Overview

This is a prospective, single-arm, single-center registry study to investigate 6-month progression-free survival with Dalpiciclib, a CDK4/6 kinase inhibitor, plus letrozole in patients with unresectable refractory or resistant recurrent HR-positive, HER2-negative gynecologic solid tumors." Dalpiciclib is a CDK4/6 kinase inhibitor that selectively inhibits the activity of CDK4/6 kinase, so that the complex with Cyclin D cannot phosphorylate the downstream Rb protein and prevent cells from entering the S phase from G1 phase, thereby inhibiting cell proliferation and anti-tumor effects.

Eligibility

Inclusion Criteria:

1. Female patients aged ≥18 years and ≤75 years;
2. Women with pathologically confirmed HR-positive, HER2-negative ovarian cancer or uterine tumors (including but not limited to high-grade serous ovarian cancer, low-grade serous ovarian cancer, ovarian endometrioid cancer, endometrioid cancer, low -grade endometrial stromal sarcoma, and uterine leiomyosarcoma) with evidence of focal recurrence or metastasis; Non-curative surgical resection or radiation therapy failing standard treatment, and no standard chemotherapy regimen. Er-positivity and/or PR-positive tumor cells were defined as 1% or more of all tumor cells that stained positively (as confirmed by the site investigator). Her2-negative was defined as 0/1+ on standard immunohistochemical (IHC) testing; An HER2/CEP17 ratio of less than 2.0 or a HER2 gene copy number of less than 4, as assessed by in situ hybridization (ISH), was confirmed by site investigator review.
3. Receipt of any previous systemic anticancer therapy for focal recurrent or metastatic disease.
4. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
5. Measurable lesions meeting RECIST 1.1 criteria or bone-only metastatic lesions (including osteolytic lesions or mixed osteolytic/osteogenic lesions).
6. Adequate organ and bone marrow function, defined as neutrophil count (ANC) ≥ 1500/mm3(1.5 × 109/L) (no growth factor administration within 14 days); Platelet count (PLT) ≥ 100,000/mm3 (100 × 109/L) (no corrective therapy within 7 days); Hemoglobin (Hb) ≥ 9 g/dL (90 g/L) (no corrective therapy used within 7 days); Serum creatinine ≤ 1.5 times the upper limit of normal (ULN) or creatinine clearance ≥ 60 ml/min; Total bilirubin (BIL) ≤ 1.5 times upper limit of normal value (ULN); Aspartate aminotransferase (AST/SGOT) or alanine aminotransferase (ALT/SGPT) ≤ 2.5 times The upper limit of normal (ULN), patients with liver metastases should be ≤ 5×ULN.
7. Use of a medically approved contraceptive method (e.g., an intrauterine device, contraceptive pill, or condom) during the study treatment period and for 3 months after the end of the study treatment period for patients with potential childbearing potential; A negative serum HCG test must have been performed within 72 hours before study entry; And had to be non-lactating.
8. All acute toxic effects prior to antineoplastic therapy resolved to grade 0-1 (according to NCICTCAE version 5.0) or to the level specified in the inclusion/exclusion criteria. Other toxicities, such as alopecia, that were deemed by the investigators not to pose a safety risk to patients were excluded.
9. There is no limit to the number of previous lines of endocrine therapy.
10. The subjects voluntarily joined the study, signed the informed consent form, had good compliance, and cooperated with the follow-up.

Exclusion Criteria:

1. Previous pathological diagnosis of HER2-positive. Patients who were not candidates for endocrine therapy as judged by the investigator. "Patients were included who were symptomatic, had spread to the viscera, and were at risk for life-threatening complications in the short term (including patients with uncontrolled massive exudates [thoracic, pericardial, abdominal], pulmonary lymphangitis, and more than 50% liver involvement)." 3.Patients with brain metastases diagnosed by head CT or MRI. 4.Patients had received any previous CDK4/6 inhibitor therapy. 5.Major surgery, chemotherapy, radiation therapy, any investigational drug, or other anticancer treatment within 2 weeks before study entry.

        6.Any other malignancy was diagnosed within 3 years before study entry, except nonmelanoma
        skin cancer, basal cell or squamous cell skin cancer, or carcinoma in situ of the cervix
        treated with curative intent 7.Human immunodeficiency virus (HIV) infection or known
        acquired immunodeficiency syndrome (AIDS), active hepatitis B (HBV DNA ≥1000 IU/ml),
        hepatitis C (positive hepatitis C antibody and HCV-RNA higher than the lower limit of
        detection of the assay), or co-infection with hepatitis B and C.
        8.In the 6 months prior to study entry, the following occurred: Myocardial infarction,
        severe
        or unstable angina, cardiac dysfunction of NYHA class 2 or higher, persistent arrhythmia of
        class 2 or higher (according to NCICTCAE, version 5.0), atrial fibrillation of any grade,
        coronary or peripheral artery bypass grafting, symptomatic congestive heart failure, or
        cerebrovascular accident (including transient ischemic attack or symptomatic pulmonary
        embolism).
        9.Severe infection (e.g., intravenous antibiotics, antifungal, or antiviral agents
        according to standard practice) within 4 weeks before the first dose or unexplained fever
        >38.5oC during screening/before the first dose.
        10.Inability to swallow, intestinal obstruction, or other factors affecting drug
        administration and absorption.
        11.Known allergies to letrozole or anastrozole, LHRH agonist (goserelin), SHR6390/ placebo,
        or any excipients.
        12.Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell
        transplantation.
        13.Known history of psychotropic drug abuse or drug use. 14.Patients with other serious
        physical or mental illnesses or laboratory abnormalities that may increase the risk of
        participating in the study or interfere with the study results, and those who are
        considered by the investigator to be unsuitable for participation in the study