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Real World Study of MPM in China

Real World Study of Diagnosis, Treatment and Prognosis of Malignant Pleural Mesothelioma in China

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05042557
Enrollment
500
Registered
2021-09-13
Start date
2021-06-01
Completion date
2022-12-20
Last updated
2021-09-13

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

Conditions

Diagnoses Disease, Malignant Pleural Mesothelioma, Prognosis, Treatments

Keywords

MPM, Prognosis, Radiotherapy

Brief summary

Malignant pleural mesothelioma (MPM) is a highly aggressive tumor with atypical clinical manifestations. Most patients with MPM are at an advanced stage at the time of diagnosis, and only a few patients can be cured by radical surgery and other treatment measures. Pemetrexed + cisplatin chemotherapy with or without bevacizumab is still the standard treatment for MPM. In recent years, multimodality therapy including surgery, radiotherapy and chemotherapy have shown certain advantages in improving patient overall survival time. Targeted and immunotherapy may bring breakthroughs in MPM therapy. However, there are still no high-quality evidence-based medical evidence reports on the treatment model and effects of MPM patients in China. Focusing on MPM, we plan to systematically review the relevant scientific literature, confirm relevant scientific research questions, and provide references for related treatments. On this basis, we will estimate MPM incidence and mortality rates from 2014 to 2025 based on the data published by the National Cancer Registry. Meanwhile, a retrospective study cohort was constructed based on the electronic medical record database, and according to the research demand, patients were followed up with their post-discharge survival status to comprehensively describe and analyze the incidence, diagnosis, treatment, and prognosis of MPM patients. Also, exploratory analysis of the therapeutic effects of existing clinical treatments was conducted.

Interventions

None listed

Sponsors

Chinese Academy of Medical Sciences
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Pathologically confirmed as malignant pleural mesothelioma * Aged over 18

Exclusion criteria

* Follow-up less than 3 months

Design outcomes

Primary

MeasureTime frameDescription
Overall survival2-year overall survivalOverall survival is defined as the time from diagnosis to death for any reason or last follow-up

Secondary

MeasureTime frameDescription
Progression-free survival2-year progression-free survivalProgression-free survival is defined as the time from diagnosis to the first event of progression

Countries

China

Contacts

Primary ContactZhouguang Hui, Ph.D.
drhuizg@163.com861067781331

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026