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Prospective, II phase clinical study with Nab-paclitaxel plus cisplatin weekly radical concurrent radiochemotherapy regimen for limited stage cervical cancer

Prospective, II phase clinical study with Nab-paclitaxel plus cisplatin weekly radical concurrent radiochemotherapy regimen for limited stage cervical cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034251
Enrollment
Unknown
Registered
2020-06-29
Start date
2020-08-01
Completion date
Unknown
Last updated
2020-07-06

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

Conditions

Cervical Cancer

Interventions

single arm:Nab-paclitaxel plus cisplatin weekly radical concurrent radiochemotherapy regimen

Sponsors

The Affiliated People's Hospital of Inner Mongolia Medical University (Inner Mongolia Cancer Hospital)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with invasive squamous cell carcinoma of the cervix confirmed by biopsy; 2. Patients with pelvic CT, MRI or PET / CT within 1-2 weeks before treatment; 3. Patients with stage ib-iii (FIGO 2018 stage) were determined based on gynecological examination and imaging examination; 4. Patients with general condition score of 0-1; 5. Laboratory examination indexes, including liver function, renal function and bone marrow examination, met the following indexes: (1) White blood cell (WBC): >= 3.5 * 10^9 / L (2) Neutrophil count (ANC): >= 1.5 * 10^9 / L (3) Platelet (PLT): >= 100 * 10^9 / L (4) Total bilirubin (TB): = 50ml / min 6. Patients must sign the informed consent before entering the group.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of malignant tumor or accompanied by a second primary tumor in recent 3 years; 2. Patients with previous history of systemic chemotherapy or pelvic / abdominal radiotherapy; 3. In patients without tumor related surgery, lymph node graft was excluded; 4. Patients with severe infection, heart, liver or kidney disease; 5. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;Safety and Tolerability;

Secondary

MeasureTime frame
overall treatment time;quality of life;

Countries

China

Contacts

Public ContactHao Yang

People's Hospital Affiliated to Inner Mongolia Medical University (Cancer Hospital of Inner Mongolia Autonomous Region)

haoyang050201@163.com+86 18686020135

Outcome results

None listed

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