Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04552977
Other study ID # GBM-IIT-SHR3162-TMZ
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date September 2020
Est. completion date August 2022

Study information

Verified date September 2020
Source Shandong Cancer Hospital and Institute
Contact Jinming Yu, Ph.D, M.D
Phone 13806406293
Email sdyujinming@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a one arm, open, single center phase II study. The main purpose of this study was to evaluate the efficacy and safety of fluzoparil combined with temozolomide in patients with recurrent glioblastoma.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date August 2022
Est. primary completion date August 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

1. Voluntary participation and written informed consent;

2. The age was 18-70 years old, with no gender limit;

3. Supratentorial space occupying lesions were diagnosed as glioblastoma by pathology;

4. Patients received standard radiotherapy and temozolomide concurrent chemotherapy after surgery, and the interval between the last radiotherapy and the last radiotherapy was = 4 weeks (pseudo progression should be excluded);

5. MRI confirmed that the tumor had definite recurrence. The diameter of the enhancement focus was more than 1 cm and more than 2 layers (layer spacing was 5 mm), or the recurrence was confirmed by pathology after re biopsy or operation;

6. The recurrence site or other reasons can not be resected;

7. The methylation status of MGMT promoter had been detected or was willing to be detected before enrollment;

8. According to recist1.1, there was at least one measurable lesion;

9. KPS score = 60 points;

10. The tablets can be swallowed normally;

11. The expected survival time was more than 3 months;

12. Sufficient organs and bone marrow function. The definition is as follows.

1. Neutrophil count (ANC) = 1500 / mm3 (1.5 ×109 / L);

2. Platelet count (PLT) = 100000 / mm3 (100 × 109 / L);

3. Hemoglobin (HB) = 9 g / dl (90 g / L);

4. Serum albumin = 2.8 g / dl;

5. Serum creatinine = 1.5 times the upper limit of normal value (ULN) or creatinine clearance rate = 60 ml / min;

6. Total bilirubin (TB) = 1.5 × ULN, or total bilirubin (TB) > 1.5 × ULN, but direct bilirubin (DBIL) = 1 × ULN; patients with liver metastasis should be = 2 × ULN;

7. The level of AST / SGOT or ALT / SGPT should be = 2.5 × ULN and = 5 × ULN in patients with liver metastasis;

8. Left ventricular ejection fraction (LVEF) = 50%, QTc < 450 ms in male and < 470ms in female;

13. The international normalized ratio (INR) of prothrombin time was =1.5 and activated partial thromboplastin time (APTT) were =1.5 times the upper limit of normal value in patients who had not received anticoagulant therapy. Patients receiving full dose or parenteral anticoagulant therapy can enter the clinical trial as long as the dosage of anticoagulant drugs is stable for at least 2 weeks before entering the clinical study, and the results of coagulation test are within the limits of local treatment;

14. Women of childbearing age should have negative pregnancy test (serum or urine) within 7 days before enrollment, and voluntarily use appropriate contraceptive methods during the observation period and within 8 weeks after the last administration of the study drug; for men, it should be surgical sterilization or agree to use appropriate contraceptive methods during the observation period and within 8 weeks after the last administration of the study drug;

15. Good compliance, can cooperate with the study and follow-up according to the requirements of the program.

Exclusion Criteria:

1. Patients had been treated with PARP inhibitors in the past;

2. Previous allergic history of temozolomide or fluzoparide, previous allergy to dacarbazine, and allergic reaction to temozolomide or fluzoparide;

3. Patients had inherited galactose intolerance, lactase deficiency and glucose galactose malabsorption;

4. The following treatments or drugs were received before the first study treatment:

1. Major surgery (biopsy is allowed due to diagnosis) or severe trauma within 4 weeks before the first use of the study drug;

2. Received strong CYP3A4 inducer or inhibitor within 2 weeks after the first use of the study drug;

3. Previously vaccinated with anti-tumor vaccine; vaccinated with live attenuated vaccine within 28 days before the first study drug treatment or within 60 days after the end of study drug treatment;

5. Currently participating in other clinical studies, unless it is an observational (non intervention) clinical study or an intervention in the follow-up of a new clinical study; or has participated in any other drug clinical study within 4 weeks before the first administration, or no more than 5 half-life from the last study medication;

