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NCT05454358Leállítva2/3. fázis

Letrozole as Maintenance Therapy for Post-surgical Endometrial Cancer Patients With NSMP

Letrozole as Maintenance Therapy Versus Observation After Adjuvant Treatment on the Prognosis for Post-surgical Endometrial Cancer Patients With Non-specific Molecular Profile: a Superiority Randomized Controlled Trial

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2025. dec. 15.

Megadott ok: No enough participants

Rövid összefoglaló (regiszter, angolul)

Aim to investigate the effect of Letrozole as maintenance after adjuvant treatment on the prognosis of post-operative endometrial cancer patients with non-specific molecular profile.

Állapot (regiszter)
Leállítva
Fázis (regiszter)
2/3. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
12 (tényleges)
Első benyújtás
2022. jún. 26.
Kezdés
2022. aug. 2.
Elsődleges befejezés
2025. dec. 1.
Fő szponzor
Fudan University
Betegségek
Méhtestrák
NCT-szám
NCT05454358

Ki nem vehet részt

Szó szerint a(z) ClinicalTrials.gov forrásból, témák szerint csoportosítva. Hogy ki vehet részt, azt csak a vizsgálat csapata dönti el.

Korábbi kezelés

  • Patients require no adjuvant therapy after surgery;
  • Received other adjuvant therapy within 6 months before surgery: including neoadjuvant therapy, hormone therapy, targeted therapy, immunotherapy and biotherapy, etc;

Más betegség

  • Recurrent endometrial cancers;
  • Patients with other malignant tumors;
  • History of vital organ transplantation;
  • History of immune disease and need to take immunosuppressor;
  • Uncontrolled psychiatric illness or other situations that would limit compliance with study requirements;
  • History of drug abuse;

Egyéb

  • Endometrial stromal tumor;
  • Patients with low prognostic risk according to post-operative clinical pathological assessment ( Stage IA endometrioid + low-grade* +LVSI negative or focal);
  • Negative expression in estrogen receptor or progesterone receptor according to post-operative Immunohistochemistry;
  • Patients with contraindications for letrozole;
  • Participated in other clinical trials;
  • No ability or intention to receive letrozole maintenance/sign the consent/obey the study requirements.

Kiket keres a vizsgálat

  • Older than 18 years old;
  • Initial diagnosed with stage I-IV(FIGO2009) endometrial epithelial cancer, regardless of pathological types;
  • Surgery must have included a hysterectomy, bilateral salpingo-oophorectomy and sentinel node biopsy; pelvic lymph node sampling and para-aortic lymph node sampling are optional;
  • Life expectancy of 2 or more years.
  • Confirmed NSMP with intermediate or higher prognostic risk according to post-operative clinical pathological assessment and molecular classification;
    • Intermediate prognostic risk group:
    • Stage lB endometrioid + Iow-grade* + LVSI negative or focal
    • Stage IA endometrioid + high-grade*+ LVSI negative or focal
    • Stage IA non-endometrioid (serous, clear cell, undifferentiated carcinoma, carcinosarcoma, mixed) without myometrial invasion
    • High-intermediate prognostic risk group:
    • Stage I endometrioid + substantial LVSI, regardless of grade and depth of invasion
    • Stage lB endometrioid high-grade*, regardless of LVSI status
    • Stage II
    • High prognostic risk group:
    • Stage Ill-IVA with no residual disease
    • Stage I-IVA non-endometrioid (serous, clear cell, undifferentiated carcinoma, carcinosarcoma, mixed) with myometrial invasion, and with no residual disease
    • Advanced Metastatic:
    • Stage III-IVA with residual disease
    • Stage IVB Low grade: G1-2; High grade:G3;
  • Received conventional adjuvant therapy after surgery according to the latest version of NCCN or ESGO/ESTRO/ESP guidelines;
  • Patients with residual tumor after surgery (any single site) must have achieved complete response or partial response after post-operative adjuvant therapy;
  • Expected start of letrozole maintenance within 3 months after adjuvant therapy;
  • Adequate organ function as defined by the following criteria:
    • White blood cell (WBC) ≥ 3000/μL or Absolute neutrophil count (ANC) ≥1500/μL
    • Platelets ≥100,000/μL
    • Serum Aspartate transaminase (AST) and/or serum alanine transaminase (ALT) ≤ 2 times upper limit of normal (ULN)
    • Serum creatinine ≤2 times ULN
  • Karnofsky score ≥60;
  • Eastern Cooperative Oncology Group (ECOG) Performance status ≤2;
  • Ability to take anti-thyroid drugs, calcium, vitamin D or bisphosphonates together.

Életkor a regiszterben: 18 év – 80 év · Nem: csak nők · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (1)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Obstetrics and Gynecology Hospital of Fudan UniversityShanghaiKínaIsmeretlen állapot

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