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Completed

NCT Number: NCT01300143

Association of Conformational High-dose Radiotherapy and of Hyperselective Transarterial Chemoembolization in the Treatment of Hepatocellular Carcinoma

Indication : Hepatocellular carcinoma, maximum size 9 cm, with single or multiple nodes whose total tumor mass can technically be irradiated, non-resectable, and not a candidate for percutaneous therapy with recommended treatment via hyperselective transarterial chemoembolisation (TACE).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

CHU Amiens, Amiens, France

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About this study

: Phase II controlled randomized trial, multicenter, comparing the benefit of additive conformational radiotherapy after therapy with hyperselective chemoembolisation (TACE) with treatment using three TACE treatments (standard of care).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years of age
  • ECOG 0-1
  • life expectancy ≥ 6 months
  • Histologically proven hepatocellular carcinoma or proven according to radiological and biochemical criteria (EASL-AASLD) in cirrhotic patients
  • Maximum lesion size ≤ 9 cm
  • Non-eligible for surgery or percutaneous therapy
  • Premature Child-Pugh A or B (7 points for the Child-Pugh score)
  • AST and ALT < 7 x UNL
  • Technical possibility of conformational external radiotherapy
  • Technical possibility of TACE
  • All the tumor mass must be able to be treated by TACE
  • Written consent signed by the patient
  • Patients affiliated to a social security system

Exclusion criteria

  • Metastatic illness
  • Minimal lesion size ≤ 5 mm
  • Non controlled viral replication B
  • History of radiotherapy at abdominal level
  • Subjects capable of procreating without efficient contraception
  • pregnancy or nursing female patient
  • Contraindication of TACE or external conformational radiotherapy
  • Any other concomitant experimental treatment
  • Contraindication of Doxorubicin
  • Patients who are unable to respect enslaving respiratory constraints if used by sites
  • Patients who are unable to understand information and to follow protocol instructions

Treatment and study plan

TACE

Other

Control arm will be treated by 2 or 3 cures of TACE DC beads at week 0, 8 and 16 (if required)

TACE+ RTC

Other

Experimental group will be treated by one cure of TACE DC Beads at week 0 then, within two weeks, by external conformational radiotherapy in 18 sessions

Primary outcomes

  1. Time of tumor progression radiologically (CTScan) measured by mRECIST (Modified Response Evaluation Criteria In Solid Tumor).

    Time frame: up to 18 months

Secondary outcomes

  1. Evaluation of the acute toxicity at the participants

    Time frame: within 90 days after the treatment

  2. Evaluation of the late toxicity at the participants

    Time frame: after 90 days of treatment

  3. Evaluation of the quality of life (assessed by QLQ-EORT C30)

    Time frame: the day of randomization (week 0), at week 12 and week 24

  4. Evaluation of the rate of complete, partial response and stable disease after treatment (by RECIST criteria )

    Time frame: at week 24,week 48 and week 72

  5. Compare the health economic implications of these regimens in these patients.

    Time frame: up to18 months (week 72)

  6. overall survival

    Time frame: within 3 years after first cure of TACE-DC BEADS

Sponsors and collaborators

Lead sponsor

Nantes University Hospital

Other

Registry information

Acronym: TACERTE

Important dates

Study start
2011
Primary completion
2018
Study completion
2018
First posted
Feb 21, 2011
Registry last updated
Dec 27, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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