[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"mesothelioma-malignant-advanced\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:mesothelioma-malignant-advanced":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":31,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100602668","partial-pleurectomy-surgery-for-unresectable-pleural-mesothelioma-100602668",false,"NCT07126509","Partial Pleurectomy (Surgery) for Unresectable Pleural Mesothelioma","A Pilot Study of Partial Pleurectomy in Borderline and Unresectable Pleural Mesothelioma","Inclusion Criteria\n\n* Patients must have histologically confirmed epithelioid subtype pleural mesothelioma, as determined by surgical (i.e. VATS) biopsy.\n* Disease confined to the unilateral hemithorax.\n* Disease that is classified as unresectable or borderline resectable:\n* Unresectable disease is defined by cross sectional imaging (CT or MRI) demonstrating invasion of unresectable mediastinal structures (heart, great vessels, esophagus) or spine, unresectable invasion of the chest wall (multifocal chest wall invasion or apical chest wall invasion), or disease outside intended resection field.\n* Borderline resectable disease is defined by cross sectional imaging (CT or MRI) demonstrating extensive pulmonary parenchymal invasion (anticipated need for anatomic resection or complex wedge resection to clear disease) or extensive\u002Fbulky disease of (1) the diaphragm or sulci (anticipated need for diaphragm resection and reconstruction to clear disease), or (2) the chest wall (anticipated need for chest wall resection and reconstruction to clear disease). Disease with pathologically proven hilar or mediastinal lymph node involvement.\n* Successful completion of at least 6 weeks of systemic induction therapy (regimen according to treating physician choice, including the below) with no unresolved adverse event that would preclude surgery:\n* Platinum agent, pemetrexed, +\u002F- bevacizumab\n* Platinum agent, pemetrexed, pembrolizumab\n* Ipilimumab\u002Fnivolumab\n* Age ≥18 years.\n* ECOG performance status ≤1.\n* Patients must have adequate organ and marrow function as defined below:\n\n  * leukocytes ≥3,000\u002FmcL\n  * absolute neutrophil count ≥1,500\u002FmcL\n  * platelets ≥100,000\u002FmcL\n  * PT\u002FINR \\>1.5\n  * PTT \\>Upper limit of normal\n  * total bilirubin within normal institutional limits\n  * AST(SGOT)\u002FALT(SGPT) ≤2.5 × institutional upper limit of normal\n  * creatinine within normal institutional limits OR\n  * creatinine clearance ≥60 mL\u002Fmin\u002F1.73 m2 for patients with creatinine levels above institutional normal.\n* Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial.\n* For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated.\n* Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load.\n* 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 Classification21. To be eligible for this trial, patients should be class 2B or better.\n* Review by multidisciplinary treatment conference consisting of mesothelioma surgeons, radiologists, pathologists, medical oncologists, and palliative care physicians. Date of review will be documented in on the patient's elgibility checklist\n* Prior or concurrent enrollment to UChicago's Mesothelioma Biobank (IRB15-0443).\n* Ability to understand and the willingness to sign a written informed consent document.\n\nExclusion Criteria\n\n* Patients with biphasic or sarcomatoid pleural mesothelioma.\n* Patients with metastatic disease or disease which extends to the abdominal cavity or subdiaphragm as identified on post-induction therapy cross sectional imaging (CT, MRI, or PET).\n* Patients who demonstrate disease progression during or following induction therapy.\n* FEV1 \\\u003C 50% and\u002For postoperative predicted DLCO \\\u003C 50%.\n* Patients who are receiving any other investigational agents.\n* Patients with uncontrolled intercurrent illness.\n* Prior malignancy active 2 years prior to registration except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the prostate, cervix, or breast, or papillary thyroid.","ALL","18 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23],"NA","Purpose of the study: The main purpose of this research study is to see if a surgery procedure (limited partial pleurectomy and decortication) helps symptoms in people who have cancer that is unresectable that might not be able to be removed completely. This is called unresectable cancer. This study will also help the research team learn more about the types of symptoms and quality of life for people who have undergone this surgery, the number of complications following , and the time from surgery to starting other therapy. Th e study team also wants to see see the overall survival of people who have had this procedure as part of their care.