Top Tweets for #Datroway
European Commission Approves Trodelvy® as a First-Line Treatment for Metastatic Triple-Negative Breast Cancer Patients Not Candidates for PD-(l)1 Inhibitors
https://t.co/KT5gQIBrPI
Learn more 👉 https://t.co/aBf3F81wPI
#LARVOL #CancerResearch #CancerData #Oncology #OncologyInsights #ClinicalTrials #TNBC #BreastCancer #BCSM | @JavierCortesMD | @stolaney1 | @PTarantinoMD | @E_de_Azambuja | @ElisaAgostinett

🆕 @AstraZeneca and @DaiichiSankyoUS’s #Datroway has received FDA approval for immunotherapy-ineligible adults with unresectable or metastatic triple-negative #BreastCancer.
❗ This is the first TROP2-directed ADC first-line option for this population. https://t.co/cVFHx3tsOk
💊FDA承認アップデート | Dato-DXd
FDAは、#DATROWAY(#DatopotamabDeruxtecan)を承認しました。本剤は、PD-1/PD-L1療法の適応外である切除不能/転移性トリプルネガティブ乳がん(#TNBC)患者における一次治療として使用される、初のTROP2標的ADCです。
🎯Datrowayは、#TROP2 を標的とする抗体と強力なトポイソメラーゼI阻害剤ペイロードを組み合わせており、腫瘍細胞に直接化学療法を送達しつつ、全身曝露を抑えるよう設計されています。
✔️治療困難な患者集団において、化学療法と比較して全生存期間の改善を示した
✔️固形がん領域におけるADCの重要性をさらに拡大
TNBCは依然として最も侵襲性の高い乳がんサブタイプの一つであり、標的治療の選択肢が限られています。本承認は、精密腫瘍学およびADC創薬における重要なマイルストーンです。TNBC研究ツールの包括的コレクションはこちら:https://t.co/wQ3vxtXdRl
Datopotamab deruxtecanの研究に興味がある方はこちら:https://t.co/oftaRMkOKq
#FDA承認 #ADC #乳がん #TROP2 #PD1 #PDL1 #抗体薬物複合体 #腫瘍学 #創薬 #医薬化学

💊#FDAApproval Update | The FDA has approved #Datroway (#datopotamabderuxtecan), the first TROP2-directed antibody-drug conjugate (#ADC) for first-line treatment of unresectable/metastatic triple-negative breast cancer (#TNBC) in patients ineligible for PD-1/PD-L1 therapy.
🎯Datroway combines a #TROP2-targeting antibody with a potent topoisomerase I inhibitor payload, delivering chemotherapy directly to tumor cells while limiting systemic exposure.
Why this matters:
📈Demonstrated overall survival benefit vs chemotherapy in a difficult-to-treat population
💊Expands the growing impact of ADCs in solid tumor oncology
TNBC remains one of the most aggressive breast cancer subtypes with limited targeted treatment options, making this approval a major milestone in precision oncology and ADC drug development.
🧪MedChemExpress offers Datopotamab deruxtecan for research use only: https://t.co/WKFdnyNci7
🧪High-quality tools for breast cancer-related research: https://t.co/ktbHH1yZUT
#BreastCancer #AntibodyDrugConjugate #Oncology #PharmaNews #DrugDiscovery #MedicinalChemistry

💊#FDAApproval Update | The FDA has approved #Datroway (#datopotamabderuxtecan), the first TROP2-directed antibody-drug conjugate (#ADC) for first-line treatment of unresectable/metastatic triple-negative breast cancer (#TNBC) in patients ineligible for PD-1/PD-L1 therapy.
🎯Datroway combines a #TROP2-targeting antibody with a potent topoisomerase I inhibitor payload, delivering chemotherapy directly to tumor cells while limiting systemic exposure.
Why this matters:
📈Demonstrated overall survival benefit vs chemotherapy in a difficult-to-treat population
💊Expands the growing impact of ADCs in solid tumor oncology
TNBC remains one of the most aggressive breast cancer subtypes with limited targeted treatment options, making this approval a major milestone in precision oncology and ADC drug development.
🧪MedChemExpress offers Datopotamab deruxtecan for research use only: https://t.co/yaxHYo95Rm
🧪High-quality tools for breast cancer-related research: https://t.co/OE0KQPsvdY
#BreastCancer #AntibodyDrugConjugate #Oncology #PharmaNews #DrugDiscovery #MedicinalChemistry

