Induction Pembrolizumab and Chemotherapy Followed by Pembrolizumab Before Chemoradiation and Pembrolizumab Maintenance Compared to Standard Chemoradiation With Pembrolizumab Followed by Pembrolizumab Maintenance in High-Risk Cervical Cancer
A legfontosabb adatok
- Ki végzi
- National Cancer Institute (NCI)
- Hol
- Manati és San Juan (Puerto Rico)Mind a 2 helyszín megnézéseMég 1 másik országban, 345 helyszínen
- Azonosító
- Állapot
- Toboroz
- Fázis
- 3. fázis
- Résztvevők
- 336 fő, tervezett
- Kezdés
- 2025. nov. 5.
- Várható befejezés
- 2030. dec. 31.
- A vizsgálat típusa
- Beavatkozással járó, 2 csoportAz egyik csoport egy már használt kezelést kap, összehasonlításként.
- A vizsgált kezelések
- Biospecimen Collection
- Brachytherapy
- Carboplatin
- Chest Radiography
- Cisplatin
- Computed Tomography
- External Beam Radiation Therapy
- Intensity-Modulated Radiation Therapy
- Magnetic Resonance Imaging
- Paclitaxel
- Pembrolizumab
- Positron Emission Tomography
- A regiszteradat frissítve
- 2026. november 9.
Ki vehet részt
MI-összefoglaló
A vizsgálat saját részvételi feltételeiből. Gép olvasta ki az oldalon álló regiszterszövegből, ezért tévedhet. Hogy ki vehet részt, azt a lenti regiszterszöveg és a vizsgálat csapata dönti el.
A vizsgálat újonnan diagnosztizált, lokálisan előrehaladott méhnyakrákos nőket keres, akiknél a daganat a közeli szövetekbe nőtt, és a nyirokcsomókat is érintheti. A vizsgálat azt hasonlítja össze, mi történik, ha a szokásos kemoradioterápia előtt kemoterápiát és pembrolizumabot is adnak.
- Életkor
- 18 éves vagy idősebb
- Nem
- Csak nők
- A betegség stádiuma
- Újonnan diagnosztizált laphámsejtes, adenocarcinoma vagy adenosquamosus méhnyakrák, IIIA, IIIB, IIIC1, IIIC2 vagy IVA stádium (T3 vagy T4 betegség, nyirokcsomó-érintettséggel vagy anélkül). Nincs áttét a T12/L1 szint feletti paraaortikus nyirokcsomókban.
- Korábbi kezelés
- Nem volt korábban műtét, sugárkezelés vagy gyógyszeres kezelés méhnyakrák miatt. Nem volt korábban immunterápia. Nem volt korábban kismedencei sugárkezelés semmilyen betegség miatt. A teljes méhet nem távolították el.
A részvétel fő kizáró okai
- Terhesség vagy szoptatás
- Aktív fertőzés, amelyhez vénán át adott antibiotikum kell
- Immunhiány, hosszú távú, napi 10 mg prednizolon-egyenértéket meghaladó szteroidkezelés vagy más immunszuppresszív kezelés
- Aktív autoimmun betegség, amelyet az elmúlt 2 évben kezeltek
- Szteroidot igénylő tüdőgyulladás (pneumonitis) a kórelőzményben, vagy jelenlegi pneumonitis
A regiszter feltételei, szó szerint
Mind a 5 feltétel megnézéseKevesebb
Ki vehet részt
- Patients must have pathologically confirmed newly diagnosed cervical cancer. Eligible pathologic types: squamous cell carcinoma, adenocarcinoma, adenosquamous cell carcinoma
- Patients must have locally advanced cervical cancer (LACC) with T3 or T4 disease with or without lymph node involvement:; IIIA (T3aN0M0); IIIB (T3bN0M0); IIIC1(T3aN1M0, T3bN1M0); IIIC2 (T3aN2M0, T3bN2M0); IVA (T4aN0M0, T4aN1M0, T4aN2M0) No prior hysterectomy defined as removal of the entire uterus; NOTE: prior partial/subtotal hysterectomy for reasons other than cervical cancer are eligible to participate in the study. No plan to perform a hysterectomy as part of initial cervical cancer therapy; No paraaortic lymph node (PALN) metastases above the T12/L1 interspace
- Note: Nodal status can be confirmed by imaging (CT, MRI, or PET/CT), fine needle aspirate/core biopsy, extra peritoneal biopsy, laparoscopic biopsy, or lymphadenectomy; Radiologic definition of lymph node staging:
- N1:; One or more pelvic lymph nodes with short axis diameter of ≥ 15 mm (axial plane) by CT or MRI, and/or; One or more pelvic lymph nodes with short axis diameter of ≥ 10 mm and standardized uptake value maximum (SUVmax) ≥ 2.5 by fludeoxyglucose (FDG)-PET
- N2:; One or more para-aortic lymph node with short axis diameter of ≥ 15 mm (axial plane) by CT or MRI, and/or; One or more para-aortic lymph node with short axis diameter of ≥ 10 mm and SUVmax ≥ 2.5 by FDG-PET; No prior definitive surgical, radiation, or systemic therapy for cervical cancer; No prior immunotherapy; No prior pelvic radiation therapy for any disease; Age ≥ 18; Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2; Not pregnant and not nursing; Absolute neutrophil count (ANC) ≥ 1,500 cells/mm\^3; Platelets ≥ 100,000 cells/mm\^3; Hemoglobin ≥ 8 g/dl (Note: The use of transfusion or other intervention to achieve hemoglobulin [Hgb] ≥ 8 g/dl is acceptable); Creatinine clearance (CrCL) of ≥ 50 mL/min by the Cockcroft-Gault formula; Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN) (patients with known Gilbert's disease who have bilirubin level ≤ 3 x institutional ULN may be enrolled); Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 x institutional ULN; Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, patients should be class 2B or better; No active infection requiring parenteral antibiotics; No live vaccine within 30 days prior to registration. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacille Calmette Guerin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines are live attenuated vaccines and are not allowed; No diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days prior registration; No active autoimmune disease that has required systemic treatment in past 2 years (i.e., with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment and is allowed; No history of (non-infectious) pneumonitis that required steroids, or current pneumonitis; No history of allergic reaction to the study agent(s) or compounds of similar chemical or biologic composition to the study agent(s) (or any of its excipients)