\n\nWhat will be done as part of research on this study:\n\n* Surgery (Partial Pleurectomy - surgery to remove lining of lungs)\n* The research team will also ask study participants questions about their symptoms through questionnaires at certain times after surgery.\n\nHow long this study will last:\n\nParticipation in this research (pre-surgery, surgery and follow-up) will last for about 2 years.\n\nConfidentiality: All personal information will be kept confidential, and data will be used only for research purposes.\n\nContact Information: For more information about this study, please contact PhaseIICRA@medicine.bsd.uchicago.edu",[26,27,28,29,30],"Mesothelioma","Mesothelioma; Lung","Mesotheliomas Pleural","Mesothelioma Malignant Advanced","Mesothelioma, Malignant",[32],"PLEURECTOMY","RECRUITING","2026-02-13",{"date":36,"type":37},"2026-02-17","ACTUAL",{"date":39,"type":37},"2025-12-02",{"date":41,"type":20},"2028-12-01",{"name":43,"class":44},"University of Chicago","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":5},"100453770","phase-2-first-line-sintilimab-combined-with-anlotinib-and-platinum-doublet-chemotherapy-in-malignant-pleural-mesothelioma-100453770","NCT05188859","First Line Sintilimab Combined With Anlotinib and Platinum Doublet Chemotherapy in Malignant Pleural Mesothelioma","Study of Sintilimab Combined With Anlotinib and Platinum-Containing Dual-Agent Chemotherapy as First Line Therapy in Malignant Pleural Mesothelioma: A Single Arm, Open-label, Prospective Phase II Trial","Inclusion Criteria:\n\n* Sign written informed consent before implementing any trial-related procedures;\n* Age ≥ 18 years old.\n* Histologically confirmed, unresectable or inoperable or locally advanced (IIIB stage), recurrent or metastatic (IV stage) malignant pleural mesothelioma.\n* According to the modified version of the evaluation criteria for the efficacy of solid tumor (mRECIST1.1 ), patients have at least one imaging lesion can be measured;\n* Patients have not received any systemic anti-tumor therapy for advanced\u002Fmetastatic diseases in the past. Patients who have previously received platinum-containing adjuvant \u002F neoadjuvant chemotherapy, or radical radiotherapy and chemotherapy for advanced diseases, such as the interval between disease progression or recurrence and the end of the last chemotherapeutic drug treatment at least 6 months, are allowed to be enrolled in this study.\n* Patients with brain metastasis who are asymptomatic or stable after local treatment are allowed to be included in this study, as long as they meet the following conditions:\n\n  1. There are measurable lesions outside the central nervous system.\n  2. No central nervous system symptoms or no aggravation within at least 2 weeks.\n  3. Those who do not need glucocorticoid therapy or stop glucocorticoid therapy within 7 days before the first study drug administration.\n* Patients are allowed to receive palliative radiotherapy, but the end of radiotherapy is within 7 days before the administration of the first study drug.\n* ECOG score 0-1 points;\n* The expected survival time was \\> 3 months,\n* For adequate organ function, the patients need to meet the following laboratory indexes:\n\n  1. the absolute value of neutrophils (ANC) ≥ 1.5x109\u002FL without granulocyte colony stimulating factor in the past 14 days.\n  2. in the last 14 days without blood transfusion, the platelet count was ≥ 100x109\u002FL.\n  3. in the absence of blood transfusion or the use of erythropoietin in the past 14 days, hemoglobin \\> 9g\u002FdL;\n  4. Total bilirubin ≤ 1.5 × normal upper limit (ULN); for example,if total bilirubin \\> 1.5 × ULN but direct bilirubin ≤ ULN is also allowed to enter the group\n  5. aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN (patients with liver metastasis allow ALT or AST ≤ 5 × ULN).\n  6. Serum creatinine ≤ 1.5 × ULN and creatinine clearance (calculated by Cockcroft-Gault formula) ≥ 60ml;\n  7. Coagulation function is good, defined as international standardized ratio (INR) or prothrombin time (PT) ≤ 1.5 times ULN;\n  8. Normal thyroid function is defined as thyroid stimulating hormone (TSH) within the normal range. If the baseline TSH is beyond the normal range, subjects with total T3 (or FT3) and FT4 within the normal range can also be enrolled.