Power Doppler Quantification in Assessing Gestational Trophoblastic Neoplasia

被引:3
作者
Li, Yuanwei [1 ]
Tang, Meng Xing [1 ]
Agarwal, Roshan [2 ]
Patel, Daksha [3 ]
Eckersley, Robert J. [1 ]
Barrois, Guillaume [1 ]
Roddie, Mary E. [3 ]
Dayal, Linda [2 ]
Savage, Philip M. [2 ]
Seckl, Michael J. [2 ]
Lim, Adrian [4 ]
机构
[1] Imperial Coll London, Bioengn, South Kensington Campus, London SW7 2AZ, England
[2] Charing Cross Hosp, Med Oncol, London, England
[3] Charing Cross Hosp, Imaging, London, England
[4] Imperial Coll, Imaging, London, England
来源
ULTRASCHALL IN DER MEDIZIN | 2018年 / 39卷 / 02期
关键词
uterus; ultrasound-power doppler; angiogenesis; neoplasms; tumor; UTERINE ARTERY; CHEMOTHERAPY; METHOTREXATE; DISEASE;
D O I
10.1055/s-0041-111065
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
Purpose The FIGO score cannot accurately stratify low-risk gestational trophoblastic neoplasia (GTN) patients who develop chemoresistance to single agent methotrexate chemotherapy. Tumour vascularisation is a key risk factor and its quantification may provide non-invasive way of complementing risk assessment. Materials and Methods 187 FIGO-staged, low-risk GTN patients were prospectively recruited. Power Doppler ultrasound was analysed using a quantification program. Four diagnostic indicators were obtained comprising the number of colour pixels (NCP), mean dB, power Doppler quantification (PDQ), and percentage of colour pixels (%CP). Each indicator performance was assessed to determine if they could distinguish the subset of low-risk patients who became chemoresistant. Results There were 111 non-resistant and 76 resistant patients. NCP performed best at distinguishing these two groups where the non-resistant group had an average 3435 (2060) pixels and the resistant group 6151 (3192) pixels (p<0.001). PDQ and %CP showed significant differences (p<0.001) but had poorer performance (area under ROC curves were 72% and 67% respectively compared with 75% for NCP). The mean dB index was not significantly different (p=0.133). Conclusion Power Doppler ultrasound quantification shows potential for non-invasive assessment of tumour vascularity and can distinguish low-risk GTN patients who become chemoresistant from those who have an uncomplicated course with first line treatment.
引用
收藏
页码:206 / 212
页数:7
相关论文
共 16 条
  • [1] Evolutionary Algorithm-Based Classifier Parameter Tuning for Automatic Ovarian Cancer Tissue Characterization and Classification
    Acharya, U. R.
    Mookiah, M. R. K.
    Sree, S. Vinitha
    Yanti, R.
    Martis, R. J.
    Saba, L.
    Molinari, F.
    Guerriero, S.
    Suri, J. S.
    [J]. ULTRASCHALL IN DER MEDIZIN, 2014, 35 (03): : 237 - 245
  • [2] Uterine artery pulsatility index: a predictor of methotrexate resistance in gestational trophoblastic neoplasia
    Agarwal, R.
    Harding, V.
    Short, D.
    Fisher, R. A.
    Sebire, N. J.
    Harvey, R.
    Patel, D.
    Savage, P. M.
    Lim, A. K. P.
    Seckl, M. J.
    [J]. BRITISH JOURNAL OF CANCER, 2012, 106 (06) : 1089 - 1094
  • [3] Agarwal R, 2002, CLIN CANCER RES, V8, P1142
  • [4] Treatment of Low-Risk Gestational Trophoblastic Neoplasia
    Aghajanian, Carol
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (07) : 786 - +
  • [5] Radiology of gestational trophoblastic neoplasia
    Allen, SD
    Lim, AK
    Seckl, MJ
    Blunt, DM
    Mitchell, AW
    [J]. CLINICAL RADIOLOGY, 2006, 61 (04) : 301 - 313
  • [6] EMA/CO for high-risk gestational trophoblastic tumors: Results from a cohort of 272 patients
    Bower, M
    Newlands, ES
    Holden, L
    Short, D
    Brock, C
    Rustin, GJS
    Begent, RHJ
    Bagshawe, KD
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (07) : 2636 - 2643
  • [7] Hallmarks of Cancer: The Next Generation
    Hanahan, Douglas
    Weinberg, Robert A.
    [J]. CELL, 2011, 144 (05) : 646 - 674
  • [8] ANDROGENETIC ORIGIN OF HYDATIDIFORM MOLE
    KAJII, T
    OHAMA, K
    [J]. NATURE, 1977, 268 (5621) : 633 - 634
  • [9] The new FIGO 2000 staging and risk factor scoring system for gestational trophoblastic disease: Description and critical assessment
    Kohorn, EI
    [J]. INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2001, 11 (01) : 73 - 77
  • [10] Lim AKP, 2008, J REPROD MED, V53, P575