Helyszínek itt: Puerto Rico
Még 1 másik országban, 345 helyszínen
- Doctors Cancer CenterManati, Puerto RicoContact: Luis J. Santos Reyes (principal investigator)Résztvevőt keres
- Centro Comprensivo de Cancer de UPRSan Juan, Puerto RicoContact: Luis J. Santos Reyes (principal investigator)Résztvevőt keres
A vizsgálatról
Mit akar kideríteni a vizsgálat
This phase III trial compares the addition of induction chemotherapy, with carboplatin, paclitaxel and pembrolizumab, to chemotherapy and radiation, with cisplatin and pembrolizumab followed by pembrolizumab maintenance for the treatment of patients with cervical cancer that has spread to nearby tissue or lymph nodes (locally advanced). Carboplatin is in a class of medications known as platinum-containing compounds. It works in a way similar to the anticancer drug cisplatin, but may be better tolerated than cisplatin. Carboplatin works by killing, stopping or slowing the growth of cancer cells. Paclitaxel is in a class of medications called antimicrotubule agents. It stops cancer cells from growing and dividing and may kill them. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Radiation therapy uses high energy x-rays, particles, or radioactive seeds to kill cancer cells and shrink tumors. Cisplatin is in a class of medications known as platinum-containing compounds. It works by killing, stopping or slowing the growth of cancer cells. Adding induction chemotherapy to the usual treatment of chemotherapy and radiation followed by maintenance may be more effective in treating patients with high risk, locally advanced cervical cancer.
A vizsgálat 2 csoportja
- Arm 1 (Standard care)Már használt kezelés, összehasonlításként
CHEMORADIATION: Patients receive cisplatin IV QW for 5 weeks and pembrolizumab IV over 30 minutes Q3W for 5 doses. Patients also undergo radiation therapy with EBRT or IMRT once daily 5 days per week for 25-29 treatments in weeks 1-5 followed by brachytherapy up to twice per week for 4-5 treatments in weeks 5-7. Treatment is given in the absence of disease progression or unacceptable toxicity MAINTENANCE: Patients receive pembrolizumab IV over 30 minutes Q6W for 14 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo PET scan, CT scan, chest x-ray and/or MRI and blood sample collection throughout the study.
Kezelés: Biospecimen Collection, Brachytherapy, Chest Radiography, Cisplatin, Computed Tomography, External Beam Radiation Therapy, Intensity-Modulated Radiation Therapy, Magnetic Resonance Imaging, Pembrolizumab és Positron Emission Tomography
- Arm 2 (induction and standard care)A vizsgált kezelés
INDUCTION: Patients receive carboplatin IV and paclitaxel IV QW on weeks 1-3 and pembrolizumab IV over 30 minutes Q3W on week 1 for each cycle. Cycles repeat every 3 weeks for 2 cycles in the absence of disease progression or unacceptable toxicity. CHEMORADIATION: Patients receive cisplatin IV QW for 5 weeks and pembrolizumab IV over 30 minutes every Q3W for 5 doses. Patients also undergo radiation therapy with EBRT or IMRT once daily 5 days per week for 25-29 treatments in weeks 7-11 followed by brachytherapy up to twice per week for 4-5 treatments in weeks 11-13. Treatment is given in the absence of disease progression or unacceptable toxicity MAINTENANCE: Patients receive pembrolizumab IV over 30 minutes Q6W for 14 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo PET scan, CT scan, chest x-ray and/or MRI and blood sample collection throughout the study.
Kezelés: Biospecimen Collection, Brachytherapy, Carboplatin, Chest Radiography, Cisplatin, Computed Tomography, External Beam Radiation Therapy, Intensity-Modulated Radiation Therapy, Magnetic Resonance Imaging, Paclitaxel, Pembrolizumab és Positron Emission Tomography
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakAdatok és források
- Regiszteradat
- Szerepel a ClinicalTrials.gov-on.
- Hivatalos cím
- A Phase III Study of Induction Pembrolizumab and Chemotherapy Followed by Chemoradiation and Pembrolizumab vs Chemoradiation and Pembrolizumab Both Followed by Pembrolizumab for High Risk Locally Advanced Cervical Cancer
- MI-összefoglaló
- A vizsgálat saját részvételi feltételeiből. Gépi kiolvasás: 2026. november 12.
- A regiszteradat frissítve
- 2026. november 9.