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🚨 #ESMO26 Lung Cancer: Top Ten by @OncoAlert 🫁 The abstracts our faculty picked as must-know from Madrid 👇 1️⃣ DeLLphi-305 (LBA3): tarlatamab + durvalumab, 1L maintenance in ES-SCLC 2️⃣ Krascendo 1 (LBA5): divarasib vs sotorasib/adagrasib in KRAS G12C NSCLC 3️⃣ SAFFRON (LBA6): osimertinib + savolitinib in EGFRm MET+ NSCLC post-osimertinib 4️⃣ OptiTROP-Lung04 (LBA67): final OS, sac-TMT vs chemo after EGFR-TKI 5️⃣ OptiTROP-Lung06 (LBA66): sac-TMT + pembro, 1L PD-L1-negative non-squamous NSCLC 6️⃣ PERSEE (2614O): pembro ± chemo, 1L PD-L1 ≥50% 7️⃣ SANOVO (LBA69): savolitinib + osimertinib, 1L EGFRm MET-overexpressed NSCLC 8️⃣ IFCT-2103 DIAL (2618RO): continue pembro vs observation at 6 months 9️⃣ PANKU-Lung01 (LBA71): iza-bren after third-generation EGFR TKI 🔟 SARON (2613O): consolidation radiotherapy in oligometastatic NSCLC #lcsm #OncoAlert #MedTwitter Pinging our OncoAlert Lung Cancer Faculty @christine_lovly, @GlopesMd, @DrSanjayPopat, @StephenVLiu, @jillfeldman4, @UOzkerim, @DrMirallas, @MartinReck2 , @bmassutis @UmbertoMalapel1 , @CharuAggarwalMD @peters_solange, @HenningWillers, @HHorinouchi, @BRicciutiMD, @PercyLeeMD, @bensolomon1, @Latinamd, @DrJNaidoo, @barlesi, @VanitaNoronha, @ChristianRolfo @Tony_Calles @s_couraud @marinagarassino @g_mountzios @BairdAM @barlesi @JFreemanDaily @Piuchagarrido @LeciaSequist @bensolomon1 @VanitaNoronha +@alexdrilon @JordiRemon @caliraf @JulienMazieres @TerriConneran
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postMONARCH 🦋 to be presented at #ESMO26 final OS: numerically longer (32.1 vs 24.6 mo) but not significant. Consistent PFS signal and no new safety concerns. Continuing CDK4/6i beyond progression still has a place, but patient selection is key. #BreastCancer
OncoAlert 4Sight Abstracts to be Presented at #ESMO26 1RO: Final Overall Survival Analysis of postMONARCH: Abemaciclib Plus Fulvestrant After Progression on Prior CDK4/6 Inhibitor in HR+, HER2– Advanced Breast Cancer @KalinskyKevin @BianchiniGP @ErikaHamilton9 @DrSGraff @drsarahsam @MuozMateu 🔬 Phase 3, double-blind trial (n=368): abemaciclib or placebo plus fulvestrant in HR+, HER2– ABC after progression on prior CDK4/6i + ET. Final OS analysis. ➡️ Median OS 32.1 vs 24.6 mo; HR 0.80 (0.60–1.06); p=0.1145, statistical significance not reached ➡️ Updated PFS HR 0.78 (0.62–0.99); nominal p=0.0390 ➡️ Safety consistent with the established abemaciclib profile; no new signals ✅ Numerically longer median OS, not statistically significant. While absolute PFS benefit was modest, overall evidence supports considering abemaciclib-based treatment after disease progression on prior CDK4/6i + ET. #BreastCancer 🎙️ Kevin Kalinsky 👥 Giampaolo Bianchini · Erika Hamilton · Stephanie Graff · Kyong Hwa Park · Rinath Jeselsohn · Umut Demirci · Miguel Martin · Rachel Layman · Sara Hurvitz · Sarah Sammons · Peter Kaufman · Montserrat Muñoz · Jiun-I Lai · Holly Knoderer · Cynthia Sandoval · Aarti Chawla · Bastien Nguyen · Yanhong Zhou · Elizabeth Ravenberg · Lacey Litchfield · Lillian Smyth · Seth Wander (4Sight Made from Abstracts publicly available at the ESMO website) Pinging OncoAlert Breast Cancer Faculty @matteolambe @aftimosp @E_de_Azambuja @DrSGraff @ErikaHamilton9 @hoperugo @stolaney1 @BianchiniGP @aftimosp @kevinpunie @ElisaAgostinett @to_be_elizabeth @GaiaGriguolo @JankovicK @raalbany @JavierCortesMD @JaniceTNBCmets @Prof_Nadia_H @LoiSher @jamecancerdoc @Lucarecco @Dr_Oncologista
