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BLADDER CANCER
Ahmed Zeeneldin
Associate Professor of Medical Oncology
INCIDENCE IN USA
¢ 4.5% of cancers
¢ M: F: 2.5:1

¢ Age: 6th-7th decade
INCIDENCE IN EGYPT
¢ NCI males:
¢ 1st , 16%
INCIDENCE
¢ NCI combined:
¢ 4th, 4.4%

¢ M: F: 4:1

¢ Median age:

¢ M: 60

¢ F: 58
RISK FACTORS
¢   Occupational exposure:
    — Aniline dyes
    — Leather, rubber and paint industries

¢   Schistosoma haematobium:
    — Associated with squamous histology
    — In Africa and middle east

¢ Smoking
¢ Pelvic irradiation

¢ Drugs: cyclophosphamide
HISTOLOGY
¢ Urothelial (transitional cell) carcinoma TCC: commonest
¢ In situ
    —   Papillary
    —   Flat
    —   With squamous metaplasia
    —   With glandular metaplasia
    —   With squamous and glandular metaplasia
¢ Squamous cell carcinoma (SCC)
¢ Adenocarcinoma

¢ Undifferentiated carcinoma
HISTOLOGY IN EGYPT
HISTOLOGY
              US                     EGY

 ¢ TCC: 90%               ¢ TCC: 63%
 ¢ SCC: 6-8%              ¢ SCC: 27%

 ¢ Adeno: 2%              ¢ Adeno: 3%

 ¢ Small cell: 1%         ¢ Undifferentiated: 2%


systemic chemotherapy regimens used to treat TCC
are ineffective in pure SCC or Adeno
If mixed tumor only TCC responds
STAGES
TNM STAGING 2010
 URINARY BLADDER
                                   ¢   T0: non-invasive
                                        —   Ta: Noninvasive papillary carcinoma
                                        —   Tis: Carcinoma in situ “flat tumor”
                                   ¢   T1: mucosa or submucosa
                                   ¢   T2: muscle
                                        —   T2a: inner half
                                        —   T2b: outer half
                                   ¢   T3: outside muscle (adventitia)
                                        —   T3a: microscopic (histology, no
                                            masses
                                        —   T3b: macroscopic (mass)
                                   ¢   T4: surroiundings
                                        —   T4a: prostate, uterus, vagina
                                        —   T4b: pelvic or abdominal

      T   T    T   T4    T4   M1
                                   ¢   N1: regional LN+
      1   2    3   a     b              —   N1: Pelvic LNs (1)
                                        —   N2 : pelvic LNS (>1)
 N0   I   II   III III   IV   IV        —   N3: common iliac LN

   N1- IV IV IV IV IV IV
                                       M1: Distant mets
SIMPLIFICATION
   3
                                   ¢


-I: T1        -II: T2
-III: T3/T4 a -IV: T4b OR LN+
OR M1
STAGING
T0: non-invasive
    Ta: Noninvasive papillary carcinoma
    Tis: Carcinoma in situ “flat tumor”
T1: sub-epithelial connective tissue
T2: Tumor invades muscle
    T2a: inner half
    T2b: outer half
T3: Tumor invades perivesical tissue
    T3a: Microscopically
    T3b: Macroscopically (extravesical mass)
T4: surroundings
    T4a: prostate, uterus, vagina
    T4b: pelvic wall, abdominal wall

N1: 1 pelvic LN
N2: > 1 pelvic LN
                                                      Tis/0   T1   T2    T3               T4          M1=IV
N3: common iliac LN
                                               N0      0      I    II        III   T4a:        T4b:    IV
M1: distant mets                                                                    III         IV

                                               N1-3                     IV
MANAGEMENT OF BLADDER CA
¢   Cystoscopy and biopsy:
    — See lesions
    — Biopsy and muscle should be included
    — We will reach to a conclusion:
    — MUSCLE IS INVADED OR NOT
        ¢ Not invaded àTURB
           ¢ Upper UT imaging

           ¢ CT if sessile or high grade T is suspected

        ¢ Invaded à CT:

           ¢ LN small (negative): T2,T3, T4a: cyatectomy

           ¢ LN large: biopsy: negative

             —   Positive:
NON MUSCLE INVASIVE
        Grade Cyctectomy TURB            IVsT+               Cystectomy
Tis     High     No             Yes      BCG                 Resistent
                                                             /relapsed
Ta      Low      No             Yes      May (chemo, mito)   //
                                         Once
                                         ? After 6ms
Ta      high     No             Yes      BCG > Chemo         //
T1      Low      No             Yes      BCG*                If residual
                                         Mito**              //
T1      high     May            Yes      BCG*                if residual
                                         Mito**              //


