Testis Flashcards
TCa
Suspicious Mass Work-up
8
- H&P
- Labs including STMs
- Scrotal US
- Radical inguinal orchiectomy
- Discuss sperm banking
- Discuss testis prostesis
- Consider CT C/A/P
- Consider contralateral biopsy if abnormal
TCa
Seminoma Stage Ia and Ib Treatment
3
- Surveillance [pT1-pT3] (p)
- Single agent carboplatin
- Radiation therapy
TCa
Seminoma Stage Is
2
- Repeat elevated STMs
- Repeat imaging
TCa
Seminoma Stage IIa
3
- RT (including para-aortic and ipsilateral iliac nodes; 30Gy)
- BEP x3 or EP x4
- NS-RPLND
TCa
Stage IIb
1
- BEP x3 or EP x4
TCa
Seminoma Stage IIc or Stage III
2
Good Risk
* BEP x3 or EP x4
Intermediate Risk
* BEP x4 or VIP x4 (Etoposide/ Ifosfamide/ Cisplatin)
TCa
Seminoma s/p Chemotherapy
6
Repeat Img and STMs
Mass 3cm or less and normal STM
* Surveillance
Mass greater than 3cm and normal STM
* Surveillance
* FDG-PET/CT negative: surveillance
* FDG-PET/CT equivocal: repeat in 6-8 weeks
* FDG-PET/ CT positive: RPLND or biopsy
Growing mass or positive STM
* VeIP x4 or TIP x4
TCa
Seminoma Second-line Chemotherapy
3
- VeIP x4 (vinblastine/ ifosfamide/ cisplatin)
- TIP x4 (Paclitaxel/ Ifosfamide/ cisplatin)
- High-dose chemotherapy
TCa
Seminoma Post-Chemotherapy RPLND Adjuvant Treatment
3
- Complete resection positive for seminoma: consider 2 cycles of chemotherapy (EP or TIP or VIP or VeIP)
- Complete resection negative for seminoma: Surveillance
- Incomplete resection or progression: VeIP x4 (Vinblastine/ Ifosfamide/ Cisplatin) or TIP x4 (Paclitaxel/ Ifosfamide/ Cisplatin)
TCa
Seminoma Third-line Chemotherapy
7
Prior first and second-line conventional dose
* High dose chemotherapy
* Third-line chemotherapy
* Microsatellite instability/ mismatch repair testing or tumor mutational burden testing
* RT (select pts)
Prior high dose chemotherapy
* Third-line conventional dose chemotherapy
* Microsatellite instability/ mismatch repair testing or tumor mutational burden testing
* RT (select pts)
TCa
NSGCT Pre-treatment Workup
3
- CT C/A/P or MRI
- Repeat STMs
- Brain MRI with and without contrast if choriocarcinoma, extensive lung mets, viceral mets, neurologic symptoms, S3 AFP or S2 bHCG
TCa
NSGCT Risk Factors
3
- Lymphovascular invasion
- Predominance of embryonal carcinoma
- pT3 or pT4
TCa
NSGCT Stage I without RFs Treatment
3
- Surveillance (p)
- NS-RPLND
- BEP x1
TCa
NSGCT Stage I with RFs Treatment
3
- Surveillance
- BEP x1
- NS-RPLND
TCa
NSGCT Stage Is Treatment
1
- BEP x3 or EP x4
TCa
NSGCT Stage IIa Treatment
3
S0
* NS- RPLND
* BEP x3 or EP x4
S1
* BEP x3 or EP x4
TCa
NSGCT Stage IIb Treatment
3
S0, normal LN distribution
* BEP x3 or EP x4
* NS-RPLND (select pts)
S1 or abnormal LN distribution
* BEP x3 or EP x4
TCa
NSGCT Stage IIc and IIIa Treatment
2
- Good Risk BEP x3 or EP x4
- Int or Poor Risk BEP x4
TCa
NSGCT Stage IIa or IIb s/p chemotherapy
3
Negative markers, Residual mass <1cm
* Surveillance (p)
* NS-RPLND (select pts)
Negative markers, Residual mass >1cm
* NS-RPLND
TCa
NSGCT Treatment s/p post-chemo RPLND
2
- Viable tumor in path: adjuvant chemotherapy x2 (EP or TIP or VIP or VeIP)
- Teratoma or necrosis: surveillance (no need to resect extra-RP masses if fibrosis in the post-chemo RPLND specimen (12% chance of discordance)
TCa
NSGCT s/p primary RPLND
4
- pN0: surveillance
- pN1: surveillance (p) or EP x2
- pN2: EP x2 (p) or surveillance
- pN3: BEP x3 or EP x4