We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
Dose escalation study of amrubicin and cisplatin with concurrent thoracic radiotherapy for limited-disease small cell lung cancer.
- Authors
Shimada, Midori; Yamaguchi, Hiroyuki; Fukuda, Minoru; Tomono, Hiromi; Honda, Noritaka; Dotsu, Yosuke; Taniguchi, Hirokazu; Gyotoku, Hiroshi; Senju, Hiroaki; Takemoto, Shinnosuke; Ikeda, Takaya; Nakatomi, Katsumi; Nakamura, Yoichi; Nagashima, Seiji; Yamazaki, Takuya; Mukae, Hiroshi
- Abstract
<bold>Background: </bold>Amrubicin and cisplatin is one of the active regimens used to treat patients with extensive-disease (ED)-small cell lung cancer (SCLC), whereas combined therapy involving chemotherapy and concurrent thoracic radiotherapy is the standard treatment for limited-disease (LD)-SCLC.<bold>Purpose: </bold>This study aimed to determine the maximum tolerated dose (MTD) and dose-limiting toxicities (DLT) of amrubicin and cisplatin with concurrent thoracic radiotherapy (TRT) for LD-SCLC.<bold>Patients and Methods: </bold>Patients that fulfilled the following eligibility criteria were enrolled: being aged ≤ 75 years and chemotherapy-naïve and having a performance status (PS) of 0-1, LD-SCLC, and adequate organ function. The patients received escalating doses of amrubicin on days 1, 2, and 3, and a fixed 60-mg/m2 dose of cisplatin on day 1. Four cycles of chemotherapy were administered, with each cycle lasting 4 weeks. TRT involving 2 Gy/day, once daily, commenced on day 2 of the first cycle of chemotherapy. The initial dose of amrubicin was 20 mg/m2 (level 1), and the dose was escalated to 25 mg/m2 (level 2) and then 30 mg/m2 (level 3).<bold>Results: </bold>Eight patients from three institutions were enrolled at three dose levels. The patients' characteristics were as follows: male/female: 3/5; median age (range): 68.5 (60-73); PS 0/1: 4/4; stage IIIA/IIIB disease: 3/5. Both level 3 patients experienced DLT (grade 4 neutropenia and/or leukopenia lasting > 4 days). Level 3 was defined as the MTD, and level 2 was recommended as the dose for this regimen. Seven patients exhibited partial responses, and 1 displayed progressive disease (response rate: 88%). The median progression-free survival and overall survival periods were 11.1 and 39.5 months, respectively. No treatment-related deaths occurred.<bold>Conclusions: </bold>When this regimen was combined with TRT for LD-SCLC, the MTD was 30 mg/m2 for amrubicin and 60 mg/m2 for cisplatin. In addition, neutropenia and leukopenia were DLT, and doses of 25 mg/m2 for amrubicin and 60 mg/m2 for cisplatin are recommended for this regimen.
- Subjects
SMALL cell lung cancer; CISPLATIN; GEFITINIB; RADIOTHERAPY
- Publication
Cancer Chemotherapy & Pharmacology, 2019, Vol 84, Issue 5, p1059
- ISSN
0344-5704
- Publication type
journal article
- DOI
10.1007/s00280-019-03940-0