Nano-crystalline Megestrol Acetate for Anorexia-Cachexia Syndrome in Advanced Lung Cancer

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorGuangzhou Institute of Respiratory Disease

About this trial

Patients with advanced lung cancer are a high-risk population for cancer-related anorexia-cachexia syndrome (CACS). Meanwhile, the adverse reactions of chemotherapy and immunotherapy potentially exacerbate the occurrence and progression of CACS. CACS seriously affects the quality of life of patients with advanced lung cancer, significantly shortens the overall survival (OS) and progression-free survival (PFS), forming a vicious cycle. A number of previous studies have shown that combined supportive therapies such as megestrol acetate during chemotherapy or concurrent chemoradiotherapy for advanced tumor patients is a clinically meaningful and feasible treatment model in clinical practice. However, the efficacy and optimal treatment timing of combination with current first-line immunochemotherapy regimens remain unclear. Although mechanistic studies have shown that anti-cachexia therapy may synergistically enhance the efficacy of immunotherapy, relevant clinical research evidence is lacking.

Therefore, this study hypothesizes that the combination of first-line immunochemotherapy regimen and nano-crystalline megestrol acetate can improve the clinical benefits of patients with advanced lung cancer. It is planned to enroll patients with advanced lung cancer who present with anorexia-cachexia, and administer nano-crystalline megestrol acetate intervention (nano-crystalline megestrol acetate or its placebo control) during first-line immunochemotherapy. The changes in body weight relative to the baseline, as well as the impact on survival benefits and quality of life of patients, will be detected. In China, megestrol acetate is mainly available in two dosage forms: oral suspension and dispersible tablets. The oral suspension of megestrol acetate adopts nano-crystal technology (referred to as nano-crystalline megestrol acetate), which reduces the particle size of megestrol acetate and improves bioavailability. Previous randomized controlled studies have shown that it is superior to non-nano-crystal dosage forms in improving body weight.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with histologically or cytologically confirmed locally advanced (Stage ⅢC) or metastatic (Stage IV) non-small cell lung cancer (NSCLC) that cannot be completely resected surgically or treated with radical chemoradiotherapy, according to the 8th edition of the TNM staging classification for lung cancer by the International Association for the Study of Lung Cancer and the American Joint Committee on Cancer Classification.

Patients with histologically or cytologically confirmed small cell lung cancer (SCLC) and diagnosed as extensive-stage SCLC based on the 8th edition of AJCC staging or the Veterans Administration Lung Group (VALG) criteria (excluding mixed small cell lung cancer).

Subjects who have not received prior systemic chemotherapy for metastatic disease. Subjects who received adjuvant/neoadjuvant chemotherapy or radical concurrent/sequential chemoradiotherapy with curative intent for non-metastatic disease are eligible if disease progression occurs >6 months after the end of the last treatment.

At least one measurable tumor lesion according to RECIST v1.1.

Disqualifiers

Women who are pregnant, lactating, or planning to become pregnant during the study.

Among patients with positive HCV antibody, only those with negative HCV RNA by polymerase chain reaction (PCR) may participate.

Patients with positive human immunodeficiency virus (HIV) test results.

Receipt of major surgery (excluding diagnostic surgery) within 28 days before randomization, or expected to undergo major surgery during the study.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Nano-crystalline Megestrol Acetate Oral Suspension

    Drug

    Nano-crystalline Megestrol Acetate+PD-(L)1 inhibitor (Q3W, until PD) + chemotherapy (based on guidelines)

  • Nano-crystalline Megestrol Acetate Oral Suspension placebo

    Other intervention

    Nano-crystalline Megestrol Acetate placebo+PD-(L)1 inhibitor (Q3W, until PD) + chemotherapy (based on guidelines)

Treatment groups

116 Participants
are divided into 2 treatment groups
Group A: Nanocrystalline megestrol acetate+immunochemotherapyExperimental treatment 1 intervention
Group B: Nanocrystalline megestrol acetate placebo+immunochemotherapyPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

The proportion of participants with a body weight increase of >5% relative to the baseline.

Time frame
From enrollment to the end of treatment at 12 weeks

Secondary outcomes

1

appetite

The proportion of participants with a better appetite \>5% relative to the baseline. Participants report a score on a scale FAACT-A/CS 12,with 4 higher scores mean a better outcome.

Time frame
From enrollment to the end of treatment at 12 week
2

QOL

Participants report a score on a scale EORTC QLQ-C30.

Time frame
From enrollment to the end of treatment at 12 week
3

Anxiety and depression

Participants report a score on a scale HADS

Time frame
From enrollment to the end of treatment at 12 week
4

PFS in 6 months and 12 months

Time frame
From enrollment to the end of treatment at 6 months and 12 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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