Retrospective Evaluation of Treatment Response in Patients with Nonmetastatic Pancreatic Cancer Using CT and CA 19-9

被引:12
|
作者
Kim, Seung-Seob [1 ,2 ]
Lee, Sunyoung [1 ,2 ]
Lee, Hee Seung [3 ]
Bang, Seungmin [3 ]
Han, Kyunghwa [4 ]
Park, Mi-Suk [1 ,2 ]
机构
[1] Yonsei Univ, Severance Hosp, Dept Radiol, Coll Med, 50-1 Yonsei Ro, Seoul 03722, South Korea
[2] Yonsei Univ, Severance Hosp, Res Inst Radiol Sci, Coll Med, 50-1 Yonsei Ro, Seoul 03722, South Korea
[3] Yonsei Univ, Dept Internal Med, Div Gastroenterol, Coll Med, Seoul, South Korea
[4] Yonsei Univ, Ctr Clin Imaging Data Sci CCIDS, Res Inst Radiol Sci, Dept Radiol,Coll Med, Seoul, South Korea
关键词
RANDOMIZED PHASE-III; DUCTAL ADENOCARCINOMA; NEOADJUVANT THERAPY; CA19-9; DECREASE; BORDERLINE; FOLFIRINOX; CHEMOTHERAPY; GEMCITABINE; CORRELATE; SURVIVAL;
D O I
10.1148/radiol.212236
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: Imaging studies have limitations in evaluating pancreatic ductal adenocarcinoma (PDAC) treatment response. Purpose: To investigate the effectiveness of combined CT and carbohydrate antigen 19-9 (CA 19-9) evaluation at 8 weeks after first-line treatment to predict overall survival (OS) of patients with nonmetastatic PDAC. Materials and Methods: Patients with nonmetastatic PDAC who received first-line treatment with either chemotherapy or concurrent chemoradiation in a single-center PDAC cohort registry were retrospectively enrolled in the study between January 2013 and December 2016. Follow-up CT images obtained 8 weeks after treatment were evaluated according to Response Evaluation Criteria in Solid Tumors. Patients with partial response (PR) or stable disease (SD) were defined as CT responders, and those with progressive disease (PD) were defined as CT nonresponders. Patients with a normalized CA 19-9 level at 8-week follow-up were defined as CA 19-9 responders, and those with a nonnormalized or nonelevated CA 19-9 level were defined as CA 19-9 nonresponders. OS was compared using the Kaplan-Meier method with Breslow analysis. Results: A total of 197 patients (mean age +/- standard deviation, 65 years +/- 10; 107 men) were evaluated. Patients with PD (n = 17) showed shorter OS than those with SD (n = 147; P,.001) or PR (n = 33; P =.003). OS did not differ between the patients with PR and those with SD (P =.60). When the CT and CA 19-9 responses were integrated, OS was longest in CT and CA 19-9 responders (group 1, n = 27; median OS, 26.6 months [95% CI: 9.0, 44.1]), followed by CT responders but CA 19-9 nonresponders (group 2, n = 153; median OS, 15.9 months [95% CI: 13.3, 18.5]; P =.007 vs group 1) and CT and CA 19-9 nonresponders (group 3, n = 17; median OS, 6.5 months [95% CI: 0.8, 12.2]; P,.001 vs group 2). Conclusion: Integrated evaluation with CT and carbohydrate antigen 19-9 response allowed more accurate stratification of survival in patients with pancreatic ductal adenocarcinoma in the early treatment period than did evaluation according to Response Evaluation Criteria in Solid Tumors. (C) RSNA, 2022
引用
收藏
页码:548 / 556
页数:9
相关论文
共 50 条
  • [31] A CLINICAL-EVALUATION OF CARBOHYDRATE ANTIGEN 19-9 (CA 19-9) AND CARCINOEMBRYONIC ANTIGEN (GEA) IN PATIENTS WITH PANCREATIC-CARCINOMA
    SATAKE, K
    KANAZAWA, G
    KOH, I
    CHUNG, YS
    UMEYAMA, K
    DIGESTIVE DISEASES AND SCIENCES, 1984, 29 (10) : 966 - 966
  • [32] CA 125 AND CA 19-9 AS TUMORAL MARKERS IN PANCREATIC-CANCER
    PASQUALI, C
    SPERTI, C
    DANDREA, AA
    PETRIN, P
    PEDRAZZOLI, S
    ITALIAN JOURNAL OF GASTROENTEROLOGY, 1986, 18 (04): : 235 - 235
  • [33] CA 19-9, miR-200 and GIP in patients with diabetes and pancreatic cancer
    Skrha, P.
    Horinek, A.
    Andel, M.
    Fric, P.
    Skrha, J.
    DIABETOLOGIA, 2020, 63 (SUPPL 1) : S452 - S452
  • [34] The impact of CA 19-9 on survival in patients with clinical stage I pancreatic cancer
    Melucci, Alexa D.
    Chacon, Alexander C.
    Burchard, Paul R.
    Ullman, Nicholas A.
    Tsagkalidis, Vasleios
    Casabianca, Anthony S.
    Reitz, Alexandra
    Swift, David A.
    Goyal, Subir
    Switchenko, Jeffrey M.
    Carpizo, Darren R.
    Shah, Mihir Maheshkumar
    JOURNAL OF CLINICAL ONCOLOGY, 2022, 40 (04)
  • [35] Diagnostic Value of CA 19-9 in Patients with Pancreatic Cancer and Nonspecific Gastrointestinal Symptoms
    Safi F.
    Schlosser W.
    Kolb G.
    Beger H.G.
    Journal of Gastrointestinal Surgery, 1997, 1 (2) : 106 - 112
  • [36] Impact of CA 19-9 on Survival in Patients with Clinical Stage I Pancreatic Cancer
    Melucci, Alexa D.
    Chacon, Alexander C.
    Burchard, Paul R.
    Ullman, Nicholas A.
    Tsagkalidis, Vasleios
    Casabianca, Anthony S.
    Reitz, Alexandra C.
    Swift, David A.
    Goyal, Subir
    Switchenko, Jeffrey
    Carpizo, Darren R.
    Shah, Mihir M.
    ANNALS OF SURGICAL ONCOLOGY, 2022, 29 (SUPPL 2) : 445 - 446
  • [37] CA 19-9 and pancreatic carcinoma, a revival?
    Ducreux, Michel
    Boige, Valerie
    Malka, David
    ONKOLOGIE, 2007, 30 (1-2): : 12 - 13
  • [38] Prognostic value of CA 19-9 serum course in pancreatic cancer
    Safi, F
    Schlosser, W
    Falkenreck, S
    Beger, HG
    HEPATO-GASTROENTEROLOGY, 1998, 45 (19) : 253 - 259
  • [39] Serum determination of CA 19-9 in diagnosing pancreatic cancer: An obituary
    Pezzilli, R.
    Casadei, R.
    Calculli, L.
    Santini, D.
    Morselli-Labate, A. M.
    DIGESTIVE AND LIVER DISEASE, 2010, 42 (01) : 73 - 74
  • [40] ELEVATED CA 19-9 PREDICTS UNRESECTABLE PANCREATIC-CANCER
    LAMBIASE, L
    VOGEL, SB
    FORSMARK, CE
    GASTROENTEROLOGY, 1993, 104 (04) : A418 - A418