Trial Title:
Clinical Study of Azacitidine Combined With Ruxolitinib in the Treatment of Higher-risk MDS/MPN
NCT ID:
NCT05817955
Condition:
MDS/MPN
Conditions: Official terms:
Azacitidine
Study type:
Interventional
Study phase:
Phase 2
Overall status:
Recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Primary purpose:
Treatment
Masking:
None (Open Label)
Intervention:
Intervention type:
Drug
Intervention name:
Azacitidine (AZA) with Ruxolitinib
Description:
1. Antibiotics: Antibiotic treatment is positively given when symptoms related to
infection, and other support treatment is strengthened.
2. Blood products: Infuse the blood products according to the patient's blood routine
test. Drugs that need to be used by other diseases must be recorded in detail in the
case report form, including the general name of the drug, the dosage of the
medication, and the frequency of administration. Drugs are not allowed to be
combined: Avoiding the use of granulocyte colony-stimulating factor (G-CSF), there
may be risk of spleen rupture.
Arm group label:
Azacitidine (AZA) with Ruxolitinib
Summary:
This study observes the safety and efficacy of Azacitidine (AZA) combined with
ruxolitinib to treat higher-risk Myelodysplastic Syndromes∕Myeloproliferative
Neoplasms(MDS/MPN)
Detailed description:
This is an open label, a multi -centered clinical trial, aiming to evaluate the safety
and efficacy of Azacitidine with Ruxolitinib to treat MDS/MPN patients Myelodysplastic
Syndromes/Myeloproliferative Neoplasms（MDS/MPN） are a set of malignant clonal diseases
that originated from hematopoietic stem cells, which have both the characteristics of MDS
and MPN. They also have the risk of transforming to Acute Myeloid Leukemia (AML).
According to the 2016 World Health Organization (WHO) classification, MDS/MPN include
Chronic myelomonocytic leukemia(CMML), Atypical chronic myeloid leukemia(aCML)，Juvenile
myelomonocytic leukemia (JMML), MDS/MPN with ring sideroblasts and
thrombocytosis(MDS/MPN-RS-T), and MDS/MPN unclassified(MDS/MPN-U). Except for JMML, other
types of MDS/MPN mainly happened in persons over 60 years old, and the heterogeneity of
the disease is large. At present, the treatment is limited. Although allo hematopoietic
stem cell transplantation is the only way to cure the diseases, a recent large series
study on CMML showed that allo hematopoietic stem cell transplantation would increase the
mortality risk of lower-risk CMML, and did not obtain survival benefit in higher-risk
CMML. Therefore, it is currently urgent to explore the new treatment for MDS/MPN.
CMML is the most common subtype of MDS/MPN, manifested the increased monocytes in
peripheral blood (absolute cell count ≥1x109/L and percentage ≥10%, which lasts more than
3 months) accompanied with at least one lineage dysplasia and bone marrow blasts ≤20%.
The median diagnosis age is (73-75) years old, and the estimated annual incidence in the
population is 4/10,000.
The treatment strategy of CMML based on the prognostic stratification. According to the
prognostic stratification, low-risk patients (low and inter-1) receive red blood cells
transfusion and cytoreductive treatment. For high-risk (inter-2 and high) patients who
are unsuitable for stem cell transplantation, hypomethylating agents and clinical trials
are recommended. The hypomethylating agents (including Decitabine, Azacitidine, and oral
Decitabine) are the only drugs approved by the FDA in the United States for CMML
treatment. The approvement were based on MDS clinical trials that included CMML, such as
CALGB Studies (including 14 patients with CMML) and European AZA-001 Studies (including
11patients with CMML). Since then, many prospective and retrospective studies containing
CMML have confirmed its efficacy. The Overall Response Rates (ORR) is 40-50% for
hypomethylating agents, while Complete Remission (CR) is less than 20%. In addition, a
recent prospective clinical trial pointed out that hypomethylating agents did not
achieved clinical response in MPN-CMML, and no significant difference was found between
hypomethylating agents group and Hydroxyurea group in Overall Survivals (OS) and Leukemia
Free Survival.
