Clinical Trial Details
— Status: Not yet recruiting
Administrative data
| NCT number |
NCT05583799 |
| Other study ID # |
XJTU1AF2022LSK-354 |
| Secondary ID |
|
| Status |
Not yet recruiting |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
October 15, 2022 |
| Est. completion date |
September 30, 2025 |
Study information
| Verified date |
September 2022 |
| Source |
First Affiliated Hospital Xi'an Jiaotong University |
| Contact |
Qiling Li, Dr. |
| Phone |
02985323849 |
| Email |
liqiling[@]mail.xjtu.edu.cn |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational [Patient Registry]
|
Clinical Trial Summary
Ovarian cancer is the second fatal gynecological cancer. More than 70% of ovarian cancer
patients are diagnosed as advanced. Niraparib was approved by the National Medical Products
Administration on December 27, 2019. It can be used as a maintenance treatment for adult
patients with platinum-sensitive recurrent epithelial ovarian cancer, fallopian tube cancer,
or primary peritoneal cancer after platinum-containing chemotherapy has achieved complete or
partial remission. On September 10, 2020, niraparib became a poly ADP-ribose polymerase
inhibitor approved in China and globally, which can be used as a single agent for the
maintenance treatment of first-line and recurrent ovarian cancer regardless of the patient's
biomarker status. On December 28, 2020, niraparib has been included in the new version of the
medical insurance catalog. At present, most studies based on niraparib are randomized
controlled trials (RCTs). RCTs often have strict inclusion and exclusion criteria and they
are implemented in a highly standardized environment. Its internal validity is high, but the
research results may not be able to be extrapolated to practice. This study is a prospective
real-world study. In this study, based on the modified Response Evaluation Criteria in Solid
Tumors v.1.1 criteria, we evaluated the use of niraparib in patients with ovarian cancer,
fallopian tube cancer, or primary peritoneal cancer in the progression-free survival, overall
survival, and objective control rate, etc. The safety and tolerability of niraparib and the
impact on the quality of life of patients are evaluated. 10ml blood samples of enrolled
patients are collected at baseline and study endpoints respectively (only for enrolled
patients who agree to blood sampling) for exploratory biological marker research and
exploratory pharmacogenetic analysis. Finally, the results will as a supplement to the
conclusions of randomized controlled trials to provide better guidance for patients.
Description:
1. Research status at domestic and foreign
Ovarian cancer is the second fatal gynecological cancer. More than 70% of ovarian cancer
patients are diagnosed as advanced. Standard treatments include optimal reduction
surgery and platinum/taxane chemotherapy. Epithelial ovarian cancer (EOC) is the most
common histological type of ovarian cancer, up to 20% of high-grade serous ovarian
cancer shows germline and/or somatic mutations in the BRCA1/BRCA2 gene. BRCA1 and BRCA2
are tumor suppressor genes that play a central role in repairing DNA double-strand
breaks (DSB) through homologous recombination (HR). Due to their increased sensitivity
to DNA damage reagents, they extend the survival period of BRCA1 and BRCA2 mutant EOCs,
among which BRCA2 vectors have the best survival rate. Poly-ADP-ribose polymerase (PARP)
1 is a key ribozyme involved in single-strand break repair through the base excision
repair pathway. In the absence of PARP activity, these lesions are considered to have
transformed into DSB. Cells lacking HR, such as BRCA mutant cells, are extremely
sensitive to PARP inhibition. This phenomenon called "synthetic lethality" has led
people to study PAPP inhibitors used as therapeutic agents in BRCA1/BRCA2 carriers.
Niraparib was approved by the National Medical Products Administration on December 27,
2019. It can be used as a maintenance treatment for adult patients with
platinum-sensitive recurrent epithelial ovarian cancer, fallopian tube cancer, or
primary peritoneal cancer after platinum-containing chemotherapy has achieved complete
or partial remission. On September 10, 2020, niraparib became a PARP inhibitor approved
in China and globally, which can be used as a single agent for the maintenance treatment
of first-line and recurrent ovarian cancer regardless of the patient's biomarker status.
