- |||||||||| Opdivo (nivolumab) / BMS, Cabometyx (cabozantinib tablet) / Exelixis, Yervoy (ipilimumab) / BMS
Trial completion, Trial completion date: Nivolumab, Cabozantinib S-Malate, and Ipilimumab in Treating Patients With Recurrent Stage IV Non-small Cell Lung Cancer (clinicaltrials.gov) - Feb 8, 2023 P2, N=3, Completed, Recruiting --> Active, not recruiting | N=144 --> 39 Active, not recruiting --> Completed | Trial completion date: Sep 2023 --> Dec 2022
- |||||||||| relatlimab (BMS-986016) / BMS, Opdivo (nivolumab) / BMS, Yervoy (ipilimumab) / BMS
Trial completion, Checkpoint inhibition: Neoadjuvant and Adjuvant Checkpoint Blockade (clinicaltrials.gov) - Feb 8, 2023 P2, N=53, Completed, Active, not recruiting --> Completed | Trial completion date: Sep 2023 --> Dec 2022 Active, not recruiting --> Completed
- |||||||||| Opdivo (nivolumab) / Ono Pharma, BMS, Tecentriq (atezolizumab) / Roche, Yervoy (ipilimumab) / Ono Pharma, BMS
Journal, Checkpoint inhibition, PD(L)-1 Biomarker, IO biomarker: Differential treatment responses to immune checkpoint inhibitor (ICI) therapy in a case of multiple primary malignancies: the programmed death ligand-1 (PD-L1) negative ureteral and lung metastasis from a clear cell renal cell carcinoma appearing after robotic-assisted partial nephrectomy progressed after ICI therapy, while synchronous PD-L1-positive primary lung squamous cell carcinoma responded very well to ICI therapy: a case report. (Pubmed Central) - Feb 8, 2023 The responses to ICI therapy of concomitant RCC and NSCLC were quite different. The PD-L1 expression status in individual tumors in cases of multiple primary malignancies (MPMs) may directly predict the response of each malignancy to ICI therapy, because the host immune system, which may affect the response to ICI therapy, could be the same in MPMs.
- |||||||||| sitravatinib (MGCD516) / BeiGene, Opdivo (nivolumab) / BMS, Yervoy (ipilimumab) / BMS
Trial completion date, Trial primary completion date: Study of Sitravatinib, Nivolumab and Ipilimumab in Advanced or Metastatic Clear-Cell Renal Cell Carcinoma or Other Solid Malignancies (clinicaltrials.gov) - Feb 6, 2023 P1, N=92, Active, not recruiting, For BRAF mutation-positive patients, more RCTs are still required to determine which is better between ICIs and targeted therapy. Trial completion date: Mar 2023 --> Jun 2023 | Trial primary completion date: Dec 2022 --> Mar 2023
- |||||||||| Yervoy (ipilimumab) / Ono Pharma, BMS
Enrollment change, Trial completion date, Trial termination, Trial primary completion date: Study of Ipilimumab After Stem Cell Transplantation in People With Relapsed/Refractory Multiple Myeloma (clinicaltrials.gov) - Feb 6, 2023 P1/2, N=3, Terminated, Trial completion date: Mar 2023 --> Jun 2023 | Trial primary completion date: Dec 2022 --> Mar 2023 N=45 --> 3 | Trial completion date: Nov 2023 --> Feb 2023 | Recruiting --> Terminated | Trial primary completion date: Nov 2023 --> Feb 2023; Lack of accrual
- |||||||||| Opdivo (nivolumab) / Ono Pharma, BMS, Yervoy (ipilimumab) / Ono Pharma, BMS
Nivolumab plus Ipilimumab Induced IPEX-like Polyendocrinopathy in Sarcomaoid Renal Cell Carcinoma () - Feb 4, 2023 - Abstract #AAAAI2023AAAAI_1790; Despite the development of an exceptionally uncommon spectrum irAEs, the patient achieved clinical remission. The following case highlights 1) the management of immunotherapy related polyendocrinopathy, 2) patients with more irAEs have improved response to therapy, 3) the critical role of FOXP3+Tregs in mediating the balance between cancer and autoimmunity.
- |||||||||| Opdivo (nivolumab) / Ono Pharma, BMS, Tecentriq (atezolizumab) / Roche, Yervoy (ipilimumab) / Ono Pharma, BMS
Journal, Adverse events, Checkpoint inhibition: Hepatic failure associated with immune checkpoint inhibitors: An analysis of the Food and Drug Administration Adverse Event Reporting System database. (Pubmed Central) - Feb 4, 2023 The following case highlights 1) the management of immunotherapy related polyendocrinopathy, 2) patients with more irAEs have improved response to therapy, 3) the critical role of FOXP3+Tregs in mediating the balance between cancer and autoimmunity. ICIs had possible strong signals associated with hepatic failure, and most cases of hepatic failure occurred within the first 3 months and had poor outcomes, which should attract clinical attention.
