Trial Title:
Nimotuzumab Combined With Paclitaxel for Recurrent Metastatic Gastric or Esophagogastric Junction Adenocarcinoma
NCT ID:
NCT05978050
Condition:
Gastric or Esophagogastric Junction Adenocarcinoma
Conditions: Official terms:
Adenocarcinoma
Paclitaxel
Albumin-Bound Paclitaxel
Nimotuzumab
Study type:
Interventional
Study phase:
Phase 3
Overall status:
Recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Treatment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Intervention:
Intervention type:
Drug
Intervention name:
nimotuzumab plus paclitaxel
Description:
Nimotuzumab injection: 50mg/10ml/stick Paclitaxel: 30mg/5ml/stick
Arm group label:
nimotuzumab
Other name:
Combined with chemotherapy
Intervention type:
Drug
Intervention name:
placebo plus paclitaxel
Description:
placebo: 50mg/10ml/stick Paclitaxel: 30mg/5ml/stick
Arm group label:
placebo
Other name:
chemotherapy alone
Summary:
In order to evaluate the efficacy and safety of nimotuzumab combined with paclitaxel as
second-line treatment for recurrent metastatic gastric or esophagogastric junction
adenocarcinoma with EGFR over-expression, investigators performed a randomized,
double-blind, placebo-controlled phase III clinical trial. Patients will be randomized
(1:1) to receive nimotuzumab plus paclitaxel in the experimental group and placebo plus
paclitaxel in the control group. The primary endpoint of this study was OS, and according
to the results of the RAINBOW-Asia gastric cancer phase III clinical study, the mOS of
paclitaxel single-agent second-line treatment for gastric cancer was 7.92 months,
assuming that the mOS increased to 10.92 months after the addition of nimotuzumab, Using
the survival module in the PASS15 software, the two-sided test level was set α=0.05,
β=0.20, enrolled for 2 years, followed up for 1.5 years, the dropout rate was 5%, the
sample size including interim analysis was 354 cases. The secondary endpoints are
progression-free survival (PFS), objective response rate (ORR), duration of response
(DOR), disease control rate (DCR), patient reported outcome (PRO), and safety.
Detailed description:
Study design:
This study is a prospective, randomized, double-blind, placebo-controlled trial designed
to evaluate the efficacy and safety of nimotuzumab combined with paclitaxel as
second-line treatment for recurrent metastatic gastric or esophagogastric junction
adenocarcinoma with EGFR over-expression.A total of 354 patients with recurrent
metastatic gastric or esophagogastric junction adenocarcinoma with EGFR over-expression
are expected to be enrolled. Patients will be randomized (1:1) to receive nimotuzumab
(600 mg for the first dose, then 400 mg, weekly) plus paclitaxel (80 mg/m2, on day 1, 8
and 15, every 4 weeks as a cycle) in the experimental group and placebo plus paclitaxel
(same as experimental group) in the control group. The study will be randomized by
stratified block randomization, stratification factors included ECOG PS (0 vs. 1),
first-line immunotherapy (yes vs. no), and EGFR expression status (IHC 2+ vs. 3+).
Treatment will continue until disease progression, intolerance, or patient withdrawal
from the trial, and each patient will be followed up until death, loss to follow-up, or
the end of study.
Quality Assurance plan： According to the GCP's guidelines, sponsors are responsible for
using and maintaining quality assurance and quality control systems in accordance with
the corresponding standard operating procedures (SOPs). The sponsor or sponsor's
representative shall conduct quality control at every stage of data processing to ensure
the accuracy, consistency, completeness and reliability of the data. In addition, the
sponsor or its representative, the appropriate regulatory body, may conduct audits and/or
inspections of the research process. During audits and/or regulatory inspections,
authorized sponsor representatives and relevant regulatory authorities have access to all
research-related documents.
