- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07571551
Perioperative Trial With IO/TKI for Multi-stage Clear Cell Renal Cell Carcinoma (TRIPLE-PATH)
A Prospective, Open-label, Phase II Clinical Trial of Perioperative Toripalimab Plus Lenvatinib for Multi-stage Clear Cell Renal Cell Carcinoma (ccRCC)
The IO/TKI regimens which combines Immune checkpoint inhibitors (IO) with Tyrosine Kinase Inhibitors (TKI) have become the standard first-line option for advanced ccRCC. Currently, IO/TKI regimens are serving as neoadjuvant treatment in arising clinical trials for ccRCC. Although anatomical change reflected by radiological response is reported in most neoadjuvant trials, only few studies focus on evaluation for pathological response in ccRCC.
The TRIPLE-PATH trial is an investigator initiated prospective, open-label phase II trial with the main objective to evaluate the clinical activity of preoperative/neoadjuvant therapy of toripalimab plus lenvatinib as mesured by pathological response of resected primary lesion in multi-stage ccRCC. Patients with ccRCC will be enrolled into 3 different cohorts based on their clinical TNM at the time of screening: localized ccRCC (cT1-2N0M0), locally advanced ccRCC (cT3-4N0M0 or cTanyN1M0), and metastatic ccRCC (cTanyNanyM1). Toripalimab (240mg Q3W) will be administered intravenously on the 1st day, and lenvatinib (20mg QD) will be administered orally once daily of each 3 weeks cycle. Patients in all cohorts will receive 4 cycles of preopertive/neoadjuvant toripalimab (240mg Q3W IV) plus lenvatinib (20mg QD PO), and a subsequent partial/radical nephrectomy 7-10 days after the last cycle. For adjuvant/postoperative treatment, patients who undergo R0 resection presented with cT1-2aN0M0G4/cT2bN0M0G3-4/cT3-4N0M0Gany/cTanyN1M0Gany will receive adjuvant doses of toripalimab (240mg Q3W IV) for 17 cycles; patients who undergo simultaneous resection of all oligometastases considered as "no evidence of disease" (M1 NED) will also receive adjuvant doses of toripalimab (240mg Q3W IV) for 17 cycles; patients who undergo R1 resection or presented with M1 disease cannot be definitely resected will receive postoperative doses of toripalimab (240mg Q3W IV) plus lenvatinib (20mg QD PO) for 17 cycles.
Specific follow-up for the enrolled patients is required in the TRIPLE-PATH trial. Longitudinal CT/MRI is utilized to assess the radiological response. Tissues and body fluid samples collected from the patients will be utilized for biomarker and multi-omic analysis.
The primary endpoint of the TRIPLE-PATH trial is major pathological response (MPR) in the primary lesion according to the pathological response reporting guidelines by the International Neoadjuvant Kidney Cancer Consortium (INKCC). Simon's two-stage minimax design is adopted by TRIPLE-PATH. An initial of 12 patients per cohort (36 in total) will be recruited, following an interim analysis. Recruitment to any cohort will be suspended if MPR is not observed in any patient at the interim analysis. If MPR is observed in at least 1 patient, additional 9 patients will be recruited in each cohort to at most 21 patients. Considering potential 15% dropout rate in each cohort, an anticipation of 25 patients will be recruited for each cohort (75 in total) in this study.
Přehled studie
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 2
Kontakty a umístění
Studijní kontakt
- Jméno: Le Qu, M.D.
- Telefonní číslo: +86 15720625951
- E-mail: septsoul@hotmail.com
Studijní místa
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Jiangsu
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Nanjing, Jiangsu, Čína, 210000
- Nábor
- Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University
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Kontakt:
- Le Qu, M.D.
- Telefonní číslo: +86 15720625952
- E-mail: septsoul@hotmail.com
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Kontakt:
- Junfu Huang
- Telefonní číslo: +86 15123894157
- E-mail: junfuh810@gmail.com
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Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
Inclusion Criteria:
- Patients have fully understood and give written informed consent prior to receive neoadjuvant therapy. Patients with history of major psychiatric disease must be judged able to fully understand the trial, and the explicit consent of family members is required;
- Patients with the ages range from 18 to 80 years old (at the time of signing informed consent);
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0 or 1;
- Patients have at least 1 measurable target lesion according to RECIST v1.1. The target lesion can be biopsied as per protocol.
