Efficacy and safety of lurbinectedin and doxorubicin in relapsed small cell lung cancer. Results from an expansion cohort of a phase I study

Summary Background A phase I study found remarkable activity and manageable toxicity for doxorubicin (bolus) plus lurbinectedin (1-h intravenous [i.v.] infusion) on Day 1 every three weeks (q3wk) as second-line therapy in relapsed small cell lung cancer (SCLC). An expansion cohort further evaluated...

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Veröffentlicht in:Investigational new drugs 2021-10, Vol.39 (5), p.1275-1283
Hauptverfasser: Olmedo, María Eugenia, Forster, Martin, Moreno, Victor, López-Criado, María Pilar, Braña, Irene, Flynn, Michael, Doger, Bernard, de Miguel, María, López-Vilariño, José Antonio, Núñez, Rafael, Kahatt, Carmen, Cullell-Young, Martin, Zeaiter, Ali, Calvo, Emiliano
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Sprache:eng
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Zusammenfassung:Summary Background A phase I study found remarkable activity and manageable toxicity for doxorubicin (bolus) plus lurbinectedin (1-h intravenous [i.v.] infusion) on Day 1 every three weeks (q3wk) as second-line therapy in relapsed small cell lung cancer (SCLC). An expansion cohort further evaluated this combination. Patients and methods Twenty-eight patients with relapsed SCLC after no more than one line of cytotoxic-containing chemotherapy were treated: 18 (64%) with sensitive disease (chemotherapy-free interval [CTFI] ≥90 days) and ten (36%) with resistant disease (CTFI
ISSN:0167-6997
1573-0646
DOI:10.1007/s10637-020-01025-x