Monday, February 23, 2009

Treatment Approaches for High Risk Prostate Cancer

Junzo Chino M.D.

Case

  • 55yo AAM presents to Primary Care for initial visit
  • He has mild HTN on exam
  • No GU symptoms
  • Erectile function intact
  • PSA is sent as a screening test and returns at 325 ng/ml
  • DRE performed revealing a moderate sized gland, firm nodule in the R apex.
  • U/S guided Biopsy performed
  • 7/8 cores reveal prostate cancer 4+4 = 8 GS
  • Pt is initially seen in Urology Clinic and offered surgery - placed on OR schedule

Further Staging

  • CT scan reveals moderate sized prostate
  • 3x4cm R pelvic lymph node just below the bifurcation of the common iliac
  • No other LAD
  • No invasion of bladder or rectum
  • Bone scan negative

Case

  • We are called by the urology chief resident, to have the patient discuss alternatives to surgery

Defining High Risk

D'Amico classification looking at T stage, GS and PSA: any of the below

  • T2c or greater
  • GS 8 or greater
  • PSA 20 or greater

Per Nguyen, IJROBP 2009: Increased # of high risk factors is associated with PCSM. Paper includes PSA velocity as an additional risk factor.


 

Surgery for High Risk Disease

Several Retrospectives series exist comparing results of surgery to radiation (see Zincke Cancer 1981, D'Amico JAMA 1998)

Duke Data (unpublished)

from 1997-2007, 146 patients with clinically high risk disease operated on

  • Median PSA 9
  • 58% had GS 8 or greater
  • 23% had T-stage T2c or greater
  • 91% had only one high risk factor

Therefore this cohort tended to have a high grade and low-middle disease burden

Pathologic Results

  • 76% had at least on indication for adjuvant RT on final path (ECE, SVI, positive margin, or PSA ≥ 0.2ng/ml)
  • 55% with ECE
  • 27% with SVI
  • 54% with positive margins
  • 20% with PSA ≥ 0.2ng/ml
  • 28% received early RT (within first 6 months postoperatively)

Outcomes at 4 years

  • 48% (95% CI 38-57%) had received postoperative radiation therapy
  • 74% (95% CI 64-83%) remained free of biochemical failure (including those salvaged with RT)
  • 98% (95% CI 96-100%) alive
  • 14% (95% CI 8-23%) undergoing indefinite ADT

Postoperative Toxicity

  • ≥ Grade 2 urinary toxicity in 42 (29%)
  • ≥ Grade 2 erectile dysfunction in 93 (64%)
  • ≥ Grade 2 rectal toxicity in 3 (2%).

Conclusions -

  1. Even in Highly selected patients, ½ of patients undergoing initial surgery had postoperative RT by 4 years.
  2. With selected adjuvant RT and salvage RT, 4 year biochemical control was reasonable at 74%
  3. Toxicity rates are not insignificant

New directions for Surgery and Radation Therapy

Neoadjuvant RT for high Risk Prostate cancer

  • Phase I/II trial is proceeding at Duke with reasonable toxicity to date


 

To Compare Approaches (Apples and Oranges)

Merglen Arch Intern Med 2007;167(18):1944

Compared results with 844 consequtive patients treated for ACP in Geneva Switzerland 1989-1998. This demonstrates high survival rates for those treated with RP vs RT, However, there were clearly significant selection biases for surgery have younger age, and a bias against RT + ADT for higher grade disease. When these factors were controlled for with a Cox Regression, the HR of RT + ADT overlapped the Surgery Cohort.

Moreover, there are multiple other factors that go into Surgical selection that are unaccounted for. No details on RT or ADT - given time frame likely these were suboptimal


 

SEER data (Lu-Yao Lancet 1997)

queried the SEER databaes 1983-1992

59,876 pts identified

Cohorts determined by reported Grade (1-3) and Therapy Received

No control for PSA, cT stage or comorbity

RT fared worse with G3-4 disease compared to RP, but again there is no systematic control for other variables.


 

External Beam Radiation Therapy and Hormone Treatment

The majority of randomized data in Prostate cancer treatment lies in this group.

Trials

  1. RTOG 8531 (non bulky)
  2. RTOG 8610 (bulky)
  3. RTOG 9202 (4 months vs 2 years ADT)
  4. EORTC 22863 (no ADT vs 3 years ADT)
  5. EORTC 22961 (6mo ADT vs 3years ADT)

RTOG 85-31 "HIgh Risk - NonBulky"

977 patients with cT3 or pT3 ACP, or N+. bulky tumors excluded.