6. Except basal cell carcinoma or squamous cell carcinoma of skin, superficial bladder cancer, carcinoma in situ of cervix, intraductal carcinoma in situ of breast and papillary thyroid carcinoma which can be treated locally and have been cured in the past 5 years or at the same time;

7. Advanced patients with symptoms, spread to the viscera, and at risk of life-threatening complications in a short period of time (including patients with uncontrollable large amount of exudate [chest, pericardium, abdominal cavity];

8. Fever of unknown origin > 38.5? occurred during the screening period / before the first administration (according to the researcher's judgment, fever caused by tumor can be included in the group);

9. Severe infection (CTCAE > Level 2) occurred within 4 weeks before the first use of the study drug, such as severe pneumonia, bacteremia, infection complications, etc. the baseline chest imaging examination revealed active pulmonary inflammation, symptoms and signs of infection within 2 weeks before the first use of the study drug, or the need for oral or intravenous antibiotic treatment (excluding prophylactic use of antibiotics);

10. Within 6 months before entering the study, the following conditions occurred: myocardial infarction, severe / unstable angina pectoris, NYHA grade 2 or above cardiac insufficiency and clinically significant supraventricular or ventricular arrhythmias requiring clinical intervention; hypertension with poor drug control (systolic blood pressure continuously increased = 150mmhg or diastolic blood pressure = 100mmhg);

11. History of gastrointestinal bleeding or tendency of gastrointestinal bleeding in the past 6 months, such as esophageal varices, local active ulcer lesions, fecal occult blood=(+) (gastroscopy is required when fecal occult blood is (+));

12. Unable to swallow the study drug, chronic diarrhea (including but not limited to irritable bowel syndrome, Crohn's disease, ulcerative colitis), intestinal obstruction and other factors affecting drug administration and absorption;

13. Urine protein = + + + or 24-hour urine protein > 1.0g;

14. History of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation or congenital immunodeficiency was known;

15. Patients with active pulmonary tuberculosis infection found through medical history or CT examination, or patients with active pulmonary tuberculosis infection within one year before enrollment, or patients with active pulmonary tuberculosis infection history one year ago but without regular treatment;

16. Human immunodeficiency virus (HIV) infection or acquired immunodeficiency syndrome (AIDS); untreated active hepatitis B (hepatitis B, defined as hepatitis B virus surface antigen [HBsAg] positive test results, HBV-DNA = 500 Hepatitis C was defined as hepatitis C antibody [HCV AB] positive, HCV-RNA higher than the detection limit of analysis method and abnormal liver function), or combined with hepatitis B and hepatitis C co infection;

17. Patients had a clear history of neurological or mental disorders, including epilepsy and dementia, and was known to have a history of psychotropic substance abuse, alcoholism or drug abuse;

18. Patients who were considered unsuitable for the study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
fluzoparil
a PARP1 inhibitor
temozolomide
an alkylating chemotherapeutic agent

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Shandong Cancer Hospital and Institute

