Skip to content

Induction chemotherapy with cisplatin and gemcitabine followed by radiation concurrent with gemcitabine for locally recurrent nasopharyngeal carcinoma: a single-arm, open-label phase II clinical study

Induction chemotherapy with cisplatin and gemcitabine followed by radiation concurrent with gemcitabine for locally recurrent nasopharyngeal carcinoma: a single-arm, open-label phase II clinical study

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-12002613
Enrollment
Unknown
Registered
2012-10-23
Start date
2011-07-01
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

Nasopharyngeal Carcinoma

Interventions

1:neoadjuvant chemotherapy of gemcitabine combined with cisplatin, concurrent chemotherapy of gemcitabine and IMRT

Sponsors

Nasopharyngeal Carcinoma Department of Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. pathologically confirmed or clinical diagnosis of recurrent nasopharyngeal carcinoma; 2. Intervals over 12 months from the first course radiotherapy; 3. aged 18 to 65 years old; 4. ECOG0~2; 5. at least one measurable lesion (RECIST 1.1); 6. without serious dysfunction of heart, lung, liver, kidney or other organ dysfunction; 7. Laboratory parameters: Bone marrow function: WBC>=4.0*10^9/L, ANC>=1.5*10^9/L; PLT >=100*10^9/L; HB>=90g/L; Hepatic function: ALT and AST=60ml/min.

Exclusion criteria

Exclusion criteria: 1. pathologically confirmed or clinical diagnosis of recurrent nasopharyngeal carcinoma; 2. Intervals over 12 months from the first course radiotherapy; 3. aged 18 to 65 years old; 4. ECOG0~2; 5. at least one measurable lesion (RECIST 1.1); 6. without serious dysfunction of heart, lung, liver, kidney or other organ dysfunction; 7. Laboratory parameters: Bone marrow function: WBC>=4.0*10^9/L, ANC>=1.5*10^9/L; PLT >=100*10^9/L; HB>=90g/L; Hepatic function: ALT and AST=60ml/min.

Design outcomes

Primary

MeasureTime frame
Progression-free survival;

Secondary

MeasureTime frame
Objective response rate;Overall survival;safety;

Countries

China

Contacts

Public ContactGuo Xiang
guoxiang@sysucc.org.cn+86 020 87343359

Outcome results

None listed

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