Abstract 158P
Background
The delivery of cancer immunotherapy often encounters complications from immune-related adverse events (irAEs). Analyzing irAEs in large clinical trials of checkpoint inhibitors (CPIs) has improved their management and surveillance. However, for non-standard cancer immunotherapies (CITs), aggregated clinical data on irAEs are scarce, and systematic exploration of these toxicities is lacking.
Methods
To systematically evaluate the pattern of irAEs across CITs and to examine the variability linked to concurrent CPI use and tumor burden metrics, we established a harmonized data mart from 23 early-phase trials, encompassing 12 molecules with diverse mechanisms targeting various cancers and involving a total of 3,568 patients.
Results
Our preliminary results reveal substantial variation in the incidence proportions of irAEs over a 3-month period across different CIT classes. Hepatitis (IQR: 17.7-34.2%), rash (IQR: 9.8-38.9%), and hypothyroidism (IQR: 0.3-2.5%) are the most common irAEs. Notably, a significant proportion of hepatitis cases are severe (grades 3-5, 44.4%), while rash and hypothyroidism are predominantly mild (grades 1-2, 92.7% and 97.2% respectively). Hepatitis is more frequent with systemic immunocytokines (50.4%) and related immune stimulators (35.1%), while targeted treatments with T-cell bispecifics (TCBs) are linked to organ-specific toxicities like rash (61.4%) and colitis (4.4%). The time-to-onset for severe irAEs, as indicated by the 10th percentile, also varied across CIT classes: TCBs and immunocytokines show effects within 1-3 days; immune modulators at 3-6 weeks; and treatments targeting the PD1/PD-L1 axis typically within 3-6 months. Finally, our analysis suggests that patients with liver metastases have a higher risk of developing hepatitis (hazard ratio [HR] = 2.0), but a lower risk of rash (HR = 0.8), a pattern also observed in patients with smaller target lesions (HR = 0.8).
Conclusions
In conclusion, our study provides insights into the occurrence of irAEs linked to non-standard CITs. More research is needed to uncover the molecular basis of these toxicities and help refine patient management and risk-benefit evaluations.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
F. Hoffmann-La Roche AG.
Funding
F. Hoffmann-La Roche AG.
Disclosure
B.P. Fairfax: Financial Interests, Institutional, Advisory Board, I sit on a scientific advisory board for Roche regarding immunotherapy toxicity: Roche; Financial Interests, Institutional, Advisory Board, I have sat on a scientific advisory board for Pathios Therapeutics: Pathios Therapeutics; Financial Interests, Institutional, Invited Speaker, I have given a talk and provided consultancy for Immunocore and may provide further input for their work as a scientific advisor: Immunocore; Financial Interests, Personal, Advisory Board, I have given a talk and provided consultancy for UCB, last in 2022.: UCB; Financial Interests, Personal, Invited Speaker, I have provided an educational talk for Bristol Myers Squibb for local Oncology meeting in Birmingham UK and may provide further such talks.: BMS; Financial Interests, Personal, Invited Speaker, I have been asked to present my group's work at GSK in 2024: GSK; Financial Interests, Personal, Advisory Board, I have been asked to sit on a scientific advisory board for TCypher BIO: TCypher BIO. V.C. Schmid: Financial Interests, Personal, Full or part-time Employment: Roche; Financial Interests, Personal, Stocks/Shares: Achilles therapeutics. D.F. Lamparter: Financial Interests, Personal, Full or part-time Employment: F. Hoffmann-La Roche AG; Financial Interests, Personal, Stocks/Shares: F. Hoffmann-La Roche AG, Verge Analytics, Lonza AG. T. Kam-Thong: Financial Interests, Personal, Full or part-time Employment: Hoffmann-La Roche; Financial Interests, Personal, Stocks/Shares: Hoffmann-La Roche. P. Scepanovic, R. Mohindra: Financial Interests, Personal, Full or part-time Employment: F. Hoffmann-La Roche Ltd; Financial Interests, Personal, Stocks/Shares: F. Hoffmann-La Roche Ltd. G. Duchateau-Nguyen: Financial Interests, Institutional, Full or part-time Employment: Hoffmann-La Roche; Financial Interests, Institutional, Stocks/Shares: Hoffmann-La Roche. A. Roller: Financial Interests, Personal, Stocks/Shares: F. Hoffmann-La Roche. V. Karanikas: Financial Interests, Personal, Full or part-time Employment: Roche; Financial Interests, Personal, Stocks/Shares: Roche. D. Heinzmann, S.L. Mycroft: Financial Interests, Institutional, Full or part-time Employment: Roche; Financial Interests, Institutional, Stocks/Shares: Roche. C. Adams: Financial Interests, Personal, Full or part-time Employment, I am a scientist at Genentech.: Genentech; Financial Interests, Personal, Stocks/Shares, I have received RSUs/SARs as part of my compensation from Genentech.: Genentech. N. Städler: Financial Interests, Personal, Full or part-time Employment, employee of Roche: F. Hoffmann-La Roche AG; Financial Interests, Personal, Stocks/Shares, Roche Holding AG Genussscheine: F. Hoffmann-La Roche AG; Non-Financial Interests, Project Lead, As employee I lead projects: F. Hoffmann-La Roche AG.
Resources from the same session
193P - Translational, PK, PD, and immunophenotyping analyses of tuvusertib + niraparib in a phase Ib open-label multicenter dose-escalation study in patients with advanced solid tumors (DDRiver Solid Tumors 301)
Presenter: Anthony Tolcher
Session: Poster session 08
194P - CD8-to-CD20 lymphocyte ratio is a predictive biomarker for lenvatinib and pembrolizumab efficacy and progression-free survival in advanced endometrial cancer: Updated data
Presenter: Liubov Tashireva
Session: Poster session 08
195P - Preclinical efficacy of the trastuzumab duocarmazine SYD985 as monotherapy or in combination with the PARP inhibitor niraparib in HER2-expressing endometrial cancer
Presenter: Eva Colas
Session: Poster session 08
196P - Randomized phase II study of trabectedin/olaparib compared to physician’s choice in subjects with previously treated advanced or recurrent solid tumors harboring DNA repair deficiencies
Presenter: Richard Schlenk
Session: Poster session 08
197P - PRIME-ROSE: Merging clinical outcome data from DRUP-like clinical trials
Presenter: Tina Kringelbach
Session: Poster session 08
198P - Inavolisib in cancers with activating PIK3CA mutations: Results from the CRAFT trial
Presenter: Christoph Heilig
Session: Poster session 08
199P - Association of homologous recombination deficiency status with outcomes for ovarian cancer patients treated with olaparib, and exploration of other biomarkers of relapse and survival
Presenter: qingsheng xie
Session: Poster session 08
200P - Outcomes of patients (pts) with unfavourable, non-squamous cancer of unknown primary (CUP) progressing after induction chemotherapy (CTX) in the global, open-label, phase II CUPISCO study
Presenter: Tilmann Bochtler
Session: Poster session 08
201P - Efficacy of antibody drug conjugate (ADC) by mRNA expression of targeted genes in advanced solid tumors: SCRUM-Japan MONSTAR-SCREEN-2
Presenter: Takao Fujisawa
Session: Poster session 08