRC for initial evaluation and management. 4. Able to provide informed consent (or proxy consent where allowed).

Exclusion criteria

Exclusion criteria: 1. Already received definitive ATC therapy elsewhere prior to navigator contact. 2. Expected survival less than 48 hours where immediate palliation supersedes study procedures. 3. Declines participation

Design outcomes

Primary

MeasureTime frame
Compliance to ATC-RETS To evaluate the effectiveness of ATC-RETS by measuring the proportion of patients who (a) Achieve a multidisciplinary treatment decision within 3 days and (b) Initiate treatment within 5 days of the index diagnostic event. (short delays between diagnosis and treatment allow tumor proliferation, vascular invasion, or airway compromise.)Timepoint: 2 years

Secondary

MeasureTime frame
To map the full patient journey from presentation to treatment and identify modifiable workflow delaysTimepoint: 2 years;To assess overall survival (OS) at 3 months and 6 months, and evaluate whether early treatment through ATC-RETS influences short-term survival outcomes.Timepoint: 2 years;To evaluate the uptake and turnaround time of essential molecular testing (including BRAF), and whether results are available in time to inform early treatment decisions.Timepoint: 2 years;To assess the proportion of patients with actionable mutations who initiate appropriate targeted therapy, and document reasons for non-initiation when indicated.Timepoint: 2 years;To identify and categorize barriers to timely care, and describe how navigator interventions address these delays.Timepoint: 2 years;To assess patient and clinician acceptability of the navigator-supported care pathway, using brief structured satisfaction surveysTimepoint: 2 years;Emergency airway intervention rateTimepoint: 2 years;Percentage receiving dabrafenib/trametinib (for BRAF V600E)Timepoint: 2 years;Percentage receiving palliative RTTimepoint: 2 years;Steroid use and acute QOL changes (if feasible)Timepoint: 2 years;Measuring surgery stress score for each patientTimepoint: 2 years

Countries

India

Contacts

Public ContactDr Srinjeeta Garg

Homi Bhabha Cancer Hospital and Research Centre

gargs@hbchrcmzp.tmc.gov.in916212100162

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026