- Histologically confirmed clear cell RCC;
Patients will be enrolled into 3 separate cohorts based on their clinical TNM at the time of baseline screening:
Cohort 1: localized ccRCC (cT1-2N0M0): the primary tumor in this cohort must meet the subsequent criteria:
The cT1a primary tumor should have ≥10 R.E.N.A.L. score, or locate in renal hilum close to renal artery or its main branch;
Patients with cT1b-2b primary tumors can be directly enrolled;
- In case of necessary, patients will undergo dual radiological examinations using contrast-enhanced CT and MRI to rule out potential invasion of the renal pelvis or perirenal fat as per protocol.
- Cohort 2: locally advanced ccRCC (cT3-4N0M0 or cTanyN1M0);
Cohort 3: metastatic ccRCC (cTanyNanyM1): the patients should be evaluated as suitable for cytoreductive nephrectomy.
Patient have no symptomatic metastatic lesions requiring urgent intervention;
- The sum of the diameters of the other target lesions (excluding the primary tumor) does not exceed the longest diameter of the primary tumor.
- The patients who are treatment-naive, and have not received systemic therapy for any tumor;
Adequate main organ function. The screening laboratory indicators must meet the following criteria:
- Hemoglobin ≥ 90 g/L (Without blood transfusion);
- Platelets count ≥ 100 x 109/L;
- Absolute neutrophil count ≥ 1.5 x 109/L;
- Serum creatinine ≤ 1.5 x ULN, or eGFR > 60 mL/min/1.73m2;
- Total bilirubin ≤ 1.5 mg/dL;
- Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) ≤ 2.5 x ULN for patients without evidence of liver metastases; AST and/or ALT ≤ 5 x ULN for patients with liver metastases;
- Normal CK;
- Normal Troponin T;
- Normal LDH.
- Willingness and ability to comply with planned visits, therapeutic laboratory testing, and other procedures.
Exclusion Criteria:
- Signs of tumor metastasis involving the central nervous system, or radiological evidence of brain metastasis;
- History of malignant tumors other than ccRCC within the previous 5 years, with the exception of malignant tumors that can be expected to be cured with treatment (including but not limited to adequately treated thyroid cancer, carcinoma in situ of the cervix, basal or squamous cell skin cancer, or ductal carcinoma in situ of the breast treated with radical surgery);
- Prior to participating in the study, patients have received prior immune checkpoint inhibitors, investigational drugs or device therapy;
- History of undergoing major surgery (judged by the investigator) within 4 weeks before the first trial dose, are recovering, or are unable to undergo baseline puncture;
- History of severe drug allergy, including but not limited to antibody drugs;
Patients with contraindications to immunotherapy restart, including but not limited to:
- Grade 2-4 immune myocarditis;
- Severe grade 4 proteinuria;
- Severe or life-threatening grade 4 immune hepatitis;
- Severe grade 3-4 immune pneumonitis;
- Severe inflammatory arthritis that significantly affects daily life or quality of life;
- Severe neurological toxicity:
- Myasthenia gravis grade 2-4;
- Guillain-Barre syndrome (GBS) or transverse myelitis of any grade;
- Grade 2-4 encephalitis;
- Severe or life-threatening grade 3-4 pancreatitis;
- Severe or life-threatening bullous disease (grade 3-4);
- Severe grade 3-4 uveitis or episcleritis.
- Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation or long-term corticosteroid therapy.
- Non-resolution of toxicity after previous antineoplastic therapy, i.e., resolution to baseline, CTCAE v5.0 grade 0-1 (excluding alopecia), or inclusion/exclusion criteria. Irreversible toxicities (e.g., hearing loss) that would not reasonably be expected to be exacerbated by the study drug can be included in the study;
- Known history of clinically significant liver disease, including active viral hepatitis (hepatitis B surface antigen (HBsAg) and/or hepatitis B core antibody (HbcAb) positive, HBV DNA>10000 copies /mL or >2000 IU/mL; Hepatitis C virus (HCV) antibody positive and HCV RNA positive), or other active hepatitis, clinically significant moderate to severe cirrhosis;
- Patients with uncontrolled third space effusion requiring repeated drainage, such as pleural effusion, ascites, pericardial effusion, etc. (Patients who do not need drainage of effusion or stop drainage for 3 days without significant increase in effusion can be enrolled);
- Receiving a systemic corticosteroid (prednisone > 10mg/ day or equivalent) or other immunosuppressive medication within 14 days before the first study medication;
Patients with any severe and/or uncontrolled disease, including:
- Hypertension that is not well controlled by antihypertensive medication;
- Unstable angina pectoris or myocardial infarction, coronary artery bypass grafting or stent implantation within 6 months before study medication;
- Grade I or above myocardial ischemia or myocardial infarction, arrhythmia (including QTc≥480ms) and ≥ grade 2 congestive heart failure (New York Heart Association (NYHA) classification); Degree II or above heart block; Left ventricular ejection fraction (LVEF) < 50%;
- Poorly controlled diabetes (fasting blood glucose > 10 mmol/L);
- Patients with urinary protein ≥++ and confirmed 24-hour urinary protein > 1.0g;
- Severe active or uncontrolled infection.
