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CA DE PRÓSTATA- MANEJO:
LOCALIZADO- ALTO RIESGO/
LOCALMENTE AVANZADO
MR YESENIA HUERTA COLLADO
ONCOLOGIA MÉDICA
BAJO RIESGO- INTERMEDIO RIESGO
• VIGILANCIA ACTIVA
• PROSTATECTOMIA RADICAL
• RT
Pelvic lymph node dissection
• pelvic lymph node dissection (PLND) during
RP failed to improveoncological outcomes,
including survival.
• However, it is generally accepted that
extended pelvic LN dissection (eLND)
provides important information for staging
and prognosis
• preoperative tolos:
• A risk of nodal metastases over 5%
• Briganti nomogram
• Roach formula
• INCONTINENCIA
• 12M:
• RALP, 21.3%
• RRP 20.2%
• The adjusted OR was 1.08 (95% CI: 0.87-1.34).
• Erectile dysfunction
• RALP : 70.4%
• RRP : 74.7
• The adjusted OR was 0.81 (95% CI: 0.66-0.98)
ESTUDIO PIVOT
ESTUDIO PIVOT
PROSTATECTOMIA RADICAL VS OBSERVACIÓN --- MORTALIDAD A 12 AÑOS
ESTUDIO PIVOT
ESTUDIO PIVOT : ACTUALIZACIÓN
CIRUGIA: > EVENTOS ADVERSOS
CIRUGIA: < PROGRESION DE ENFERMEDAD
CIRUGIA: POTENCIAL BENEFICIO EN RIESGO INTERMEDIO
RADIOTERAPIA
BAJO RIESGO
 VIGILACIA ACTIVA
 RT
 PR
• Dosis de Rt externa debe de ser mínimo 74gY, engloando toda la rosa
base de las vesículas seminales
• No hay beneficio de asocioacn con bloqueo hormonal
• No hay benefcio de asociación de rt
PR VS (RT+ADT)
Among patients with Gleason score 9-10 prostate cancer,
treatment
with EBRT+BT with androgen deprivation therapy was associated
with significantly better prostate cancer–specific mortality and
longer time to distant metastasis compared with EBRT with
androgen deprivation therapy or with radical prostatectomy.
It is POSSIBLE!!!
All boils down to expertise
RT + ADT
In summary, we found that dose-
escalated EBRT was associated with
improved survival for men with
intermediate- and
high-risk, but not low-risk, prostate
cancer.
CONVENTIONAL FRACTIONS
 Low-risk cancers : A dose of 75.6 to 79.2 Gy.
 Intermediate-risk and high-risk: up to 81.0 Gy
freedom from biochemical
failure.
Cancer-Specific–Survival (%)
estudio DURACION
BRAZOS
N SOBREVIDA
ESPECIFICA -CANCER
SG
Neoadjuvant docetaxel for M0 disease
primary endpoint was relapse-free survival
follow-up of 12 years showed :
clinical RFS (metastases, local relapse or death) was also
improved with docetaxel (median cRFS 13.9 years versus
12.5 years; HR 0.75; 95% CI 0.56-1.00; P= 0.0491)
HR 0.71; 95% CI 0.54-0.94,
P=0.017).
• RTOG 0521:
 Tested RT plus 2 years ADT with or without 6 cycles of docetaxel
 reported a borderline improved RFS [HR 0.76;(95% CI 0.57-1.00); P=0.05].
 OS did not reach significance.
• STAMPEDE :
- A subset of men randomised had high-risk locali sed disease (and/or pelvic enlarged lymph nodes)
- RFS was improved in men randomised to receive docetaxel (HR 0.60; 95% CI 0.45-0.80; P= 0.283 x10-3)
Based on the available data, offering docetaxel
based ChT may be a reasonable option for younger,
fit men with multiple risk factors for recurrence.
RT - POST PR
Adverse laboratory/pathologic
features include:
 positive margin(s);
 seminal vesicle invasion;
 extracapsular extensión
 detectable PSA.
