Sentinel Node Mapping in High Risk Endometrial Cancer (ALICE)
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ClinicalTrials.gov Identifier: NCT03366051 |
Recruitment Status :
Recruiting
First Posted : December 8, 2017
Last Update Posted : February 18, 2022
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Condition or disease | Intervention/treatment | Phase |
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Endometrial Cancer Lymph Node Metastases | Procedure: Sentinel Node Mapping Procedure: Lymphadenectomy | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 178 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Intervention Model Description: | Randomized Controlled Non-Inferiority Trial |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Sentinel Node Mapping Versus Sentinel Node Mapping With Systematic Lymphadenectomy in High Risk Endometrial Cancer: a Open Label, Non-inferiority, Randomized Trial. |
Actual Study Start Date : | December 22, 2017 |
Estimated Primary Completion Date : | December 20, 2024 |
Estimated Study Completion Date : | December 20, 2024 |
Arm | Intervention/treatment |
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Active Comparator: Sentinel Node Mapping plus Lymphadenectomy
Patients with high risk endometrial cancer will undergo Sentinel Node Mapping followed by Systematic Pelvic and Para-Aortic Lymphadenectomy
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Procedure: Sentinel Node Mapping
At least one sentinel node should be retrieved in both hemipelvis. If no sentinel node is found in one hemipelvis, a side specific lymphadenectomy will be performed. Procedure: Lymphadenectomy Systematic Pelvic and Para-Aortic Lymphadenectomy |
Experimental: Sentinel Node Mapping
Patients with high risk endometrial cancer will undergo Sentinel Node Mapping per NCCN algorithm
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Procedure: Sentinel Node Mapping
At least one sentinel node should be retrieved in both hemipelvis. If no sentinel node is found in one hemipelvis, a side specific lymphadenectomy will be performed. |
- Recurrence [ Time Frame: 3 years ]Recurrence Free Survival
- Survival [ Time Frame: 5 years ]Overall Survival
- Early morbidity [ Time Frame: <30 days after surgery ]Surgical and clinical morbidity
- Late morbidity [ Time Frame: >30 days after surgery ]Surgical and clinical morbidity
- Lymphedema [ Time Frame: Evaluation before surgery and after 6 and 12 months of follow-up ]Presence and lymphedema graduation
- Quality of Life Questionary (QLQ) [ Time Frame: Evaluation before surgery and after 1 and 6 months of follow-up ]EORTC QLQ-C30

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Ages Eligible for Study: | 18 Years to 75 Years (Adult, Older Adult) |
Sexes Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- High grade histologies (endometrioid grade 3, serous, clear cell and carcinosarcoma)
- Endometrioid grades 1 or 2 with myometrial invasion of ≥50%
- Endometrioid grades 1 or 2 with cervical invasion
- Clinically suitable to receive systematic lymphadenectomy
- Consent statement
Exclusion Criteria:
- Previous hysterectomy in other institution
- Presence of extra-uterine disease (peritoneal, visceral or suspicious lymph node metastasis)
- Previous pelvic node dissection

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03366051
Contact: Bruna Goncalves, RN, MSc | 551121895110 | bruna.goncalves@accamargo.org.br |
Brazil | |
Hospital Erasto Gaertner | Recruiting |
Curitiba, Parana, Brazil | |
Contact: Reitan Ribeiro, MD reitanribeiro@hotmail.com | |
Hospital do Cancer de Barretos | Recruiting |
Barretos, Sao Paulo, Brazil | |
Contact: Carlos Andrade, MD, PhD mdcarlosandrade@gmail.com | |
AC Camargo Cancer Center | Recruiting |
Sao Paulo, SP, Brazil, 01509010 | |
Contact: Glauco Baiocchi, MD, PhD 551121895110 glauco.baiocchi@accamargo.org.br | |
Albert Einstein Hospital | Recruiting |
São Paulo, SP, Brazil | |
Contact: Renato Moretti-Marques, MD, PhD morettimarques@gmail.com | |
Sao Camilo Oncologia | Recruiting |
São Paulo, SP, Brazil | |
Contact: Andre Lopes, MD, PhD andrelopes.cirurgia@gmail.com |
Principal Investigator: | Glauco Baiocchi, MD, PhD | Department of Gynecologic Oncology - AC Camargo Cancer Center |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Glauco Baiocchi Neto, Director, Department of Gynecologic Oncology, AC Camargo Cancer Center |
ClinicalTrials.gov Identifier: | NCT03366051 |
Other Study ID Numbers: |
2.392.088 |
First Posted: | December 8, 2017 Key Record Dates |
Last Update Posted: | February 18, 2022 |
Last Verified: | February 2022 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Endometrial Cancer Sentinel Lymph Node Lymphadenectomy |
Endometrial Neoplasms Lymphatic Metastasis Neoplasm Metastasis Neoplastic Processes Neoplasms Pathologic Processes |
Uterine Neoplasms Genital Neoplasms, Female Urogenital Neoplasms Neoplasms by Site Uterine Diseases |