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🚨 @OncoAlert 4Sight Abstracts to be presented at #ESMO26 🇪🇸 | Final OS results from #postMONARCH ✨👀 👇 Abemaciclib + fulvestrant after progression on prior CDK4/6i: 🎀 OS: 32.1 🆚 24.6 months (HR 0.80; p=0.1145) 🎀 updated PFS (HR 0.78)
OncoAlert 4Sight Abstracts to be Presented at #ESMO26 1RO: Final Overall Survival Analysis of postMONARCH: Abemaciclib Plus Fulvestrant After Progression on Prior CDK4/6 Inhibitor in HR+, HER2– Advanced Breast Cancer @KalinskyKevin @BianchiniGP @ErikaHamilton9 @DrSGraff @drsarahsam @MuozMateu 🔬 Phase 3, double-blind trial (n=368): abemaciclib or placebo plus fulvestrant in HR+, HER2– ABC after progression on prior CDK4/6i + ET. Final OS analysis. ➡️ Median OS 32.1 vs 24.6 mo; HR 0.80 (0.60–1.06); p=0.1145, statistical significance not reached ➡️ Updated PFS HR 0.78 (0.62–0.99); nominal p=0.0390 ➡️ Safety consistent with the established abemaciclib profile; no new signals ✅ Numerically longer median OS, not statistically significant. While absolute PFS benefit was modest, overall evidence supports considering abemaciclib-based treatment after disease progression on prior CDK4/6i + ET. #BreastCancer 🎙️ Kevin Kalinsky 👥 Giampaolo Bianchini · Erika Hamilton · Stephanie Graff · Kyong Hwa Park · Rinath Jeselsohn · Umut Demirci · Miguel Martin · Rachel Layman · Sara Hurvitz · Sarah Sammons · Peter Kaufman · Montserrat Muñoz · Jiun-I Lai · Holly Knoderer · Cynthia Sandoval · Aarti Chawla · Bastien Nguyen · Yanhong Zhou · Elizabeth Ravenberg · Lacey Litchfield · Lillian Smyth · Seth Wander (4Sight Made from Abstracts publicly available at the ESMO website) Pinging OncoAlert Breast Cancer Faculty @matteolambe @aftimosp @E_de_Azambuja @DrSGraff @ErikaHamilton9 @hoperugo @stolaney1 @BianchiniGP @aftimosp @kevinpunie @ElisaAgostinett @to_be_elizabeth @GaiaGriguolo @JankovicK @raalbany @JavierCortesMD @JaniceTNBCmets @Prof_Nadia_H @LoiSher @jamecancerdoc @Lucarecco @Dr_Oncologista
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10-year data settle it: upfront AI vs switch makes no real difference. The surprise is exemestane trailing on DFS. GIM3 FATA to be presented at #ESMO26
OncoAlert 4Sight Abstracts to be Presented at #ESMO26 Final Analysis of the GIM3 FATA Trial: Treatment Schedule and Three Aromatase Inhibitors in Postmenopausal HR+ Early Breast Cancer @PietroDePlacido @antoniorusso_pa @delmastro_lucia @MicheleDelauren @fperrone62 🔬 Randomized trial (n=3697): 5 years of anastrozole, exemestane or letrozole, upfront or after 2 years of tamoxifen. Co-primary: DFS by schedule and by AI. ➡️ Upfront vs switch: DFS HR 0.95 (0.82–1.09); OS HR 0.88 (0.74–1.06) ➡️ 10-year DFS 79.1% anastrozole, 76.6% letrozole, 74.2% exemestane (global p=0.028) ➡️ Exemestane vs anastrozole: adjusted DFS HR 1.23 (1.04–1.46). 