+ not if extensive TURB or perforation
* Whether residual or no residual
** chemotherapy only if no residaul
INTRAVESICAL CHMOTHERAPY
¢   Drugs
    —   Chemotherapy
        ¢   Alkylating agents: thiotepa, mitomycin C (40mg in 20 cc st
            Water),
        ¢   Anthracyclines: doxorubicin (50 mg in 25 cc St water),
            epirubicin, valrubicin
¢   Value:
    — Acts by diffusion
    — Prevent seeding and Reduce recurrence by 6%
    — No reduction in disease progression or mortality
    — Within 6 Hrs post TUR, Not if extensive TURB or
      perforation
    — Overnight fast, empty bladder before
    — Keep for .5 hr (post TUR) or 2Hrs, supine and prone (air
      bubble)
    — Alkalanize urine with mitomycin
INTRAVESICLA IMMUNOTHERAPY
 —   Immunotherapy
     ¢   BCG (81 mg for TheraCys and 50 mg for TICE, both in 50 cc
         physiologic saline)
 —   Value:
     ¢ Acts by enhancing immune response, drawing lymphocytes
       and macrophages to the bladder and stimulating a cellular
       (TH1) immune response
     ¢ Not immediate (at least 1-2 wks post TUR)

     ¢ Weekly x 6 w

     ¢ Maintenance

        ¢ (3 app x q 3ms)

        ¢ 3 weekly at 2, 6, 12, 18, 24, 30, 36 ms XXXX?

        ¢ NOT WITH CIPRO
MUSCLE INVASIVE
N            Cystectomy Chemotherapy             Radiotherapy
N-     T2*   Radical        Neoadj or adjuvant   No
             Partial        Neoadj or adjuvant   May be used instead of CT
             No             CRT                  CRT
N-     T3*   Radical        Neoadj or adjuvant   No

             No             CRT                  CRT
N-     T4a   If possible    CRT or chemo         CRT or chemo
             1st or after   (Neoadj or adj)      (Neoadj or adj)
             Neoadj
N-     T4b   If possible    CRT or chemo         CRT or chemo
             after Neoadj   (Neoadj or adj)      (Neoadj or adj)
N+           If possible    CRT or chemo         CRT or chemo
             after Neoadj   (Neoadj or adj)      (Neoadj or adj)
M1           No             Yes                  may
PROGNOSTIC FACTORS
¢   Stage :
    —   depth of invasion
¢   Grade:
    — Low grade: 1-2
    — High grade: 3-4
TREATMENT
Non-Muscle-invasive               Muscle-invasive

    —  Ta                         ¢ T2
     — Tis
                                  ¢ T3
     — T1
                                  ¢ T4
¢   Treatment:
     — Resection: Repeat TUR
                                  ¢ Treat.

     — +/- intravesical therapy       —   Resection: cystectomy
        ¢   Grade                         ¢   Partial or complete
        ¢   depth                     — Chemo: adjuvant/neoadj
                                      — RT:
TREATMENT MODALITIES
¢   Resection:
    — TURBT: ONLY FOR non-muscle invasive
    — Cystectomy:
        ¢ Partial cystectomy : selected cases of muscle invasion
        ¢ Radical cystectomy: standard treatment of muscle invasive

          tumors and as salvage therapy
¢   Drug therapy:
    —   Local (intravesical): ONLY FOR non-muscle invasive
        ¢ Immunotherapy: BCG or INF
        ¢ Chemotherapy: MMC, Doxorubicin or Valrubicin, thiotepa

    —   Systemic (IV) chemotherapy: ONLY for muscle
        invasive
¢   Radiotherapy: ONLY for muscle invasive
TREATMENT: NON-MUSCLE INVASIVE
¢ Includes: Ta, Tis, T1
¢ Tx:
    — Repeated TURB
    — Post TURB intravesical therapy:
        ¢ depends on grade and depth of invasion that determines:
           ¢ Bladder recurrence risk

           ¢ Progression to muscle invasion risk

        ¢ Modes:

           ¢ Adjuvant: to prevent bladder recurrence: MAINLY

           ¢ Complementary: to eradicate residual disease: RARELY

    —   Cystectomy: rare
TREATMENT: NON-MUSCLE INVASIVE
¢   Tis (CIS), always high grade
¢   Tx:
     — TURB
     — Post TURB intravesical BCG
      therapy Weekly x 6
    — Follow up: cystectoscopy +
      cytology + imaging of upper
      Urinary tract q3 m x 24m,
      then increase intervals

    —   Recurrence:
        ¢   TURB +
        ¢   Adjuvant intravesical therapy
            according to grade and
            depth of invasion
        ¢   Follow up: cystectoscopy q3
            m
TREATMENT: NON-MUSCLE INVASIVE
¢   Ta (papilloma), low grade                  ¢   Ta (papilloma), high grade
¢   Tx:                                        ¢   Tx:
    —   TURB                                       —   TURB
    —   Post TURB intravesical therapy:            —   Post TURB intravesical therapy:
         ¢   None                                       ¢   None
         ¢   Adjuvant intravesical                      ¢   Adjuvant intravesical BCG:
             chemotherapy (Mitomycin C):                ¢   Adjuvant intravesical
              ¢ Single                                      chemotherapy (Mitomycin C):
              ¢ Within 24 Hours form TURB                    ¢ Single