- Patients with or suspected to have active autoimmune diseases, including but not limited to systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, etc.;
- Renal failure requiring hemodialysis or peritoneal dialysis;
- Patients with a history of immunodeficiency, including HIV positive patients, other acquired immunodeficiency diseases, congenital immunodeficiency diseases, or organ transplantation history;
- History of live attenuated vaccine inoculation within 4 weeks before the first study drug or the expected vaccination during the study period;
- History of psychiatric drug abuse and can not quit or have a history of mental disorders;
- Women who are of childbearing potential. Women of childbearing potential must have a negative serum or urine pregnancy test, and must use appropriate methods of contraception.
- The presence of any other severe, acute or chronic medical disease or mental illness or laboratory abnormality, as judged by the investigator, that may increase the risk associated with participation in the study or that may interfere with the interpretation of the results of the study.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
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Experimentální: Experimental: Perioperative toripalimab + lenvatinib followed by a partial/radical nephrectomy
Toripalimab (240mg Q3W) will be administered intravenously on the 1st day of each 3 weeks cycle, and lenvatinib (20mg QD) will be administered orally once daily of each 3 weeks cycle. The patients will receive preoperative/neoadjuvant 4 cycles of toripalimab (240mg Q3W IV) plus lenvatinb (20mg QD PO) followed by a partial/radical nephrectomy 7-10 days after the last cycle. Adjuvant 17 cycles of toripalimab (240mg Q3W IV) will start at 4-8 weeks after surgery, for patients who undergo R0 resection but presented with cT1-2aN0M0G4/cT2bN0M0G3-4/cT3-4N0M0Gany/cTanyN1M0Gany, or undergo simultaneous resection of all oligometastases considered as "no evidence of disease" (M1 NED). Postoperative 17 cycles of toripalimab (240mg Q3W IV) plus lenvatinb (20mg QD PO) will start at 4-8 weeks after surgery, for patients who undergo R1 resection or presented with M1 disease cannot be definitely resected. |
Patients will receive 4 cycles of preoperative/neoadjuvant toripalimab (240mg Q3W IV) followed by a partial/radical nephrectomy 7-10 days after the last cycle. Patients who undergo R0 resection but presented with cT1-2aN0M0G4/cT2bN0M0G3-4/cT3-4N0M0Gany/cTanyN1M0Gany, or undergo simultaneous resection of all oligometastases considered as "no evidence of disease" (M1 NED), will receive 17 cycles of adjuvant toripalimab (240mg Q3W IV), starting at 4-8 weeks after surgery. Patients who undergo R1 resection or presented with M1 disease cannot be definitely resected will receive 17 cycles of postoperative toripalimab (240mg Q3W IV), starting at 4-8 weeks after surgery. Adjustment of dose: For patients with grade 3 or greater adverse events according to CTCAE v5.0 suspected to be caused by toripalimab, the dose can be postponed. In case of SAE, the dose can be discontinued. Dose de-escalation can be decided in patients who achieve MPR in primary lesions by investigators as per protocol.
Ostatní jména:
Patients will receive 4 cycles of preoperative/neoadjuvant lenvatinib (20mg QD PO) of each 3 weeks cycle followed by a partial/radical nephrectomy 7-10 days after the last cycle. Patients who undergo R1 resection or presented with M1 disease cannot be definitely resected will receive 17 cycles of postoperative lenvatinib (20mg) orally once daily of each 3 weeks cycle, starting at 4-8 weeks after surgery. Adjustment of dose: For patients with grade 3 or greater adverse events according to CTCAE v5.0 suspected to be caused by lenvatinib, the dosage can be gradually reduced to 16mg, 12mg and a minimal of 8mg. In case of SAE, the dose can be discontinued. Dose de-escalation can be decided in patients who achieve MPR in primary lesions by investigators as per protocol.
Ostatní jména:
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Major Pathological Response Rate
Časové okno: Within 1 week after nephrectomy
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MPR is defined as the total proportion of viable residual tumor cells in the tumor bed via H-E stained sections of the resected tumor according to the guidelines by INKCC.
Major pathological response rate is defined as the proportion of patients achieving MPR in their primary lesion.
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Within 1 week after nephrectomy
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Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Safety according to Adverse Events
Časové okno: From baseline to 12 weeks after last dose
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The frequency and percentage of patients experiencing adverse events (AEs) according to Common Terminology Criteria for Adverse Events version 5.0 (CTCAE v5.0).
