Benjamin J. Solomon
MBBS, PhD, FRACP
Medical Oncologist and Head of Lung Service
👥Biography 个人简介
Benjamin J. Solomon, MBBS, PhD, FRACP, is a Medical Oncologist and Head of the Lung Service at Peter MacCallum Cancer Centre in Melbourne, Australia, and one of the leading global authorities on ALK-positive non-small cell lung cancer. He has been a principal investigator on multiple pivotal clinical trials evaluating ALK inhibitors, including PROFILE 1014 with crizotinib and the ALEX and J-ALEX trials with alectinib, which transformed the treatment landscape for this molecular subtype. His translational research bridges molecular genomics with clinical drug development to identify and validate novel therapeutic targets in thoracic malignancies. Solomon's contributions to the ALEX trial, which demonstrated the superiority of alectinib over crizotinib in previously untreated ALK-positive NSCLC—including superior CNS activity—were instrumental in establishing alectinib as the preferred first-line standard worldwide. He has also contributed to studies of third-generation ALK inhibitors including lorlatinib, and has worked extensively on understanding and overcoming resistance to ALK-directed therapy. His laboratory programs investigate mechanisms of resistance through genomic analysis of serial biopsies and liquid biopsy platforms, seeking to rationalize sequencing of ALK inhibitors and rational combination strategies. As a leading voice from the Asia-Pacific region in thoracic oncology, Solomon has helped shape global clinical guidelines through his involvement with IASLC and major cooperative groups. He is a prolific author and frequent presenter at ASCO, ESMO, and WCLC, and serves as a mentor for medical oncology trainees at Peter MacCallum and across Australia. His work exemplifies the integration of academic rigor with patient-centered clinical trial conduct.
🧪Research Fields 研究领域
🎓Key Contributions 主要贡献
First-Line ALK Inhibitor Therapy
Principal investigator on the ALEX trial demonstrating superior progression-free survival and CNS efficacy of alectinib over crizotinib in treatment-naive ALK-positive NSCLC, establishing alectinib as the global standard of care.
Crizotinib Development
Contributed to the PROFILE 1014 trial establishing crizotinib as first-line therapy in ALK-positive NSCLC and to studies defining its efficacy against ROS1 fusions, broadening the scope of MET/ALK/ROS1 targeting.
ALK Resistance Mechanisms
Led genomic analyses of resistance to first- and second-generation ALK inhibitors, characterizing on-target ALK mutations and bypass resistance pathways to inform rational next-line therapy selection and drug development.
Next-Generation ALK Inhibitor Trials
Contributed to clinical evaluation of lorlatinib and other third-generation ALK inhibitors in the second-line and first-line settings, including studies in patients with CNS metastases, expanding treatment options across lines of therapy.
Representative Works 代表性著作
Alectinib versus Crizotinib in Untreated ALK-Positive Non–Small-Cell Lung Cancer (ALEX)
New England Journal of Medicine (2017)
Phase III trial establishing alectinib as superior to crizotinib for first-line treatment of ALK-positive NSCLC, with improved progression-free survival and CNS control.
First-Line Crizotinib versus Chemotherapy in ALK-Positive Lung Cancer (PROFILE 1014)
New England Journal of Medicine (2014)
Pivotal phase III trial demonstrating superior response rate and progression-free survival with crizotinib over platinum-based chemotherapy in ALK-positive NSCLC.
Lorlatinib in Previously Treated ALK-Positive Non–Small-Cell Lung Cancer
Lancet Oncology (2018)
Phase II data supporting the activity of lorlatinib in patients with ALK-positive NSCLC after progression on prior ALK inhibitors, including those with CNS disease.
🏆Awards & Recognition 奖项与荣誉
📄Data Sources 数据来源
Last updated: 2026-04-05 | All information from publicly available academic sources
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