Trilaciclib for the Prevention of Chemoradiotherapy-Induced Myelosuppression in Esophageal Squamous Cell Carcinoma

ConditionESCC
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe First Affiliated Hospital with Nanjing Medical University

About this trial

Clinical data of patients with synchronous radiotherapy for esophageal cancer in the Department of Radiology of Jiangsu Provincial People's Hospital were collected. Patients were divided into trilaciclib group (34 cases) and control group (169 cases) based on whether trilaciclib was used or not. Patients in the trilaciclib group were given trilaciclib before each chemotherapy treatment. Propensity score matching (PSM) was used to balance the baseline characteristics between the two groups on a 1:1 ratio. After pairing, the rates of bone marrow suppression and other adverse events were compared between the two groups.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

age ≥18 years;

pathological diagnosis of esophageal squamous cell carcinoma;

failure to undergo surgical treatment;

completion of definitive chemoradiotherapy or chemoradiotherapy combined with immunotherapy.

Disqualifiers

history of other malignant tumors;

difficulty in follow-up;

insufficient clinical information.

Trial population

Patients with esophageal squamous carcinoma who received concurrent chemoradiotherapy with or without trilaciclib.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Trilaciclib Injection [Cosela]

    Drug

    Trilaciclib Combined chemoradiotherapy

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Observation group1 intervention
Group B: Control group0 interventions

Trial outcomes

Primary outcomes

1

Incidence of grade ≥3 neutropenia

Incidence of grade ≥3 neutropenia

Time frame
during Trilaciclib plus chemotherapy assessed up to 1 years

Secondary outcomes

1

Incidence of Adverse Events

The incidence of Adverse Events according to Common Terminology Criteria for Adverse Events

Time frame
during Trilaciclib plus chemotherapy assessed up to 1 years

Other outcomes

Sponsors and contacts

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