🌟 This week's #OncFive 🌟:
🎗️ @US_FDA approves Dato-DXd (#Datroway) in PD-L1–ineligible TNBC
🫁 Priority review for sevabertinib in 1L HER2-mutant NSCLC
🔵 sBLA accepted for nogapendekin (#Anktiva) + BCG in papillary NMIBC
🧬 Fast track for suplexa in MSI-H CRC
🩸 Orphan designation for CLN-049 in r/r AML
Learn more 🔗: https://t.co/GUUosMzHNW
✅ The #FDA has approved @AstraZeneca and @DaiichiSankyoUS’s #Datroway for certain adults with triple-negative #BreastCancer.
👀 Compared with chemotherapy, the agent improved PFS by 4️⃣3️⃣% and OS by 2️⃣1️⃣% https://t.co/qDiTzZgUIZ
Avacta Group (AIM: AVCT) delivers preCISION payload data that challenges Enhertu and Datroway tumor selectivity at Science Day 2026 https://t.co/RC53TcdD8d #Avacta #AVCT #Enhertu #Datroway #ADC #Oncology #Biotech #PreCISION #DaiichiSankyo #AstraZeneca #LSE #AIM #CancerResearch
Agree! 👍 TROPION-Lung14 /Lung15
Datopotamab deruxtecan–based strategies in EGFR-mutant NSCLC, including combinations with EGFR TKIs. These trials test whether ADC-based intensification can outperform established TKI-centric first-line approaches. #osimertinib #datroway

And what will 2026 bring? Trials Likely to Shape Lung Cancer Care in 2026
EGFR-Mutant NSCLC: Beyond MARIPOSA and FLAURA2
1.TROPION-Lung14 / TROPION-Lung15
Datopotamab deruxtecan–based strategies in EGFR-mutant NSCLC, including combinations with EGFR TKIs. These trials test whether ADC-based intensification can outperform established TKI-centric first-line approaches.
2.FURVENT (ex20)
Furmonertinib versus platinum-pemetrexed chemotherapy. A positive result would further validate next-generation EGFR TKIs as chemotherapy-replacing options in earlier lines.
3.Post-osimertinib combination studies (various sponsors)
Several phase III programs are evaluating rational combinations aimed at delaying or overcoming resistance, with PFS and OS readouts expected to mature in 2026.
⸻
ADC Expansion Across Molecular Subsets
4.DESTINY-Lung04
Trastuzumab deruxtecan in earlier-line HER2-mutant NSCLC. A key test of whether HER2-targeted ADCs move from salvage to frontline-adjacent settings.
5.TROPION-Lung01 / Lung05 (mature OS analyses)
Datopotamab deruxtecan across biomarker-unselected and selected NSCLC populations. These readouts will determine how broadly TROP2 ADCs can be deployed.
6.MET-directed ADC and combination programs
Follow-on trials building on telisotuzumab vedotin, including combinations and earlier-line use, with efficacy and tolerability data expected to mature.
⸻
Immunotherapy: Refinement
7.Ivonescimab + chemotherapy phase III programs
Bispecific PD-1/PD-L1 targeting strategies aimed at improving outcomes in PD-L1–low disease. Results will test whether bispecific checkpoint modulation adds meaningful benefit.
8.Novel checkpoint combinations (post-PD-1 era)
Multiple large trials combining PD-1/PD-L1 blockade with new immune targets are expected to read out. These will clarify whether immunotherapy still has headroom in unselected NSCLC.
⸻
Early-Stage and Curative-Intent Disease
9.Perioperative targeted therapy trials (EGFR, ALK)
Neoadjuvant and adjuvant studies incorporating TKIs or targeted combinations, with disease-free and overall survival endpoints maturing. These have the potential to reshape curative-intent care.
10.Perioperative immunotherapy intensification studies
Trials evaluating extended or intensified neoadjuvant/adjuvant immunotherapy beyond current chemo-IO standards, testing whether deeper pathologic responses translate into cure.
⸻
Small-Cell Lung Cancer: Incremental but Real Movement
11.Post-platinum maintenance and consolidation strategies
Trials building on atezolizumab maintenance and DLL3-targeted approaches, including combinations and sequencing studies, with interim or final results expected.
12.Next-generation T-cell engager programs in SCLC
Follow-up phase II/III studies evaluating durability, safety, and survival beyond early DLL3 successes.
⸻
Detection, Stratification, and Minimal Residual Disease
13.Prospective AI-assisted lung cancer screening studies
Trials validating AI-enhanced low-dose CT interpretation and risk stratification, with implications for screening scale-up rather than treatment per se.
14.ctDNA-guided intervention trials
Minimal residual disease–directed escalation or de-escalation strategies in early-stage NSCLC, potentially redefining adjuvant therapy decision-making.
⸻
What to watch most closely
•Whether ADC-based intensification improves survival without unacceptable pulmonary toxicity
•Whether combination EGFR strategies prove deliverable outside ideal trial populations
•Whether perioperative systemic therapy meaningfully increases cure, not just DFS
•Whether SCLC gains durability, not just response
•Whether AI and MRD quietly change who gets treated, and when
The ADC Era Enters Its Sequencing Phase - Amol Akhade (@SuyogCancer)
@AstraZeneca @DaiichiSankyoUS
https://t.co/clqo3Jc9Si
#OncoDaily #Oncology #Cancer #Health #Medicine #MedTwitter #MedEd #MedOnc #MedNews #ADC #TNBC #BreastCancer #Datroway @CancerWorldmag