10-year OS across AIs: no statistically significant difference (p=0.25) ✅ No schedule superior; exemestane associated with worse DFS. Choice should be individualized by tolerability, comorbidities and cost. #BreastCancer 🎙️ Pietro De Placido 👥 Laura Arenare · Erica Pietroluongo · Giancarlo Bisagni · Maria Sarobba · Antonio Russo · Ferdinando Riccardi · Lucia Del Mastro · Antonio Pazzola · Francesco Cognetti · Jennifer Foglietta · Stefania Gori · Francesco Nuzzo · Adriano Gravina · Michelino De Laurentiis · Roberto Bianco · Grazia Arpino · Sabino De Placido · Ciro Gallo · Francesco Perrone (4Sight Made from Abstracts publicly available at the ESMO website) Pinging OncoAlert Breast Cancer Faculty @matteolambe @aftimosp @E_de_Azambuja @DrSGraff @ErikaHamilton9 @hoperugo @stolaney1 @BianchiniGP @aftimosp @kevinpunie @ElisaAgostinett @to_be_elizabeth @GaiaGriguolo @JankovicK @raalbany @JavierCortesMD @JaniceTNBCmets @Prof_Nadia_H @LoiSher @jamecancerdoc @Lucarecco @Dr_Oncologista
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OncoAlert 4Sight Abstracts to be Presented at #ESMO26 2875O: Pembrolizumab or Placebo Plus Concurrent Definitive Chemoradiotherapy in Esophageal and Gastroesophageal Junction (GEJ) Cancer: The Phase 3 Randomized KEYNOTE-975 Study @MDmanishshah @BennounaJaafar @cbcbc1971 🔬 Phase 3, double-blind trial (n=703): pembrolizumab or placebo plus definitive chemoradiotherapy in untreated, unresectable esophageal/GEJ cancer. Dual primary endpoints: EFS and OS. ➡️ CPS ≥10 EFS: median 15.2 vs 14.7 mo; HR 0.97 (0.77–1.23); P=0.3994 ➡️ CPS ≥10 OS: median 32.2 vs 35.0 mo; HR 1.00 (0.77–1.30); nominal P=0.5003 ➡️ Grade 5 AEs 13% vs 10%; discontinuation due to AEs 34% vs 27% ✅ Pembrolizumab + dCRT did not significantly improve EFS in PD-L1 CPS ≥10; no new safety signals observed. 🎙️ Manish Shah 👥 Jaafar Bennouna · Toshihiko Doi · Lin Shen · Ken Kato · Antoine Adenis · Harvey Mamon · Markus Moehler · Xiaolong Fu · Byoung Chul Cho · Sonal Bordia · Pooja Bhagia · Chie-Schin Shih · Anjali Desai · Peter Enzinger (4Sight Made from Abstracts publicly available at the ESMO website) Pinging OncoAlert Faculty @CathyEngMD, @BenWestphalen, @graokane, @NiuSanford, , @GillSharlene, @pashtoonkasi, @DrVilmaPBarcia, @Erman_Akkus, @GIMedOnc, @UOzkerim, @MarioBalsaMD, @p_ciracimd, @DraMartinezLago, @DaisukeKotani, @Aiims1742, @ARosen380, @realbowtiedoc, @KoheiShitara,
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Can pembrolizumab monotherapy still be considered the optimal control arm in actual and future phase III trials for chemotherapy-eligible patients with advanced NSCLC and PD-L1 ≥50%? Looking forward to detailed results! #LCSM @decroisette @myGFPC @myESMO @Larvol @OncoAlert
🆙#ESMO26 Proffered Paper I: #LCSM Mets 🔥PERSEE (GFPC 01-2020): Pembrolizumab With or Without Platinum-Based Chemotherapy as First-Line Treatment in Advanced NSCLC With PD-L1 ≥50%, Phase 3 Trial 🎙️ @decroisette 🔢2614O 🎯Pembro-Chemo Improved BCR-PFS vs Pembro Alone 🎯PFS HR 0.56, mPFS 16.1 vs 6.9m 🎯OS HR 0.77 not significant; mOS 50.2 vs 29.9mo 🎯Grade≥3 TRAEs 53.8% vs 19.3% ☑️NCT04547504 🔗 cslide.ctimeetingtech.com/es… @OncoAlert @Larvol @myESMO @IASLC
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Kudos to @ChadTangMD @PavlosMsaouel for this paper on a rare variant of RCC. Data absolutely useful for clinical practice! @EurUrolOncol @OncoAlert @KidneyCancer.
