Observational Study
Copyright ©The Author(s) 2021.
World J Clin Oncol. Mar 24, 2021; 12(3): 183-194
Published online Mar 24, 2021. doi: 10.5306/wjco.v12.i3.183
Table 1 Characteristics of patients with testicular germ cell tumors at our Institution
Metric

Number of patients (n = 68)
Demographics
Mean age at orchiectomy (yr)31 (16-53)
Mean BMI at 1st medical oncology visit, n (%)29 (18.6-58.4)
Cigarette smoker or ex-smoker35 (51)
Current cannabis user, n (%)16 (23.5)
Clinicopathologic characteristics
Histology, n (%)Seminoma19 (28)
Non-seminoma49 (72)
Pathologic stage, n (%)IA1 (1.5)
IB1 (1.5)
IS6 (9)
IIA31 (45.5)
IIB10 (14.5)
IIC8 (11.5)
III1 (1.5)
IIIA2 (3)
IIIB4 (6)
IIIC 4 (6)
Laterality, n (%)Left35 (52)
Right33 (48)
RPLN ≥ 3.0 cm before chemotherapy, n (%)Yes18 (26)
No50 (74)
Type of chemotherapyBEP58 (85.3%)
EP4 (5.9%)
BEP + EP6 (8.8%)
Cycles of chemotherapy11 (1.5%)
23 (4.4%)
349 (72.0%)
413 (19.1%)
61 (1.5%)
71 (1.5%)
RPLNDYes18 (26.5%)
No50 (73.5%)
Recurrence after initial chemotherapyYes5 (7.4%)
No63 (92.6%)
Table 2 Thromboembolic events in patients with testicular germ cell tumors who underwent cisplatin-based chemotherapy at our Institution (n = 19)
Type/pathologic stage of testicular tumor
RPLN ≥ 3.0 cm before chemotherapy
Type/number of cycles of chemotherapy
PE/DVT
Timing of PE/DVT in relation to chemotherapy
Anticoagulant
Hospitalization
Seminoma IIBYesBEP (2 cycles), EP (1 cycles)DVTSame day immediately prior to Cycle 1 Fondaparinux sodiumYes
Seminoma IIANoEP (3 cycles)DVT1During (Cycle 1)Heparin → apixabanYes
Seminoma IIIBNoEP (4 cycles)PE + DVT23 yr after initial chemotherapy, recurrent diseaseEnoxaparin sodiumYes
Non-seminoma IIBYesBEP (2 cycles)DVT2During (Cycle 2)Warfarin →enoxaparin sodiumYes
Non-seminoma IIBNoBEP (3 cycles)PEDuring (Cycle 2)Heparin → enoxaparin sodium → rivaroxaban → apixabanYes
Non-seminoma IICYesEP (4 cycles)PE + DVT1 wk before Cycle 1Heparin (lovenox) → warfarinYes
Non-seminoma IIANoBEP (3 cycles)DVT2During (Cycle 2)Fondaparinux sodiumNo
Non-seminoma IIBYesBEP (3 cycles)PE1During (Cycle 3)Fondaparinux sodium → warfarinNo
Seminoma IIANoBEP (3 cycles)DVT2During (Cycle 3)NoneNo
Seminoma IIINoBEP (3 cycles)PEDuring (Cycle 3)Enoxaparin sodiumNo
Non-seminoma IIICYesBEP (4 cycles)PEDuring (Cycle 4)Enoxaparin sodiumNo
Non-seminoma IIICYesBEP (4 cycles)DVTDuring (Cycle 3)Enoxaparin sodiumNo
Non-seminoma IIANoBEP (3 cycles)PEDuring (Cycle 3)Heparin → rivaroxabanYes
Non-seminoma IIANoBEP (2 cycles)PEDuring (Cycle 2)Enoxaparin sodiumNo
Seminoma IICYesBEP (3 cycles)PE1 mo after chemotherapy endedHeparin → enoxaparin sodiumYes
Seminoma IIANoBEP (3 cycles)PE + DVTDuring (Cycle 2)Heparin → enoxaparin sodiumYes
Non-seminoma IIBNoBEP (3 cycles)DVT1 d prior to Cycle 1Heparin → fondaparinux sodiumYes
Non-seminoma IIIANoBEP (3 cycles)PE2 wk after chemotherapy endedWarfarin + enoxaparin sodiumNo
Seminoma IICYesEP (4 cycles)DVT2During (Cycle 2)Enoxaparin sodium → fondaparinuxYes
Table 3 Comparison of metrics between patients with testicular germ cell tumors at our Institution stratified by those who experienced a thromboembolic event and those who did not

Thromboembolic event
Metric
No (%)
Yes (%)
P value
n4919
Age [mean (SD)]30.9 (7.86)30.79 (8.67)0.909
BMI [mean (SD)]27.87 (6.38)30.22 (9.25)0.237
Cigarette smoker = Yes (%)27 (55.1)8 (42.1)0.421
Marijuana use = Yes (%)13 (26.5)3 (15.8)0.526
Side of orchiectomy = Right (%)27 (55.1)6 (31.6)0.107
Pathology = Seminoma (%)11 (22.4)8 (42.1)0.135
Pathologic stage (%)0.050
I10 (20.4)0 (0.0)
II33 (67.3)14 (73.7)
III6 (12.2)5 (26.3)
Port = Yes (%)4 (8.2)3 (15.8)0.390
Type of chemotherapy (%)
BEP X 345 (91.8)13 (68.4)
BEP X 3 + EP X 14 (8.2)2 (10.5)
EP X 40 (0.0)4 (21.1)
RPLN ≥ 3.0 cm = Yes (%)10 (20.4)8 (42.1)0.123
RPLND = Yes (%)12 (24.5)6 (31.6)0.555
Recurrence after chemotherapy = Yes (%)3 (6.1)2 (10.5)0.614
Table 4 Patients with testicular germ cell tumors who underwent cisplatin-based chemotherapy and experienced a thromboembolic event in the literature
Ref.
Number of patients
Percentage of patients with TE
Main findings
Piketty et al[9], 2005100 patients with GCT; 100 controls with various neoplasms19 (19%)> All stages of TGCT;
> TE: 1st day of chemo to 6 mo after;
> Of 19 TEE, 14 occurred during chemotherapy, 5 after chemo;
> Risk factors for TEE: High body surface area, elevated serum LDH
Honecker et al[6], 201319322 (11%)> All stages of TGCT;
> TEE: Considered therapy-associated if occurred from start of chemotherapy to 6 wk after;
> 18 (%) TEE occurred before chemotherapy;
> Risk factors for TEE: Pure seminoma, retroperitoneal or supraclavicular lymph node metastases, elevated LDH, CVC
Bezan et al[18], 201765734 (5.2%)> All stages of TGCT;
> TEE: During 1st year of follow-up;
> Risk factors for TEE: Higher clinical stage and RPLN, increased number of cycles of chemotherapy
Tran et al[19], 20191135150 (10%)> Metastatic TGCT;
> TEE: During or within 90 d of chemotherapy;
> Risk factors for TEE: Large RPLN, CVC
Paffenholz et al[16], 201922549 (19%)> All stages of TGCT;
> TEE: Start of chemotherapy to 6 mo after;
> Risk factors for TEE: Higher clinical stage, elevated serum LDH, febrile neutropenia, CVC;
> Patients with TEE had significantly reduced overall survival during median follow-up of 8 mo
Current Study, 20206818 (26.5%)> All stages of TCGT;
> TEE: Following orchiectomy;
> Risk factors for TEE: Higher pathologic stage, greater number of chemotherapy cycles