Prostate Flashcards

1
Q

What are the three main observation trials in prostate cancer?

A
  1. Swedish Trial (Bill-Axelson)
  2. PIVOT
  3. Klotz
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2
Q

PIVOT trial: P/D/R

A

P: 45% low, 35% intermediate, 20% high risk
D: prostatectomy vs. observation
R: marginal / nonsignificant benefit in OS with prostatectomy

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3
Q

Klotz: P/D/R

A

P: mostly low risk, some intermediate risk if >70yrs
D: single arm PSA every 6mo, biopsy every 3-4 years, definitive treatment for progression of disease
R: no difference in overall survival

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4
Q

MDACC dose escalation: P/D/R

A

P: T1-T3
D: 70Gy vs. 78Gy
R: PFS improved in all groups, most significant in high risk group, worse GI toxicity, nonsignificant trend for worse GU toxicity

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5
Q

Fox Chase / Gerry Hanks dose escalation: P/D/R

A

P: nonmetastatic / clinically localized
D: stepwise dose escalation, 68-79Gy
R: BPFS with dose escalation, increased grade 2 GI with higher dose

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6
Q

What three trials examined the utility of long term ADT?

A
  1. EORTC 22863 (Bolla)
  2. RTOG 8531 (Lawton)
  3. RTOG 9202 (Hanks)
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7
Q

EORTC 22863 (Bolla) long term ADT: P/D/R

A

P: GS 7+, T3-4
D: RT +/- 36mo adjuvant ADT (goserelin/cyproterone)
R: OS improved with ADT (58% vs 40%)

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8
Q

RTOG 9202 long term ADT: P/D/R

A

P: T2c-T4
D: neoadjuvant and concurrent ADT with RT +/- 28mo adjuvant ADT (goserelin)
R: long term ADT improved PFS and BPFS but no improvement in OS

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9
Q

RTOG 8531 long term ADT: P/D/R

A

P: cT3, pT3 or N+ (some post RP)
D: RT +/- indefinite ADT (goserelin)
R: OS improved with ADT (49% vs 39%)

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10
Q

What two trials examined the utility of short term ADT?

A
  1. RTOG 8610

2. D’Amico hormone trial

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11
Q

RTOG 8610 short term ADT: P/D/R

A

P: bulky T2-T4, mostly intermediate risk, some high risk
D: RT +/- 4mo ADT (2mo neoadjuvant, 2mo concurrent)
R: improved DM and PFS with ADT, no OS benefit

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12
Q

D’Amico hormone trial short term ADT: P/D/R

A

P: intermediate risk with some low risk
D: RT +/- 6mo ADT
R: OS improved with ADT (74% vs 61% at 8yrs)

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13
Q

RTOG 9413 whole pelvis and hormones: P/D/R

A

P: PSA < 100, risk of LN+ > 15% (Roach formula)
D: 4 arm +/- whole pelvis, neoadj/conc ADT (4mo) vs. adj ADT (4mo)
R: PFS and OS improved in whole pelvis + neoadj/conc ADT but this was unplanned analysis with statistical flaws

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14
Q

What three trials examined the utility of adjuvant RT?

A
  1. ARO 96-02
  2. EORTC 22911
  3. SWOG 8794
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15
Q

ARO 96-02 adjuvant RT: P/D/R

A

P: postop, pT3N0, undetectable PSA
D: adjuvant RT 60Gy vs. observation
R: improved BPFS with RT (56% vs 35% at 10yrs), no OS improvement

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16
Q

EORTC 22911 adjuvant RT: P/D/R

A

P: postop, pT3N0 or positive margin
D: adjuvant RT 60Gy vs. observation (70Gy if failed obs)
R: BPFS improved with adjuvant RT, 56% of obs group got salvage RT

17
Q

SWOG 8794 adjuvant RT: P/D/R

A

P: postop, pT3N0 or positive margin
D: adjuvant RT 60-64Gy vs. observation
R: OS benefit with RT (47% vs. 37% at 15yrs), 30% of obs group got salvage RT

18
Q

What RTOG trial examined ADT in the setting of salvage RT?

A

RTOG 9601, final results pending, BPFS appears to be improved with ADT

19
Q

What two trials examined the utility of RT in N+ disease?

A
  1. RTOG 8531 (N+ subset)
  2. Messing study
    both showed OS benefit with ADT + RT
20
Q

MDACC/Zagars N+ study: P/D/R

A

P: postop, N+
D: ADT +/- RT 70Gy
R: OS improved with RT (67% vs. 46% at 10yrs)

21
Q

Swedish trial (Bill-Axelson): P/D/R

A

P: T1/T2, age less than 75
D: prostatectomy vs. observation
R: OS benefit with RP if younger than 65, unclear benefit if older