Datopotamab Deruxtecan Improves Outcomes in IO-Ineligible mTNBC - Paolo Tarantino (@PTarantinoMD)
@AstraZeneca
https://t.co/hedA6T9qtU
#OncoDaily #Oncology #Cancer #Health #Medicine #MedTwitter #MedEd #MedOnc #MedNews #TNBC #BreastCancer #Datroway @CancerWorldmag

Big Step Forward in TNBC - @JadChahoud
@AstraZeneca
https://t.co/nqKmrPeAr6
#OncoDaily #Oncology #Cancer #Health #Medicine #MedTwitter #MedEd #MedOnc #MedNews #TNBC #BreastCancer #TROPIONBreast02 #Datroway @CancerWorldmag

🔔 Breakthrough in Triple-Negative #BreastCancer
#Datroway significantly improves overall & progression-free survival in patients with metastatic TNBD who are ineligible for immunotherapy. @US_FDA
Learn more about Datroway in the full article from CURE! https://t.co/dg4G8knvK4
Kanserle mücadelede kritik adım: Göğüs kanseri tedavisinde yeni umut
📌Datroway, metastatik üçlü negatif göğüs kanserinde yaşam süresini uzatan umut verici bir seçenek oldu.
...
#kanser #datroway #metastatiküçlünegatifmemekanseri
https://t.co/nyT667xSBW
#AstraZeneca and its partner #DaiichiSankyo have won approval from #US regulators for their precision drug #Datroway to treat a type of #lungcancer, marking the first approval of the therapy in this indication and expanding access for patients.
https://t.co/eggJYOUngY
#FDA has approved #Datroway (#datopotamab #deruxtecan-dlnk) for adult patients with unresectable or metastatic HR+, HER2- #breastcancer. This innovative #TROP2-directed antibody-drug conjugate (#ADC) provides a much-needed treatment option for patients
https://t.co/1WbpqZwS2p
حصلت شركتا #أسترازينيكا و #Daiichi_Sankyo على موافقة إدارة الغذاء والدواء الأميركية (FDA) على علاج جديد لسرطان الثدي، يحمل اسم #Datroway.
العلاج الجديد هو الأول من نوعه الذي يحصل على الموافقة في #الولايات_المتحدة بعد أن تم اعتماده الشهر الماضي في #اليابان.

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