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OUTCOME AND TOXICITY OF TOTAL NEOADJUVANT THERAPY IN RECTAL CANCER

OUTCOME AND TOXICITY OF TOTAL NEOADJUVANT THERAPY IN RECTAL CANCER - TNTox

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033000
Enrollment
350
Registered
2023-11-07
Start date
2024-01-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

C20

Interventions

Group 1: A retrospective cohort of patients with rectal cancer who underwent (chemo)radiation followed by consolidating chemotherapy (so-called "total neoadjuvant therapy") between 2010 and January 20

Sponsors

Universitätsklinikum Jena
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with locally advanced rectal cancer (LARC), UICC stage II/III who underwent total neoadjuvant therapy (TNT) adequately measured tumor response (histologically and / or radiologically plus endoscopically) available follow-up data (min. 6 months)

Exclusion criteria

Exclusion criteria: Enrollment in other ongoing clinical trials

Design outcomes

Primary

MeasureTime frame
complete remission rate

Secondary

MeasureTime frame
treatment schedule (i.e. fractionation of radiation, duration of radiation and chemotherapy respectively, chemotherapy dosing, cumulative chemotherapy dose) toxicity during and after therapy quality / results of surgery survival rates (overall, disease-free, colostomy-free), relapse rate quality of life

Countries

Germany

Contacts

Public ContactGeorg Wurschi

Klinik für Strahlentherapie und Radioonkologie, Universitätsklinikum Jena

georg.wurschi@med.uni-jena.de0049 3641 9 32 84 01

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 19, 2026