A phase I study of weekly doxorubicin and oral topotecan for patients with relapsed or refractory small cell lung cancer (SCLC): A Fred and Pamela Buffet Cancer Center Clinical Trials Network study

•Topotecan and doxorubicin provide sequential topoisomerase I and II inhibition.•Hematologic side effects were the most common. There were no therapy-related grade 5 toxicities.•The maximum tolerated dose of oral topotecan was 1.35 mg/m2.•The response rate was 20% (4/20); median PFS and OS were 3.6...

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Veröffentlicht in:Cancer treatment and research communications 2020-01, Vol.22, p.100162-100162, Article 100162
Hauptverfasser: Ernani, Vinicius, Jahan, Rahat, Smith, Lynette M., Marr, Alissa S., Kimbrough, Sarah E., Kos, Mary E., Tijerina, Jolene, Pivovar, Shannon, Lakshmanan, Imayavaramban, Ketcham, Marsha, Rauth, Sanchita, Mallya, Kavita, Nasser, Mohd W, Jain, Maneesh, Kessinger, Anne, Batra, Surinder K., Ganti, Apar Kishor
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Sprache:eng
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Zusammenfassung:•Topotecan and doxorubicin provide sequential topoisomerase I and II inhibition.•Hematologic side effects were the most common. There were no therapy-related grade 5 toxicities.•The maximum tolerated dose of oral topotecan was 1.35 mg/m2.•The response rate was 20% (4/20); median PFS and OS were 3.6 months and 6 months, respectively.•The combination of topotecan and doxorubicin is safe and effective in relapsed SCLC. Relapsed/refractory small cell lung cancer (SCLC) has a poor prognosis, with no good options. We evaluated a novel combination of topotecan and doxorubicin, providing sequential topoisomerase I and II inhibition, in this setting. Adult patients (>19 years) with relapsed/refractory SCLC, who had received at least one prior chemotherapy regimen were eligible. Patients received escalating doses of oral topotecan on days 1–5 of each three week cycle (maximum - 5 cycles). The dosing cohorts were: 0.85 mg/m2, 1.05 mg/m2, 1.35 mg/m2, 1.65 mg/m2 and 2.30 mg/m2. All patients received weekly doxorubicin 20 mg/m2 intravenously starting day 6 of the first cycle and continued weekly for a maximum of 15 weeks. In the absence of pre-specified dose limiting toxicities (DLT), patients were enrolled serially to escalated dose level cohorts. Twenty-two patients were enrolled, of which 20 were evaluable. Median age was 61 years; 74% were male and 95% were Caucasian. Hematologic side effects were the most common adverse events. There were no therapy-related Grade 5 toxicities. Incidence of DLT based on cohorts were: DL2: 1/6 (Grade 4 thrombocytopenia), DL3: 1/6 (AST elevation) and DL4: 2/4 (Grade 4 thrombocytopenia). Response rate was 20% (4/20) and disease control rate (SD + PR) was 36%. The median progression free and overall survival were 3.6 months and 6 months, respectively. The combination of topotecan and doxorubicin was safe and effective in relapsed/refractory SCLC. The maximum tolerated dose of oral topotecan was 1.35 mg/m2 when given concurrently with weekly doxorubicin.
ISSN:2468-2942
2468-2942
DOI:10.1016/j.ctarc.2019.100162