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1/5 New in @EurUrolOncol: the largest series yet of metastasis-directed radiation therapy in SMARCB1-deficient #RenalMedullaryCarcinoma. Key finding that this cancer appears far more radiosensitive than clear cell kidney cancer: authors.elsevier.com/c/1n~As… #endRMC #MsaouelLab
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A benefit of working with @PavlosMsaouel is that we treat many variant RCCs. Renal Medullary Carcinoma is one such variant (0.5% of RCC), which has remarkably different RT sensitivity. MDT to 30gy/5 often achieves a CR and with minimal toxicity even with high dose chemo.
1/5 New in @EurUrolOncol: the largest series yet of metastasis-directed radiation therapy in SMARCB1-deficient #RenalMedullaryCarcinoma. Key finding that this cancer appears far more radiosensitive than clear cell kidney cancer: authors.elsevier.com/c/1n~As… #endRMC #MsaouelLab
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Published today @TheLancet NICHE-2: 4 weeks of immunotherapy + surgery ➡️ 100% 3-year DFS and 100% 5-year OS in dMMR colon cancer. Congratulations to @MyriamChalabi et al ⭐️ Pleased to author the editorial commentary with @jonathanloree on these remarkable results and potential Implications of what comes next. doi.org/10.1016/S0140-6736(2… @BCCancer
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Circulating Eosinophils in HR+/HER2− #BreastCancer A @JCO_ASCO study of 23,170 patients links higher preoperative eosinophil counts to lower recurrence risk, with added prognostic value beyond the 21-gene RS. ascopubs.org/doi/abs/10.1200… @OncoAlert @ASCO #BCSM
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Tumor biology in #BreastCancer is important, but anatomic extent of disease still has a role in determining prognosis. A recent study from @JenniferPlichta and @DukeSurgery investigators explains more: acsjournals.onlinelibrary.wi… @OncoAlert @DukeCancer CC: @oreganruth #BCSM
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🚨 New ESMO 2026 data challenge our understanding of perioperative therapy in MIBC! KEYNOTE-866 (phase III, n=707), ENERGIZE (phase III, n=653): Adding perioperative pembro or nivolumab to neoadjuvant gemcitabine/cisplatin did not significantly improve EFS and OS, despite numerically higher pCR! Yet NIAGARA demonstrated significant EFS (HR 0.68) and OS (HR 0.75) benefits with perioperative durvalumab. Why does one chemoimmunotherapy strategy succeed while others fails? Different patient populations, trial designs, or underlying biology? We urgently need predictive biomarkers—not just another checkpoint inhibitor. Meanwhile, new KEYNOTE-905 data in cisplatin-ineligible MIBC (ad hoc, n=255) show: • Pembrolizumab alone: pCR 25.3%; EFS HR 0.71 vs surgery alone. • EV+pembrolizumab: pCR 58.8%; EFS HR 0.40 vs surgery alone. The key question is no longer simply whether to add immunotherapy—but which patients need chemotherapy, ADC-based therapy, or both. Histology, NECTIN4/HER2 biology, and longitudinal ctDNA deserve prospective evaluation as treatment-selection tools. Exciting times for MIBC—but precision must catch up with therapeutic progress. @OncoAlert Faculty @DrChoueiri , @tompowles1 , @apolo_andrea , @neerajaiims , @montypal , @Silke_Gillessen , @AOmlin , @brian_rini , @PGrivasMDPhD , @TiansterZhang , @amerseburger , @DrDanielHeng , @HHammersMD , @scocmem , @AndreaNecchi , @AmandaNizamMD , @drenriquegrande , @nataliagandur , @AlbigesL , @cdanicas , @declangmurphy , @seanmmcbride , @shilpaonc , @DrRanaMcKay , @scserendipity1 , @DrYukselUrun , @ravikanesvaran , @BraunMDPhD , @EfstathiouEleni , @mzugman , @crisbergerot