In addition to hypomethylating agents, clinical trials are also recommended for patients
with higher risks CMML. At present, several clinical trials including Lenzilumab (GM-CSF
monoclonal antibody, NCT02546284), Tipifarnib (Fennec metastases inhibitor, NCT02807272),
Ruxolitinib (JAK1/2 inhibitors, NCT03722407) and Cobimetinib (MEK inhibitor, NCT04409639)
are carried on in CMML. The results show that they have good efficacy and safety in CMML.
In addition, a series of clinical trials combined hypomethylating agents with other drugs
to explore the way to increase the efficacy in CMML.
Some MDS/MPN patients have the clinical manifestations of MPNs such as increased blood
cells, large spleen sizes, and constitutional symptom. Meanwhile, activated inflammatory
cytokine secretion also exists in MDS/MPN. Ruxolitinib is JAK1/JAK2 inhibitor used for
the treatment of myelofibrosis. A multi -center phase I clinical trial of ruxolitinib
including 20 CMML patients showed that 4 patients obtained hematopoietic improvement, and
1 patient obtained bone marrow PR. Of the 9 patients with splenomegaly, 5 patients
received spleen reduction > 50%. 10 of 11 patients with constitutional symptom were
significantly improved. The ORR was 35% combining spleen response and MDS/MPN
International Working Group (IWG) efficacy criteria. Only one patient had level 3
platelet decrease, indicating that ruxolitinib had less impact on platelet counts in
CMML. Based on this, the phase I/II clinical trial was included 50 patients with CMML.
The ORR according to MDS/MPN IWG was 38%, and 43% patients achieved spleen reduction. The
most common adverse events were anemia (10%) and platelet decrease (6%), further
confirming the safety and efficacy of ruxolitinib in the treatment of CMML.
In addition, a phase II clinical trial explores the efficacy of ruxolitinib in aCML (n =
23) and chronic neutrophilic leukemia (CNL) (n = 22). The ORR was 35% (11 PR[9 CNL and 2
aCML], 4 CR [CNL]). The most common 3/4 adverse event was anemia (34%) and platelet
decrease (14%). It is worth noting that the efficacy was better in CNL compared with
aCML.
Based on previous studies, we intend to further investigate the safety and efficacy of
azacitidine combined with ruxolitinib in the treatment of higher-risk myelodysplastic
syndromes/myelodysplastic diseases (MDS/MPN).
Criteria for eligibility:
Criteria:
Inclusion Criteria:
• According to WHO (2016) classification, researchers made the diagnosis of CMML based on
clinical and morphological characteristics. Other criteria should be met: 1) Neut
≥2x109/L, PLT ≥25x109/L, 2) belongs to the following prognostic risk group according to
CPSS-MOL or MMM : CPSS-MOL: inter-2 risk (2 to 3 points); high risk (≥4 points);
MMM: inter-2 risk (2.5 to 4.5 points); high risk (≥5 points), or:
- According to the WHO (2016) classification standards (Arber 2016), researchers made
the diagnosis of other types of MDS/MPN (including aCML and MDS /MPN-U) based on
clinical and morphological characteristics. Other criteria should be met: 1) Neut
≥2x109/L, PLT ≥25x109/L, 2) Bone marrow blasts ≥5%;
- Patients who are not suitable for hematopoietic stem cell transplantation (HSCT)
according to the local medical standards and treatment guidelines;
- Patients who are suitable for Azacitidine(AZA) treatment according to the local
medical standards and treatment guidelines;
- BCR-ABL positive Chronic Myelogenous Leukemia (CML) and Ph chromosomal negative
classic myeloproliferative Neoplasms, such as essential thrombocytosis (ET),
polycythemia vera (PV) and primary myelofibrosis (PMF) are excluded;
- Age is between 18 to 80 years old;
- ALT, AST and serum bilirubin is no more than 2 times of the upper limit of normal
values (ULN), serum creatinine is no more than 150 μmol/L, and serum myocardial
enzyme is less than (the same age) 2 times of normal value upper limit;
- The LVEF determined by the echocardiography is no less than 50%;
- Estimated glomerular filtration rate (EGFR) is no less than 30ml · min · 1.73m2;
- Eastern Tumor Collaboration Group (ECOG) physical states score is 0 to 2;
- Informed Consent Form is signed by patients or legal agents.
