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To evaluate Neoadjuvant chemotherapy in treatment of unresectable cervical cancer patients

To evaluate Neoadjuvant chemotherapy followed by chemoradiation in patients with unresectable cervical cancer

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210808052110N1
Enrollment
74
Registered
2021-10-21
Start date
2021-10-23
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

cancer of cervix. Malignant neoplasm of cervix uteri

Interventions

Intervention group:Recieving 4 course chemotherapy with carboplatin (Area under curve
AUC:5)and paclitaxel (175mg per square meter)every three week before chemoradiation with External beam radiation and brachytherapy up to 80 to 90Gy to high risk Clinical target volume (CTV)with prescr

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Unresectable cervical cancer(IIB toIVA,IB3,IIAmore than 4cm) 2.No history of metastasis 3.Adequate renal function(GFR more than 60ml per min per1.73) 4.Adequate hepatic function(Liver enzyme1500) 6-Without history of systemic disease 7.Absence of active infection 8.Absence of previous or concurrent oncology pathology 9.ECOG performance status 0 and 1 10.Age 18 to 75 years

Exclusion criteria

Exclusion criteria: 1-Previous pelvic radiation 2-Pregnancy 3-Serious medical illness 4-Hypersensitivity to chemotherapy agent

Design outcomes

Primary

MeasureTime frame
Response to treatment 3 months after fulfilling it. Timepoint: 3 months after fulfilling treatment. Method of measurement: To do MRI and evaluate response to treatment by recist 1.1 guideline.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzieh Heidarpourfard

Shiraz University of Medical Sciences

heidarpourfard@sums.ac.ir+98 71 3648 8332

Outcome results

None listed

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