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ICYMI: A conversation with @PedAYAJournal Associate Editors @JGladeBender and Dr. Jonathan Metts, hosted by our Editor-in-Chief Dr. Nirali Shah 💜 Hear their perspectives on pediatric & AYA cancer research on CancerSpeak:️ cancerspeak.podbean.com/e/ad… @OncoAlert #pedonc #ayacancer
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🧬 Lenvatinib + pembrolizumab | Phase II | Advanced GC/GEJ 👥 24 ICI-naïve pts 🎯 ORR 25% (5/20), incl. 2 CPS<1 ⏳ mPFS 12.9 wk | mOS 21.4 wk ❌ Primary efficacy threshold not met 💡 Exploratory signal in CPS<1 tumors. 🔗 doi.org/10.1016/j.esmogo.202… @OncoAlert
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We know immunotherapy works in MSI-H colorectal cancer. The question is, how long do we actually need to treat patients? Well, grateful we’re finally getting some answers ahead of #ESMO2026 A new multicenter study from China published in @jitc evaluated 129 patients with dMMR/MSI-H CRC who achieved a clinical complete response to PD-1 inhibition and pursued non-operative management. 66 stopped treatment, 63 continued maintenance. At 3 years: ▪️DFS: 96.2% vs 98.3% (p=0.508) ▪️OS: 100% vs 98.3% ▪️Only 2 local regrowths, both in the observation group and both successfully salvaged. ▪️No distant metastases. Meanwhile, 15.9% of patients continuing maintenance developed grade ≥2 treatment-related toxicity during maintenance. But what actually constitutes a complete response? Radiographically, patients may have persistent abnormalities due to fibrosis rather than viable tumor. In my practice, I use ctDNA and biopsy, alongside imaging and endoscopy, to help guide these decisions. A residual mass doesn’t necessarily mean residual cancer. Yes, China only. Yes, retrospective. And importantly, these were predominantly patients with localized disease who achieved cCR, not all patients with mCRC. I’ve been using these data in abstract form to guide discussions with patients almost weekly. In fact, I was literally discussing this study with a colleague a few hours ago, without realizing the full paper had come out (@patel_riya7 ). We know immunotherapy can produce durable responses. Maybe we don’t need to keep treating patients for years… @OncoAlert @TheGutOncLab jitc.bmj.com/content/14/10/e…
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Revisão narrativa (Front Oncol, 2026) sobre a eficácia, segurança e preferências do paciente nas opções de 1ª linha do NSCLC EGFR-mutado (del19/L858R) para apoiar a decisão compartilhada, com atenção à realidade do Brasil e de países de baixa e média renda. •FLAURA (osimertinibe vs 1ª geração): SLP 18,9 vs 10,2 meses (HR 0,46); SG 38,6 vs 31,8 meses (HR 0,80); eventos G≥3 em 31% vs 41% •MARIPOSA (amivantamabe + lazertinibe vs osimertinibe): SLP 23,7 vs 16,6 meses (HR 0,70); SG em 3 anos 60% vs 51% (HR 0,75); G≥3 ~80% vs ~52%; TEV 37% vs 9%; reação infusional 63% •FLAURA2 (osimertinibe + quimio vs osimertinibe): SLP 25,5 vs 16,7 meses (HR 0,62); SG 47,5 vs 37,6 meses (HR 0,77); G≥3 64% vs 27% •SNC (FLAURA2): SLP 24,9 vs 13,8 meses nos pacientes com metástases cerebrais •Brasil: no SUS, sem incorporação pela CONITEC, o acesso segue restrito a TKIs de 1ª geração; as combinações estão disponíveis apenas no setor privado Os ganhos de eficácia das combinações vêm acompanhados de mais toxicidade e maior carga de tratamento. O desafio deixou de ser a falta de opções e passou a ser como empregá-las: individualizar conforme perfil de risco, preferências do paciente e acesso. @IASLC @SBOC_Oncologia @OncoAlert #GBOT #CancerDePulmao #EGFR #NSCLC #OncologiaToracica
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Registration is now OPEN! Follow the link here to join us for #SoCalGU27, featuring the litany of terrific speakers noted below - with several surprise guests to come: cme.cityofhope.org/2027-SCGU
⭐️SAVE THE DATE: MARCH 5, 2027⭐️ We will be convening the 2027 So Cal GU Research Forum on this date at the Waterfront Hilton in #HuntingtonBeach, CA. If you are a clinician with interest in GU cancers in the #Socal area, you will not want to miss this. Our format is different: our agenda focuses exclusively on #clinicaltrials in the area, and we leave lots of time on the agenda for collaboration. Looking forward to seeing you there!
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More pCR didn’t translate into EFS or OS. KEYNOTE-866: an important negative phase 3 in cisplatin-eligible MIBC. #ESMO26 #BladderCancer
OncoAlert 4Sight Abstracts to be Presented at #ESMO26 Perioperative Pembrolizumab or Placebo + Neoadjuvant Cisplatin and Gemcitabine in Muscle-Invasive Bladder Cancer: The Double-Blind, Phase 3 KEYNOTE-866 Study @garysteinbergmd @DrChrisHoimes 🔬 Phase 3, double-blind (n=907): perioperative pembrolizumab or placebo + neoadjuvant gemcitabine-cisplatin and RC + PLND in cisplatin-eligible MIBC. Primary endpoint: EFS. ➡️ Median EFS 74.1 mo vs NR; HR 0.88 (0.71–1.10); P=.1366 ➡️ pCR 44.4% vs 35.8%; OS HR 1.00 (0.79–1.27); neither formally tested ➡️ Grade 3–5 TEAEs 80.2% vs 75.1% ✅ Perioperative pembrolizumab did not confer a statistically significant EFS benefit; safety profile manageable and consistent with prior reports. #BladderCancer 🎙️ Jens Bedke 👥 Arlene Siefker-Radtke · Gary Steinberg · Hiroyuki Nishiyama · Xiao Fang · Ritesh Kataria · Blanca Homet Moreno · Christopher Hoimes (4Sight Made from Abstracts publicly available at the ESMO website) Pinging Our Faculty @DrChoueiri, @tompowles1, @apolo_andrea, @neerajaiims, @montypal, @Silke_Gillessen, @AOmlin, @brian_rini, @PGrivasMDPhD, @TiansterZhang, @amerseburger, @DrDanielHeng, @HHammersMD, @scocmem, @AndreaNecchi, @AmandaNizamMD, @drenriquegrande, @nataliagandur, @AlbigesL, @cdanicas, @declangmurphy, @seanmmcbride, @shilpaonc, @DrRanaMcKay, @scserendipity1, @DrYukselUrun, @ravikanesvaran, @BraunMDPhD, @EfstathiouEleni, @mzugman, @crisbergerot, @niklas_kluemper
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Replying to @DrChoueiri