On December 28, 2020, niraparib has been included in the new version of the medical
insurance catalog. The results of the international phase III clinical trial (NOVA) of
niraparib showed that niraparib can prolong the median progression-free survival of
ovarian cancer patients regardless of whether the patients have germline BRCA mutations.
Among patients with gBRCA mutations, the risk of disease progression was reduced by 73%
and progression-free survival was 4-fold longer than in the placebo group (21 months vs.
5.5 months). In patients without the gBRCA mutation, the risk of disease progression was
reduced by 55% and progression-free survival was more than 2-fold longer (9.3 months vs
3.9 months). The PRIMA clinical study showed that niraparib, as single-agent maintenance
therapy, can significantly prolong the progression-free survival of first-line
platinum-responsive ovarian cancer patients. The risk of disease progression and death
was reduced by 38% across all treated patient populations. In BRCA-mutated,
HRD-positive, and HRD-negative patients, niraparib reduced the risk of disease
progression or death by 60%, 57%, and 32%, respectively. This study proves that
niraparib becomes the first PARP inhibitor that can significantly improve the
progression-free survival of patients regardless of biomarker status, which is expected
to change the treatment of ovarian cancer in China. Recently, the first all-round,
multicenter phase III clinical study in a Chinese population (NORA) showed that in
patients with gBRCA mutations, median progression-free survival (PFS) was significantly
longer with niraparib as second-line maintenance therapy, compared with placebo (not
reached vs. 5.5 months, HR: 0.22) and those without gBRCA mutation at ESMO 2020(11.1 vs.
3.9 months, HR: 0.40). The QUADRA study shows that niraparib has a substantial survival
benefit in women treated for ovarian cancer, especially in HRD-positive
platinum-sensitive patients, including not only BRCA-mutated patients but also the BRCA
wild-type population.
The above-mentioned studies based on niraparib are mostly randomized controlled trials
(RCTs). Because RCTs often have strict inclusion and exclusion criteria, they are
carried out in a highly standardized environment, so that the research subjects have
good homogeneity. The validity is high, but the research results may not be able to be
extrapolated to practice. Therefore, it is necessary to evaluate the role of treatments
for advanced diseases in the real environment. To provide better guidance for patients,
real-world evidence is needed to make up for the lack of randomized controlled trials.
At present, in real-world research, there are only retrospective studies on the use of
niraparib in ovarian cancer at home and abroad, and the results are consistent with
their corresponding RCTs. There is a lack of prospective real-world evidence with higher
levels of evidence.
2. Study drugs
The drug name is niraparib Tosylate capsules. This product is a 100mg capsule.
3. Research programs
3.1 Overall design
This study is a prospective real-world product registration study. It is an
observational study. The main research content is to evaluate the efficacy and adverse
reactions of PAPP inhibitors niraparib in patients with ovarian cancer, fallopian tube
cancer, or primary peritoneal cancer. According to the inclusion and exclusion criteria,
we collect various information about the target research participants, organize the data
and perform statistical analysis under the guidance of epidemiologists and statistical
experts. The curative effect is evaluated by indicators such as PFS, overall survival,
and objective response rate. Moreover, we collect and analyze the adverse reactions of
study participants after taking niraparib. 10ml blood samples of enrolled patients are
collected at baseline and study endpoints respectively (only for enrolled patients who
agree to blood sampling) for exploratory biological marker research and exploratory
pharmacogenetic analysis.
3.2 Sample size
This research is an observational study. 222 study participants are expected to be
included.
3.3 Stratification factors
This research can set up different plans according to the following different
stratification factors and research purposes.1) Number of treatment lines: first-line
maintenance, second-line maintenance, back-line treatment, excess indications. 2)
BRCA1/2 mutation status: positive, negative. 3) Platinum sensitive status: platinum
sensitive, platinum resistant. 4) carbohydrate antigen 125 (CA125) level, etc.
3.4 Treatment plan
This study is a non-interventional study that only collects data and does not interfere
with clinical treatment. The medication is administered according to clinical
instructions, guidelines, and local treatment routines.
