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NCT Number: NCT06205472

Phase II Study of Adjuvant SIB Radiotherapy Following Narrow-Margin Hepatectomy in Patients With HCC.

This is a single-arm prospective phase II clinical trial to investigate the efficacy and safety of adjuvant simultaneouslyintegrated boost radiotherapy following narrow-margin(<1cm) hepatectomy in patients with HCC. Eligibility patients will receive IMRT or VMAT to high risk area of tumor bed and tumor bed. The prescription dose to 95% GTVtb boost was planned at 55-60Gy, with PTV 45-50Gy, in 23-25 fractions, mainly depending on the dose constraints of OARs. The primary endpoint is the 3-year OS, the secondary endpoints are disease-free survival, patterns of failure, toxic events and local control rate.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Bo Chen

Beijing, China

Location status: Recruiting

Location contact

Bo Chen

CONTACT

[email protected]

00861324000876

Bo Chen

PRINCIPAL_INVESTIGATOR

Yirui Zhai

SUB_INVESTIGATOR

About this study

Surgical resection is the primary treatment for HCC. However, it is associated with a high rate of recurrence and death. Based on the results of our retrospective study and phase II study, adjuvant radiotherapy is an effective, tolerable, and promising adjuvant regimen in patients with narrow-margin(<1cm) after hepatectomy. The 3-year and 5-year OS rates of 88.2% and 72.2% were significantly higher than the expected rates based on published reports and exceeded our predetermined threshold. However, there is no standard for the prescription dose. The high risk area of recurrence is mostly close to the blood vessels in the tumor bed, and simultaneously integrated boost (SIB) technique can optimize the target dose while protecting normal tissues. So, the investigators conducted this single-arm prospective phase II clinical trial to investigate the efficacy and safety of adjuvant SIB radiotherapy following narrow-margin(<1cm) hepatectomy in patients with HCC.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Pathological diagnosis of HCC after hepatectomy with narrow pathological margins (< 1 cm)
  • Age > 18 years
  • Recovery from surgery with an Eastern Cooperative Oncology Group performance status score of 0 or 1
  • Child-Push Score: A5-A6
  • Estimated life expectancy > 3 months
  • No distant metastasis (M0)
  • Blood routine examination: Hb≥80g/L, ANC≥1.0x10^9/L, PLT≥50x10^9/L
  • Hepatic function: alanine transaminase(ALT) and aspartate transaminase(AST) ≤1.5 times ULN; or ALT ≤ULN and AST ≤6 times ULN exclude possibility of heart disease
  • Renal function: creatinine(CRE) and blood urea nitrogen(BUN)≤1.5 times ULN
  • Voluntary to participate and sign informed consent

Exclusion criteria

  • History of malignancies, except for basal cell skin carcinoma and in situ carcinoma of the cervix
  • Had prior abdominal irradiation
  • Had prior liver transplantation
  • Had serious myocardial disease or renal failure
  • Had moderate or severe ascites with obvious symptoms
  • Duration from surgery ≥ 3 months

Treatment and study plan

Adjuvant SIB radiotherapy

Radiation

Eligibility patients will receive IMRT or VMAT to high risk area of tumor bed and tumor bed. The prescription dose to 95% GTVtb boost was planned at 55-60Gy, with PTV 45-50Gy, in 23-25 fractions,mainly depending on the dose constraints of OARs.

Primary outcomes

  1. The 3-year Overall Survival

    Time frame: up to 36 months

    The 3-year overall survival was calculated from the date of surgical resection to the date of death from any cause.

Secondary outcomes

  1. Disease-free Survival (DFS)

    Time frame: up to 36 months

    Disease-free survival (DFS) was calculated from the date of surgical resection to the date of the first recurrence or death from HCC

  2. Pattern of Failure

    Time frame: up to 36 months

    The type of recurrence (locoregional failures or distant failure)

  3. Toxic Events

    Time frame: up to 36 months

    Toxic events was evaluated during received protocol therapy according to CTCAE 4.03

  4. Local Control Rate

    Time frame: up to 36 months

    Patients with stable disease [SD], partial response [PR] or complete response[CR] were recorded as local control.

Study contacts

Contact information is provided by the study sponsor or research team.

Bo Chen, MD

CONTACT

[email protected]

00861324000876

Sponsors and collaborators

Lead sponsor

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Other

Registry information

Official study title

Phase II Study of Adjuvant Simultaneously Integrated Boost Radiotherapy Following Narrow-Margin Hepatectomy in Patients With HCC.

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Jan 16, 2024
Registry last updated
Jan 16, 2024

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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