@MediHumdani@DunleavyKieron@TheIACH There is accumulating retrospective data that RCHOP and even abbreviated therapy (less than 6 cycles) may be adequate for patients with early stage DHL/THL.
Do you treat all patients with HGBCL with DA-EPOCH-R, or only those with advanced stage disease?
What is your choice of salvage chemotherapy in a 28 yo patient with primary refractory classical Hodgkins lymphoma after 6 cycles of ABVD?
We go through the current data and our approach in a recent review: https://t.co/v2mwMpYO8M
Treatment Outcomes and Roles of Transplantation and Maintenance Rituximab in Patients With Previously Untreated Mantle Cell Lymphoma: Results From Large Real-World Cohorts https://t.co/0c5SEk6v4B
Updated analysis of ECHELON-1 at #ASCO22 showed OS benefit to BV-AVD arm compared to ABVD in untreated advanced stage cHL!
- Median fu 73 mo
- 6 yr OS 93.9% vs. 89.%
- HR for OS 0.59 (95%CI 0.396-0.879; p=0.009)
- Fewer secondary malignancies w BV-AVD
@MediHumdani Data from Tandem 2022 on alloSCT post Cd19 CART in RR DLBCL (Zurko et al):
1 yr OS/PFS: 51%, 40%
1 yr non relapse mortality 27%
10% G3/4 acute GVHD
28% chronic GVHD at 1 yr
Allo is very toxic but reasonable--need longer follow up! Alternatively, consider bispecifics or trials.
@AaronGoodman33 @matthew_mei@graham74GC I have started to lean more towards sequential BV-AVD-BV (particularly in stage IV, high IPS score) as it is a challenge to know how best to tx after 2 ABVD per RATHL if PET2 positive...Can't escalate to beacopp, shouldn't continue bleo.
@AaronGoodman33 I would avoid ICE since relapse so quickly after 1st line tx. Would use Pembro-GVD: all output, high response rates.
Data that CPIs resenitize tumor to cytotoxic chemo and benefit to autoSCT.
:https://t.co/Ba6iQDQ1sw
Question is whether you do BV maint post auto per ATHERA??
@BijoyTelivala@Berninini @AaronGoodman33 @emouMD Agree- approach to 2nd line Auto vs. CART will depend on:
- Duration of CR1
- Disease burden (need to use salvage chemo vs bridging steroids)
- How quickly can be referred to cellular therapies program, obtain insurance auth and undergo apheresis
- Co morbidites precluding auto
CART now approved in the 2nd line setting for DLBCL, for pts with relapse <12 mo after 1st line tx or primary refractory disease based on Zuma 7 data.
@AaronGoodman33, @Berninini, @emouMD How would you now treat a 60 yo patient with DLBCL relapsed 9 mo after RCHOP?
@emouMD @AaronGoodman33 @Berninini Agreed! There is still a role for autoSCT in 2nd line setting. In Zuma-7, similar duration of response in Axi-cel vs. SOC arms in responding patients.
So #twitterx doesn't throw me in Twitter jail, here are 10 #ASH21 abstracts...as HARRY POTTER characters.
I couldn't decide if I should rank based on "impactful" or "practice changing", so these are some that I think everyone should *read carefully*, and I tried to make it fun!
On round today, seeing a patient with altered mental status:
Me: Who is the president of the US?
Team behind me: *cumulative sigh of relief*
...Four years later, it's a nice feeling to not cringe during neuro exams again.
Grateful to have received the CancerLinQ Discovery Award from @ASCO. Excited about the work and feel so fortunate to be part of a great QI team at Stanford!