- |||||||||| Opdivo (nivolumab) / BMS, anetumab ravtansine (BAY 94-9343) / Bayer, Yervoy (ipilimumab) / BMS
Enrollment closed, Tumor mutational burden, IO biomarker: NCI10208: Testing the Combination of Anetumab Ravtansine With Either Nivolumab, Nivolumab and Ipilimumab, or Gemcitabine and Nivolumab in Advanced Pancreatic Cancer (clinicaltrials.gov) - Feb 3, 2023 P1/2, N=74, Active, not recruiting, ICIs had possible strong signals associated with hepatic failure, and most cases of hepatic failure occurred within the first 3 months and had poor outcomes, which should attract clinical attention. Recruiting --> Active, not recruiting
- |||||||||| MODULE 2: Evidence-Based Selection of First-Line Therapy for Metastatic RCC (San Francisco Marriott Marquis, Yerba Buena Ballroom ) - Feb 2, 2023 - Abstract #ASCOGU2023ASCO_GU_915;
CME Provider and Supporter(s): This event is organized and accredited by Research to Practice and supported through educational grants provided by Aveo Pharmaceuticals, Eisai Inc, Exelixis Inc, and Merck. Key clinical and biologic factors guiding the selection of first-line therapy for patients with newly diagnosed metastatic RCC Published efficacy and safety findings with nivolumab/ipilimumab, pembrolizumab/axitinib and avelumab/axitinib for treatment-na
- |||||||||| MODULE 1: Available Data with and Ongoing Investigation of Immune Checkpoint Inhibitors in Nonmetastatic Renal Cell Carcinoma (RCC) (San Francisco Marriott Marquis, Yerba Buena Ballroom ) - Feb 2, 2023 - Abstract #ASCOGU2023ASCO_GU_914;
CME Provider and Supporter(s): This event is organized and accredited by Research to Practice and supported through educational grants provided by Aveo Pharmaceuticals, Eisai Inc, Exelixis Inc, and Merck. Historical data with tyrosine kinase inhibitors (TKIs) as adjuvant therapy for high-risk RCC Biologic rationale for the assessment of immune checkpoint inhibitors as adjuvant therapy for RCC Design, eligibility criteria and primary and secondary endpoints of the Phase III KEYNOTE-564 trial of pembrolizumab versus placebo as adjuvant treatment for patients with clear cell RCC at increased risk of recurrence following nephrectomy Published efficacy and safety findings from KEYNOTE-564 showing a disease-free survival advantage with adjuvant pembrolizumab FDA approval of and identification of patients for treatment with adjuvant pembrolizumab Primary data from the Phase III IMmotion010 and CheckMate 914 studies demonstrating a lack of benefit with atezolizumab monotherapy and nivolumab/ipilimumab, respectively, versus placebo as adjuvant therapy for localized RCC; implications for clinical practice Ongoing Phase III studies (eg, PROSPER RCC, RAMPART trials) evaluating immune checkpoint inhibition as neoadjuvant and/or adjuvant therapy for patients with high-risk RCC
- |||||||||| Opdivo (nivolumab) / Ono Pharma, BMS, Yervoy (ipilimumab) / Ono Pharma, BMS
Journal, Metastases: Utility of prognostic prediction by early assessment of response to combined treatment with nivolumab plus ipilimumab in patients with treatment-naïve metastatic renal cell carcinoma. (Pubmed Central) - Feb 2, 2023 Historical data with tyrosine kinase inhibitors (TKIs) as adjuvant therapy for high-risk RCC Biologic rationale for the assessment of immune checkpoint inhibitors as adjuvant therapy for RCC Design, eligibility criteria and primary and secondary endpoints of the Phase III KEYNOTE-564 trial of pembrolizumab versus placebo as adjuvant treatment for patients with clear cell RCC at increased risk of recurrence following nephrectomy Published efficacy and safety findings from KEYNOTE-564 showing a disease-free survival advantage with adjuvant pembrolizumab FDA approval of and identification of patients for treatment with adjuvant pembrolizumab Primary data from the Phase III IMmotion010 and CheckMate 914 studies demonstrating a lack of benefit with atezolizumab monotherapy and nivolumab/ipilimumab, respectively, versus placebo as adjuvant therapy for localized RCC; implications for clinical practice Ongoing Phase III studies (eg, PROSPER RCC, RAMPART trials) evaluating immune checkpoint inhibition as neoadjuvant and/or adjuvant therapy for patients with high-risk RCC No abstract available
- |||||||||| renvistobart (BMS-986207) / BMS, Opdivo (nivolumab) / BMS, Yervoy (ipilimumab) / BMS
Enrollment change, Trial completion date, Trial termination, Trial primary completion date: A Study to Assess BMS-986207 in Combination With Nivolumab and Ipilimumab as First-line Treatment for Participants With Stage IV Non-Small Cell Lung Cancer (clinicaltrials.gov) - Feb 1, 2023 P2, N=1, Terminated, Trial primary completion date: Dec 2022 --> Dec 2023 N=180 --> 1 | Trial completion date: Aug 2026 --> Dec 2022 | Active, not recruiting --> Terminated | Trial primary completion date: Sep 2024 --> Dec 2022
- |||||||||| Yervoy (ipilimumab) / Ono Pharma, BMS
Journal: Research landscape and trends of melanoma immunotherapy: A bibliometric analysis. (Pubmed Central) - Jan 27, 2023 "Improved survival with ipilimumab in patients with metastatic melanoma" by Hodi et al...The researchers can benefit in selecting journals and in finding potential collaborators. This study can help researchers gain a comprehensive impression of the research landscape, historical development, and current hotspots in melanoma immunotherapy and can provide inspiration for future research.
|