- |||||||||| Tuoyi (toripalimab) / Shanghai Junshi Biosci, Coherus Biosci, Lenvima (lenvatinib) / Eisai, Merck (MSD)
P2 data, Retrospective data, Clinical Trial,Phase II, Journal: Lenvatinib, toripalimab plus hepatic arterial infusion chemotherapy in patients with high-risk advanced hepatocellular carcinoma: A biomolecular exploratory, phase II trial. (Pubmed Central) - Sep 21, 2022 Lenvatinib, toripalimab and FOLFOX-HAIC showed safe and encouraging antitumour activity for advanced HCC with high-risk features. The levels of CCL28 and BTC might be the predictive biomarkers for the triple combination therapy.
- |||||||||| 5-fluorouracil / Generic mfg., leucovorin calcium / Generic mfg., irinotecan / Generic mfg.
Journal: Incidence of and risk factors for severe neutropenia during treatment with the modified FOLFIRINOX therapy in patients with advanced pancreatic cancer. (Pubmed Central) - Sep 21, 2022 Although FOLFIRINOX (L-Leucovorin/5-FU/Irinotecan/Oxaliplatin) is established as one of the standard therapies for patients with metastatic pancreatic cancer, the modified FOLFIRINOX (mFOLFIRINOX) is often used in clinical practice to reduce the incidence of toxicities...The incidences of severe neutropenia and FN in patients receiving mFOLFIRINOX in our clinical practice were comparable to previous reports. The risk factors for severe neutropenia in patients receiving mFOLFIRINOX were a low baseline white blood cell count and presence of heterozygosity for UGT1A1*28 or UGT1A1*6 polymorphism.
- |||||||||| Onivyde (nanoliposomal irinotecan) / Servier, Ipsen, Takeda
Trial completion date, Trial primary completion date, Metastases: NCI-2018-02122: Liposomal Irinotecan, Fluorouracil and Leucovorin in Treating Patients With Refractory Advanced High Grade Neuroendocrine Cancer of Gastrointestinal, Unknown, or Pancreatic Origin (clinicaltrials.gov) - Sep 19, 2022 P2, N=37, Recruiting, ATRA plus FOLFOX4 significantly improves the overall survival and time to disease progression in patients with advanced HCC. Trial completion date: Sep 2024 --> Jun 2026 | Trial primary completion date: Sep 2023 --> Jun 2026
- |||||||||| Bylantra (devimistat) / Cornerstone Pharma, Ono Pharma
Trial completion date, Combination therapy, Metastases: CPI-613 in Combination With Modified FOLFIRINOX in Locally Advanced Pancreatic Cancer (clinicaltrials.gov) - Sep 16, 2022 P1/2, N=49, Active, not recruiting, Trial completion date: Oct 2026 --> Jan 2027 | Initiation date: Aug 2022 --> Nov 2022 | Trial primary completion date: Dec 2025 --> Mar 2026 Trial completion date: Dec 2023 --> Apr 2024
- |||||||||| Review, Journal, BRCA Biomarker, IO biomarker: Therapeutic advances in metastatic pancreatic cancer: a focus on targeted therapies. (Pubmed Central) - Sep 14, 2022
The current treatment of metastatic PDAC in fit patients is based on two chemotherapy combinations (FOLFIRINOX and gemcitabine plus nab-paclitaxel) which were validated more than 8 years ago...This review evaluates the current expectations and limits of available treatments and analyses the existing trials. A permanent search for actionable vulnerabilities in PDAC tumor cells and microenvironments will probably result in a more personalized therapeutic approach, keeping in mind that supportive care must also play a major role if real clinical efficacy is to be achieved in these patients.
- |||||||||| 5-fluorouracil / Generic mfg., oxaliplatin / Generic mfg.
Retrospective data, Review: Chinese herbal medicine combined with oxaliplatin-based chemotherapy for advanced gastric cancer: A systematic review and meta-analysis of contributions of specific medicinal materials to tumor response. (Pubmed Central) - Sep 14, 2022 Subgroup analysis showed that compare to SOX, FOLFOX, and XELOX regimens alone, CHM plus SOX, CHM plus FOLFOX, and CHM plus XELOX could significantly increase the ORR and DCR...To support this conclusion, these seven herbs are worthy of further clinical research. Systematic Review Registration: [http://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=262595], identifier [CRD42022262595].