    —   Follow up: cystectoscopy +                           ¢ Within 24 Hours form TURB

        cytology q3 m x 12 m, then                 — Follow up: cystectoscopy +
        increase intervals                           cytology + imaging of upper
                                                     Urinary tract q3 m x 24m, then
    —   Recurrence:                                  increase intervals
         ¢   TURB +                                — Recurrence:
         ¢   Adjuvant intravesical therapy              ¢   TURB +
             according to grade and depth of            ¢   Adjuvant intravesical therapy
             invasion                                       according to grade and depth of
         ¢   Follow up: cystectoscopy q3 m                  invasion
                                                        ¢   Follow up: cystectoscopy q3 m
TREATMENT: NON-MUSCLE INVASIVE
¢   Persistent or recurrent Ta and Tis
    —     TURB+/- IVTà recurrence/persistence at W12à TURB+IVT à still recurrence or
          persistence at W 24
¢   Tx:
    — Cystectomy is the first option
    — TURB and Post TURB intravesical therapy may be considered to avoid cyctectomy
           ¢   Use different agents
           ¢   Chemo: MMC, Valrubicin
           ¢   BCG + INF a
           ¢   Follow up: cystectoscopy + cytology + imaging of upper Urinary tract q3 m x 24m, then q 6m x 24
               m
                ¢   Recurrence/persistence: cystectomy

¢   Another scenario:
    — TURB+/- IVTà recurrence/persistence at W12à TURB+IVT à CR:
    — Maintenance BCG
    —     Follow up: cystectoscopy + cytology + imaging of upper Urinary tract q3 m x
          24m, then q 6m x 24 m
                ¢   Recurrence/persistence: TRUB + different IVT or cystectomy
TREATMENT: NON-MUSCLE INVASIVE
¢   T1 , low risk                                   ¢   T1, high risk
     —    No high risk features                          —    multifocal lesions,
                                                         —    vascular invasion,
                                                         —    recurrence after BCG
¢   Tx:
                                                         —    High grade.
     —    TURB
     —    Post TURB intravesical therapy:           ¢   Tx:
           ¢   Adjuvant intravesical BCG:                —    TURB
           ¢   Adjuvant intravesical chemotherapy        —    Post TURB intravesical therapy:
               (Mitomycin C):                                  ¢   Adjuvant intravesical BCG:
                ¢ Single                                       ¢   Adjuvant intravesical chemotherapy
                ¢ Within 24 Hours form TURB                        (Mitomycin C):
     —    Follow up: cystectoscopy + cytology                       ¢ Single

          q3 m x 12 m, then increase intervals                      ¢ Within 24 Hours form TURB

                                                         —    Cystectomy
     —    Recurrence:                                    — Follow up: cystectoscopy + cytology
           ¢   TURB +                                      + imaging of upper Urinary tract q3
           ¢   Adjuvant intravesical therapy               m x 24m, then increase intervals
               according to grade and depth of           — Persistence after conservative
               invasion                                    management :
           ¢   Follow up: cystectoscopy q3 m                   ¢   Cystectomy
FOLLOW UP
¢   Low risk lesion:      high risk lesions+
    Cystoscopy and cytology   Cystoscopy and cytology
¢                                imaging upper tract
¢ q3 m x 12                     q3 m x24
¢ Then increasing         q 6m x 24
TREATMENT: MUSCLE INVASIVE DISEASE
¢   Workup:
    — Lab: CBC, chemistry, Alk phos
    — Cystoscopy, EAU/TRUBT
    — Imaging:
        ¢ Chest Xray
        ¢ CT/MRI of abdomen and pelvis