Data checks:
Investigators should collect complete participant data as required by the protocol,
recorded in the original record. This study will use an electronic data acquisition (EDC)
system, and the library builder will build an electronic database according to the plan,
set up the corresponding logic verification, and data management personnel will conduct
data verification according to the corresponding verification plan.
Source data verification:
The research data will be entered into the eCRF by the researcher or authorized research
center staff. Investigators review the data to ensure the accuracy of all data entered
into the eCRF. The eCRF will be reviewed by the Inspector and assessed for completeness
and consistency, and the Auditor will compare the eCRF with the original documentation to
ensure consistency of critical data. All data entry, correction and modification will be
the responsibility of the researcher or its designee, and the supervisor will not have
this authority. The data in the eCRF is submitted to the data server, and any changes to
the data will be recorded in the audit track, that is, the reason for the change, the
operator account number, the modification time and date will be recorded. If there is a
data challenge, the monitor, medical or data management personnel will issue the
challenge in the EDC according to the corresponding verification plan, and the research
center staff will be responsible for answering the question, and conduct data
verification from multiple parties and angles to ensure data quality. After all data has
been entered into the EDC in its entirety, the monitor has completed the SDV on all data
in the EDC, the medical and data administrator has completed the review of all data in
the EDC, and all challenges have been closed, the data administrator freezes the data.
Data dictionary:
The combined medication and medical history will be encoded using the Anatomical,
Therapeutic, and Chemical Taxonomy of Drugs (ATC 2021 and above) and the Regulatory
Activities Medical Dictionary (MedDRA V24.0 and above), respectively.
Standard Operating Procedures:
Informed consent approved by the Independent Ethics Committee (IEC)/Institutional Review
Board (IRB) must be obtained prior to carrying out any research-specific procedures.
Potentially eligible subjects will be screened within 4 weeks prior to the first dose,
and after qualified subject screening, they will be enrolled through an interactive web
response system (IWRS). Investigators should collect complete participant data (e.g.,
laboratory tests, vital signs, physical examination, electrocardiogram, imaging tests,
adverse effects, quality of life assessment scale evaluation, etc.) as required by the
protocol and record them in the original record.
Investigators are required to submit a completed eCRF for each participant enrolled in
the study. Study numbers and subject numbers submitted with the eCRF should be carefully
verified and all private information (including subject names) removed or rendered
illegible to protect subject privacy. When researching data entry into eCRF, the system
will automatically add the identity of the data entry user by the ID of the login user.
The investigator proves that it has reviewed the record through an electronic signature
record and guarantees the accuracy of the data in the record. After all data in the EDC
is reviewed and all doubts have been closed, the data is locked and analyzed.
Adverse events were monitored throughout the study and it was the responsibility of the
investigator to document all AEs observed during the study. From the beginning of the
subject's signing of informed consent to 30 days after the last dose of the
investigational drug, all AEs, regardless of severity and causal relationship with the
investigational drug, need to be recorded in the original data and the corresponding AE
page in the eCRF. According to the relevant regulations of ICH and China GCP (2020
edition), during this study, investigators should complete the SAE report form provided
by the sponsor and report to the sponsor in writing within 24 hours after learning of SAE
or relevant new follow-up information.
Sample size:
The primary endpoint of this study was OS, and according to the results of the
RAINBOW-Asia gastric cancer phase III clinical study, the mOS of paclitaxel single-agent
second-line treatment for gastric cancer was 7.92 months, assuming that the mOS increased
to 10.92 months after the addition of nimotuzumab, and an interim analysis was set up
during the trial. Using the survival module in the PASS15 software, the two-sided test
level was set α=0.05, β=0.20, enrolled for 2 years, followed up for 1.5 years, the
dropout rate was 5%, the single-stage sample size was 354 cases, and the required sample
size for each group was 177.
Plan for missing data:
For participants who had not reported death at the time of analysis, the last known
surviving follow-up date was used as the censoring date. For subjects who have not yet
progressed, the date of the last radiographic evaluation is used as the date of
censoring. For participants who had not undergone tumour assessment after baseline, the
date of randomisation was used as the date of censoring.