SWOG-8794
EORTC-22911
ARO-96-02
Finn Prostate Group Study
2.151 pacientes
PR- compromiso linfático
April 2018
BJU Int 123:252, 2019].
recibieron tratamiento combinado tuvieron
Gleason más alto
T más alto
márgenes positivos
mayor número de GL afectados.
mejor supervivencia en comparación con
*los individuos que permanecieron en observación
(HR = 0,77; IC del 95%: 0,64-0,94; p = 0,008)
*aquellos que recibieron ADT
(HR = 0,76 ; IC del 95%: 0,63-0,93; p = 0,007)
Patients with LNM after RP were identified
using the National Cancer Database
(2004–2013).
Exclusion criteria included any
 radiation therapy
 ADT before RP
 clinical M1 disease
patients with node-positive disease represent a heterogeneous population
Patients with the most adverse pathological features demonstrated the greatest benefit
from adjuvant ADT + EBRT.

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ca de prostata_ alto riesgo _ localmente avanzado.pptx

  • 1. CA DE PRÓSTATA- MANEJO: LOCALIZADO- ALTO RIESGO/ LOCALMENTE AVANZADO MR YESENIA HUERTA COLLADO ONCOLOGIA MÉDICA
  • 2.
  • 3.
  • 4.
  • 5. BAJO RIESGO- INTERMEDIO RIESGO • VIGILANCIA ACTIVA • PROSTATECTOMIA RADICAL • RT
  • 6.
  • 7.
  • 8.
  • 9.
  • 10. Pelvic lymph node dissection • pelvic lymph node dissection (PLND) during RP failed to improveoncological outcomes, including survival. • However, it is generally accepted that extended pelvic LN dissection (eLND) provides important information for staging and prognosis • preoperative tolos: • A risk of nodal metastases over 5% • Briganti nomogram • Roach formula
  • 11. • INCONTINENCIA • 12M: • RALP, 21.3% • RRP 20.2% • The adjusted OR was 1.08 (95% CI: 0.87-1.34). • Erectile dysfunction • RALP : 70.4% • RRP : 74.7 • The adjusted OR was 0.81 (95% CI: 0.66-0.98)
  • 13. ESTUDIO PIVOT PROSTATECTOMIA RADICAL VS OBSERVACIÓN --- MORTALIDAD A 12 AÑOS
  • 15. ESTUDIO PIVOT : ACTUALIZACIÓN CIRUGIA: > EVENTOS ADVERSOS CIRUGIA: < PROGRESION DE ENFERMEDAD CIRUGIA: POTENCIAL BENEFICIO EN RIESGO INTERMEDIO
  • 16.
  • 18. BAJO RIESGO  VIGILACIA ACTIVA  RT  PR
  • 19. • Dosis de Rt externa debe de ser mínimo 74gY, engloando toda la rosa base de las vesículas seminales • No hay beneficio de asocioacn con bloqueo hormonal • No hay benefcio de asociación de rt
  • 20.
  • 21.
  • 22.
  • 23.
  • 25.
  • 26.
  • 27.
  • 28. Among patients with Gleason score 9-10 prostate cancer, treatment with EBRT+BT with androgen deprivation therapy was associated with significantly better prostate cancer–specific mortality and longer time to distant metastasis compared with EBRT with androgen deprivation therapy or with radical prostatectomy.
  • 29.
  • 30.
  • 31. It is POSSIBLE!!! All boils down to expertise
  • 32.
  • 33.
  • 34.
  • 36.
  • 37. In summary, we found that dose- escalated EBRT was associated with improved survival for men with intermediate- and high-risk, but not low-risk, prostate cancer. CONVENTIONAL FRACTIONS  Low-risk cancers : A dose of 75.6 to 79.2 Gy.  Intermediate-risk and high-risk: up to 81.0 Gy
  • 39.
  • 40.
  • 42.
  • 43.
  • 45. primary endpoint was relapse-free survival
  • 46. follow-up of 12 years showed : clinical RFS (metastases, local relapse or death) was also improved with docetaxel (median cRFS 13.9 years versus 12.5 years; HR 0.75; 95% CI 0.56-1.00; P= 0.0491) HR 0.71; 95% CI 0.54-0.94, P=0.017).
