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OPTIMA: An Open-Label, Noncomparative Pilot Trial of Inhaled Molgramostim in Pulmonary Nontuberculous Mycobacterial Infection.
Thomson, Rachel M; Loebinger, Michael R; Burke, Andrew J; Morgan, Lucy C; Waterer, Grant W; Ganslandt, Cecilia.
Afiliação
  • Thomson RM; School of Clinical Medicine, University of Queensland, Brisbane, Queensland, Australia.
  • Loebinger MR; Gallipoli Medical Research Foundation, Greenslopes Private Hospital, Greenslopes, Queensland, Australia.
  • Burke AJ; The Prince Charles Hospital, Brisbane, Queensland, Australia.
  • Morgan LC; National Heart and Lung Institute, Imperial College and Royal Brompton Hospital, London, United Kingdom.
  • Waterer GW; School of Clinical Medicine, University of Queensland, Brisbane, Queensland, Australia.
  • Ganslandt C; The Prince Charles Hospital, Brisbane, Queensland, Australia.
Ann Am Thorac Soc ; 21(4): 568-576, 2024 Apr.
Article em En | MEDLINE | ID: mdl-37948736
ABSTRACT
Rationale Inhaled granulocyte-macrophage colony-stimulating factor (GM-CSF) has been proposed as a potential immunomodulatory treatment for nontuberculous mycobacterial (NTM) infection.

Objectives:

This open-label, noncomparative pilot trial investigated the efficacy and safety of inhaled GM-CSF (molgramostim nebulizer solution) in patients with predominantly treatment-refractory pulmonary NTM infection (Mycobacterium avium complex [MAC] and M. abscessus [MABS]), either in combination with ongoing guideline-based therapy (GBT) or as monotherapy in patients who had stopped GBT because of lack of efficacy or intolerability.

Methods:

Thirty-two adult patients with refractory NTM infection (MAC, n = 24; MABS, n = 8) were recruited into two cohorts those with (n = 16) and without (n = 16) ongoing GBT. Nebulized molgramostim 300 µg/d was administered over 48 weeks. Sputum cultures and smears and clinical assessments (6-min-walk distance, symptom scores, Quality of Life-Bronchiectasis Questionnaire score, and body weight) were collected every 4 weeks during treatment and 12 weeks after the end of treatment. The primary endpoint was sputum culture conversion, defined as three consecutive monthly negative cultures during the treatment period.

Results:

Eight patients (25%) achieved culture conversion on treatment (seven [29.2%] patients with MAC infection, one [12.5%] patient with MABS infection); in four patients, this was durable after the end of treatment. Of the 24 patients with MAC infection, an additional 4 patients had a partial response, converting from smear positive at baseline to smear negative at the end of treatment, and time to positivity in liquid culture media increased. Two of these patients sustained negative cultures from the end of treatment. Other clinical endpoints were unchanged. Serious adverse events were mainly pulmonary exacerbations or worsening NTM infection. Three deaths, not treatment related, were reported.

Conclusions:

In this population of patients with severe NTM disease, molgramostim was safe and well tolerated. Sputum culture conversion rates for patients with MAC infection (29.2%) were greater than reported for similar refractory MAC cohorts managed with GBT alone. Less benefit was seen for MABS infection. No serious safety concerns were identified. Further evaluation in a larger cohort is warranted.Clinical trial registered with www.clinicaltrials.gov (NCT03421743).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecção por Mycobacterium avium-intracellulare / Infecções por Mycobacterium não Tuberculosas Limite: Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecção por Mycobacterium avium-intracellulare / Infecções por Mycobacterium não Tuberculosas Limite: Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article