Statistical analysis plan:
The main overall survival (OS) analysis will be performed when 306 death events occur,
optimality test and blind sample size adjustment will be performed when 50% of death
events occur.
The primary endpoint of this study was mOS. OS is the time between the date of
randomization and death from any cause. A stratified log-rank test was used to compare OS
in the nilotuzumab plus paclitaxel and placebo plus paclitaxel group at a bilateral
significance level of 0.05. The Kaplan-Meier (KM) method was used to estimate the OS of
each treatment group, and the Kaplan-Meier curve was plotted to show the survival
difference description. Efficacy estimates of OS will be expressed by risk ratios (HR)
estimated by the hierarchical Cox proportional hazards model and their 95% confidence
intervals.
Secondary endpoints: PFS, ORR, DOR, DCR，PRO and safety. The Kaplan-Meier (KM) method was
used to estimate the PFS of each treatment group, and the Kaplan-Meier curve was plotted
to show the difference description. The stratification factors are the same as for OS
analysis. Efficacy estimates of PFS will be expressed by risk ratios (HR) estimated by
the hierarchical Cox proportional hazards model and their 95% confidence intervals. The
Clopper-Pearson exact probability method was used to calculate the ORR and DCR estimates
and their 95% confidence intervals for each treatment group, respectively. The
Cochran-Mantel-Haenszel (CMH) method was used to calculate the odds ratio and its 95%
confidence interval and p. The stratification factors used in the CMH test are the same
as in the OS analysis. If the number of objective remission or disease control cases is
insufficient to support the CMH test, stratified precision testing is considered and
precise confidence intervals for odds ratios are calculated. DOR is only available for
participants with objective response (CR/PR) for descriptive analysis of TOR. Results
will be shown using the Kaplan-Meier method for each treatment group to estimate the
median DOR and the distribution curve.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
-
1. Age: 18-75 years old (including boundary value), male or female;
-
2. The physical status score ECOG is 0-1;
-
3. Histopathologically or cytologically confirmed gastric or esophagogastric
junction adenocarcinoma;
-
4. Recurrent metastatic disease, previous treatment with first-line standard
chemotherapy regimens (including platinum-containing and/or fluorouracil
regimens) (recurrence or metastasis during adjuvant therapy or within 6 months
after completion is considered first-line therapy), or received anti-HER2
therapy, or received immunotherapy, and has been confirmed by the investigator
or has a clear disease progression in the medical history;
-
5. At least one evaluable tumor lesion according to the RECIST version 1.1
evaluation criteria;
-
6. Detection of primary or metastatic lesions during the screening period (when
multiple specimens exist at the same time, the bulk specimen is preferred over
the biopsy specimen, and the metastasis is preferred over the primary lesion)
tissue is determined to be EGFR high expression (IHC2+ or IHC3+);
-
7. Estimated survival≥ 12 weeks;
-
8. Have proper organ function, defined as:Total bilirubin ≤ 1.5 times the upper
normal limit (ULN); glutamyltransferase (ALT) or aspartate aminotransferase
(AST) ≤ 2.5 times ULN in the absence of liver metastases; ALT or AST ≤ 5 times
ULN in the presence of liver metastases;Serum creatinine level≤ 1.5 times ULN;
neutrophil count ≥1.5×109/L; WBC count≥ 3.0×109/L; platelets≥ 100×109/L;
Hemoglobin≥ 90g/L;
-
9. Patients of childbearing age and their spouses are willing to use
contraception;
-
10. Women of potential fertility have negative serum hCG within 72 hours prior to
randomization (postmenopausal women with amenorrhea for at least 12 months are
considered infertile, and women who are known to have undergone tubal ligation
are not required to undergo a pregnancy test);
-
11. The subject understands and complies with the study process, voluntarily
participates, and signs the informed consent form.