        ¢ +/- Bone scan


¢   Aim:
                                                 Tis/0   T1   T2    T3           T4          M1=IV
    — Organ confined T2, N0, M0           N0      0      I    II    III   T4a:        T4b:    IV
                                                                           III         IV
    — Non-organ confined T3, T4, N1, M0
                                          N1-3                     IV
    — Metastatic disease M1
ORGAN CONFINED (T2) DISEASE
¢   Surgery (cyctectomy):
    —   Primary Tx
    —   radical : standard particularly in recurrence
    —   Partial (segmental)
          ¢   More in dome and solitary
          ¢   Less in neck, trigone and multiple or associated Tis
¢   Chemotherapy:
    —   Cisplatin-based
          ¢   Neoadjuvant: in T3 or T2 or
          ¢   Adjuvant :    pT3 and pT4 and LN+
¢   RT:
          ¢   Adjuvant:       pT3 and pT4, LN+, SM+ or high grade
¢   Concurrent chemoradiotherapy (CCRT):
    —   Preoperative: in advanced disease
    —   Definitive:     in severe comorbidities and poor PS
    —   If CCRT is not tolerable: chemo or radio can be given alone
ORGAN CONFINED (T2 N0)
NON-ORGAN CONFINED (T3, N0)
NON-ORGAN CONFINED (T4 OR N1-3 OR M1)
CYSTECTOMY
¢   Radical cystectomy: standard
    —   Male:
         ¢   removes bladder, prostate, seminal vesicles
    —   Females:
         ¢   Removes bladder and maybe uterus, ovaries and tubes
    —   Pelvic LND:
         ¢   decreases recurrence and
         ¢   increase OS
    —   Urinary diversion or neobladder
¢   Partial systectomy: selective
    —   More in dome and solitary
    —   Less in neck, trigone and multiple or associated Tis
    —   Recurrence after partial cystectomy:
         ¢   Consider as new cancer
         ¢   Non-M invasive: TURB and IVT
         ¢   M invasive: as usual but do not consider conservation
             again
NEOADJUVANT CHEMO
¢   Cisplatin-based
    —   MVAC
    —   CMV
    —   Cis-Gem
    —   Cis-adia
    —   Cis-Mtx
¢ 3 cycles
¢ In T3 (category 1) or T2 (category 2A)
NEOADJUVANT M-VAC CHEMO
¢   Grossman et al, N Engl J Med. 2003;349(9):859-66.
¢   MVAC x 3 q 28d
    — Mtx:       30 mg sm d1, 15, 22
    — Vinblastine: 3 mg sm d2, 15, 22
    — Adrai:       30 mg sm d2
    — Cisplatin:   70 mg sm d2
¢ T2-T4a
¢ Pathological CR: 38%
ADVERSE EVENTS OF MVAC
COMPLICATIONS AFTER SURGERY
Figure 1. Survival
among Patients
Randomly Assigned
to Receive
Methotrexate,
Vinblastine,
Doxorubicin, and
Cisplatin (M-VAC)
Followed by
Cystectomy or
Cystectomy Alone,
According to an
Intention-to-Treat
Analysis.
OS in pT0 vs RD
NEOADJ CIS-ADRIA OR CIS-MTX
¢ Sherif et al, Eur Urol 2004;45:297–303.
¢ Combined analysis of 2 trials

¢ Regimens:
    — Cis 70 mg/sm & A 30 mg/sm q 3w x2 + RT
    — Cis 100mg/m & Mtx 250mg/sm q3w x 3 NO RT

¢ OS HR 0.80 (95% CI 0.64–0.99) in favor of neoadjuvant
  treatment.
¢ 5 Y OS was 56% for neoadjuvant and 48% in the control
  group,
¢ 8% reduction in risk of death.
OS
NEOADJ CMV
¢ 967 pts
¢ 16% reduction in mortality with NACT
NEOADJUVANT   CHEMOTHERAPY FOR TRANSITIONAL CELL
               CARCINOMA OF THE BLADDER:
         A SYSTEMATIC REVIEW AND META-ANALYSIS.

¢   Winquist et al, J Urol. 2004 Feb;171(2 Pt 1):561-9.
¢   11 trials (2,605 patients)
¢   Conducted between 1984 and 2002
¢   TCC stages II and III (T2-T4, Nx-N3, M0)
¢   Pooled HR of death was 0.90 (95% CI 0.82 to 0.99, p =
    0.02).
¢   Absolute OS benefit of 6.5% (95% CI 2 to 11%) from
    50% to 56.5%
¢   PFS benefit consistent with OS benefit
¢   CR rates: 14-38%, Major Pathological response: 43%
¢   Major pathological response was associated with
    improved OS in 4 trials
REGIMENS
NEOADJUVANT CHEMO
CONCURRENT CHEMORADIOTHERAPY
     ¢   Improved local control of invasive bladder
            cancer by concurrent cisplatin and
          preoperative or definitive radiation. The
        National Cancer Institute of Canada Clinical
                       Trials Group.

¢   Coppin et al, J Clin Oncol. 1996 Nov;14(11):2901-7.
¢   RCT in 99 patients
¢   T2 to T4b TCC
¢   Randomized to CCRT or RT
    —    (cisplatin 100 mg/m2 at 2-week intervals x 3 cycles
         concurrent with pelvic radiation), or RT (radiation without
         chemotherapy)
DESIGN
CCRT VS RT IN TCC OF BLADDER
¢ Pelvis relapse significantly lower in CCRT
¢ Distant relapse were similar

¢ PFS better with CCRT (P 0.08)

¢ 3 y OS rates 47% in CCRT and 33% in RT (P0.34)
OS & PFS
ADJUVANT CHEMOTHERAPY
¢   Non-urothelial CA
    —   No data in any stage
¢   Urothelial CA
    — Conflicting data
    — Many trials showing benefit are not randomized
    — Metaanalysis of 6 trails
        ¢ 25% mortality reduction
        ¢ But many limitations