\n  9. Myocardial enzyme spectrum is within the normal range (if the researchers comprehensively judge that there is no clinical significance of simple laboratory abnormalities can also be included in the group); (optional)\n* For female patients at childbearing age, they should undergo a urine or serum pregnancy test within 3 days before receiving the first study drug administration (day 1 of cycle 1) and the results be negative. If the urine pregnancy test results cannot be confirmed as negative, a blood pregnancy test is required. Women of non-childbearing age are defined as at least 1 year after menopause or have undergone surgical sterilization or hysterectomy.\n* If there is a risk of pregnancy, all patient (male or female) are required to use contraception with an annual failure rate of less than 1% during the entire treatment period until 120 days after the last study drug administration (or 180 days after the last chemotherapy drug administration).\n\nExclusion Criteria:\n\n* Diagnosis of malignant diseases other than malignant pleural mesothelioma (excluding radical skin basal cell carcinoma, skin squamous cell carcinoma, and \u002F or radical resection of carcinoma in situ) within 5 years before the first administration\n* Currently participating in interventional clinical research treatment, or receiving other research drugs or using research instruments within 4 weeks before the first administration;\n* Previous usage of the following treatments: anti-PD-1, anti-PD-L1 or anti-PD-L2 drugs, for another stimulating or synergistic inhibition of T cell receptors (for example, CTLA-4, OX-40, CD137) drug;\n* Within 2 weeks before the first administration, they received systemic systemic therapy with anti-tumor indications of proprietary Chinese medicine or immunomodulatory drugs (including thymosin, interferon, interleukin, except for controlling local use of pleural effusion)\n* Active autoimmune diseases requiring systemic treatment (such as the use of disease-relieving drugs, glucocorticoids or immunosuppressants) occurred within 2 years before the first administration. Alternative therapy (such as thyroxine, insulin or physiological glucocorticoids for adrenal or pituitary insufficiency) are not considered systemic therapy.\n* The patients are received systemic glucocorticoid therapy (excluding nasal, inhaled or other topical glucocorticoids) or any other form of immunosuppressive therapy within 7 days before the first administration.\n\nNote: The use of physiological doses of glucocorticoids (≤10 mg\u002Fday prednisone or equivalent drugs) is allowed;\n\n* There are clinically uncontrollable pleural effusion \u002F ascites (patients who do not need drainage or stop drainage for 3 days without a significant increase in effusion can be enrolled in the group)\n* Known allogeneic organ transplantation (except corneal transplantation) or allogeneic hematopoietic stem cell transplantation;\n* Those who are known to be allergic to the active ingredients or excipients of Sintilimab in this study.\n* Patients with multiple factors affecting oral drugs (such as inability to swallow, gastrointestinal resection, chronic diarrhea and intestinal obstruction, etc.)\n* Symptomatic or uncontrolled brain metastasis;\n* Active hemoptysis (at least 2.5ml or 1\u002F2 teaspoon of blood was spit out at a time) 3 months before the first study drug administration;\n* Imaging showed that there were tumors invading \u002F infiltrating large blood vessels or bleeding tendency assessed by researchers or radiologists;\n* Received major surgery (except for surgery for the purpose of biopsy) within 4 weeks before the first study drug administration, or is expected to undergo major surgery during the study period;\n* Severe unhealed wound ulcers or fractures;\n* Minor surgery was performed within 48 hours before first receiving the study drug (outpatient \u002F inpatient surgery requiring local anesthesia, including central venous catheterization);\n* Use aspirin (\\>325 mg\u002Fday) or other non-steroidal anti-inflammatory drugs that are known to inhibit platelet function for 10 consecutive days (within 10 days before receiving the first dose of study drug) at present or in the near future;\n* Current or recent treatment with full-dose oral or parenteral anticoagulants or thrombolytic agents for 10 consecutive days (within 10 days before receiving the first study drug) Note: Prophylactic use of low-dose anticoagulants is permitted: low-dose warfarin (≤ 1mg\u002Fd) is allowed for preventive purposes on the premise that the international standardized ratio of prothrombin time (INR) ≤ 1.5. Low-dose heparin (≤ 12000 U\u002Fe d) or low-dose aspirin (≤ 100mg\u002Fd).