Outcome

Type Measure Description Time frame Safety issue
Primary 6-months PFS rate in all participants by RECIST 1.1 6-months progression-free survival rate in all participants by RECIST 1.1 Up to approximately 24 months
Secondary ORR in all paients by RECIST Version 1.1 ORR was assessed by performing study imaging every 6-9 weeks after the first dose of study treatment. ORR was defined as the proportion of participants in the analysis population who had a CR defined as a disappearance of all target lesions with pathological lymph nodes having a reduction in short axis to <10 mm) or PR defined as at least a 30% decrease in the sum of diameters of target lesions, using the baseline sum diameters as a reference. Up to approximately 24 months
Secondary Disease control rate in all patients by RECIST Version 1.1 Disease control rate is defined as the proportion of patients whose best curative effect reaches complete remission, partial remission or disease control. Maintain for at least 4 weeks by RECIST Version 1.1 Up to approximately 24 months
Secondary Overall survival (OS) in all participants OS was defined as the time from the first day of study treatment to death due to any cause. OS was analyzed by the Kaplan-Meier method for censored data and reported in months. Up to approximately 24 months
Secondary mPFS in all participants mPFS was defined as as the median time from the first day of study treatment to the first documented PD per RECIST 1.1 or death due to any cause, whichever occurred first. Up to approximately 24 months
Secondary mOS in all participants mOS was defined as the time from the first day of study treatment to death due to any cause. Up to approximately 24 months
Secondary Number of participants experiencing an adverse event (AE) An AE was defined as any untoward medical occurrence in a participant administered a pharmaceutical product and which did not necessarily have to have a causal relationship with this treatment. An AE could therefore be any unfavorable and unintended sign, symptom, or disease temporally associated with the use of a medicinal product/protocol-specified procedure, whether or not considered related to the medicinal product/protocol-specified procedure. Any worsening of a preexisting condition temporally associated with the use of the product was also an AE. A serious adverse event (SAE) was an AE that resulted in death, was life threatening, resulted in persistent or significant disability/incapacity, resulted in or prolonged an existing inpatient hospitalization, was a congenital anomaly/birth defect, was a cancer, was associated with an overdose, was another important medical event. From first dose to last dose of treatment plus 2 months of follow-up, up to 24 months
Secondary Number of participants experiencing a serious adverse event (SAE) Any event which causes death, permanent damage, birth defects, or requires hospitalization is considered an SAE. From first dose to last dose of treatment plus 2 months of follow-up, up to 24 months
See also
  Status Clinical Trial Phase
Recruiting NCT05664243 - A Phase 1b / 2 Drug Resistant Immunotherapy With Activated, Gene Modified Allogeneic or Autologous γδ T Cells (DeltEx) in Combination With Maintenance Temozolomide in Subjects With Recurrent or Newly Diagnosed Glioblastoma Phase 1/Phase 2
Completed NCT02768389 - Feasibility Trial of the Modified Atkins Diet and Bevacizumab for Recurrent Glioblastoma Early Phase 1
Recruiting NCT05635734 - Azeliragon and Chemoradiotherapy in Newly Diagnosed Glioblastoma Phase 1/Phase 2
Completed NCT03679754 - Evaluation of Ad-RTS-hIL-12 + Veledimex in Subjects With Recurrent or Progressive Glioblastoma, a Substudy to ATI001-102 Phase 1
Completed NCT01250470 - Vaccine Therapy and Sargramostim in Treating Patients With Malignant Glioma Phase 1
Terminated NCT03927222 - Immunotherapy Targeted Against Cytomegalovirus in Patients With Newly-Diagnosed WHO Grade IV Unmethylated Glioma Phase 2
Recruiting NCT03897491 - PD L 506 for Stereotactic Interstitial Photodynamic Therapy of Newly Diagnosed Supratentorial IDH Wild-type Glioblastoma Phase 2
Active, not recruiting NCT03587038 - OKN-007 in Combination With Adjuvant Temozolomide Chemoradiotherapy for Newly Diagnosed Glioblastoma Phase 1
Completed NCT01922076 - Adavosertib and Local Radiation Therapy in Treating Children With Newly Diagnosed Diffuse Intrinsic Pontine Gliomas Phase 1
Recruiting NCT04391062 - Dose Finding for Intraoperative Photodynamic Therapy of Glioblastoma Phase 2
Active, not recruiting NCT03661723 - Pembrolizumab and Reirradiation in Bevacizumab Naïve and Bevacizumab Resistant Recurrent Glioblastoma Phase 2
Active, not recruiting NCT02655601 - Trial of Newly Diagnosed High Grade Glioma Treated With Concurrent Radiation Therapy, Temozolomide and BMX-001 Phase 2
Completed NCT02206230 - Trial of Hypofractionated Radiation Therapy for Glioblastoma Phase 2
Completed NCT03493932 - Cytokine Microdialysis for Real-Time Immune Monitoring in Glioblastoma Patients Undergoing Checkpoint Blockade Phase 1
Terminated NCT02709889 - Rovalpituzumab Tesirine in Delta-Like Protein 3-Expressing Advanced Solid Tumors Phase 1/Phase 2
Recruiting NCT06058988 - Trastuzumab Deruxtecan (T-DXd) for People With Brain Cancer Phase 2
Completed NCT03018288 - Radiation Therapy Plus Temozolomide and Pembrolizumab With and Without HSPPC-96 in Newly Diagnosed Glioblastoma (GBM) Phase 2
Withdrawn NCT03980249 - Anti-Cancer Effects of Carvedilol With Standard Treatment in Glioblastoma and Response of Peripheral Glioma Circulating Tumor Cells Early Phase 1
Withdrawn NCT02876003 - Efficacy and Safety of G-202 in PSMA-Positive Glioblastoma Phase 2
Terminated NCT02905643 - Discerning Pseudoprogression vs True Tumor Growth in GBMs