- |||||||||| Cyramza (ramucirumab) / Eli Lilly
P4 data, Journal: A post-marketing safety study of ramucirumab with FOLFIRI in patients with metastatic colorectal cancer. (Pubmed Central) - Sep 14, 2022 P3 Ramucirumab [human vascular endothelial growth factor (VEGF) receptor-2 monoclonal antibody] + levofolinate, fluorouracil, and irinotecan (FOLFIRI) was approved for the treatment of metastatic colorectal cancer (CRC) in Japan based on the results from the phase 3 RAISE trial (NCT01183780)...Approximately 83.7% (n=303) and 25.4% (n=92) of patients had medication history of bevacizumab and anti-epidermal growth factor receptor (EGFR) antibodies, respectively...Although the current observational study enrolled patients with various medication history, the regimen of ramucirumab + FOLFIRI was manageable under clinical practice. No new safety concerns beyond the findings observed in previous clinical trials were reported.
- |||||||||| 5-fluorouracil / Generic mfg., leucovorin calcium / Generic mfg., irinotecan / Generic mfg.
Journal: Establishment of a human 3D pancreatic adenocarcinoma model based on a patient-derived extracellular matrix scaffold. (Pubmed Central) - Sep 14, 2022 Finally, both PANC-1 and AsPC-1 cells cultured in 3D matrices showed a reduced response to treatment with FOLFIRINOX if compared to conventional bi-dimensional culture. Our 3D culture system with patient-derived tissue-specific decellularized ECM better recapitulates the pancreatic cancer microenvironment compared to conventional 2D culture conditions and represents a relevant approach for the study of pancreatic cancer response to chemotherapy agents.
- |||||||||| Onivyde (nanoliposomal irinotecan) / Servier, Ipsen
Trial completion date, Trial primary completion date, Combination therapy, Metastases: Liposomal Irinotecan in Combination With Oxaliplatin, Leucovorin, and 5-fluorouracil for Patients With Locally Advanced Pancreatic Carcinoma: (clinicaltrials.gov) - Sep 14, 2022 P2, N=28, Recruiting, The MEND-IT study aims to evaluate the CR rate after intensified chemotherapy prior to concomitant chemoradiotherapy in a homogeneous group of patients with locally advanced rectal cancer and indisputably unfavourable characteristics, defined as hr-LARC, in order to improve their prognosis. Trial completion date: Mar 2023 --> Sep 2023 | Trial primary completion date: Sep 2022 --> Mar 2023
- |||||||||| spartalizumab (PDR001) / Novartis
Enrollment closed, Combination therapy: GASPAR: Perioperative Treatment in Resectable Gastric Cancer With Spartalizumab (PDR001) in Combination With Fluorouracil, Leucovorin, Oxaliplatin, and Docetaxel (FLOT) (clinicaltrials.gov) - Sep 13, 2022 P2, N=67, Active, not recruiting, Not yet recruiting --> Recruiting Recruiting --> Active, not recruiting
- |||||||||| 5-fluorouracil / Generic mfg., oxaliplatin / Generic mfg., leucovorin calcium / Generic mfg.
A CASE OF FATAL FOLINIC ACID, FLUOROURACIL, AND OXALIPLATIN (FOLFOX)-INDUCED PNEUMONITIS (Convention Center Exhibit Hall: Rapid Area 2D) - Sep 11, 2022 - Abstract #CHEST2022CHEST_3773; FOLFOX related pulmonary toxicity is a rare but potentially lethal complication. Data concerning mechanism of injury and optimal therapy is limited, warranting further investigation.
- |||||||||| oxaliplatin / Generic mfg., capecitabine / Generic mfg.
CORONARY VASOSPASM FROM COMBINATION CAPECITABINE AND OXALIPLATIN THERAPY (Convention Center Exhibit Hall: Rapid Area 4C) - Sep 11, 2022 - Abstract #CHEST2022CHEST_3704; Within one hour of administration of FOLFOX, he developed ST segment elevations that resolved with nitroglycerin... Capecitabine, with or without, oxaliplatin increases the risk of chemotherapy-induced cardiotoxicity, specifically coronary vasospasm, which can present as acute coronary syndrome.
- |||||||||| Rituxan (rituximab) / Biogen, Zenyaku Kogyo, Roche
INVASIVE FUNGUS AMONG US: A RARE CASE OF CEREBRAL PHAEOHYPHOMYCOSIS (Convention Center Exhibit Hall: Rapid Area 3D) - Sep 11, 2022 - Abstract #CHEST2022CHEST_3495; The invasive fungus C. Bantiana carries a high mortality rate. Any evidence of this organism must raise concern in immunocompromised individuals and empiric treatment should not be delayed.
|