        ¢ Regimens

           ¢ GC

           ¢ MVAC, MVEC

           ¢ CAP

        ¢ No. of cycles: at least 3
ADJUVANT CHEMOTERAPY FOR TCC OF
BLADDER
CHEMOTHERAPY IN METASTATIC TCC
ADJ RT
¢ Dat are scarce
¢ Possible role in T3a, T3b, T4a
    —   Due to High recurrence (30% that increase to 60% if
        SM+)
¢ May be given with concurrent cisplatin
¢ Adj chemotherapy is also indicated in these cases

¢ Adj RT and Adj CT are not give together
BLADDER PRESERVATION
¢ Partial cystectomy alone
¢ Chemotherapy then partial cystectomy
¢ TUR alone
¢ TUR followed by
    —   Chemotherapy and radiotherapy (BEST)
        ¢   Cisplatin w1, 4 +/-8
    — Chemo only
    — Radio only


¢   Indications
    — Urothelial ca
    — Unfit pts
    — Refusing pts

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Bladder cancer 12 2012

  • 1. BLADDER CANCER Ahmed Zeeneldin Associate Professor of Medical Oncology
  • 2. INCIDENCE IN USA ¢ 4.5% of cancers ¢ M: F: 2.5:1 ¢ Age: 6th-7th decade
  • 3. INCIDENCE IN EGYPT ¢ NCI males: ¢ 1st , 16%
  • 4. INCIDENCE ¢ NCI combined: ¢ 4th, 4.4% ¢ M: F: 4:1 ¢ Median age: ¢ M: 60 ¢ F: 58
  • 5. RISK FACTORS ¢ Occupational exposure: — Aniline dyes — Leather, rubber and paint industries ¢ Schistosoma haematobium: — Associated with squamous histology — In Africa and middle east ¢ Smoking ¢ Pelvic irradiation ¢ Drugs: cyclophosphamide
  • 6. HISTOLOGY ¢ Urothelial (transitional cell) carcinoma TCC: commonest ¢ In situ — Papillary — Flat — With squamous metaplasia — With glandular metaplasia — With squamous and glandular metaplasia ¢ Squamous cell carcinoma (SCC) ¢ Adenocarcinoma ¢ Undifferentiated carcinoma
  • 8. HISTOLOGY US EGY ¢ TCC: 90% ¢ TCC: 63% ¢ SCC: 6-8% ¢ SCC: 27% ¢ Adeno: 2% ¢ Adeno: 3% ¢ Small cell: 1% ¢ Undifferentiated: 2% systemic chemotherapy regimens used to treat TCC are ineffective in pure SCC or Adeno If mixed tumor only TCC responds
  • 10. TNM STAGING 2010 URINARY BLADDER ¢ T0: non-invasive — Ta: Noninvasive papillary carcinoma — Tis: Carcinoma in situ “flat tumor” ¢ T1: mucosa or submucosa ¢ T2: muscle — T2a: inner half — T2b: outer half ¢ T3: outside muscle (adventitia) — T3a: microscopic (histology, no masses — T3b: macroscopic (mass) ¢ T4: surroiundings — T4a: prostate, uterus, vagina — T4b: pelvic or abdominal T T T T4 T4 M1 ¢ N1: regional LN+ 1 2 3 a b — N1: Pelvic LNs (1) — N2 : pelvic LNS (>1) N0 I II III III IV IV — N3: common iliac LN N1- IV IV IV IV IV IV M1: Distant mets SIMPLIFICATION 3 ¢ -I: T1 -II: T2 -III: T3/T4 a -IV: T4b OR LN+ OR M1
  • 11. STAGING T0: non-invasive Ta: Noninvasive papillary carcinoma Tis: Carcinoma in situ “flat tumor” T1: sub-epithelial connective tissue T2: Tumor invades muscle T2a: inner half T2b: outer half T3: Tumor invades perivesical tissue T3a: Microscopically T3b: Macroscopically (extravesical mass) T4: surroundings T4a: prostate, uterus, vagina T4b: pelvic wall, abdominal wall N1: 1 pelvic LN N2: > 1 pelvic LN Tis/0 T1 T2 T3 T4 M1=IV N3: common iliac LN N0 0 I II III T4a: T4b: IV M1: distant mets III IV N1-3 IV
  • 12. MANAGEMENT OF BLADDER CA ¢ Cystoscopy and biopsy: — See lesions — Biopsy and muscle should be included — We will reach to a conclusion: — MUSCLE IS INVADED OR NOT ¢ Not invaded àTURB ¢ Upper UT imaging ¢ CT if sessile or high grade T is suspected ¢ Invaded à CT: ¢ LN small (negative): T2,T3, T4a: cyatectomy ¢ LN large: biopsy: negative — Positive:
