JSKN033 Combination Therapy in Subjects With Advanced Cervical Cancer

Inclusion Criteria: 1. Voluntarily participate and sign the informed consent form. 2. Age ≥ 18 years old, male or female. 3. Eastern Cooperative Oncology Group performance status (ECOG PS) score of 0 or 1. 4. Expected survival ≥ 3 months. 5. Histologically or cytologically confirmed persistent, recurrent, or metastatic (FIGO stage IVB) cervical cancer unsuitable for curative surgery and/or curative radiotherapy, meeting the following criteria: 1. Pathological types include squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma; 2. No prior systemic therapy for recurrent or metastatic cervical cancer. 6. At least one measurable lesion per RECIST 1.1 at baseline. 7. Agree to provide recently archived or fresh tumor tissue samples. 8. Adequate organ function. 9. Female subjects of childbearing potential or male subjects whose partners are of childbearing potential agree to use effective contraceptive measures. Female subjects of childbearing potential must have a negative serum/urine pregnancy test within 7 days before the first dose. 10. Be able and willing to comply with the visits, treatment plans, laboratory tests, and other study-related procedures specified in the study protocol. Exclusion Criteria: 1. Complicated with other malignant tumors within 3 years before the first dose, except for tumor types that have achieved clinical cure through local treatment with extremely low recurrence risk. 2. History of brainstem, meningeal metastasis, spinal cord metastasis or compression, or carcinomatous meningitis; presence of active brain metastasis. 3. Screening imaging shows tumor invasion, compression, or occurrence in surrounding important organs or risk of esophagotracheal fistula or esophagopleural fistula, except those judged by the investigator and medical monitor to not affect the patient's enrollment and administration. 4. Prior treatment with topoisomerase I inhibitors or antibody-drug conjugates containing topoisomerase I inhibitors. 5. Inadequate washout period of previous therapy. 6. Presence of the risk factors related to interstitial lung disease (ILD) or non-infectious pneumonia: 7. Presence of clinically severe respiratory impairment caused by pulmonary disease complications. 8. Presence of cardiovascular and cerebrovascular diseases or cardiovascular and cerebrovascular risk factors. 9. Gastrointestinal abnormalities with obvious clinical manifestations. 10. Significant serous effusion. 11. Active autoimmune diseases requiring systemic treatment. 12. Uncontrolled infection. 13. Toxicity of previous anti-tumor treatment has not fully or partially recovered. 14. History of allogeneic bone marrow or organ transplantation. 15. Known allergy to any component of the study drug/platinum, or history of severe allergic reactions to other antibody drugs. 16. Pregnant and/or lactating women, or planning to become pregnant during the study period. 17. Known history of mental illness, substance abuse, alcoholism, etc., or other situations that the investigator deems may affect the safety or compliance of the study drug treatment. 18. Any other previous or current diseases, treatments, or laboratory test abnormalities that the investigator deems may confuse the study results, affect the patient's full participation in the study, or participation in the study may not be in the best interest of the patient. 19. Local or systemic diseases caused by non-malignant tumors, or diseases or symptoms secondary to tumors, which may lead to high medical risks and/or uncertainty in survival assessment, such as tumor-related leukemia reaction (white blood cell count \> 20×10⁹/L), cachexia manifestations, etc. 20. Known contraindications to bevacizumab or allergy to its components, or the medical conditions affecting its safe use (Note: Applicable only to subjects planned to receive bevacizumab).