\n* Hereditary bleeding tendency or coagulation dysfunction, or history of thrombosis;\n* Did not fully recover from toxicity and \u002F or complications caused by any intervention (i.e., ≤ level 1 or reached baseline, excluding fatigue or hair loss) before starting treatment;\n* Known human immunodeficiency virus (HIV) infection history (i.e. HIV 1\u002F2 antibody positive)\n* Untreated active hepatitis B (defined as HBsAg positive and the number of HBV-DNA copies detected is greater than the upper limit of the normal value of the laboratory in the research center).\n\nNote: hepatitis B subjects who meet the following criteria can also be enrolled in the group:\n\n1. Before the first administration, the HBV viral load is less than 1000 copies\u002Fml (200 IU\u002Fml), and the patients should receive anti-HBV treatment during the entire study drug treatment period to avoid viral reactivation;\n2. For patients with anti-HBc (+), HBsAg (-), anti-HBs (-) and HBV viral load (-), there is no need to receive preventive anti-HBV therapy. However, the virus needs to be closely monitored for reactivation\n\n   * Active HCV infection subjects (HCV antibody positive and HCV-RNA level higher than the lower limit of detection)\n   * Live vaccine is given within 30 days before the first administration (cycle 1, day 1).\n\nNote: It is allowed to receive inactivated virus vaccine for seasonal influenza within 30 days before the first administration; however, it is not allowed to receive live attenuated influenza vaccine for intranasal administration..\n\n* Pregnant or lactating women;\n* There are any serious or uncontrollable systemic diseases, such as\n\n  1. significant abnormalities in rhythm, conduction, or morphology of resting electrocardiogram and serious and uncontrollable symptoms, such as complete left bundle branch block, second-degree cardiac block, ventricular arrhythmia or atrial fibrillation.\n  2. unstable angina pectoris, congestive heart failure, chronic heart failure with New York Heart Association (NYHA) grade ≥ 2;\n  3. any arterial thrombosis, embolism or ischemia occurred within 6 months before treatment, such as myocardial infarction, unstable angina pectoris, cerebrovascular accident or transient ischemic attack;\n  4. Blood pressure control is not satisfactory (systolic blood pressure \\> 140mmHg, diastolic blood pressure \\> 90mmHg).\n  5. within 1 year before the first administration, there is a history of non-infectious pneumonia requiring glucocorticoid treatment, or currently there is clinically active interstitial lung disease;\n  6. active pulmonary tuberculosis;\n  7. active or uncontrolled infections requiring systemic treatment;\n  8. clinically active diverticulitis, abdominal abscess, gastrointestinal obstruction.\n  9. liver diseases such as liver cirrhosis, decompensated liver disease, acute or chronic active hepatitis;\n  10. poorly controlled diabetes (fasting blood glucose (FBG) \\> 10mmol\u002FL);\n  11. patients with urinary protein ≥ + + and confirmed 24-hour urinary protein quantity \\> 1.0g;\n  12. patients with mental disorders and unable to cooperate with treatment\n* At the discretion of the investigator, there are patients with serious concomitant disease that compromises patient safety or affects the patient's completion of the study; The investigator believes that there are other potential risks and is not suitable for participation this research.",{"count":54,"type":20},29,[56],"PHASE2","This study is a single-arm, open-lable, single-center phase II clinical trial for patients with advanced or metastatic pleural mesothelioma. The aim of this study was to observe and evaluate the efficacy and safety of Sintilimab combined with Anlotinib hydrochloride and platinum-containing dual-agent chemotherapy as first-line therapy in malignant pleural mesothelioma.",[30,59,29],"Mesothelioma, Malignant Pleural","2025-05-27",{"date":62,"type":37},"2025-05-31",{"date":64,"type":37},"2024-09-01",{"date":66,"type":20},"2027-09",{"name":68,"class":44},"Cancer Institute and Hospital, Chinese Academy of Medical Sciences"]