Stephen V Liu, MD Profile picture
Apr 23 11 tweets 7 min read Twitter logo Read on Twitter
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 Image
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 Image
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 ImageImage
NEOTORCH included 90% men, 78% squamous NSCLC. This is a far cry from AEGEAN (46% squamous) and CheckMate 816 (49% squamous). Includes 67% stage IIIA and 32% stage IIIB. 66% were PDL1 positive (no breakdown on high vs low yet). #ASCOPlenarySeries Image
NEOTORCH interim results (for stage III NSCLC) show addition of perioperative toripalimab to chemotherapy improves event free survival with EFS HR 0.40 (same by IRC). Median EFS not reached for tori arm but 1y EFS rate 84% vs 57% and 2y EFS rate 65% vs 39%. Curves separate early. Image
NEOTORCH subgroup analysis (for stage III) shows more benefit with adding toripalimab for PDL1+ subset (EFS HR 0.31 in PDL1+ and HR 0.59 in PDL1-) and squamous (this trial was mostly squamous, mostly male). #ASCOPlenarySeries ImageImage
NEOTORCH: Adding neoadjuvant toripalimab for resectable stage III NSCLC (mostly squamous) improves major pathologic response (MPR) rate from 8.4% to 48.5% and improves pathologic complete response (pCR) rate from 1% with chemotherapy to 28.2% with chemo-immunotherapy. #LCSM ImageImage
NEOTORCH survival analysis very immature but with 18m median follow up (for stage III), OS HR 0.62 with 2y OS rate 81% vs 74%. Image
NEOTORCH: Among pts with resectable stage III NSCLC treated with neoadjuvant toripalimab + chemo x 3 cycles, 18% did not get to surgery (27% in placebo + chemo arm). Of the 82.2% that had surgery, 95.8% ha R0 resection. Similar to overall AEGEAN numbers. #ASCOPlenarySeries Image
Note that 28% in the toripalimab + chemo arm had TEAEs leading to interruption (vs 14%) with 9% discontinuation (vs 7%) but most AEs were low grade and chemotherapy-related (myelosuppression). Higher rates of (low grade) thyroid and rash AEs and few with G3 pneumonitis. ImageImageImageImage
NEOTORCH shows that addition of anti-PD1 toripalimab to 3 cycles of neoadjuvant chemotherapy for resectable stage III NSCLC improves MPR and pCR rate and when coupled with 1 adjuvant cycle and 13 maintenance cycles, significantly improves EFS. #ASCOPlenarySeries Image

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More from @StephenVLiu

Apr 16
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. Image
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. Image
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). ImageImageImage
Read 9 tweets
Dec 8, 2022
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 Image
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 Image
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 ImageImage
Read 10 tweets
Sep 19, 2022
Dr. @ZPiotrowskaMD presents initial results from the ELIOS trial at #ESMO22 - molecular profiling of #EGFR mutant NSCLC after progression on 1L osimertinib. ImageImage
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 Image
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 ImageImageImage
Read 5 tweets
Sep 11, 2022
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
Read 4 tweets
Sep 11, 2022
Dr. @marinagarassino presents 5-year efficacy and safety update of KEYNOTE-189 (1L carboplatin plus pemetrexed +- pembrolizumab in non-squamous NSCLC) #ESMO22
KEYNOTE 189 is our SOC and has shown a consistent benefit including improving OS even with a crossover rate of 57%. #ESMO22
KEYNOTE 189 shows sustained OS benefit with longer follow up and a 5y OS rate of 18.4% with an OS HR of 0.60. Better PFS and OS also observed. Benefit across PDL1 strata. No new safety signals . #ESMO22
Read 5 tweets
Sep 11, 2022
Dr. Baohui Han presents SUNRISE: randomized phase II study of sintilimab (PD1) and anlotinib (anti-angiogenic TKI) in metastatic NSCLC. #ESMO22
Study design here shows randomization to first-line sintilimab + anlotinib or chemo (with sintilimab at progression). Some concerns about randomization to chemotherapy without immunotherapy in a modern day study. #ESMO22
Baseline characteristics show a fairly high proportion of never smokers. SUNRISE excluded EGFR, ALK, and ROS1 - would like details on testing methods and presence of other drivers. More pts with brain and liver metastases in the sintilimab + anlotinib arm. #ESMO22
Read 5 tweets

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