Randomized to

  • RT alone (44-46 WPRT + boost to 65-70Gy)
  • RT + adjuvant goserelin indefinitely

10 year results:

  • OS 49% ADT vs 39% (SS)
  • LF 23% ADT vs 38% (SS)
  • DM 24% vs 39% (SS)

RTOG 86-10 "High Risk Bulky"

471 pts with T2-T4 ACP, bulky randomized to

  • RT alone (45Gy pelvis, boost to 65-70 Gy)
  • goserelin + flutamide x 4months (neoadjuvant and concurrent) + RT

10 year results:

  • OS ADT 43% vs 34% (NS) (primary endpoint)
  • DSM ADT 23% vs 36% (SS)
  • DM ADT 35% vs 47% (SS)
  • BR ADT 65% vs 80% (SS)

RTOG 92-02: Short vs Long ADT

1554 pts with T2c-T4 ACP, psa < 150 Randomized to:

  • Goserelin + Flutamide x 4 months (neoadjuvant and concurrent) + RT WPRT 45Gy boost to 65-70Gy
  • Same + 2 years goserelin thereafter

10 year results

  • OS 52% LTADT vs 54% STADT (NS)
  • GS 8-10: OS 45% LTADT vs 32% STADT (SS)
  • DFS 22% LTADT vs 13% STADT (SS)

EORTC 22863: Bolla

415 pts with t1-2 G3, or T3-4 any grade (majority T3), randomized to

  • RT 50Gy WPRT, boost to 70Gy
  • Same RT + goserelin x 3 years (start with RT)

5 year results

  • OS ADT 78% vs 62% (SS)
  • DSS ADT 94% vs 79% (SS)
  • DFS ADT 74% vs 40% (SS)

D'Amico Study

206 men with Intermediate-High Risk - T1-T2b PSA>= 10, GS >=10, ECE or T3 by MRI

  • 70 GY RT (no pelvis)
  • Same + 6 months leuprolide/goserelin + flutamide (start 2 months prior to RT)

8 year results

  • OS 74% (ADT) vs 61% (no ADT) SS
  • Difference seen primarily in men without significant comorbidities

What about 6 months vs 3 years? ADT: Bolla EORTC 22961

970 pts with pT2c-T4 or N+ prostate cancer PSA <150, randomized to

  • 70Gy + 6 months ADT
  • 70Gy + 3 years ADT

at 5.2 years f/u interim analysis demonstrated futility. 5y OS was 85% LTADT, 81% STADT, failing to prove non-inferiority. 5y bRFS was 78% vs 59%, which was SS for inferiority of STADT

WPRT?

Currently Three Trials exist on +/- WPRT

  1. RTOG 77-06
  2. RTOG 94-13
  3. GETUG-01

None of these trials are perfect

None of these trials demonstrate a benefit to WPRT

However, the EORTC trials and RTOG trials demonstrating benefit of ADT used WPRT


 

ADT summary table

Study

n

stage

ADT

Dose

WPRT

yrs fu

DFS

OS

RTOG

85-31

977

c or p T3, or N+

none

∞ A

65-70Gy

if N+

10

 

39%*

49%*

RTOG

86-10

471

bulky T2-4

none

4mo NA/C

65- 70Gy

yes

8

10%*

24%*

bRFS

44%†

53%†

EORTC 22863

415

T1-2 G3 or T3-4

none

3yr C/A

70Gy

yes

5

40%*

74% *

62%*

78%*

RTOG

92-02

1500

T2c-T4

4mo NA/C

2yr NA/C/A

65-70Gy

yes

5

28%*

46%*

78%‡

80%‡

D'Amico

206

T1-T2b

none

6mo NA/C/A

70Gy

no

5

57%*

82%*

78%*

88%*

A- Adjuvant, C- Concurrent, NA- Neoadjuvant, * SS, † SS for GS2-6, ‡ SS for GS8-10


 

At this point I ran out of time, but wanted to cover EBRT with brachy boost as another RT based option which has had good preliminary results - Stay tuned!


 

Case Resolution

Pt started on ADT

To be rescanned for potential RT + LTADT in 2 months


 

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