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From baseline to 12 weeks after last dose
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Surgical morbidity
Časové okno: Up to 4 weeks after nephrectomy
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Surgical morbidity or complications rate after neoadjuvant therapy.
Intraoperative adverse incidents are defined as adverse events due to surgical intervention occurring between skin incision and closure and are evaluated according to the EAU intraoperative AI classification (EAUiaiC).
Postoperative complications are evaluated according to Clavien-Dindo classification system.
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Up to 4 weeks after nephrectomy
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Best Overall Response
Časové okno: From baseline to 12 weeks
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BOR is defined as the best response state among all the longitudinal evaluation according to RECIST v1.1.
A modified BOR only focusing on metastases will be specially utilized for patients in cohort 3.
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From baseline to 12 weeks
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Down-staging Rate of Primary T Stage
Časové okno: From baseline to 12 weeks
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The T stage of the primary lesion will be evaluated according to the 8th edition of AJCC at baseline and surgery to reflect the change in T stage of the primary lesion after neoadjuvant therapy.
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From baseline to 12 weeks
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Change in R.E.N.A.L. Score of Primary Lesion
Časové okno: From baseline to 12 weeks
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The R.E.N.A.L. score can reflect the difficulty of the nephrectomy.
The R.E.N.A.L. scores of the patients before and after neoadjuvant therapy will be evaluated based on the CT/MRI scan.
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From baseline to 12 weeks
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Rate of R0 Resection
Časové okno: Within 1 week after nephrectomy
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R0 resection is defined as no visible tumor cells were observed at the surgical margins of the pathological specimens.
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Within 1 week after nephrectomy
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Change in Tumor Thrombus
Časové okno: From baseline to 12 weeks
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For patients with TT at baseline, the change of TT according to Mayo's classification will be recorded.
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From baseline to 12 weeks
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Change in Renal Function
Časové okno: Up to 1 year after nephrectomy
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The change in renal function before and after neoadjuvant therapy,also before and after nephrectomy will be evaluated by eGFR.
The eGFR will be calculated using the CKD-EPI formula.
Split renal function recovery rate will be report in patients who undergo partial nephrectomy.
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Up to 1 year after nephrectomy
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Progression Free Survival
Časové okno: Up to 5 years after treatment
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PFS is defined as the time from enrollment to progression disease, recurrence, distant metastasis or death from any cause.
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Up to 5 years after treatment
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Disease Free Survival
Časové okno: Up to 5 years after nephrectomy
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DFS is defined as the time from completion of nephrectomy to recurrence, distant metastasis or death from any cause.
DFS will only be reported in the cohort 1 and 2.
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Up to 5 years after nephrectomy
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Overall Survival
Časové okno: Up to 5 years after treatment
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OS is defined as the time from enrollment to death from any cause.
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Up to 5 years after treatment
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Další výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Tissue-based Biomarker Analysis
Časové okno: Up to 2 years after treatment
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Biopsied and resected tumor specimens will be collected for revealing changes in the tumor microenvironment.
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Up to 2 years after treatment
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Peripheral Plasma-based Biomarker Analysis
Časové okno: Up to 2 years after treatment
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Baseline, during-treatment, pre-operative, and postoperative peripheral plasma will be collected for revealing potential cycling biomarkers.
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Up to 2 years after treatment
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Radiological and Pathological Biomarker Analysis
Časové okno: Up to 2 years after treatment
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The radiological and pathological information during the treatment process will be collected.
A prediction model related to therapeutic efficacy and prognosis is anticipated to be developed.
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Up to 2 years after treatment
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Spolupracovníci a vyšetřovatelé
Sponzor
Vyšetřovatelé
- Vrchní vyšetřovatel: Le Qu, M.D., Jinling Hospital, China
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Aktuální)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Urogenitální onemocnění
- Urogenitální novotvary
- Novotvary podle místa
- Novotvary
- Mužská urogenitální onemocnění
- Onemocnění ledvin
- Urologická onemocnění
- Ženské urogenitální onemocnění
- Ženské urogenitální onemocnění a těhotenské komplikace
- Novotvary podle histologického typu
- Novotvary, žlázové a epiteliální
- Adenokarcinom
- Urologické novotvary
- Karcinom
- Novotvary ledvin
- Karcinom, renální buňka
- Toripalimab
- Spartalizumab
- Lenvatinib
- multi-kinase inhibitor 108600
Další identifikační čísla studie
- DZQH-KYLL-26-05
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
produkt vyrobený a vyvážený z USA
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