Integrated Analysis of the RASH Study with the Use of the "Burden of Therapy" (BOTh ®TM ) Methodology-A Novel Tool for Assessing Adverse Events in Metastatic Pancreatic Cancer

• Published in: Current oncology (Toronto) Vol. 30; no. 6; pp. 5828 - 5834
• Main Authors: Dorman, Klara, Boeck, Stefan, Snijder, Robert J, Siveke, Jens T, Schenk, Michael, Mayerle, Julia, Caca, Karel, Freiberg-Richter, Jens, Fischer von Weikersthal, Ludwig, Kullmann, Frank, Reinacher-Schick, Anke, Fuchs, Martin, Kanzler, Stephan, Kunzmann, Volker, Ettrich, Thomas J, Zhang, Danmei, Held, Swantje, Abdul-Ahad, Ayad, von Bergwelt-Baildon, Michael, Heinemann, Volker, Haas, Michael
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.06.2023; MDPI
• Subjects: Antineoplastic Combined Chemotherapy Protocols - adverse effects; burden of therapy; Clinical Trials as Topic; Communication; Complications and side effects; erlotinib; Erlotinib Hydrochloride - adverse effects; Exanthema - chemically induced; Exanthema - drug therapy; FOLFIRINOX; gemcitabine; Humans; Metastasis; Methods; Pancreatic cancer; Pancreatic Neoplasms; Pharmaceutical industry; quality of life; Rash (Dermatology); United States; United Kingdom; Germany; rash; FOLFIRINOX; pancreatic cancer; burden of therapy; erlotinib; gemcitabine; quality of life
• ISSN: 1718-7729; 1198-0052; 1718-7729
• DOI: 10.3390/curroncol30060436

This analysis of the RASH trial (NCT01729481) aimed at gaining a better understanding of the "Burden of Therapy" (BOTh ) in pancreatic ductal adenocarcinoma (PDAC). In the RASH study, 150 patients with newly diagnosed metastatic PDAC were treated with gemcitabine plus erlotinib (gem/erlotinib) for four weeks. Patients who developed a skin rash during this four-week run-in phase continued with the gem/erlotinib treatment, while rash-negative patients were switched to FOLFIRINOX. The study demonstrated a 1-year survival rate of rash-positive patients who received gem/erlotinib as first-line treatment that was comparable to previous reports of patients receiving FOLFIRINOX. To understand whether these comparable survival rates may be accompanied by better tolerability of the gem/erlotinib treatment compared to FOLFIRINOX, the BOTh methodology was used to continuously quantify and depict the burden of therapy generated by treatment emergent events (TEAEs). Sensory neuropathy was significantly more common in the FOLFIRINOX arm, and prevalence as well as severity increased over time. In both arms, the BOTh associated with diarrhea decreased over the course of treatment. The BOTh caused by neutropenia was comparable in both arms but decreased in the FOLFIRINOX arm over time, possibly due to chemotherapy dose reductions. Overall, gem/erlotinib was associated with a slightly higher overall BOTh , but the difference was not statistically significant ( = 0.6735). In summary, the BOTh analysis facilitates the evaluation of TEAEs. In patients fit for intense chemotherapeutic regimens, FOLFIRINOX is associated with a lower BOTh than gem/erlotinib.