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Exploring the clinical efficacy and mechanism of anti-tumor formula in the treatment of diffuse large B-cell lymphoma based on mir-296-5p/PTEN signaling axis

Exploring the clinical efficacy and mechanism of anti-tumor formula in the treatment of diffuse large B-cell lymphoma based on mir-296-5p/PTEN signaling axis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089701
Enrollment
Unknown
Registered
2024-09-13
Start date
2022-11-28
Completion date
Unknown
Last updated
2024-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diffuse large B cell lymphoma

Interventions

Control Group:Subjects were followed up regularly every 3 months for a total of 12 months as prescribed by the physician.
Test Group: The above Chinese medicinal herbs were all provided by the Chinese herbal pharmacy of Yueyang Hospital of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, and dec
the frequency of the follow-up observation time was consistent with that of the control group.

Sponsors

Shanghai University of Traditional Chinese Medicine, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
29 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with diffuse large B-cell lymphoma definitively diagnosed on the basis of tissue biopsy, clinical symptoms, and laboratory tests and clinically assessed to be in complete remission (CR) or indeterminate complete remission (CRu) after completion of the R-CHOP/CHOP chemotherapy regimen; 2. 18 years = age = 75 years, gender is not limited; 3. TCM disease identification consistent with phlegm-toxicity disease, meeting the diagnostic criteria of Zhengxu phlegm coagulation syndrome; 4. Kanofskky score (KPS) =70 points (can take care of themselves, but cannot live and work normally); 5. Understanding, agreeing to participate in this study and signing the informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe vital organ insufficiency (NYHA cardiac function class 3-4; pulmonary hypoplasia class 3-4; hepatic function Child-Pugh class C; renal function CKD class 3-5); 2. Previous diagnosis of a malignancy other than non-Hodgkin's lymphoma; 3. Pregnant or lactating patients; 4 .Active or uncontrolled serious infection (= CTCAE grade 2 infection); 5. Consciousness and mental disorders and lack of independent judgment; 6. Those who have participated or are participating in other clinical trials within 2 weeks prior to enrollment.

Design outcomes

Primary

MeasureTime frame
Relapse;

Secondary

MeasureTime frame
1-year progression-free survival (PFS) rate;TCM Symptom Score;Karnofsky score;Tumor load indicators (LDH, ß2-MG, ferritin);Cytokines (IL-2, IL-6, IFN-?, TNF-a);

Countries

China

Contacts

Public ContactLi Jiekai; Zhou Yongming

Yueyang Hospital of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, China

623640299@qq.com+86 166 2119 0513

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026