Weekly cabazitaxel plus prednisone is effective and less toxic for 'unfit' metastatic castration-resistant prostate cancer: Phase II Spanish Oncology Genitourinary Group (SOGUG) trial

被引:20
作者
Angel Climent, Miguel [1 ]
Perez-Valderrama, Begona [2 ]
Mellado, Begona [3 ]
Fernandez Parra, Eva Maria [4 ]
Fernandez Calvo, Ovidio [5 ]
Ochoa de Olza, Maria [6 ]
Muinelo Romay, Laura [7 ]
Anido, Urbano [8 ]
Domenech, Montserrat [9 ]
Hernando Polo, Susana [10 ]
Arranz Arija, Jose Angel [11 ]
Caballero, Cristina [12 ]
Juan Fita, Maria Jose [1 ]
Castellano, Daniel [13 ]
机构
[1] Inst Valenciano Oncol, Valencia 46009, Spain
[2] Hosp Univ Virgen Del Rocio, Med Oncol Dept, Seville, Spain
[3] Univ Barcelona, Hosp Clin, IDIBAPS, Med Oncol Dept, Barcelona, Spain
[4] Hosp Univ Nuestra Senora de Valme, Med Oncol Dept, Seville, Spain
[5] Complejo Hosp Univ Ourense, Med Oncol Dept, Orense, Spain
[6] Inst Catalan Oncol, Med Oncol Dept, Barcelona, Spain
[7] CIBERONC, Hlth Res Inst Santiago de Compostela IDIS, Liquid Biopsy Anal Unit, Translat Med Oncol, Santiago De Compostela, Spain
[8] Complexo Hosp Univ Santiago de Compostela, Santiago De Compostela, Spain
[9] Hosp Althaia, Med Oncol Dept, Manresa, Spain
[10] Hosp Univ Fdn Alcorcon, Med Oncol Dept, Alcorcon, Spain
[11] Hosp Gen Univ Gregorio Maranon, Med Oncol Dept, Madrid, Spain
[12] Hosp Gen Univ Valencia, Med Oncol Dept, Valencia, Spain
[13] Hosp Univ 12 Octubre, Med Oncol Dept, Madrid, Spain
关键词
Cabazitaxel; Castration-resistant prostate cancer; Circulating tumour cells; Dosing schedule; Toxicity; CIRCULATING TUMOR-CELLS; CLINICAL-TRIALS; SAFETY DATA; DOCETAXEL; SURVIVAL; RECOMMENDATIONS; BENEFIT;
D O I
10.1016/j.ejca.2017.09.028
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: Cabazitaxel (CBZ), a novel tubulin-binding taxane, improves overall survival in metastatic castration-resistant prostate cancer (mCRPC) that progresses during or after docetaxel treatment. We have designed a phase II study to evaluate the efficacy and safety of CBZ as a weekly schedule for 'unfit' mCRPC patients after docetaxel failure. Methods: In this single arm phase II study. CBZ was weekly administered in 1-hour infusion on days 1, 8, 15 and 22, every 5 weeks at 10 mg/m(2) to eligible 'unfit' patients; oral prednisone (5 mg) was administered twice a day. Circulating tumour cells (CTCs) were also collected. New treatment scheme was considered effective if at least 65% of patients met a clinical benefit criteria based on prostate-specific antigen (PSA)-progression-free survival (PFS) values at week 12. Results: Seventy patients (median age: 73.9 years) were enrolled; overall, 71.4% had an Eastern Cooperative Oncology Group Performance Status (ECOG-PS) of 2; and 84%, 16% and 11% had bone, liver and lung metastases, respectively. Objective partial response or stable disease was achieved in 61% of patients, while PSA responses of >= 50% and >= 80% were observed in 34.8% and 10.6%, respectively. The median PSA-PFS was 4.8 months; and 68.6% of patients had no progression at week 12. The most frequent grade 3/4 toxicities were neutropenia (2.8%), leukopenia (5.7%) and thrombocytopaenia (9%); no cases of febrile neutropenia were reported. Early CTC response was significantly correlated with PSA-PFS. Conclusions: CBZ/prednisone administered weekly to 'unfit' mCRPC patients appears to be as effective as classical standard 3-week scheme (TROPIC study) but with significantly lower toxicities and better tolerance. Early CTC response appears to be valuable as an early end-point of therapeutic efficacy. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:30 / 37
页数:8
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