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A randomized multicenter trial on Alternating-IMRT VS Conventional IMRT for massive hepatocellular carcinoma

A randomized multicenter trial on Alternating-IMRT VS Conventional IMRT for massive hepatocellular carcinoma

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OIC-16009726
Enrollment
Unknown
Registered
2016-11-03
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Massive hepatocellular carcinoma

Interventions

group A:alternating intensity modulated radiotherapy
group B:intensity modulated radiotherapy

Sponsors

The Fifth Hospital of Wuhan (Wuhan Cancer Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients of unresectable advanced stage massive HCC are discussed by multidisciplinary team (including at least one hepatic surgeon). Lesion is confirmed by image examinations and its volume must be smaller than 2/3 of the liver volume; age=18 years; KPS=70 before registered two weeks ago; Bone marrow hematopoietic function tests before entered group two weeks ago, including: WBC=1.5×10^9/L, PLT=100×10^9/L; HGB=10.0 g/dl (HGB=10.0 g/dl under the supportive therapy is accepted), SCR or CCR=60 ml/min,Child-Pugh A or B, ALT<90U/L; AST<90U/L, TBil<160umol/L.

Exclusion criteria

Exclusion criteria: Patients were accepted abdominal radiotherapy or potential radiation fields overlap due to radiation therapy; A large number of peritoneal effusion suggested by color ultrasound; intrahepatic metastasis; metastasis in other distant organs; fertile female and male who are not willing to contracept; patients are not suitable to enhance contrast MRI or CT examinations (cardiac pacemaker, allege to enhance contract agents and so forth); unstable angina pectoris and /or chronic congestive heart-failure happened within six months; transmural myocardial infarction happened in six months.

Design outcomes

Primary

MeasureTime frame
clinical benefit rate;overall survival rate;objective response rate;local control rates;local control rates;

Secondary

MeasureTime frame
progression-free survival;Alpha-fetoprotein;

Countries

China

Contacts

Public ContactLong Zhixiong

The Fifth Hospital of Wuhan (Wuhan Cancer Hospital)

2428850630@qq.com+86 18507199619

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026