The Efficacy of Adjuvant Chemotherapy in Locally Advanced Cervical Cancer
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- STATUS
- Recruiting
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- End date
- Apr 5, 2028
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- participants needed
- 120
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- sponsor
- Chongqing University Cancer Hospital
Summary
The aim of this trial was to evaluate the efficacy of adjuvant chemotherapy in the locally advanced cervical cancer with residual lesions after concurrent chemoradiation therapy.
Description
- Objective:
To compare response rate and survivals of locally advanced stage cervical cancer patients with residual lesions who had CCRT alone to those who had adjuvant chemotherapy after CCRT.
2. Patients:
- Cervical cancer stage IIb to IVa with a histopathology of squamous cell carcinoma, adenosquamous cell carcinoma, adenocarcinoma
- Complete CCRT(Radiation Does: A point 85Gy(+/-10%)B50Gy(+/-10%)concurrent paclitaxel and cisplatin once a week for six cycles)
- MRI is performed within 4 weeks after CCRT and shows residual lesions (non-lymph node10mmlymph node shortest diameter15mm).
- Methods:
The patients who have residual lesions after CCRT are randomized to arm A by observation or arm B by adjuvant chemotherapy with paclitaxel plus cisplatin every 3 weeks for 3 cycles.
Details
Condition | Cervical Cancer, Cervical Cancer, Uterine Cancer, Uterine Cancer |
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Age | 18years - 75years |
Treatment | CCRT, Paclitaxel, Cisplatin |
Clinical Study Identifier | NCT04409860 |
Sponsor | Chongqing University Cancer Hospital |
Last Modified on | 19 February 2024 |
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