  • 13. NON MUSCLE INVASIVE Grade Cyctectomy TURB IVsT+ Cystectomy Tis High No Yes BCG Resistent /relapsed Ta Low No Yes May (chemo, mito) // Once ? After 6ms Ta high No Yes BCG > Chemo // T1 Low No Yes BCG* If residual Mito** // T1 high May Yes BCG* if residual Mito** // + not if extensive TURB or perforation * Whether residual or no residual ** chemotherapy only if no residaul
  • 14. INTRAVESICAL CHMOTHERAPY ¢ Drugs — Chemotherapy ¢ Alkylating agents: thiotepa, mitomycin C (40mg in 20 cc st Water), ¢ Anthracyclines: doxorubicin (50 mg in 25 cc St water), epirubicin, valrubicin ¢ Value: — Acts by diffusion — Prevent seeding and Reduce recurrence by 6% — No reduction in disease progression or mortality — Within 6 Hrs post TUR, Not if extensive TURB or perforation — Overnight fast, empty bladder before — Keep for .5 hr (post TUR) or 2Hrs, supine and prone (air bubble) — Alkalanize urine with mitomycin
  • 15. INTRAVESICLA IMMUNOTHERAPY — Immunotherapy ¢ BCG (81 mg for TheraCys and 50 mg for TICE, both in 50 cc physiologic saline) — Value: ¢ Acts by enhancing immune response, drawing lymphocytes and macrophages to the bladder and stimulating a cellular (TH1) immune response ¢ Not immediate (at least 1-2 wks post TUR) ¢ Weekly x 6 w ¢ Maintenance ¢ (3 app x q 3ms) ¢ 3 weekly at 2, 6, 12, 18, 24, 30, 36 ms XXXX? ¢ NOT WITH CIPRO
  • 16. MUSCLE INVASIVE N Cystectomy Chemotherapy Radiotherapy N- T2* Radical Neoadj or adjuvant No Partial Neoadj or adjuvant May be used instead of CT No CRT CRT N- T3* Radical Neoadj or adjuvant No No CRT CRT N- T4a If possible CRT or chemo CRT or chemo 1st or after (Neoadj or adj) (Neoadj or adj) Neoadj N- T4b If possible CRT or chemo CRT or chemo after Neoadj (Neoadj or adj) (Neoadj or adj) N+ If possible CRT or chemo CRT or chemo after Neoadj (Neoadj or adj) (Neoadj or adj) M1 No Yes may
  • 17. PROGNOSTIC FACTORS ¢ Stage : — depth of invasion ¢ Grade: — Low grade: 1-2 — High grade: 3-4
  • 18. TREATMENT Non-Muscle-invasive Muscle-invasive — Ta ¢ T2 — Tis ¢ T3 — T1 ¢ T4 ¢ Treatment: — Resection: Repeat TUR ¢ Treat. — +/- intravesical therapy — Resection: cystectomy ¢ Grade ¢ Partial or complete ¢ depth — Chemo: adjuvant/neoadj — RT:
  • 19. TREATMENT MODALITIES ¢ Resection: — TURBT: ONLY FOR non-muscle invasive — Cystectomy: ¢ Partial cystectomy : selected cases of muscle invasion ¢ Radical cystectomy: standard treatment of muscle invasive tumors and as salvage therapy ¢ Drug therapy: — Local (intravesical): ONLY FOR non-muscle invasive ¢ Immunotherapy: BCG or INF ¢ Chemotherapy: MMC, Doxorubicin or Valrubicin, thiotepa — Systemic (IV) chemotherapy: ONLY for muscle invasive ¢ Radiotherapy: ONLY for muscle invasive
  • 20. TREATMENT: NON-MUSCLE INVASIVE ¢ Includes: Ta, Tis, T1 ¢ Tx: — Repeated TURB — Post TURB intravesical therapy: ¢ depends on grade and depth of invasion that determines: ¢ Bladder recurrence risk ¢ Progression to muscle invasion risk ¢ Modes: ¢ Adjuvant: to prevent bladder recurrence: MAINLY ¢ Complementary: to eradicate residual disease: RARELY — Cystectomy: rare
  • 21. TREATMENT: NON-MUSCLE INVASIVE ¢ Tis (CIS), always high grade ¢ Tx: — TURB — Post TURB intravesical BCG therapy Weekly x 6 — Follow up: cystectoscopy + cytology + imaging of upper Urinary tract q3 m x 24m, then increase intervals — Recurrence: ¢ TURB + ¢ Adjuvant intravesical therapy according to grade and depth of invasion ¢ Follow up: cystectoscopy q3 m
