Multimodal treatment for high-risk locally-advanced prostate cancer following radical prostatectomy and extended lymphadenectomy

被引:8
|
作者
Zattoni, Fabio [1 ]
Morlacco, Alessandro [1 ,2 ]
Matrone, Fabio [3 ]
Arcicasa, Mauro [3 ]
Buttazzi, Lorenzo [4 ]
Maruzzi, Daniele [4 ]
Fratino, Lucia [5 ]
Lo Re, Giovanni [5 ]
Bortolus, Roberto [3 ]
机构
[1] Univ Padua, Dept Surg Oncol & Gastroenterol, Padua, Italy
[2] Univ Padua, Dept Oncol & Surg Sci, Clin Urol, Padua, Italy
[3] Natl Canc Inst CRO, Dept Radiotherapy, Aviano, Pordenone, Italy
[4] Gen Hosp Pordenone, Dept Urol, Pordenone, Italy
[5] Natl Canc Inst CRO, Dept Med Oncol, Aviano, Pordenone, Italy
关键词
Prostatic neoplasms; Prostatectomy; Radiotherapy; Drug therapy; Combined modality therapy; CONFORMAL RADIATION-THERAPY; PHASE-I TRIAL; WEEKLY DOCETAXEL; NATURAL-HISTORY; CONCURRENT; MITOXANTRONE; PREDNISONE; RECURRENCE;
D O I
10.23736/S0393-2249.19.03388-5
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: The aim of this study was to prospectively evaluate the safety and oncologic outcomes of multimodal treatment in high risk-locally advanced prostate cancer patients (PCa). METHODS: High-risk-locally advanced prostate cancer patients without distant metastases before radical prostatectomy (RP) were included. Adjuvant high-dose intensity-modulated radiation therapy (IMRT) with concurrent docetaxel and long-term androgen-deprivation therapy (ADT) were started after 3-6 months from RP. ADT was maintained for two years. Acute and late toxicity were evaluated with the Common Terminology Criteria for Adverse Events (v. 3.0). Biochemical and clinical recurrence-free survival were explored by using the Kaplan-Meier method. RESULTS: Overall 42 patients were included. Acute genitourinary toxicity was observed with Grade I, II, and III in four (9.5%), two (4.8%), and one (2.3%) patients, respectively. Acute gastrointestinal toxicity was reported to be of Grade I and II in 12 (29.3%) and three (7.2%) patients, respectively. In these patients, concomitant genito-urinary and gastrointestinal toxicity occurred in three (7.2%) cases. A residual GU Grade I toxicity was present only in one patient. Toxicity due to CHT was found in four (9.5%) patients. Complete continence after RP and IMRT was achieved in 32 patients (76.2%). After a median follow-up of 3.4 years, BCR and clinical recurrence were observed in 16.7% and 9.5% of patients, respectively. A 5-year biochemical and clinical recurrence-free survival rate were 70.7% and 84.0%, respectively. Five-year overall survival was 93.6%. None of the patients died for prostate cancer during follow-up. CONCLUSIONS: This novel multimodal treatment paradigm for high-risk locally advanced prostate cancer has an acceptable level of toxicity and good oncological outcomes observed after a long follow-up.
引用
收藏
页码:508 / 515
页数:8
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