GU CA Flashcards

1
Q

What high-risk features may prompt early initiation of ADT for biochemical recurrence? (3)

A
  • Gleason 8 to 10 disease
  • PSA doubling time less than one year
  • Biochemical relapse less than 18 months following local therapy
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2
Q

Name treatment options for high-volume mCSPC. (3)

A

1) ADT, docetaxel
2) ADT, docetaxel, darolutamide
3) ADT, docetaxel, abiraterone

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3
Q

Name the treatment options for low volume mCSPC (3)

A

1) ADT +Abi
2) ADT + enza
3) ADT + apalutamide

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4
Q

What are treatment options for nmCRPC?

A

1) ADT + Enzalutamide
2) ADT + Apalutamide
3) ADT + Darolutamide

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5
Q

What are common genes implicated in homologous recombination repair that may indicate PARP inhibitor responsiveness (7)

A

BRCA1, BRCA2, PALB2,CHEK2,RAD51B, ATM, FANCA

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6
Q

What defines Stage III RCC (2)

A
  • node positive
  • T3
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7
Q

What defines high risk mRCC? (5)

A
  • KPS <80
  • time from dx to tx <12m
  • Hb<12
  • PLT >400
  • WBC >12
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8
Q

what are preferred tx for first line mRCC (4)

A

IPI / nivo (High risk)
Nivo / Cabo
Pembro / Axi
Pembro / lenvatinib

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9
Q

What is the benefit of adjuvant pembrolizumab in stage III RCC?

A

Improved DFS only

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10
Q

Who is a candidate for TMT for bladder CA?

A

T2-3a
N0
Low grade
No CIS
Unifocal

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11
Q

What defines high Vs low risk non muscle invasive bladder CA (3)

A

Multiple lesions
Size >3cm
T1 (vs Ta)

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12
Q

Tx of low risk non muscle invasive bladder cancer

A

TURBT

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13
Q

Tx of high risk non muscle invasive bladder cancer

A

BCGx6 > TURBT > BCG x 3y

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14
Q

What defines cisplatin eligibility in muscle invasive bladder CA? (4)

A
  • EGFR > 60
  • no hearing loss
  • PS < 2
  • NYHA CHF 2 or less
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15
Q

Who should get adjuvant chemo for bladder cancer

A
  • T2+ or n+ upstaged at cystectomy
  • cisplatin eligible

Cisplatin Gemcitabine or ddMVAC

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16
Q

What neoadjuvant regimens are used in bladder cancer?

A

Cisplatin - gemcitabine
ddMVAC

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17
Q

When is adjuvant Nivolumab recommended in bladder CA?

A

Residual disease at cystectomy

18
Q

Metastatic urothelial cell tx (4)

A
  • gem - cis (no prior platinum or >12m)
    • consider avelumab maintenance
  • pembrolizumab
  • Erdafitinib (FGFRmut)
  • Enfortumab vedotin
  • Sacituzumab govitecan
19
Q

What are the two biggest principles in muscle invasive bladder CA

A

1) cisplatin based regimens are the only option
2) neoadjuvant is preferred

20
Q

What is total medical therapy TMT for muscle invasive bladder cancer

A

Maximal TURBT
Rads
Cis or taxol

21
Q

Three factors needed to stratify risk for non metastatic prostate cancer

A
  • grade group
  • PSA
  • T stage
22
Q

nmPC - define favorable prognosis

A
  • grade group 1 (3+3=6)
  • PSA < 10
  • T1 or T2a
23
Q

nmPC - define high risk

A

Grade group 4/5
- Gleason 4+4
- Gleason 4+5 / 5+5
PSA > 20
T3 or T4

24
Q

nmPC - what defines intermediate risk? (Fav and unfav)

A

Grade group 2-3
PSA 10-20
T2b-3
Fav - <50% cores
Unfav - >50% cores

25
Prostate cancer T staging
1 - imaging 2 - palpable 3 - extraprostatic ext 4 - invasion of other structures
26
ADJ prostate cancer treatment
FAV - observation FAV-INT - obs or ADT x 6m UnFAV-INT - ADT x 6m HIGH - ADT x 18m
27
Penile cancer treatment by stage - CIS - I/II (node negative) - III (node positive) - IV or recurrent
- topical - resection - resection w ILND (consider adj TIP but no data) - TIP or CRT with cisplatin
28
How to evaluate an adrenal module
1) is it likely to be a met? If so stop here 2) if not, is it large or secretory? - evaluate for aldosteronism, bushings, pheo 3) if large, secretory, and unilateral respect
29
Tx of pheocheomocytoma
Resection or cytoreductive subtotal resection if unresectable
30
Tx or adrenocortical carcinoma
1) resection, consider mitotatne ( no OS benefit) 2) Mitotane based systemic therapy
31
Tx for mCSPC
ADT with - doce - doce abi - doce dara - abi - apa - enza
32
treatment for mCRPC (ASIs)
ADT with Enza Abi
33
Define high volume metastatic prostate cancer
>4 lesions 1 extra axial lesion Visceral lesions
34
What questions should you ask about every testis cancer?
1) seminoma or NSGCT 2) nodal status? I, IIA, IIB+ 3) risk Sem - m0-1 NSGCT - non pulm Mets, biomarker levels
35
What defines favorable vs intermediate seminoma risk
Favorable Intermediate - non pulm Mets
36
Define fav/int/high risk for NSGCT
FAV - INT - AFP>1k, hcg > 5k HIGH- mediastinal primary, non pulm Mets, AFP>10k, hcg>50k
37
Treatment for stage I seminoma
Surgery then Obs > carbo x2 > RT
38
Treatment for stage IIA seminoma
Surgery then 1) RT 2) BEPx3 or EPx4
39
Treatment for stage IIB+ seminoma
Surgery then Fav risk - BEPx3 or EPx4 Int risk - BEPx4 or VIP x4
40
Treatment for stage I NSGCT
Surgery then 1) observation 2) RPLND (esp if teratoma) 3) BEP x 1
41
Treatment for stage IIA NSGCT
Surgery then 1) RPLND 2) BEP x3 or EPx 4
42
What is residual disease after frontline treatment for seminoma and NSGCT? What are tx options
S >3cm mass - RT or RPLND NSGCT >1cm - RPLND