Intensified therapies improve survival and identification of novel prognostic factors for placental-site and epithelioid trophoblastic tumours

被引:63
作者
Froeling, Fieke E. M. [1 ,2 ]
Ramaswami, Ramya [1 ,2 ]
Papanastasopoulos, Panagiotis [1 ,2 ]
Kaur, Baljeet [1 ,2 ]
Sebire, Neil J. [1 ,2 ]
Short, Dee [1 ,2 ]
Fisher, Rosemary A. [1 ,2 ]
Sarwar, Naveed [1 ,2 ]
Wells, Michael [3 ]
Singh, Kam [3 ]
Ellis, Laura [3 ]
Horsman, Janet M. [3 ]
Winter, Matthew C. [3 ]
Tidy, John [3 ]
Hancock, Barry W. [3 ]
Seckl, Michael J. [1 ,2 ]
机构
[1] Imperial Coll NHS Healthcare Trust, Charing Cross Gestat Trophoblast Dis Ctr, Dept Med Oncol, London, England
[2] Imperial Coll London, London, England
[3] Weston Pk Hosp, Trophoblast Dis Ctr, Sheffield, S Yorkshire, England
关键词
FREE BETA-SUBUNIT; RELIABLE MARKER; DISEASE; CHEMOTHERAPY; PSEUDOTUMOR; MANAGEMENT;
D O I
10.1038/s41416-019-0402-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Placental-site trophoblastic (PSTT) and epithelioid trophoblastic tumours (ETT) are the rarest malignant forms of gestational trophoblastic disease (GTD). Our prior work demonstrated that an interval of >= 48 months from the antecedent pregnancy was associated with 100% death rate, independent of the stage. Here, we assess whether modified treatments for these patients have increased survival and identify new prognostic factors. METHODS: The United Kingdom GTD database was screened to identify all PSTT/ETT cases diagnosed between 1973 and 2014. Data and survival outcomes from our prior patient cohort (1976-2006) were compared to our new modern cohort (2007-2014), when intensified treatments were introduced. RESULTS: Of 54,743 GTD patients, 125 (0.23%) were diagnosed with PSTT and/or ETT. Probability of survival at 5 and 10 years following treatment was 80% (95% CI 72.8-87.6%) and 75% (95% CI 66.3-84.3%), respectively. Univariate analysis identified five prognostic factors for reduced overall survival (age, FIGO stage, time since antecedent pregnancy, hCG level, mitotic index) of which stage IV disease (HR 6.18, 95% CI 1.61-23.81, p = 0.008) and interval >= 48 months since antecedent pregnancy (HR 14.57, 95% CI 4.17-50.96, p < 0.001) were most significant on multivariable analysis. No significant differences in prognostic factors were seen between the old and new patient cohort. However, the new cohort received significantly more cisplatin-based and high-dose chemotherapy, and patients with an interval >= 48 months demonstrated an improved median overall survival (8.3 years, 95% CI 1.53-15.1, versus 2.6 years, 95% CI 0.73-4.44, p = 0.005). CONCLUSION: PSTT/ETT with advanced FIGO stage or an interval = 48 months from their last known pregnancy have poorer outcomes. Platinum-based and high-dose chemotherapy may help to improve survival in poor-prognosis patients.
引用
收藏
页码:587 / 594
页数:8
相关论文
共 34 条
[11]  
Hancock BW, 2015, ISSTD 18 WORLD C GES
[12]  
Harvey RA, 2008, J REPROD MED, V53, P643
[13]  
Hoekstra AV, 2004, J REPROD MED, V49, P447
[14]   Placental site trophoblastic tumors and epithelioid trophoblastic tumors: Biology, natural history, and treatment modalities [J].
Horowitz, Neil S. ;
Goldstein, Donald P. ;
Berkowitz, Ross S. .
GYNECOLOGIC ONCOLOGY, 2017, 144 (01) :208-214
[15]   Placental site trophoblastic tumor: Analysis of presentation, treatment, and outcome [J].
Hyman, David M. ;
Bakios, Lauren ;
Gualtiere, Gina ;
Carr, Christina ;
Grisham, Rachel N. ;
Makker, Vicky ;
Sonoda, Yukio ;
Aghajanian, Carol ;
Jewell, Elizabeth L. .
GYNECOLOGIC ONCOLOGY, 2013, 129 (01) :58-62
[16]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[17]   Placental site trophoblastic tumour [J].
Kim, SJ .
BEST PRACTICE & RESEARCH IN CLINICAL OBSTETRICS & GYNAECOLOGY, 2003, 17 (06) :969-984
[18]   The new FIGO 2000 staging and risk factor scoring system for gestational trophoblastic disease: Description and critical assessment [J].
Kohorn, EI .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2001, 11 (01) :73-77
[19]  
KURMAN RJ, 1976, CANCER-AM CANCER SOC, V38, P1214, DOI 10.1002/1097-0142(197609)38:3<1214::AID-CNCR2820380323>3.0.CO
[20]  
2-J