A prospective study of cognitive function in men with non-seminomatous germ cell tumors

被引:50
|
作者
Wefel, Jeffrey S. [1 ]
Vidrine, Damon J. [2 ]
Marani, Salma K. [2 ]
Swartz, Richard J. [3 ]
Veramonti, Tracy L. [4 ]
Meyers, Christina A. [1 ]
Hoekstra, Harald J. [5 ]
Hoekstra-Weebers, Josette E. H. M. [6 ,7 ]
Gritz, Ellen R. [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Neurooncol, Houston, TX 77230 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Behav Sci, Houston, TX 77230 USA
[3] Rice Univ, Jesse H Jones Grad Sch Business, Houston, TX USA
[4] Mentis Neuro Rehabil, Houston, TX USA
[5] Univ Groningen, Univ Med Ctr Groningen, Dept Surg Oncol, Groningen, Netherlands
[6] Univ Groningen, Univ Med Ctr Groningen, Wenkebach Inst, Groningen, Netherlands
[7] Comprehens Canc Ctr North Netherlands, Groningen, Netherlands
关键词
chemotherapy; cognitive function; neurotoxicity; quality of life; testicular cancer; oncology; BREAST-CANCER; ADJUVANT CHEMOTHERAPY; PROSTATE-CANCER; IMPAIRMENT; WOMEN; CARCINOMA;
D O I
10.1002/pon.3453
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ObjectiveLongitudinal neuropsychological assessments were performed to determine if adjuvant chemotherapy was associated with cognitive dysfunction in men with non-seminomatous germ cell tumors (NSGCT). MethodsPatients with NSGCT status post-orchiectomy that either received adjuvant chemotherapy (n=55) or did not (n=14) were recruited. Patients were tested before chemotherapy, 1week post-chemotherapy (or 3months later in the surveillance group) and 12months after the baseline evaluation. ResultsCompared with the surveillance group, patients treated with chemotherapy had higher rates of cognitive decline at 12months (overall cognitive decline: 0%, 52%, and 67% in the surveillance, low exposure (LE), and high exposure (HE) group, respectively), greater number of tests that declined (mean of 0.1, 1.4, and 2.0 in the surveillance, LE, and HE group, respectively), and more frequent worsening in motor dexterity (0%, 48%, and 46% in the surveillance, LE, and HE group, respectively). Compared with the surveillance group, patients receiving more cycles of chemotherapy demonstrated worse psychomotor speed and learning and memory. Younger age was associated with greater incidence of overall cognitive decline at 12-month follow-up. ConclusionsMen with NSGCT that received chemotherapy demonstrated greater rates of cognitive decline in a dose-response manner. Reductions in motor dexterity were most common. Decline in learning and memory also was evident particularly at later follow-up time points and in men receiving more chemotherapy. Men that receive chemotherapy for NSGCT are at risk for cognitive decline and may benefit from monitoring and referral for psychosocial care. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:626 / 633
页数:8
相关论文
共 50 条
  • [41] Primary mediastinal non-seminomatous germ-cell tumors: From clinics to biology
    Fizazi, K
    Culine, S
    Droz, JP
    LeChevalier, T
    Ruffie, P
    Theodore, C
    BULLETIN DU CANCER, 1997, 84 (03) : 313 - 327
  • [42] DECREASING UTILIZATION OF RPLND FOR CLINICAL STAGE I NON-SEMINOMATOUS GERM CELL TUMORS
    Navai, Neema
    Shikanov, Sergey
    Pisters, Louis
    Eggener, Scott
    JOURNAL OF UROLOGY, 2012, 187 (04): : E305 - E305
  • [43] TUMOR-MARKERS IN PATIENTS WITH NON-SEMINOMATOUS GERM-CELL TUMORS OF THE TESTIS
    WILLEMSE, PHB
    SLEIJFER, DT
    KOOPS, HS
    DEBRUIJN, HWA
    OOSTERHUIS, JW
    BROUWERS, TM
    OCKHUIZEN, T
    MARRINK, J
    ONCODEVELOPMENTAL BIOLOGY AND MEDICINE, 1981, 2 (1-2): : 117 - 128
  • [44] INTENSIVE INDUCTION CHEMOTHERAPY FOR POOR RISK NON-SEMINOMATOUS GERM-CELL TUMORS
    HORWICH, A
    BRADA, M
    NICHOLLS, J
    JAY, G
    HENDRY, WF
    DEARNALEY, D
    PECKHAM, MJ
    EUROPEAN JOURNAL OF CANCER & CLINICAL ONCOLOGY, 1989, 25 (02): : 177 - 184
  • [45] Radiomics model to predict teratoma in metastatic non-seminomatous testicular germ cell tumors
    Scavuzzo, A.
    Crescio, E.
    Figueroa Rodriguez, P. A.
    Duran Chable, D. L.
    Rios Garcia, C. A.
    Jimenez Guedulain, N.
    Calvo Vazquez, I
    Jimenez Rios, M. A.
    EUROPEAN UROLOGY, 2023, 83
  • [46] Results of multimodality therapy in poor risk non-seminomatous germ cell tumors (NSGCT)
    Omuro, Y
    Sasaki, E
    Hayashi, C
    Okamoto, R
    Kobayashi, T
    Maeda, Y
    Sasaki, T
    INTERNATIONAL JOURNAL OF CANCER, 2002, : 430 - 430
  • [47] COMPUTED-TOMOGRAPHY IN PRIMARY NON-SEMINOMATOUS GERM-CELL TUMORS OF THE MEDIASTINUM
    BLOMLIE, V
    LIEN, HH
    FOSSA, SD
    JACOBSEN, AB
    STENWIG, AE
    ACTA RADIOLOGICA, 1988, 29 (03) : 289 - 292
  • [48] Surveillance for Boys with Localized Testicular Non-Seminomatous Germ Cell Tumors: Hacettepe Experience
    Yalcin, B.
    Aydin, B.
    Tanyel, C.
    Orhan, D.
    Cemaloglu, M.
    Kurucu, N.
    Varan, A.
    Kutluk, T.
    Akyuz, C.
    PEDIATRIC BLOOD & CANCER, 2018, 65 : S495 - S495
  • [49] MANAGEMENT OF NON-SEMINOMATOUS TUMORS
    GITTES, RF
    RICHIE, JP
    GARNICK, MB
    BRITISH JOURNAL OF UROLOGY, 1981, 53 (01): : 68 - 68
  • [50] Fatty acid synthase overexpression in adult testicular germ cell tumors: potential role in the progression of non-seminomatous germ cell tumors
    Miyai, Kosuke
    Iwaya, Keiichi
    Asano, Tomohiko
    Tamai, Seiichi
    Matsubara, Osamu
    Tsuda, Hitoshi
    VIRCHOWS ARCHIV, 2014, 464 (02) : 221 - 228