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A prospective clinical study to evaluate the feasibility and safeness of the chemotherapy with weekly paclitaxel administration in cases with anaplastic thyroid cancer

A prospective clinical study to evaluate the feasibility and safeness of the chemotherapy with weekly paclitaxel administration in cases with anaplastic thyroid cancer - ATCCJ-TXL-P2

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008574
Enrollment
50
Registered
2012-07-31
Start date
2012-04-20
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

anaplastic thyroid cancer

Interventions

Chemotherapy with weekly paclitaxel administration. 80mg/m2 once every week. One course consisted of 3 administrations. At least 1 course of the therapy is necessary. Therapy may continue when availab

Sponsors

Anaplastic Thyroid Carcinoma Consortium Japan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patient who fulfills all following criterion. (1) pathologically proven anaplastic thyroid cancer (2) aged 20 and over (3) ECOG performance status 0-2 (4) suffient organ function(e.g. marrow,liver, kidney,bone) (5) written informed consent

Exclusion criteria

Exclusion criteria: Patient who matches one of these criterion. (1) suspision for interstitial pneumonia or pulmonary fibrosis by chest radiograph (2) brain metastasis with symptom (3) presence of the active peptic ulcer (4) presence of the active other malignancies (5) fever more than 38C (6) severe complication (e.g. myocardial infarction within 3 months, heart failure with clinically problem, poorly controlled diabetes mellitus, severe infectious disease. (7) past history for severe drug allergy (8) past history of hypersisitivity to polyoxyethylated or hydrogenated castor oil (9) hypersisitivity to alcohol (10) pregnant or nursing women (11) difficult to entry due to psychological problem (12) previous chemotherapy or radiation therapy to the present illness (13) physician judged improper to entry this trial

Design outcomes

Primary

MeasureTime frame
Relative dose intensity and safety of the chemotherapy will be evaluated. Overall response rate, time to failure, type of recurrence, overall survival.

Countries

Japan

Contacts

Public ContactIwao Sugitani

Anaplastic Thyroid Carcinoma Consortium Japan Department of Endocrine Surgery, Nippon Medical School

isugitani@nms.ac.jp03-5814-6219

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026