  • 22. TREATMENT: NON-MUSCLE INVASIVE ¢ Ta (papilloma), low grade ¢ Ta (papilloma), high grade ¢ Tx: ¢ Tx: — TURB — TURB — Post TURB intravesical therapy: — Post TURB intravesical therapy: ¢ None ¢ None ¢ Adjuvant intravesical ¢ Adjuvant intravesical BCG: chemotherapy (Mitomycin C): ¢ Adjuvant intravesical ¢ Single chemotherapy (Mitomycin C): ¢ Within 24 Hours form TURB ¢ Single — Follow up: cystectoscopy + ¢ Within 24 Hours form TURB cytology q3 m x 12 m, then — Follow up: cystectoscopy + increase intervals cytology + imaging of upper Urinary tract q3 m x 24m, then — Recurrence: increase intervals ¢ TURB + — Recurrence: ¢ Adjuvant intravesical therapy ¢ TURB + according to grade and depth of ¢ Adjuvant intravesical therapy invasion according to grade and depth of ¢ Follow up: cystectoscopy q3 m invasion ¢ Follow up: cystectoscopy q3 m
  • 23. TREATMENT: NON-MUSCLE INVASIVE ¢ Persistent or recurrent Ta and Tis — TURB+/- IVTà recurrence/persistence at W12à TURB+IVT à still recurrence or persistence at W 24 ¢ Tx: — Cystectomy is the first option — TURB and Post TURB intravesical therapy may be considered to avoid cyctectomy ¢ Use different agents ¢ Chemo: MMC, Valrubicin ¢ BCG + INF a ¢ Follow up: cystectoscopy + cytology + imaging of upper Urinary tract q3 m x 24m, then q 6m x 24 m ¢ Recurrence/persistence: cystectomy ¢ Another scenario: — TURB+/- IVTà recurrence/persistence at W12à TURB+IVT à CR: — Maintenance BCG — Follow up: cystectoscopy + cytology + imaging of upper Urinary tract q3 m x 24m, then q 6m x 24 m ¢ Recurrence/persistence: TRUB + different IVT or cystectomy
  • 24. TREATMENT: NON-MUSCLE INVASIVE ¢ T1 , low risk ¢ T1, high risk — No high risk features — multifocal lesions, — vascular invasion, — recurrence after BCG ¢ Tx: — High grade. — TURB — Post TURB intravesical therapy: ¢ Tx: ¢ Adjuvant intravesical BCG: — TURB ¢ Adjuvant intravesical chemotherapy — Post TURB intravesical therapy: (Mitomycin C): ¢ Adjuvant intravesical BCG: ¢ Single ¢ Adjuvant intravesical chemotherapy ¢ Within 24 Hours form TURB (Mitomycin C): — Follow up: cystectoscopy + cytology ¢ Single q3 m x 12 m, then increase intervals ¢ Within 24 Hours form TURB — Cystectomy — Recurrence: — Follow up: cystectoscopy + cytology ¢ TURB + + imaging of upper Urinary tract q3 ¢ Adjuvant intravesical therapy m x 24m, then increase intervals according to grade and depth of — Persistence after conservative invasion management : ¢ Follow up: cystectoscopy q3 m ¢ Cystectomy
  • 25. FOLLOW UP ¢ Low risk lesion: high risk lesions+ Cystoscopy and cytology Cystoscopy and cytology ¢ imaging upper tract ¢ q3 m x 12 q3 m x24 ¢ Then increasing q 6m x 24
  • 26. TREATMENT: MUSCLE INVASIVE DISEASE ¢ Workup: — Lab: CBC, chemistry, Alk phos — Cystoscopy, EAU/TRUBT — Imaging: ¢ Chest Xray ¢ CT/MRI of abdomen and pelvis ¢ +/- Bone scan ¢ Aim: Tis/0 T1 T2 T3 T4 M1=IV — Organ confined T2, N0, M0 N0 0 I II III T4a: T4b: IV III IV — Non-organ confined T3, T4, N1, M0 N1-3 IV — Metastatic disease M1
  • 27. ORGAN CONFINED (T2) DISEASE ¢ Surgery (cyctectomy): — Primary Tx — radical : standard particularly in recurrence — Partial (segmental) ¢ More in dome and solitary ¢ Less in neck, trigone and multiple or associated Tis ¢ Chemotherapy: — Cisplatin-based ¢ Neoadjuvant: in T3 or T2 or ¢ Adjuvant : pT3 and pT4 and LN+ ¢ RT: ¢ Adjuvant: pT3 and pT4, LN+, SM+ or high grade ¢ Concurrent chemoradiotherapy (CCRT): — Preoperative: in advanced disease — Definitive: in severe comorbidities and poor PS — If CCRT is not tolerable: chemo or radio can be given alone
  • 28.
  • 31. NON-ORGAN CONFINED (T4 OR N1-3 OR M1)
