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Osama E. Rahma

AstraZeneca (South Korea) · US
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Area of research
Oncology · Immunology
Research interest
Research interests include Cancer Immunotherapy and Biomarkers, Pancreatic and Hepatic Oncology Research, Colorectal Cancer Treatments and Studies, and CAR-T cell therapy research.
h-index
44
citations
7,497
works
308
NIH funding
primary concept
Medicine
email

Recent publications

A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer.
2025cited by 3position: contributordoi
Table S1 from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
Figure S3 from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
Figure S2 from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
Figure S5 from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
Table S2 from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
Data from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
Figure S1 from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
Figure S4 from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
Table S4 from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
Table S3 from A Phase I Trial of Trebananib, an Angiopoietin 1 and 2 Neutralizing Peptibody, Combined with Pembrolizumab in Patients with Advanced Ovarian and Colorectal Cancer
2025cited by 0position: contributordoi
PD-1 Blockade Induces Reactivation of Nonproductive T-Cell Responses Characterized by NF-κB Signaling in Patients with Pancreatic Cancer.
2024cited by 22position: contributordoi
Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor.
2024cited by 17position: contributordoi
Figure S6 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Table S1 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Figure S4 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Figure S2 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Figure S4 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Figure S7 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Figure S7 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Table S2 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Data from PD-1 Blockade Induces Reactivation of Nonproductive T-Cell Responses Characterized by NF-κB Signaling in Patients with Pancreatic Cancer
2024cited by 0position: contributordoi
Table S1 from PD-1 Blockade Induces Reactivation of Nonproductive T-Cell Responses Characterized by NF-κB Signaling in Patients with Pancreatic Cancer
2024cited by 0position: contributordoi
Figure S3 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Table S3 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Arm A count matrices 3 from PD-1 Blockade Induces Reactivation of Nonproductive T-Cell Responses Characterized by NF-κB Signaling in Patients with Pancreatic Cancer
2024cited by 0position: contributordoi
Figure S1 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi
Table S1 from PD-1 Blockade Induces Reactivation of Nonproductive T-Cell Responses Characterized by NF-κB Signaling in Patients with Pancreatic Cancer
2024cited by 0position: contributordoi
Data from PD-1 Blockade Induces Reactivation of Nonproductive T-Cell Responses Characterized by NF-κB Signaling in Patients with Pancreatic Cancer
2024cited by 0position: contributordoi
Figure S2 from Blockade of IL1β and PD1 with Combination Chemotherapy Reduces Systemic Myeloid Suppression in Metastatic Pancreatic Cancer with Heterogeneous Effects in the Tumor
2024cited by 0position: contributordoi

Grants

No grants ingested yet.

Frequent collaborators

· 15 papers (2020–2025)F. Stephen Hodi · Harvard University14 papers (2018–2025)Joanna Baginska · Brigham and Women's Hospital11 papers (2025–2025)Harshabad Singh · Dana-Farber/Harvard Cancer Center11 papers (2025–2025) · 11 papers (2025–2025)James M. Cleary · University of Missouri11 papers (2025–2025)Marios Giannakis · Dana-Farber Brigham Cancer Center11 papers (2025–2025)Brandon M. Huffman · Winchester Hospital11 papers (2025–2025)Benjamin L. Schlechter · Dana-Farber Brigham Cancer Center11 papers (2025–2025)Yvonne Li · Blacktown & Mount Druitt Hospital11 papers (2025–2025)Adrián Mariño-Enríquez · Dana-Farber Cancer Institute11 papers (2025–2025)Kevin Tyan · Harvard University Press11 papers (2025–2025)Bruno Bockorny · Boston Medical Center11 papers (2025–2025)Andrew D. Cherniack · Van Andel Institute11 papers (2025–2025)Kimmie Ng · University of Jyväskylä11 papers (2025–2025)Michael P. Manos · Brigham and Women's Hospital11 papers (2025–2025)Scott J. Rodig · Massachusetts Institute of Technology11 papers (2025–2025)Anita Giobbie-Hurder · Boston University11 papers (2025–2025)Kathleen L. Pfaff · Dana-Farber Brigham Cancer Center11 papers (2025–2025)Allison Ferro · Dana-Farber Cancer Institute11 papers (2025–2025)
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