#OncoAlert Randomized cohort from CheckMate 032 now available @JTOonline. Included 243 patients with relapsed #SCLC (1-2 prior lines), no PDL1 selection. Randomized 3:2 to nivo 3mg/kg q2w or nivo 1mg/kg with ipi 3mg/kg q3w x 4 (then nivo maint). #LCSM
@JTOonline#OncoAlert Primary endpoint ORR (side bar: what is the best endpoint?). Early results from @ASCO 2017 showed ORR 12% nivo and 21% with nivo/ipi with improved 3 month PFS rate but no diff in 3 month OS, presented then as bar graphs instead of KM curves (?!)
@JTOonline@ASCO#OncoAlert Now, with a median f/u of 11.9m, we see similar trends. ORR 11.6% with nivo (DOR 15.8m) and 21.9% with nivo/ipi (DOR 10m). mPFS similar (1.4 and 1.5m) but landmark PFS slightly better with nivo/ipi (3m: 32% vs 22%; 6m: 16% vs 22%, 1y: 10% vs 12%). Meaningful? #LCSM
@JTOonline@ASCO#OncoAlert No difference in overall survival. mOS 5.7m with nivo and 4.7m with nivo/ipi. 12m and 24m OS rates 30.5% and 17.9% with nivo compared to 30.2% and 16.9% with nivo/ipi. No breakdown by PD-L1 status as only 24 patients had PD-L1 > 1%. And no difference by #TMB#LCSM
@JTOonline@ASCO#OncoAlert Clear difference in safety. Grade 3-4 adverse events in 12.9% with nivo and 37.5% with nivo/ipi. Any event leading to discontinuation: 2.7% with nivo and 13.5% with nivo/ipi. Note: further therapy received in 32% nivo arm, 17% nivo/ipi. Could this be due to toxicity?
@JTOonline@ASCO#OncoAlert Ultimately, 2y OS rate is still meaningful, just not different between the arms. Is this due to higher discontinuation with ipi? Would it be better at the low doses used in CM227? Or is there no benefit to CTLA4 in this salvage population? Clear need for biomarker.
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Dr. @marinagarassino at #WCLC24 Presidential Plenary presents Normalized Membrane Ratio of TROP2 as a biomarker for datopotamab deruxtecan in TROPION-Lung01 (Dato-DXd vs docetaxel in previously treated NSCLC which previously showed PFS benefit with Dato-DXd.
#WCLC24 TROP2 IHC has been a poor predictive marker. Normalized Membrane Ratio (NMR) factors in receptor internalization. Ratio is membrane expression over membrane plus cytoplasmic expression (using optical density from digitized slide) and lower would be more favorable.
#WCLC24 TROP2 QCS-NMR seems to be a much better predictor of benefit with datopotamab deruxtecan in BEP and in non-sq non-AGA subset: in NMR+, PFS HR 0.57 and KM shows clear separation.
Dr. Shun Lu presents interim results from the perioperative NEOTORCH study at the #ASCOPlenarySeries. Randomized pts with resectable stage II/III NSCLC to perioperative chemotherapy with toripalimab (anti-PD1) vs placebo. Another entry in the perioperative space? #LCSM
Includes resectable stage II/III (AJCC v8), EGFR/ALK wild type NSCLC. Pts receive 3 cycles of neoadjuvant chemotherapy + toripalimab vs placebo then surgery then 1 more cycle of adjuvant chemo (+tori/pbo) then 13 doses of maintenance toripalimab vs placebo. #ASCOPlenarySeries
First interim EFS analysis only for stage III. Includes 404 pts - but 926 screened. Would be interesting to see specific eligibility criteria not met in screening process. Reminder of how selected trial populations are and value of future real-world analyses. #ASCOPlenarySeries
Impressive data from #AEGEAN at #AACR23 from Dr. John Heymach and colleagues. This is the first of several phase III peri-operative IO studies in resectable NSCLC combining neoadjuvant chemo-immunotherapy followed by adjuvant immunotherapy.
Included stage IIA-IIIB (AJCC v8) with no EGFR/ALK & excluded pts who would require pneumonectomy. Large study with n=801 (CM816 was n=358). Pts received 4 cycles (not 3) of platinum-based chemo with durvalumab (anti-PDL1) or placebo, then surgery, then durvalumab / placebo x 1y.
Almost 75% received carboplatin over cisplatin. Global study; fairly even PDL1 distribution. 80% of pts went to surgery, 78% completed resection (90-95% of those were R0). Overall, 66% of pts began adjuvant phase (but 90% of those who had an R0 resection had adjuvant therapy).
There is a lot to consider in this first-line study of the #KRAS G12C inhibitor adagrasib plus pembrolizumab from #ESMOImmuno22. Some pleasant surprises in terms of safety. Definitely encouraging but need to see a bit more to be sold on this strategy. 🤔 #LCSM
We're looking for synergy with the two agents - more than an additive effect. Reason to believe there will be based on preclinical data showing the effect on T-cell infiltration from #KRAS inhibition. Similar to what has been shown with MEK inhibition. #ESMOImmuno22
The first-line dataset includes the phase Ib KRYSTAL-1 and the phase II KRYSTAL-7. In KRYSTAL-1 (n=7), 4/7 had a response and all were durable (>9m). G3 TRAEs in 4 pts (lipase elevation, LFTs, muscular pain, pneumothorax). #ESMOImmuno22
Dr. @ZPiotrowskaMD presents initial results from the ELIOS trial at #ESMO22 - molecular profiling of #EGFR mutant NSCLC after progression on 1L osimertinib.
In this study of highly motivated pts at esteemed sites, evaluable paired biopsy at PD only available in 46/115 pts (40%). Interestingly, 75 pts (65%) had paired biopsy but 27 failed NGS (23%). Speaks somewhat to the real world feasibility of a repeat biopsy approach. #ESMO22
Common co-mutations at baseline included TP53, EGFR amp, and CDKN2A loss. Acquired alterations included MET amp, EGFR C797S, ALK fusion, NKX2-1 amp. Mostly mutually exclusive. #ESMO22
Dr. Silvia Novello presents 5y update on KEYNOTE 407 (platinum plus tax and +/- pembrolizumab for 1L squamous NSCLC #ESMO22
With longer follow up, OS favors pembrolizumab arm with mOS 17.2 vs 11.6m (OS HR 0.71) in squamous NSCLC. 5y OS rate 18.4% vs 9.7%. PFS benefit (HR 0.62) and higher RR across PDL1 strata. #ESMO22
For patients who complete 2y of pembrolizumab, 3y OS rate (after completing 2y pembro) was 70% - though not all of those patients are cured (44% were alive without PD or subsequent therapy). #ESMO22