Chronic Lymphocytic Leukemia (CLL)- Chronic Relapsing Remitting
Most common leukemia in adults
Incurable but treatable
*Remember Supportive Care*
Median age of 72
M > F
80% incidental
SLL: lymphocytes in lymph nodes and spleen instead of blood
Presentation:
1) Fatigue
2) B symptoms
3) High WC
4) Cytopenias (Marrow infiltrate, AIHA, ITP, Hyposplenism)
Rule out: Reactive (viral serology)- Hepatitis, HIV
Investigate:
1) FBC + blood film (mature lymphocytes) w/ trend
2) Haemolysis screen + Coombs test
3) B2 Microglobulin (prognostic marker)
4) IGs + serum electrophoresis
5) Flow cytometry (immunophenotyping)
6) LN Bx (core) especially if lymphadenopathy (*SLL)
7) BMBx
8) Tp53 (17p del or mut)
9) CTNTAP if treatment indicated
Confirm :
1) Lymphocyte morphology (blood film)- monomorphic mature small w/out nucleolous r/o aggressive pro-lymphocytes r/o prominent nucleoli in reactive lymphocytosis
2) 5x10^9 / L circulating clonal B cells for over 3 months on Flow…if below, need annual FBC monitoring
3) Immunophenotype scoring out of 5 (1 point each): +ve CD5, +ve CD23, weak IG expression, absent/weak CD22, absence of FMC-7...need 4 or 5/5
Staging :
1) BINIT A/B/C
2) RAI 0-4
Prognosis: CLL International Prognostic Index
1) Age
2) B2 Microglobulin
3) TP53 status- continuous therapy better if TP53 mut
4) IGHV mutation- better if present
5) RAI or BINIT
The International Working Group for CLL (iwCLL) treatment- Risk vs. Benefit
1) Cytopenias Hb <100, Plts <100
2) Bulky disease >10cm LN length
3) Constitutional sx disease related
4) AIHA (10-20%) and ITP (2-5%)
5) Symptomatic or fnxnal extranodal involvement
6) Massive Splenomegaly >6cm from costal margin or progressive SM + Sx
7) Lymphocyte doubling time < 6 months or > 50 percent rise in 2 months
WATCH and WAIT if not reaching criteria
Infection risk (bacterial):
1) Vaccination (NB: NO LIVE VACCINES)
2) IVIG in immune paresis
3) Prophylactic Abx (azithromycin)
4) PCP prophylaxis while on treatment
Need IRRAD blood products
Trials for Traditional treatments vs. BTK1 and BCL2
1) Alliance
2) Mayo clinic study
3) FLARE
4) CLL14 (German) and Illuminate trials
Treatment:
1) Traditional: FCR
2) Targeted:
a. 1st gen BTK1- Ibrutinib 420mg OD (continuous)
b. 2nd gen BTK1- Acalabrutonib 100mg BD (continuous)
c. BCL-2 inhibitor- Venetoclax 400mg OD
i. Frontline : OVen.. Ven + Obinutuzumab (CD20 mAb) - 1 yr
ii. Relapse: VenR... Ven + Rituximab (CD20 mAb)- 2 yrs
d. PI3K inhibitor- Idelalisib - 3rd line as bridging for 2x refractory/2x exposed
*High Risk*: Doublet therapy (targeted combined)
i. Jain et al. – Phase 2 trial
ii. CAPTIVATE trial: Ibru + Ven <65, TP53 mut/del OR unmutated IGHV
TRIPLET Therapy trials
-ALLO SCT- early referrals in high risk with first progression
· Primary Progression: <6m of response
· Relapse: >6m response and then….look at iwCLL for treatment…class switching….
