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Combination Chemotherapy of Paclitaxel and Carboplatin With or Without Anthracycline as Aneo Adjuvant Treatment in Advanced Endometrial Carcinoma

S

Sohag University

Status

Not yet enrolling

Conditions

Endometrial Carcinoma

Treatments

Drug: Paclitaxel/epirubcin/carboplatin
Drug: Paclitaxel/carboplatin

Study type

Interventional

Funder types

Other

Identifiers

NCT06102252
Soh-Med-24-7-01MD

Details and patient eligibility

About

Endometrial cancer, the most common gynecologic cancer worldwide, is steadily increasing in developed countries.The early-stage forms of endometrial cancer are usually highly curable by surgical treatment alone, whereas advanced stages require adjuvant interdictions such as radiotherapy and chemotherapy. Platinum and anthracycline drugs have long been used as standard adjuvant chemotherapy drugs for advanced and recurrent endometrial carcinomas. In one study, the standard combination adjuvant treatment with AP was found to be more effective as an adjuvant therapy than whole abdominal irradiation

Enrollment

80 estimated patients

Sex

Female

Ages

20 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:• Age group: Histologically diagnosed with primary endometrial carcinoma

  • more than 20 years old.

    • Any histological type of endometrial carcinoma

    • Stage III, IV

    • Stage one I or II with one or more of the following factors:

      1. Histologic grade 3 endometroid carcinoma with myometrial invasion still within half of the myometrium
      2. histological grade 1,2 endometroid carcinomas with invasion of over half of myometrium
      3. cervical stromal invasion
      4. vascular invasion; or
      5. serous carcinoma, clear cell carcinoma, or undifferentiated carcinoma
    • performance status 0-2

    • adequate function of all major organs

Exclusion Criteria:

  • • Pt has received prior radiation or chemotherapy.

    • Pt with sarcomatous component
    • Metastatic endometrial carcinoma
    • Other malignancy
    • Unfit patient for chemotherapy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 3 patient groups

group A
Active Comparator group
Description:
will receive the TEC regimen: paclitaxel 150mg/m2 infused for 3 hours, epirubicin 50mg/m2 infused for 30 minutes, and carboplatin 4mg/ml/min for one hour on day 1 every 3 weeks.
Treatment:
Drug: Paclitaxel/epirubcin/carboplatin
group B
Active Comparator group
Description:
) will receive a ddTC regimen: paclitaxel 80mg/m2 for 3 hours on day 1,8,15. Carboplatin AUC 5 over one hour on day 1 repeated at 3-week intervals
Treatment:
Drug: Paclitaxel/carboplatin
group C
Active Comparator group
Description:
: paclitaxel 175 mg/m2 over 3 hours infusion on day 1-carboplatin AUC 5 over 1 hour on day 1 at 3 weeks intervals
Treatment:
Drug: Paclitaxel/carboplatin

Trial contacts and locations

1

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Central trial contact

ELSAYED M MOSTAFA, professor; ASMAA G GAMAL, assistant lecutrer

Data sourced from clinicaltrials.gov

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