Open AccessMulticentric phase II trial of TI‐CE high‐dose chemotherapy with therapeutic drug monitoring of carboplatin in patients with relapsed advanced germ cell tumors
Author(s) -
Chevreau Christine,
Massard Christophe,
Flechon Aude,
Delva Rémy,
Gravis Gwenaëlle,
Lotz JeanPierre,
Bay JacquesOlivier,
GrossGoupil Marine,
Fizazi Karim,
Mourey Loïc,
Paci Angelo,
Guitton Jérôme,
Thomas Fabienne,
Lelièvre Bénédicte,
Ciccolini Joseph,
Moeung Sotheara,
Gallois Yohan,
Olivier Pascale,
Culine Stéphane,
Filleron Thomas,
Chatelut Etienne
Publication year - 2021
Publication title -
cancer medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.403
H-Index - 53
ISSN - 2045-7634
DOI - 10.1002/cam4.3687
Subject(s) - carboplatin , medicine , etoposide , ifosfamide , regimen , chemotherapy , phases of clinical research , urology , germ cell tumors , clinical endpoint , area under the curve , surgery , paclitaxel , gastroenterology , clinical trial , cisplatin
Background High‐dose chemotherapy (HDCT) with TI‐CE regimen is a valid option for the treatment of relapsed advanced germ cell tumors (GCT). We report a phase II trial with therapeutic drug monitoring of carboplatin for optimizing area under the curve (AUC) of this drug. Methods Patients with unfavorable relapsed GCT were treated according to TI‐CE regimen: two cycles combining paclitaxel and ifosfamide followed by three cycles of HD carboplatin plus etoposide administered on 3 days. Carboplatin dose was adapted on day 3 based on carboplatin clearance (CL) at day 1 in order to reach a target AUC of 24 mg.min/mL per cycle. The primary endpoint was the complete response (CR) rate. Results Eighty‐nine patients who received HDCT were included in the modified intent‐to‐treat (mITT) analysis. Measured mean AUC was 24.4 mg.min/mL per cycle (22.4 and 26.8 mg.min/mL for 10th and 90th percentiles). Thirty‐five (44.3%) patients achieved a CR with or without surgery of residual masses and 20 patients achieved a partial response with negative tumor markers. With a median follow‐up of 44 months (m), median PFS was 12.3 m (95% CI: 7.5–25.9) and OS was 46.3 m (95% CI: 18.6–not reached). For high‐ and very high‐risk patients, according to the International Prognostic Score at first relapse or treated after at least one salvage treatment (n = 51), 2‐year PFS rate was 41.1%. Conclusion The rates of complete and favorable responses were clinically relevant in this very poor risk population. Individual monitoring of carboplatin plasma concentration permitted to control more accurately the target AUC and avoided both underexposure and overexposure to the drug.