Exclusion Criteria:
- BCR-ABL positive Chronic Myelogenous Leukemia (CML) and Ph chromosomal negative
classic myeloproliferative Neoplasms, such as essential thrombocytosis (ET),
polycythemia vera (PV) and primary myelofibrosis (PMF) ;
- Low risk or inter-1 risk CMML patients according to CPSS-MOL or MMM scores; other
types of MDS/MPN with less than 5% bone marrow blasts;
- Patients with Neut<2x109/L, PLT<25x109/L;
- Secondary acute leukemia, myeloid sarcoma, and blast phase of aCML;
- Patients who are allergic to any drug involved in the trial;
- Pregnancy, lactating Women, and patients who are unwilling to use contraceptives;
- Patients with abnormal Liver and kidney function which exceeded the inclusion
criteria;
- Patients with organic heart disease with clinical symptoms or heart dysfunction
(NYHA ≥ level 2);
- Patients with other malignancies at the same time except the following situations:
Patients had received treatment for the purpose of cure and had no active malignancies
for at least 5 years prior to enrollment; 2)Patients had received sufficient treatment,
non-melanoma skin cancer or malignant freckles -like moles with no signs of illness (even
if random grouping is less than 3 years); 3)Received sufficient treatment, in situ cancer
without signs of illness (even if the random group is less than 3 years);
- Patients with AIDS, syphilis, active hepatitis B (HBV-DNA can be measured) and
hepatitis C;
- Patients with cardiovascular diseases with clinical significance, such as arrhythmia
that have not been controlled or have symptoms, congestive heart failure or
myocardial infarction within 6 months, or level 3 (moderate) or level 4 (Severe)
heart disease (NYHA according to the New York Heart Society's functional grading
method);
- Patients with any situations that might interfere with research procedures or
results, or have the medical status or disease that will bring a certain risk to
participating in this study judged by researchers (such as activity systemic
infection);
- Patients who can't understand or follow the research plan;
- Patients who are under 18 or over 80 years old;
- Patients who underwent a major surgery within 4 weeks before the random grouping;
- Patients who are participating in other clinical trials one month before joining the
group;
- Patients who rely on illegal drugs;
- Patients with psychological disorders or cognitive disorders
Gender:
All
Minimum age:
18 Years
Maximum age:
80 Years
Healthy volunteers:
No
Locations:
Facility:
Name:
The First Affiliated Hospital of Nanjing Medical University
Address:
City:
Nanjing
Zip:
210000
Country:
China
Status:
Recruiting
Contact:
Last name:
Zhongxun Shi, MD
Phone:
+8613502187429
Email:
shizhongxun1@hotmail.com
Start date:
November 1, 2022
Completion date:
December 30, 2026
Lead sponsor:
Agency:
The First Affiliated Hospital with Nanjing Medical University
Agency class:
Other
Collaborator:
Agency:
Jiangbin Hospital Affiliated to Jiangsu University
Agency class:
Other
Collaborator:
Agency:
Nanjing Second Hospital
Agency class:
Other
Collaborator:
Agency:
Jiangning Hospital Affiliated to Nanjing Medical University
Agency class:
Other
Source:
The First Affiliated Hospital with Nanjing Medical University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05817955
