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Stefan C. Grant

Researcher at Wake Forest University

Publications -  39
Citations -  1307

Stefan C. Grant is an academic researcher from Wake Forest University. The author has contributed to research in topics: Lung cancer & Cancer. The author has an hindex of 17, co-authored 36 publications receiving 1083 citations. Previous affiliations of Stefan C. Grant include Cornell University & Memorial Sloan Kettering Cancer Center.

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Phase III Study of Adjuvant Vaccination With Bec2/Bacille Calmette-Guerin in Responding Patients With Limited-Disease Small-Cell Lung Cancer (European Organisation for Research and Treatment of Cancer 08971-08971B; Silva Study)

TL;DR: Vaccination with Bec2/BCG has no impact on outcome of patients with limited-disease small-cell lung cancer responding to combined-modality treatment and vaccination strategies in SCLC may still be warranted using vaccines that produce a better immunologic response.
Journal Article

Long Survival of Patients with Small Cell Lung Cancer after Adjuvant Treatment with the Anti-Idiotypic Antibody BEC2 Plus Bacillus Calmette-Guérin

TL;DR: Immunization of patients with SCLC after standard therapy using BEC2 plus BCG can induce anti-GD3 antibodies and is safe, and the survival and relapse-free survival in this group of patients are substantially better than those observed in a prior group of similar patients.
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Immunogenicity of a Fucosyl-GM1-Keyhole Limpet Hemocyanin Conjugate Vaccine in Patients with Small Cell Lung Cancer

TL;DR: The Fuc-GM1-KLH + QS-21 vaccine is safe and immunogenic in patients with SCLC, and all patients demonstrated a serological response, with induction of both IgM and IgG antibodies against Fuc -GM1, despite prior treatment with chemotherapy with or without radiation.
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Phase I study of green tea extract in patients with advanced lung cancer

TL;DR: This study suggests that while relatively nontoxic at a dose of 3 g/m2 per day, GTE likely has limited activity as a cytotoxic agent, and further study of GTE as a single-agent in established malignancies may not be warranted.
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Enhancement of Antitumor Immunity in Lung Cancer by Targeting Myeloid-Derived Suppressor Cell Pathways

TL;DR: This approach offers a new paradigm to inhibit immunosuppression by direct targeting of MDSC function, to generate effector and persistent memory cells for tumor eradication, and to prevent lung cancer relapse.