医学
前列腺切除术
泌尿科
前列腺癌
列线图
阶段(地层学)
新辅助治疗
雄激素剥夺疗法
活检
生存分析
内科学
妇科
外科
肿瘤科
癌症
乳腺癌
古生物学
生物
作者
James A. Eastham,Glenn Heller,Susan Halabi,Paul Monk,Steven K. Clinton,Russell Z. Szmulewitz,Jonathan Coleman,Martin Gleave,Christopher P. Evans,David W. Hillman,Himisha Beltran,Mary‐Ellen Taplin,Olwen Hahn,J. Kellogg Parsons,Eric J. Small,James L. Mohler,Michael J. Morris
标识
DOI:10.1200/jco.2019.37.15_suppl.5079
摘要
5079 Background: Neoadjuvant CHT followed by RP did not increase 3-year biochemical progression free-survival (bPFS) compared to RP alone in men with CLHRPC. However, there is evidence that bPFS and overall survival over time was improved. In the current analysis we assessed whether CHT followed by RP improved pathological specimen features compared to RP alone. Methods: CALGB 90203 (Alliance) is a Phase III study which randomly assigned, in a 1:1 fashion, men with CLHRPC [biopsy Gleason Grade Group (GGG) 4 or 5 or Kattan pre-op nomogram bPFS < 60%] to RP alone or RP plus neoadjuvant CHT [androgen deprivation plus docetaxel (75 mg/m 2 every 3 weeks for 6 cycles)]. We conducted an exploratory analysis comparing histologic findings, determined at the treating center, in the RP specimens of men receiving CHT plus RP and men treated with RP alone. We used the Chi-square test, with P-values adjusted by the Holm method for multiple comparisons. Results: A total of 788 men (median age, 62; range: 32-83 years) were randomized, with 738 ultimately undergoing RP. There was no difference in pathologic GGG (Table). Men treated with neoadjuvant CHT had a lower pathologic T-stage and lower likelihood of having seminal vesicle invasion (SVI), positive pelvic lymph nodes, or positive surgical margins (SM) (Table). Conclusions: Most pathologic features in the RP specimen were improved in men receiving neoadjuvant CHT compared to RP alone. The relationship between pathologic changes and the development of metastasis and survival require further analysis. RP pathologic outcomes. Summary statistics are calculated for the number of patients with non-missing data for each characteristic. Clinical trial information: NCT00430183. [Table: see text]
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