  • 32. CYSTECTOMY ¢ Radical cystectomy: standard — Male: ¢ removes bladder, prostate, seminal vesicles — Females: ¢ Removes bladder and maybe uterus, ovaries and tubes — Pelvic LND: ¢ decreases recurrence and ¢ increase OS — Urinary diversion or neobladder ¢ Partial systectomy: selective — More in dome and solitary — Less in neck, trigone and multiple or associated Tis — Recurrence after partial cystectomy: ¢ Consider as new cancer ¢ Non-M invasive: TURB and IVT ¢ M invasive: as usual but do not consider conservation again
  • 33. NEOADJUVANT CHEMO ¢ Cisplatin-based — MVAC — CMV — Cis-Gem — Cis-adia — Cis-Mtx ¢ 3 cycles ¢ In T3 (category 1) or T2 (category 2A)
  • 34. NEOADJUVANT M-VAC CHEMO ¢ Grossman et al, N Engl J Med. 2003;349(9):859-66. ¢ MVAC x 3 q 28d — Mtx: 30 mg sm d1, 15, 22 — Vinblastine: 3 mg sm d2, 15, 22 — Adrai: 30 mg sm d2 — Cisplatin: 70 mg sm d2 ¢ T2-T4a ¢ Pathological CR: 38%
  • 37. Figure 1. Survival among Patients Randomly Assigned to Receive Methotrexate, Vinblastine, Doxorubicin, and Cisplatin (M-VAC) Followed by Cystectomy or Cystectomy Alone, According to an Intention-to-Treat Analysis.
  • 38.
  • 39. OS in pT0 vs RD
  • 40. NEOADJ CIS-ADRIA OR CIS-MTX ¢ Sherif et al, Eur Urol 2004;45:297–303. ¢ Combined analysis of 2 trials ¢ Regimens: — Cis 70 mg/sm & A 30 mg/sm q 3w x2 + RT — Cis 100mg/m & Mtx 250mg/sm q3w x 3 NO RT ¢ OS HR 0.80 (95% CI 0.64–0.99) in favor of neoadjuvant treatment. ¢ 5 Y OS was 56% for neoadjuvant and 48% in the control group, ¢ 8% reduction in risk of death.
  • 41. OS
  • 42. NEOADJ CMV ¢ 967 pts ¢ 16% reduction in mortality with NACT
  • 43. NEOADJUVANT CHEMOTHERAPY FOR TRANSITIONAL CELL CARCINOMA OF THE BLADDER: A SYSTEMATIC REVIEW AND META-ANALYSIS. ¢ Winquist et al, J Urol. 2004 Feb;171(2 Pt 1):561-9. ¢ 11 trials (2,605 patients) ¢ Conducted between 1984 and 2002 ¢ TCC stages II and III (T2-T4, Nx-N3, M0) ¢ Pooled HR of death was 0.90 (95% CI 0.82 to 0.99, p = 0.02). ¢ Absolute OS benefit of 6.5% (95% CI 2 to 11%) from 50% to 56.5% ¢ PFS benefit consistent with OS benefit ¢ CR rates: 14-38%, Major Pathological response: 43% ¢ Major pathological response was associated with improved OS in 4 trials
  • 46. CONCURRENT CHEMORADIOTHERAPY ¢ Improved local control of invasive bladder cancer by concurrent cisplatin and preoperative or definitive radiation. The National Cancer Institute of Canada Clinical Trials Group. ¢ Coppin et al, J Clin Oncol. 1996 Nov;14(11):2901-7. ¢ RCT in 99 patients ¢ T2 to T4b TCC ¢ Randomized to CCRT or RT — (cisplatin 100 mg/m2 at 2-week intervals x 3 cycles concurrent with pelvic radiation), or RT (radiation without chemotherapy)
  • 48. CCRT VS RT IN TCC OF BLADDER ¢ Pelvis relapse significantly lower in CCRT ¢ Distant relapse were similar ¢ PFS better with CCRT (P 0.08) ¢ 3 y OS rates 47% in CCRT and 33% in RT (P0.34)
  • 50. ADJUVANT CHEMOTHERAPY ¢ Non-urothelial CA — No data in any stage ¢ Urothelial CA — Conflicting data — Many trials showing benefit are not randomized — Metaanalysis of 6 trails ¢ 25% mortality reduction ¢ But many limitations ¢ Regimens ¢ GC ¢ MVAC, MVEC ¢ CAP ¢ No. of cycles: at least 3
  • 51. ADJUVANT CHEMOTERAPY FOR TCC OF BLADDER
  • 53.
  • 54. ADJ RT ¢ Dat are scarce ¢ Possible role in T3a, T3b, T4a — Due to High recurrence (30% that increase to 60% if SM+) ¢ May be given with concurrent cisplatin ¢ Adj chemotherapy is also indicated in these cases ¢ Adj RT and Adj CT are not give together
  • 55. BLADDER PRESERVATION ¢ Partial cystectomy alone ¢ Chemotherapy then partial cystectomy ¢ TUR alone ¢ TUR followed by — Chemotherapy and radiotherapy (BEST) ¢ Cisplatin w1, 4 +/-8 — Chemo only — Radio only ¢ Indications — Urothelial ca — Unfit pts — Refusing pts