FUTURE :
- Zanibrutinib
- Time limited therapies – STATIC trial
- MRD for CLL
NOTE:
- AIHA treatment algorithm 1st THEN CLL treatment
- Richters transformation to DLBCL
Chronic Lymphocytic Leukemia (CLL)- Chronic Relapsing Remitting
Most common leukemia in adults
Incurable but treatable
*Remember Supportive Care*
Median age of 72
M > F
80% incidental
SLL: lymphocytes in lymph nodes and spleen instead of blood
Presentation:
1) Fatigue
2) B symptoms
3) High WC
4) Cytopenias (Marrow infiltrate, AIHA, ITP, Hyposplenism)
Rule out: Reactive (viral serology)- Hepatitis, HIV
Investigate:
1) FBC + blood film (mature lymphocytes) w/ trend
2) Haemolysis screen + Coombs test
3) B2 Microglobulin (prognostic marker)
4) IGs + serum electrophoresis
5) Flow cytometry (immunophenotyping)
6) LN Bx (core) especially if lymphadenopathy (*SLL)
7) BMBx
8) Tp53 (17p del or mut)
9) CTNTAP if treatment indicated
Confirm :
1) Lymphocyte morphology (blood film)- monomorphic mature small w/out nucleolous r/o aggressive pro-lymphocytes r/o prominent nucleoli in reactive lymphocytosis
2) 5x10^9 / L circulating clonal B cells for over 3 months on Flow…if below, need annual FBC monitoring
3) Immunophenotype scoring out of 5 (1 point each): +ve CD5, +ve CD23, weak IG expression, absent/weak CD22, absence of FMC-7...need 4 or 5/5
Staging :
1) BINIT A/B/C
2) RAI 0-4
Prognosis: CLL International Prognostic Index
1) Age
2) B2 Microglobulin
3) TP53 status- continuous therapy better if TP53 mut
4) IGHV mutation- better if present
5) RAI or BINIT
The International Working Group for CLL (iwCLL) treatment- Risk vs. Benefit
1) Cytopenias Hb <100, Plts <100
2) Bulky disease >10cm LN length
3) Constitutional sx disease related
4) AIHA (10-20%) and ITP (2-5%)
5) Symptomatic or fnxnal extranodal involvement
6) Massive Splenomegaly >6cm from costal margin or progressive SM + Sx
7) Lymphocyte doubling time < 6 months or > 50 percent rise in 2 months
WATCH and WAIT if not reaching criteria
Infection risk (bacterial):
1) Vaccination (NB: NO LIVE VACCINES)
2) IVIG in immune paresis
3) Prophylactic Abx (azithromycin)
4) PCP prophylaxis while on treatment
Need IRRAD blood products
Trials for Traditional treatments vs. BTK1 and BCL2
1) Alliance
2) Mayo clinic study
3) FLARE
4) CLL14 (German) and Illuminate trials
Treatment:
1) Traditional: FCR
2) Targeted:
a. 1st gen BTK1- Ibrutinib 420mg OD (continuous)
b. 2nd gen BTK1- Acalabrutonib 100mg BD (continuous)
c. BCL-2 inhibitor- Venetoclax 400mg OD
i. Frontline : OVen.. Ven + Obinutuzumab (CD20 mAb) - 1 yr
ii. Relapse: VenR... Ven + Rituximab (CD20 mAb)- 2 yrs
d. PI3K inhibitor- Idelalisib - 3rd line as bridging for 2x refractory/2x exposed
*High Risk*: Doublet therapy (targeted combined)
i. Jain et al. – Phase 2 trial
ii. CAPTIVATE trial: Ibru + Ven <65, TP53 mut/del OR unmutated IGHV
TRIPLET Therapy trials
-ALLO SCT- early referrals in high risk with first progression
· Primary Progression: <6m of response
· Relapse: >6m response and then….look at iwCLL for treatment…class switching….
FUTURE :
- Zanibrutinib
- Time limited therapies – STATIC trial
- MRD for CLL
NOTE:
- AIHA treatment algorithm 1st THEN CLL treatment
- Richters transformation to DLBCL