Correlation Between Driver Gene Abnormalities and Clinicopathological Characteristics and Disease Prognosis in Lymphoma

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorHenan Cancer Hospital

About this trial

Correlation Between Driver Gene Abnormalities and Clinicopathological Characteristics and Disease Prognosis in Lymphoma

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosed as lymphoma (according to WHO 2017 classification criteria)

Life expectancy no less than 3 months

Agreeing to sign the written informed consents

Disqualifiers

Other malignant tumor history or active malignant tumor need be treated

Researchers determine unsuited to participate in this trial

Trial population

Including demographic characteristics / clinical characteristics / pathological characteristics / treatment and efficacy evaluations.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Incidence of driver gene abnormalities

the incidence of driver gene abnormalities by fixed gene testing technology

Time frame
from the day of the first patient was included to the date of the end of this trial, assessed up to 36 months

Secondary outcomes

1

objective response rate

the total proportion of patients with complete response (CR) and partial response (PR)

Time frame
from the date of the first patient was included to the date of the end of this trial, assessed up to 36 months
2

5-year overall survival

from the date of first patient was included to the date of death by any cause

Time frame
from the date of the first patient was included to the date of the end of this trial, assessed up to 5 years
3

Clinicopathological Characteristics

study data on clinicopathological characteristics related to incidence of driver gene abnormalities

Time frame
from the date of the first patient was included to the date of the end of this trial, assessed up to 36 months

Other outcomes

Sponsors and contacts

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