Histologic predictors of renal cell carcinoma response to interleukin-2-based therapy

被引:167
作者
Upton, MP
Parker, RA
Youmans, A
McDermott, DF
Atkins, MB
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Biometr Ctr, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Div Hematol Oncol, Boston, MA 02115 USA
关键词
renal cancer; IL-2; histologic features;
D O I
10.1097/01.cji.0000170357.14962.9b
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The authors examined pathology from patients with renal cancer (RCC) treated with IL-2 to determine response rates for clear cell and variant RCC and to identify histologic features that predict response. Pathology specimens were reviewed by a single pathologist who was blinded to both the prior pathology interpretation and the therapeutic response. Findings were correlated with response to IL-2 therapy. Evaluable pathology specimens were obtained from 231 patients. Of 163 primary RCCs, the response rate was 21% (30/146) for patients with clear cell versus 6% (1/17) for patients with variant or indeterminate type RCC (P = 0.20). For clear cell carcinomas, response to IL-2 was associated with the presence of alveolar features and the absence of papillary and granular features. Patients with more than 50% alveolar features and no granular or papillary features had a 39% response rate (14/36). Patients with alveolar and granular features representing less than 50% of the specimen and no papillary features had a 19% response rate (15/77). The response rate for the others was 3% (1/33). This model was then applied to an independent sample of 68 metastasis specimens. Response rates in the three prognostic groups and for patients with non-clear cell cancers were 25% (5/20), 9% (2/22), 0% (0/16), and 0% (0/10), respectively. Median survivals for all patients with clear cell tumors by risk group were 2.87, 1.36, and 0.87 years, respectively (P < 0.001). These data suggest that patients with non-clear cell RCC or with clear cell RCC with papillary, no alveolar, and/or more than 50% granular features respond poorly to IL-2 and should be considered for alternative treatments. Investigation of other tumor-related predictors of IL-2 responsiveness is warranted.
引用
收藏
页码:488 / 495
页数:8
相关论文
共 43 条
[1]  
Almand B, 2000, CLIN CANCER RES, V6, P1755
[2]  
Atkins MB, 2001, MED ONCOL, V18, P197
[3]  
BOSTWICK D, 1997, UROLOGIC SURG PATHOL, P88
[4]   RENAL-CARCINOMA - COMPUTER-ANALYSIS OF 96 PATIENTS TREATED BY NEPHRECTOMY [J].
BOXER, RJ ;
WAISMAN, J ;
LIEBER, MM ;
MAMPASO, FM ;
SKINNER, DG .
JOURNAL OF UROLOGY, 1979, 122 (05) :598-601
[5]   Sarcomatoid renal cell carcinoma: Biologic behavior, prognosis, and response to combined surgical resection and immunotherapy [J].
Cangiano, T ;
Liao, J ;
Naitoh, J ;
Dorey, F ;
Figlin, R ;
Belldegrun, A .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (02) :523-528
[6]   Sarcomatoid differentiation in renal cell carcinoma - A study of 101 cases [J].
de Peralta-Venturina, M ;
Moch, H ;
Amin, M ;
Tamboli, P ;
Hailemariam, S ;
Mihatsch, M ;
Javidan, J ;
Stricker, H ;
Ro, JY ;
Amin, MB .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (03) :275-284
[7]   RENAL-CELL CARCINOMA .2. HISTOLOGICAL INDICATORS OF PROGNOSIS [J].
DELAHUNT, B ;
NACEY, JN .
PATHOLOGY, 1987, 19 (03) :258-263
[8]  
Delahunt B, 1997, MODERN PATHOL, V10, P537
[9]  
Figlin R, 1997, CANCER J SCI AM, V3, pS92
[10]  
FISHER AS, 1997, ADV ATOM SP, V3, P1