Long-term Survivorship of Discharged Patients With Malignant Tumor Based on Single-institutional Cancer Registry

NCT ID: NCT04996732

Last Updated: 2021-08-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

500000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-01-01

Study Completion Date

2041-12-31

Brief Summary

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Real-world studies on long-term prognosis in patients who underwent anti-tumor treatments during hospitalization from a hospital-based cancer registry in china.

Detailed Description

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This is a single-center continuous enrollment cohort study. The overall survival and disease-free survival of patients with malignant tumors in the target tumor hospital undergoing surgery, radiotherapy, chemotherapy, and immunotherapy were observed. Follow-up methods include medical records review, telephone call interview, and data linkage to the related provincial death certificate registries. This study will provide real world data-sets for researches on long-term survival and prognosis of cancer patients, and expend exploration on the cancer survival determinants both from clinical and social-economic prospective.

Conditions

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Neoplasms Survival Surgery Radiotherapy Drug Therapy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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All Cancers

subgroups according to cancer sites

hospitalization

Intervention Type PROCEDURE

Including various treatments such as surgery, radiotherapy, chemotherapy and immunotherapy during hospitalization

Interventions

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hospitalization

Including various treatments such as surgery, radiotherapy, chemotherapy and immunotherapy during hospitalization

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* All patients who completed tumor treatment (including surgery, radiotherapy, chemotherapy, immunotherapy, etc.) due to malignant tumors based on preoperative or intraoperative evaluation in Fudan University Shanghai Cancer Center during the study period.

Exclusion Criteria

* Patients who have not been treated during hospitalization;
* Patients with non-malignant tumors.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Fudan University

OTHER

Sponsor Role lead

Responsible Party

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Ying Zheng

Director of Cancer Prevention Department, Fudan University Shanghai Cancer Center

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Fudan University Shanghai Cancer Center

Shanghai, , China

Site Status RECRUITING

Countries

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China

Central Contacts

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Ying Zheng, Dr.

Role: CONTACT

+8618121299522

Facility Contacts

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Ying Zheng, Dr.

Role: primary

+8618121299522

Other Identifiers

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YF-2021-01

Identifier Type: -

Identifier Source: org_study_id

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