OncoAlert 4Sight Abstracts to be Presented at #ESMO26 First-Line Pembrolizumab + Lenvatinib + Belzutifan or MK-1308A + Lenvatinib in Advanced RCC: The Randomized Open-Label Phase 3 LITESPARK-012 Study @DrChoueiri @tompowles1 @MVossMD @ERPlimackMD @HowardGurney @brian_rini 🔬 Phase 3 (n=1688), untreated advanced ccRCC: pembrolizumab + lenvatinib + belzutifan (Arm A) or MK-1308A + lenvatinib (Arm B) vs pembrolizumab + lenvatinib. Dual primary: PFS by BICR and OS. ➡️ Arm A: PFS HR 1.08 (0.93–1.26); OS HR 1.04 (0.87–1.25) ➡️ Arm B: PFS HR 1.07 (0.92–1.25); OS HR 1.12 (0.94–1.35) ➡️ Discontinuation due to AEs: 51.6% (A), 51.4% (B), 36.2% (control) ✅ Neither belzutifan nor CTLA-4 blockade added to pembrolizumab + lenvatinib improved efficacy; pembrolizumab + lenvatinib remains a 1L SOC. #KidneyCancer 🎙️ Toni Choueiri 👥 Thomas Powles · Martin Voss · Elizabeth Plimack · Howard Gurney · Yue Song · Rodolfo Perini · Karla Rodriguez-Lopez · Brian Rini (4Sight Made solely from Abstracts publicly available at the ESMO website) Pinging Our Faculty @tompowles1, @apolo_andrea, @neerajaiims, @montypal, @Silke_Gillessen, @AOmlin, @PGrivasMDPhD, @TiansterZhang, @amerseburger, @DrDanielHeng, @HHammersMD, @scocmem, @AndreaNecchi, @AmandaNizamMD, @drenriquegrande, @nataliagandur, @AlbigesL, @cdanicas, @declangmurphy, @seanmmcbride, @shilpaonc, @DrRanaMcKay, @scserendipity1, @DrYukselUrun, @ravikanesvaran, @BraunMDPhD, @EfstathiouEleni, @mzugman, @crisbergerot, @niklas_kluemper
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postMONARCH: CDK4/6 Inhibition Beyond Progression — Modest PFS Benefit, No Significant OS Benefit @OncoAlert #ESMO26 #BreastCancer
OncoAlert 4Sight Abstracts to be Presented at #ESMO26 1RO: Final Overall Survival Analysis of postMONARCH: Abemaciclib Plus Fulvestrant After Progression on Prior CDK4/6 Inhibitor in HR+, HER2– Advanced Breast Cancer @KalinskyKevin @BianchiniGP @ErikaHamilton9 @DrSGraff @drsarahsam @MuozMateu 🔬 Phase 3, double-blind trial (n=368): abemaciclib or placebo plus fulvestrant in HR+, HER2– ABC after progression on prior CDK4/6i + ET. Final OS analysis. ➡️ Median OS 32.1 vs 24.6 mo; HR 0.80 (0.60–1.06); p=0.1145, statistical significance not reached ➡️ Updated PFS HR 0.78 (0.62–0.99); nominal p=0.0390 ➡️ Safety consistent with the established abemaciclib profile; no new signals ✅ Numerically longer median OS, not statistically significant. While absolute PFS benefit was modest, overall evidence supports considering abemaciclib-based treatment after disease progression on prior CDK4/6i + ET. #BreastCancer 🎙️ Kevin Kalinsky 👥 Giampaolo Bianchini · Erika Hamilton · Stephanie Graff · Kyong Hwa Park · Rinath Jeselsohn · Umut Demirci · Miguel Martin · Rachel Layman · Sara Hurvitz · Sarah Sammons · Peter Kaufman · Montserrat Muñoz · Jiun-I Lai · Holly Knoderer · Cynthia Sandoval · Aarti Chawla · Bastien Nguyen · Yanhong Zhou · Elizabeth Ravenberg · Lacey Litchfield · Lillian Smyth · Seth Wander (4Sight Made from Abstracts publicly available at the ESMO website) Pinging OncoAlert Breast Cancer Faculty @matteolambe @aftimosp @E_de_Azambuja @DrSGraff @ErikaHamilton9 @hoperugo @stolaney1 @BianchiniGP @aftimosp @kevinpunie @ElisaAgostinett @to_be_elizabeth @GaiaGriguolo @JankovicK @raalbany @JavierCortesMD @JaniceTNBCmets @Prof_Nadia_H @LoiSher @jamecancerdoc @Lucarecco @Dr_Oncologista
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