Impact of Fat-free Mass in the Carboplatin Calculated Dose and Chemotherapeutic Toxicity in Patients With Advanced NSCLC

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInstituto Nacional de Cancerologia de Mexico

About this trial

This study evaluate the association of body composition (mainly free-fat mass), clinical and biochemical parameters with development of toxicity in patients under treatment with Carboplatin/Paclitaxel in advanced NSCLC.

Eligibility criteria

Qualifiers

Diagnosis of NSCLC Stage IV (stratification according to the American Joint Committee on Cancers - 7th edition)

Candidates for treatment with carboplatin plus paclitaxel 1st line

Performance status (ECOG 0-2)

Laboratory studies that demonstrate adequate renal, hepatic and hematologic function (blood chemistry and blood count)

Disqualifiers

Patients with renal impairment (KDOQI 3-5)

Patients who do not have computed tomography study at baseline

Uncontrolled blood pressure (> 140 mmHg)

Uncontrolled diabetes (> 130 mg / dL)

Trial design

Treatments tested in this trial

  • Carboplatin

Treatment groups

132 Participants
are divided into 2 treatment groups