Marwan Fakih
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Marwan Fakih has a total of 877 co-authors. Here are the top co-authors by number of shared publications:
- Chongkai Wang
City of Hope National Medical Center 1 Department of Medical Oncology and Therapeutics Research Duarte, California
35 shared publications - Neil Howard Segal
Memorial Sloan Kettering Cancer Center, New York, NY
30 shared publications - Peter P. Lee
Department of Immuno-Oncology, Beckman Research Institute, City of Hope, Duarte, USA
30 shared publications - Wells A. Messersmith
University of Colorado School of Medicine 6 Division of Medical Oncology, Department of Medicine Aurora, Colorado
30 shared publications - Jian Ye
Department of Infectious Diseases and Immunology, College of Veterinary Medicine, University of Florida, Gainesville, FL 32608, USA
29 shared publications - Colt A. Egelston
Department of Immuno-Oncology, Beckman Research Institute of the City of Hope, Duarte, California
28 shared publications
Latest Publications
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
C-800-01 SAP 1 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Statistical analysis plan to support the main manuscript.
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessC-800-01 SAP 1 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Statistical analysis plan to support the main manuscript.
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
C-800-01 Protocol 1 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Clinical trial protocol to support the main manuscript.
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessC-800-01 Protocol 1 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Clinical trial protocol to support the main manuscript.
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Figure 1 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
(A) Best overall response, (B) response over time, and (C) DOR in the overall population of patients with MSS mCRC NLM receiving either dose of BOT + BAL. Data cutoff: December 13, 2025. an = 121 patients with percent change from baseline in tumor measurement. bResponse data for this patient were corrected because of a documented database error identified after database lock; correction reflects validated source data.
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure 1 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
(A) Best overall response, (B) response over time, and (C) DOR in the overall population of patients with MSS mCRC NLM receiving either dose of BOT + BAL. Data cutoff: December 13, 2025. an = 121 patients with percent change from baseline in tumor measurement. bResponse data for this patient were corrected because of a documented database error identified after database lock; correction reflects validated source data.
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Figure 2 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
(A) PFS and (B) OS in the overall population of patients with MSS mCRC NLM receiving either dose of BOT + BAL. Data cutoff: December 13, 2025.
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure 2 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
(A) PFS and (B) OS in the overall population of patients with MSS mCRC NLM receiving either dose of BOT + BAL. Data cutoff: December 13, 2025.
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Figure 3 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
(A) Best overall response, (B) response over time, and (C) DOR in patients with MSS mCRC NLM previously exposed to available late-line therapiesa who received either dose of BOT + BAL. Data cutoff: December 13, 2025. aReceived ≥1 prior regimen of regorafenib, trifluridine/tipiracil ± bevacizumab, or fruquintinib. This was an exploratory, post hoc subgroup analysis.
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessFigure 3 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
(A) Best overall response, (B) response over time, and (C) DOR in patients with MSS mCRC NLM previously exposed to available late-line therapiesa who received either dose of BOT + BAL. Data cutoff: December 13, 2025. aReceived ≥1 prior regimen of regorafenib, trifluridine/tipiracil ± bevacizumab, or fruquintinib. This was an exploratory, post hoc subgroup analysis.
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Table 1 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Demographics and baseline disease characteristics of all patients with MSS mCRC NLM (N = 123).
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable 1 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Demographics and baseline disease characteristics of all patients with MSS mCRC NLM (N = 123).
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Table 2 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Safety overview, including the most common treatment-related imAE and TRAE (occurred in ≥10% of patients with MSS mCRC NLM; N = 123).
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable 2 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Safety overview, including the most common treatment-related imAE and TRAE (occurred in ≥10% of patients with MSS mCRC NLM; N = 123).
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Table 3 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Efficacy overview in all patients with MSS mCRC NLM (N = 123).
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable 3 from Extended Follow-up of Botensilimab plus Balstilimab in an Expanded Cohort of Microsatellite-Stable Metastatic Colorectal Cancer without Active Liver Metastases
Efficacy overview in all patients with MSS mCRC NLM (N = 123).
- Open Access
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Table 4 from A Phase I Study of PF-07062119, an Anti-GUCY2C/Anti-CD3 Bispecific Fc Antibody, in Patients with Advanced Gastrointestinal Cancers
Descriptive summary of serum PF-07062119 PK parameters (with 400 μg priming dose) for cycle 1.
- 1 October 2026
- Published by American Association for Cancer Research (AACR)
Open AccessTable 4 from A Phase I Study of PF-07062119, an Anti-GUCY2C/Anti-CD3 Bispecific Fc Antibody, in Patients with Advanced Gastrointestinal Cancers
Descriptive summary of serum PF-07062119 PK parameters (with 400 μg priming dose) for cycle 1.