Exclusion Criteria:
-
1. Received the following treatments before this study:
1. The disease has progressed after previous paclitaxel chemotherapy or molecular
targeted drug (anti-EGFR antibody) treatment, or received paclitaxel
chemotherapy or molecular targeted drug (anti-EGFR antibody) treatment within 4
weeks before randomization;
2. Within 4 weeks before randomization or participating in other
therapeutic/intervention clinical trials or receiving combined treatment
prohibited by the protocol;
-
2. Received major surgical treatment, incision biopsy (such as laparotomy) or
obvious traumatic injury within 4 weeks before randomization;
-
3. Brain metastases or meningeal metastases;
-
4. Has a history of malignant tumors other than gastric adenocarcinoma or
esophagogastric junction adenocarcinoma (except for cured cervical carcinoma in
situ or skin basal cell carcinoma and other malignant tumors that have been
cured for 5 years);
-
5. Known to have suffered from severe bleeding disorders (such as severe
gastrointestinal bleeding) and vasculitis within 3 months before randomization;
-
6. Known to be accompanied by other serious diseases, including but not limited
to:
1. Refractory congestive heart failure (NYHA classification III or IV, see
Appendix 2), unstable angina, poorly controlled arrhythmia, uncontrolled
moderate or high blood pressure (SBP>160mmHg or DBP>100mmHg );
2. Uncontrolled diabetes;
3. Mental illness that affects informed consent and/or protocol compliance;
4. There are serious diseases that other researchers believe are not suitable for
participating in this study;
-
7. Known allergies or contraindications to anti-EGFR antibody preparations,
paclitaxel and other components;
-
8. Patients who have previously used immune checkpoint inhibitors (such as
anti-PD-1, anti-PD-L1, anti-CTLA-4 antibodies), such as the following adverse
events related to immune checkpoint inhibitors and have not recovered to grade
1 And below, not suitable for inclusion: Grade ≥3 ocular adverse events,
abnormal liver function in line with Hy's Law standard adverse events, ≥3
neurological toxicity, ≥3 grade colitis, ≥3 grade renal toxicity;
-
9. Those who are known to have third space effusion (including a large amount of
pleural effusion or ascites) that cannot be controlled by drainage or other
methods;
-
10. Known NCI CTC grade 2-4 peripheral neuropathy;
-
11. Known history of primary or secondary immunodeficiency or current active
primary or secondary immunodeficiency;
-
12. Patients with untreated chronic hepatitis B or chronic hepatitis B virus (HBV)
DNA ≥ 1000 IU/ml or hepatitis C virus (HCV) RNA positive (inactive hepatitis B
surface antigen carriers, treated And stable hepatitis B patients [HBV DNA
<1000 IU/ml and cured hepatitis C patients can be selected]); Treponema
pallidum antibody positive or human immunodeficiency virus antibody positive or
any uncontrolled infection By;
-
13. Women of childbearing age who are pregnant, breast-feeding, planning to become
pregnant, or who have not taken reliable birth control measures and men in the
sexually active period who are unwilling to take birth control measures during
the study period and within 3 months after the last medication, and during the
above-mentioned specified time Sperm donors;
-
14. Any medical, psychiatric or other condition or situation that the investigator
believes that the subject's participation in this clinical research may have a
negative impact on the safety of the subject or the reliability of the research
data.
Gender:
All
Gender based:
Yes
Minimum age:
18 Years
Maximum age:
75 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
National Sun Yat-sen University Cancer Center
Address:
City:
Guangzhou
Country:
China
Status:
Recruiting
Contact:
Last name:
ruihua Xu
Phone ext:
020-87343333
Email:
xurh@sysucc.org.cn
Start date:
August 1, 2024
Completion date:
March 1, 2026
Lead sponsor:
Agency:
Biotech Pharmaceutical Co., Ltd.
Agency class:
Other
Source:
Biotech Pharmaceutical Co., Ltd.
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05978050
