Skip to content

Gendicine intratumoral injection combined with radiotherapy for advanced cervical carcinoma

recombinant adenoviral-p53 intratumoral injection combined with radiotherapy for advanced cervical carcinoma

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-08000091
Enrollment
Unknown
Registered
2008-04-22
Start date
2008-02-01
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

Advanced cervical carcinoma

Interventions

RT:the conventional fractionation 2Gy/day, five fractions a week, with a total dose of 70-80Gy was given to the primary tumor
GTRT:In the GTRT group, Gendicine 1*10^12 virus particle (vp) was intratumorally injected once a week for six weeks and concurrently irradiation was given. the conventional fractionation 2Gy/day, five

Sponsors

Beijing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients should be 18 to 80 years old. All patients were staged as unresectable IIB, III, or IVA according PICO staging system. Initial treatment with radiotherapy was judged to be the accepted standard of care. Patients must have a projected life expectancy of at least 6 months and a Karnofsky performance score of at least 70%. Patients were required to have adequate bone marrow function (WBC count 4.0*10^9/L, hemoglobin 7g/L, platelet count 70*10^9/L) and adequate liver and renal function (AST, ALT, BUN and Cr <1.5 time the upper limit of normal).

Exclusion criteria

Exclusion criteria: Pregnant or nursing women, patients with uncontrolled serious infections, or with serious heart and lung failure were excluded.

Design outcomes

Primary

MeasureTime frame
Local-regional recurrence;Survival rate;

Secondary

MeasureTime frame
Tumor response;

Countries

China

Contacts

Public ContactZhang Shanwen
zhangshw4641@sina.com+86 010 88196218

Outcome results

None listed

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