Key phrases for RM1 and RM2

 

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To Summary

RM1: Describing Research Results

RM1-Step1: Describing methods

To Map

RM1-Step1aProcedure

a total of * patients were EtoJ

ex. a total of * patients were enrolled EtoJ

were randomly assigned to EtoJ

ex. a total of * patients were randomly assigned to receive EtoJ

ex. participants were randomly assigned to one of

were available for EtoJ

ex. data were available for * patients EtoJ

 

the median duration EtoJ

ex. the median duration of follow-up was * months EtoJ

the most common EtoJ

ex. the most common reason for discontinuation EtoJ

 

 

RM1-Step2: Indicating specific observations

To Map

RM1-Step2aPresentation of results

Table 1 shows EtoJ

ex. Table 1 shows the characteristics of EtoJ

shown in EtoJ

ex. are shown in Table 1

presented in EtoJ

ex. are presented in Table 1

the baseline characteristics of EtoJ

the baseline characteristics of the patients EtoJ

ex. Table 1 shows the baseline characteristics of EtoJ

 

RM1-Step2bFindings

we found EtoJ

ex. we found that EtoJ

we noted EtoJ

ex. we noted a significant EtoJ

were observed in EtoJ

ex. responses were observed in EtoJ

were found EtoJ

were detected EtoJ

 

patients had EtoJ

survival was * months EtoJ

ex. median progression-free survival was * months EtoJ

 

RM1-Step2cPossibility

were more likely to EtoJ

were more likely to have EtoJ

were more likely to be EtoJ

were less likely to EtoJ

 

 

RM1-Step3: Indicating comparison or changes

To Map

RM1-Step3aComparison

was associated with EtoJ

ex. was associated with a lower risk of EtoJ

significantly associated with EtoJ

there was a significant EtoJ

ex. there was a significant difference EtoJ

ex. there was a significant interaction between EtoJ

was significantly EtoJ

was significantly higher EtoJ

was significantly lower EtoJ

was higher in EtoJ

was highest EtoJ

group than in the EtoJ

ex. higher in the * group than in the EtoJ

 

after adjustment for EtoJ

compared with EtoJ

as compared with

as compared with patients EtoJ

 

RM1-Step3bChanges

increase in EtoJ

ex. associated with a significant increase in EtoJ

increased significantly EtoJ

ex. increased significantly in the cohort EtoJ

significantly increased EtoJ

ex. had a significantly increased risk EtoJ

ex. was/were significantly increased EtoJ

increased by EtoJ

decreased by EtoJ

increased from * to

decreased from * to

increased in

accounted for EtoJ

 

RM1-Step3cSimilarity

was/were similar EtoJ

was/were similar in

were similar in the two groups EtoJ

characteristics were similar in EtoJ

was/were similar between

was similar between groups EtoJ

was/were similar to

were similar to those

were well balanced EtoJ

ex. were well balanced between EtoJ

baseline characteristics were EtoJ

ex. baseline characteristics were similar between EtoJ

ex. baseline characteristics were well balanced between EtoJ

were consistent with EtoJ

 

RM1-Step3dNo difference

did not differ EtoJ

did not differ significantly EtoJ

did not differ significantly between

did not differ between

was not significant EtoJ

ex. difference was not significant EtoJ

there was no

there was no significant difference EtoJ

there was no evidence EtoJ

there were no

there were no significant differences EtoJ

did not change EtoJ

ex. did not change substantially EtoJ

 

 

 

 

RM2: Describing Adverse Events

RM2-Step1: Describing adverse events

To Map

RM2-Step1aAdverse events

the most common adverse events EtoJ

ex. the most common adverse events were fatigue, EtoJ

the incidence of adverse events EtoJ

ex. the incidence of adverse events was similar in the two groups EtoJ

rate of serious adverse events EtoJ

serious adverse events occurred in * patients EtoJ

adverse events were reported in * patients EtoJ

had a serious adverse event EtoJ

ex. patients had a serious adverse event EtoJ

one or more serious adverse EtoJ

ex. participants had one or more serious adverse event

adverse events related to EtoJ

 

are summarized in EtoJ

ex. adverse events are summarized in Table 1

limit of the normal range EtoJ

ex. times the upper limit of the normal range EtoJ

 

RM2-Step1bNo adverse events

no serious adverse events EtoJ

ex. no serious adverse events were reported EtoJ

did not differ significantly between EtoJ

ex. rate of serious adverse events did not differ significantly between

there were no

there were no significant differences EtoJ

we noted no EtoJ

ex. we noted no significant difference between EtoJ

 

 

RM2-Step2: Indicating discontinuation

To Map

RM2-Step2aDiscontinuation

discontinuation of the study drug EtoJ

ex. led to discontinuation of the study drug EtoJ

discontinued the study drug EtoJ

ex. patient discontinued the study drug EtoJ

 

 

 

 

To Map