Phase I study of etoposide, cisplatin and irinotecan triplet in patients with advanced-stage small-cell lung cancer
Ημερομηνία
2005Συγγραφέας
Briassoulis, E. ChSamantas, E.
![ORCID logo](https://orcid.org/sites/default/files/images/orcid_16x16.png)
Skarlos, Dimosthenis V.
Makatsoris, T.
Christodoulou, C.
Fountzilas, George
Bamias, A. T.
Dimopoulos, M. A.
Kosmidis, Paraskevas A.
![ORCID logo](https://orcid.org/sites/default/files/images/orcid_16x16.png)
Source
Cancer chemotherapy and pharmacologyVolume
56Issue
5Pages
521-528Google Scholar check
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Εμφάνιση πλήρους εγγραφήςΕπιτομή
The irinotecan-cisplatin combination has emerged as a new standard for the treatment of advanced-stage small-cell lung cancer (AS-SCLC). To move forward we developed a 3-day regimen of cisplatin, etoposide and irinotecan. Successive cohorts of AS-SCLC patients were treated with irinotecan administered as a single 1-h infusion in combination with fixed doses of cisplatin (20 mg/m 2) and etoposide (75 mg/m2), both given for three consecutive days (ECI regimen). Irinotecan dose was escalated from 60 mg/m 2 by 40-mg/m2 increments. At mid-step between the maximum tolerated dose (MTD) and the previous dose level, patients were randomized for the day of administration of irinotecan (day 1 vs day 3). A total of 36 AS-SCLC patients received 166 courses of treatment at four dose levels. The MTD of irinotecan was 140 mg/m2 (three dose-limiting toxicities, DLTs), and the recommended optimal dose (ROD) 120 mg/m2 (two DLTs). DLTs were febrile neutropenia and grade 3 diarrhea. Other toxicities were mild. No difference in toxicity was seen between the two time schedules. A 77% (95% CI 63.25-90.75%) response rate was recorded among 31 evaluable patients and the median survival was 12 months. The ECI regimen was well tolerated and showed considerable activity in patients with AS-SCLC. Phase II/III evaluation is ongoing. © Springer-Verlag 2005.
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