Coaltered Ras/B-raf and TP53 Is Associated with Extremes of Survivorship and Distinct Patterns of Metastasis in Patients with Metastatic Colorectal Cancer

被引:64
作者
Datta, Jashodeep [1 ,2 ]
Smith, J. Joshua [1 ,2 ]
Chatila, Walid K. [3 ,4 ]
McAuliffe, John C. [1 ,5 ]
Kandoth, Cyriac [4 ]
Vakiani, Efsevia [6 ]
Frankel, Timothy L. [1 ,7 ]
Ganesh, Karuna [3 ,8 ]
Wasserman, Isaac [1 ]
Lipsyc-Sharf, Marla [8 ]
Guillem, Jose [1 ]
Nash, Garrett M. [1 ]
Paty, Philip B. [1 ]
Weiser, Martin R. [1 ]
Saltz, Leonard B. [8 ]
Berger, Michael F. [3 ,4 ,6 ]
Jarnagin, William R. [1 ]
Balachandran, Vinod [1 ]
Kingham, T. Peter [1 ]
Kemeny, Nancy E. [8 ]
Cercek, Andrea [8 ]
Garcia-Aguilar, Julio [1 ]
Taylor, Barry S. [3 ,4 ,9 ]
Viale, Agnes [4 ]
Yaeger, Rona [8 ]
Solit, David B. [3 ,4 ,8 ]
Schultz, Nikolaus [3 ,4 ,9 ]
D'Angelica, Michael, I [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10065 USA
[2] Univ Miami, Miller Sch Med, Dept Surg, Sylvester Comprehens Canc Ctr, Miami, FL 33136 USA
[3] Mem Sloan Kettering Canc Ctr, New York, NY 10065 USA
[4] Mem Sloan Kettering Canc Ctr, Marie Josee & Henry R Kravis Ctr Mol Oncol, New York, NY 10065 USA
[5] Montefiore Med Ctr, Dept Surg, 111 E 210th St, Bronx, NY 10467 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10065 USA
[7] Univ Michigan, Sch Med, Dept Surg, Ann Arbor, MI USA
[8] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10065 USA
[9] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
关键词
MICROSATELLITE INSTABILITY; HEPATIC RESECTION; LIVER METASTASES; PROGNOSTIC ROLE; APC MUTATIONS; COLON-CANCER; SURVIVAL; DEFINES; RECURRENCE; OUTCOMES;
D O I
10.1158/1078-0432.CCR-19-2390
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We aimed to investigate genomic correlates underlying extremes of survivorship in metastatic colorectal cancer and their applicability in informing survival in distinct subsets of patients with metastatic colorectal cancer. Experimental Design: We examined differences in oncogenic somatic alterations between metastatic colorectal cancer cohorts demonstrating extremes of survivorship following complete metastasectomy: <= 2-year (n = 17) and >= 10-year (n = 18) survivors. Relevant genomic findings, and their association with overall survival (OS), were validated in two independent datasets of 935 stage IV and 443 resected stage I-IV patients. Results: In the extremes-of-survivorship cohort, significant co-occurrence of KRAS hotspot mutations and TP53 alterations was observed in <= 2-year survivors (P < 0.001). When validating these findings in the independent cohort of 935 stage IV patients, incorporation of the cumulative effect of any oncogenic Ras/B-raf (i.e., either KRAS, NRAS, or BRAF) and TP53 alteration generated three prognostic clusters: (i) TP53-altered alone (median OS, 132 months); (ii) Ras/B-raf-altered alone (65 months) or Ras/B-raf- and TP53 pan-wild-type (60 months); and (iii) coaltered Ras/B-raf-TP53 (40 months; P < 0.0001). Coaltered Ras/B-raf-TP53 was independently associated with mortality (HR, 2.47; 95% confidence interval, 1.91-3.21; P < 0.001). This molecular profile predicted survival in the second independent cohort of 443 resected stage I-IV patients. Coaltered Ras/B-raf-TP53 was associated with worse OS in patients with liver (n = 490) and lung (n = 172) but not peritoneal surface (n = 149) metastases. Moreover, coaltered Ras/B-raf-TP53 tumors were significantly more likely to involve extrahepatic metastatic sites with limited salvage options. Conclusions: Genomic analysis of extremes of survivorship following colorectal cancer metastasectomy identifies a prognostic role for coaltered Ras/B-raf-TP53 and its association with distinct patterns of colorectal cancer metastasis.
引用
收藏
页码:1077 / 1085
页数:9
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