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Combining Genomics and Imageomics to Predict the Sensitivity of Neoadjuvant Pemetrexed and Cisplatin Chemotherapy in Patients With Lung Adenocarcinoma

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Fudan University

Status

Not yet enrolling

Conditions

Sensitivity

Treatments

Other: Neoadjuvant pemetrexed and cisplatin chemotherapy

Study type

Observational

Funder types

Other

Identifiers

NCT05185544
B2021-Zhan

Details and patient eligibility

About

Combining genomics and imageomics to predict the sensitivity of neoadjuvant pemetrexed and cisplatin chemotherapy in patients with lung adenocarcinoma

Enrollment

50 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

    1. Aged between 18 and 75 years;
    1. Lung adenocarcinoma;
    1. The patient is able to receive neoadjuvant pemetrexed and cisplatin chemotherapy
  • 4 .The patient is able to understand and comply with the study and has provided written informed consent.

Exclusion criteria

    1. Patients with a history of lung surgery;
    1. Postoperative pathology showed non-primary lung cancer;
    1. Patients with a history of other tumors;
    1. Patients with severe complications (coronary heart disease, valvular heart disease, end-stage renal disease, severe liver cirrhosis);
    1. Unable to cooperate with the researchers because of dementia or cognitive decline
    1. Other situations that are not in conformity with the standards and requirements of this trial.

Trial design

50 participants in 1 patient group

neoadjuvant pemetrexed and cisplatin chemotherapy in patients with lung adenocarcinoma
Description:
neoadjuvant pemetrexed and cisplatin chemotherapy in patients with lung adenocarcinoma
Treatment:
Other: Neoadjuvant pemetrexed and cisplatin chemotherapy

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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