  • 47. • RTOG 0521:  Tested RT plus 2 years ADT with or without 6 cycles of docetaxel  reported a borderline improved RFS [HR 0.76;(95% CI 0.57-1.00); P=0.05].  OS did not reach significance. • STAMPEDE : - A subset of men randomised had high-risk locali sed disease (and/or pelvic enlarged lymph nodes) - RFS was improved in men randomised to receive docetaxel (HR 0.60; 95% CI 0.45-0.80; P= 0.283 x10-3) Based on the available data, offering docetaxel based ChT may be a reasonable option for younger, fit men with multiple risk factors for recurrence.
  • 48. RT - POST PR
  • 49. Adverse laboratory/pathologic features include:  positive margin(s);  seminal vesicle invasion;  extracapsular extensión  detectable PSA. SWOG-8794 EORTC-22911 ARO-96-02 Finn Prostate Group Study
  • 50.
  • 51.
  • 53.
  • 55.
  • 57. BJU Int 123:252, 2019]. recibieron tratamiento combinado tuvieron Gleason más alto T más alto márgenes positivos mayor número de GL afectados. mejor supervivencia en comparación con *los individuos que permanecieron en observación (HR = 0,77; IC del 95%: 0,64-0,94; p = 0,008) *aquellos que recibieron ADT (HR = 0,76 ; IC del 95%: 0,63-0,93; p = 0,007) Patients with LNM after RP were identified using the National Cancer Database (2004–2013). Exclusion criteria included any  radiation therapy  ADT before RP  clinical M1 disease
  • 58. patients with node-positive disease represent a heterogeneous population Patients with the most adverse pathological features demonstrated the greatest benefit from adjuvant ADT + EBRT.

Editor's Notes

  1. PROSTATECTOMIA :: The goal of RP by any approach must be eradication of disease, while, whenever possible, preserving continence and potency [341]. Increasing comorbidity greatly increases the risk of dying from non-PCa-related causes [326]. An estimation of life expectancy is paramount in counselling a patient about surgery [331] (see also Section 5.4 – Evaluating health status and life expectancy).
  2. RADICALS, incluindo pacientes operados com PSA pós-operatório ≤ 0,2 ng/mL dentro de 4 a 22 semanas e pelo menos umas das seguintes características: pT3/4, margem positiva, escore de Gleason 7-10, PSA ≥ 0,1 ng/mL, randomizou 1.396 pacientes para RT adjuvante versus RT de resgate. Nesse estudo, somente 17% dos indivíduos apresentavam tumores com escore de Gleason 8-10, e 19% invasão de vesícula seminal, mas 63% de margens comprometidas. Primariamente era uma população N0/Nx. A SLP bioquímica foi similar entre os braços (HR=1,10; IC de 95%: 0,81-1,49; p=0,56). Do mesmo modo, o número de casos livres de posteriores tratamentos hormonais foi similar. Aproximadamente dois terços dos pacientes randomizados para RT de resgate ainda não precisaram ser tratados e, em consequência, as taxas de toxicidade gastrintestinal e geniturinária foram menores nesse braço em comparação com os indivíduos randomizados para RT adjuvante [Ann Oncol 30:abstr LBA49_PR, 2019]. A metanálise ARTISTIC, incluindo 2.151 pacientes provenientes de três estudos randomizados (RADICALS, GETUG-AFU 17, RAVES), tampouco demonstrou benefício da sobrevida livre de evento em favor da RT adjuvante (HR=1,12; IC de 95%: 0,88-1,42), sendo que aproximadamente 60% dos casos randomizados para RT de resgate foram poupados de serem tratados [Ann Oncol 30:abstrLBA48_PR, 2019]. Por esse motivo, como exceção, o uso da RT adjuvante pode ser considerado em pacientes com múltiplos fatores de risco (não tão bem representados no estudo RADICALS ou na metanálise ARTISTIC) e elevada expectativa de vida. Em um estudo retrospectivo em dez centros americanos, foram comparados os desfechos da RT adjuvante ou de resgate. Nesse estudo, 1.195 pacientes receberam RT de resgate com valores de PSA entre 0,1 e 0,5 ng/mL e 371 receberam RT adjuvante com valores de PSA < 0,1 ng/mL. A RT adjuvante quando comparada à de resgate demonstrou menor falência bioquímica, menor recorrência metastática e melhor SG (91 versus 79