To synthesize clinical-trial, post-marketing, and real-world data to create a unified, organ-system–based framework for anticipating, preventing, and managing toxicities associated with antibody-drug conjugates (ADCs) in breast cancer treatment.
Key Findings:
Remove unsupported claims about practical algorithms.
Interpretation:
Remove unsupported conclusions about implications.
Limitations:
Make limitations more concise.
Conclusion:
Revise to remove unsupported claims about addressing practice gaps.