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American Society of Clinical Oncology (ASCO)
American Society of Clinical Oncology (ASCO)
The
American Society of Clinical Oncology
(
ASCO
) is a professional organization representing physicians of all oncology sub-specialties who care for people with cancer. Founded in 1964 by Fred Ansfield, Harry Bisel, Herman Freckman, Arnoldus Goudsmit, Robert Talley, William Wilson, and Jane C. Wright, it has nearly 45,000 members worldwide.
Wrap-Up
NeoSTAR Arm A2: Evaluating Sacituzumab Govitecan and Pembrolizumab as Neoadjuvant Therapy for Early-Stage TNBC
ASCO 2025 - Wrap-Up: Triple-Negative Breast Cancer
Sacituzumab govitecan and pembrolizumab combination therapy showed promising clinical benefit in early-stage triple-negative breast cancer (TNBC).
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Wrap-Up
Efficacy and Safety of Camrelizumab, Apatinib, and Chemotherapy as Neoadjuvant Therapy for Stage II-III TNBC
ASCO 2025 - Wrap-Up: Triple-Negative Breast Cancer
The combination of camrelizumab, apatinib, and chemotherapy shows favorable outcomes in the neoadjuvant setting for stage II-III triple-negative breast cancer (TNBC), particularly in patients with programmed death-ligand 1 positivity.
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Wrap-Up
Phase 3 Trial of Benmelstobart Plus Anlotinib Versus Nab-Paclitaxel in First-Line Treatment of Recurrent or Metastatic TNBC
ASCO 2025 - Wrap-Up: Triple-Negative Breast Cancer
The combination of benmelstobart and anlotinib showed a numerical, though not a statistically significant improvement in progression-free survival and overall survival over nab-paclitaxel in recurrent or metastatic triple-negative breast cancer (TNBC).
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Wrap-Up
Phase 3 ASCENT-04/KEYNOTE-D19 Study: Sacituzumab Govitecan Plus Pembrolizumab Versus Chemotherapy Plus Pembrolizumab in First-Line, PD-L1–Positive, Advanced TNBC
ASCO 2025 - Wrap-Up: Triple-Negative Breast Cancer
The ASCENT-04/KEYNOTE-D19 trial highlights sacituzumab govitecan plus pembrolizumab as a promising first-line therapy for patients with programmed death-ligand 1 (PD-L1)-positive, advanced triple-negative breast cancer (TNBC).
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Phase 3 DeLLphi-304: Primary Analysis of Tarlatamab Versus Chemotherapy as Second-Line Treatment for Patients With SCLC
ASCO 2025 - Small Cell Lung Cancer
The DeLLphi-304 trial shows tarlatamab significantly improves survival with a manageable adverse-event profile over chemotherapy, establishing a new standard of care for patients with small cell lung cancer (SCLC) after platinum-based chemotherapy.
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A Randomized, Phase 2 Trial Evaluating Atezolizumab Maintenance Therapy Following Chemoradiotherapy in LS-SCLC
ASCO 2025 - Small Cell Lung Cancer
A randomized, phase 2 study found atezolizumab maintenance after chemoradiotherapy in limited-stage small cell lung cancer (LS-SCLC) did not improve survival outcomes and caused additional toxicities.
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IMforte Phase 3 Study: Lurbinectedin Plus Atezolizumab Improves Survival in Extensive-Stage Small Cell Lung Cancer
ASCO 2025 - Small Cell Lung Cancer
The IMforte study showed clinically meaningful improvements in progression-free survival and overall survival with lurbinectedin plus atezolizumab compared with atezolizumab alone in patients with extensive-stage small cell lung cancer.
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Promising Phase 2 Results for ZG006, a Trispecific T-Cell Engager, in Advanced Small Cell Lung Cancer
ASCO 2025 - Small Cell Lung Cancer
ZG006 demonstrated promising efficacy and a tolerable safety profile in patients with advanced small cell lung cancer, supporting further evaluation in the ongoing phase 2 study.
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Wrap-Up
MDS/Neoplasms: Time Toxicity for Patients Receiving Oral Versus Parenteral HMAs
ASCO 2024 - Wrap Up: Myelodysplastic Syndrome
At the ASCO 2024 Annual Meeting, researchers presented the differences in time toxicity among patients undergoing myelodysplastic syndromes/neoplasms with oral hypomethylating versus parenteral hypomethylating agents.
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Wrap-Up
Phase 2 Results From the ASTREON Trial: Preliminary Safety and Efficacy of Oral AZA in Patients With Low-/Intermediate-Risk MDS
ASCO 2024 - Wrap Up: Myelodysplastic Syndrome
At the ASCO 2024 Annual Meeting, researchers presented oral azacitidine’s safety and efficacy results in patients with low-/intermediate-risk myelodysplastic syndromes, as documented in the ASTREON trial.
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