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In the provided material, the specific side effects that caused treatment delays for lurbinectedin are described as “hematologic and non-hematologic toxicities,” but the text does not list which exact adverse events (e.g., specific lab abnormalities or symptoms) were responsible for the delays. [1]
No. The available excerpt groups the cause of delays into two broad categories—hematologic toxicities and non-hematologic toxicities—without naming particular side effects. [1]
The same excerpt frames these toxicities as part of the safety findings for lurbinectedin, with treatment delays occurring in association with those hematologic and non-hematologic effects. [1]
To identify the exact side effects that led to delays, you would need the full safety/results text (often the “Dose modifications,” “Treatment delays,” or “Adverse events” subsection) from the source document. The excerpt available here does not include that level of detail. [1]
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