4. Research process
4.1 Subject informed
Patients should sign an informed consent form before the start of the study. The
researchers need to explain the contents of the informed consent to the subjects in
detail. After the candidate has fully read and understood the informed consent, if she
agrees to participate in the study, the subject should sign and date the informed
consent. Researchers also need to sign and date the informed consent form.
4.2 Interview on selection
Within 7 days of the subjects' enrollment, the investigator collected baseline data,
including general information; medical history diagnosis; past tumor treatment history;
family history; whether it meets the admission criteria.
4.3 Interview during treatment and the last interview
- After the subjects are enrolled, the investigator will conduct a visit every 12
weeks. The data include: Efficacy evaluation: computed tomography/magnetic
resonance imaging examination and tumor marker CA125 examination are required.
- Safety evaluation: whether there are adverse events (AE).
- At baseline, at the same time as the Response Evaluation Criteria In Solid Tumors
assessment time (once every 12 weeks) until the objective radiation disease
progression or the end of the study treatment interview, a functional assessment of
cancer treatment-ovarian cancer questionnaire survey.
5. Safety evaluation
5.1 Definition of Adverse Events
AE refers to all the adverse medical events that occur after the subject receives the
experimental drug. It can be manifested as symptoms and signs, diseases, or abnormal
laboratory tests, but it may not be causally related to the experimental drug.
5.2 Severity of adverse events
During the study period, the severity of AEs will be classified according to Common
Terminology Criteria for Adverse Events version 5.0, and AE of grade ≥3 will be
collected.
5.3 Relationship with study drug
When judging the correlation between AEs and study drugs, the following factors should
be considered: 1) It is definitely related; 2) It may be related; 3) Possibly
irrelevant; 4) Definitely irrelevant; 5) Undecidable.
5.4 Adverse event records
All adverse events that occur from the subject's first use of niraparib to 4 weeks after
the last dose, including observed by the investigator, obtained by inquiries, and
spontaneously reported by the subject should be fully recorded.
Researchers need to continue to follow up all AEs until the event is cured, returns to
baseline, reaches a stable state, or no more information is available. The researcher
needs to monitor and record the outcome of the AE in the subject's source file. After
the study, there is no need to actively collect new AEs.
6. Drug management
This study is a real-world study, and niraparib is a marketed drug, so niraparib needs
to be purchased and used by patients according to the normal procedures in the hospital.
7. Data recording and monitoring
7.1 Data logging
This project uses table records. According to Good Clinical Practice requirements, in
order to ensure patient privacy, patient names should not appear. All patients' names
should be filled with name codes, and the codes should be abbreviated in Chinese names.
The specific dosage and time of medication are unknown and should be filled in unknown
rather than blank or missing items. The researcher should ensure that all data must be
consistent with the "inpatient medical record".
7.2 Data monitoring
During the test process, the research unit will review the completed test case data,
check whether the data is correct, complete, and standardized, and assess the
traceability of all data.
8. Statistical analysis
8.1 Definition of statistical analysis data sets
The study includes cases that have received at least one trial drug and have a safety
evaluation in the primary and secondary endpoint analysis. Those who have not used a
trial drug or have no research data after being selected can be eliminated. Excluded
cases should be kept for future reference and no statistical analysis should be
performed.
8.2 Statistical analysis methods
The continuous variables in this study are described by median and interquartile ranges.
Categorical variables are described by absolute value and the proportion of the total
number of patients. Χ2 test is used for comparison between groups. The method of
survival analysis is used to statistically process the follow-up data. Kaplan-Meier
method is used to draw the survival curve of the follow-up subjects. The log-Rank test
was used to evaluate the survival difference between each group. The Cox regression
model was used to analyze the influencing factors of the survival time of each group of
follow-up subjects. Candidate influencing factors with a significance level of 0.05 in
the univariate analysis were selected for the multivariate analysis. For all analyses,
the test level α=0.05, when p<0.05 is considered statistically significant. All analyses
were performed using Statistical Product and Service Solutions software (version 22.0).
9. Quality control and quality assurance
All research processes should establish standardized operating procedures.
