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Table 1 Responses and adverse events

From: Treatment strategy for reducing the risk of rituximab-induced cytokine release syndrome in patients with intravascular large B-cell lymphoma: a case report and review of the literature

Study/report

Timing of administration of rituximab

Response

Adverse events

Shimada et al. [3]

1st: 23 cases

NA

10 of 23 cases developed infusion reactions; hypoxia was observed in 3 of the 10 cases and Grade 3 severe hypoxia in 1 case

Shimada et al. [3]

2nd: 25 cases

NA

4 of 25 cases developed infusion reactions

Ohkubo et al. [23]

1st

CR

None

Imahashi et al. [15]

1st

CR

NA

Aoyama et al. [14]

1st

NC

Grade 3 sick sinus syndrome

Kaku et al. [16]

1st

CR

None

Okachi et al. [24]

1st: 2 cases

CR

NA

Wakamatsu et al. [34]

1st

CR

NA

Shimizu et al. [27]

1st: 5 cases

CR

NA

Takahashi et al. [31]

1st

CR

NA

Tanikawa et al. [33]

1st

NC

NA

Sawa et al. [26]

1st

CR

NA

Watanabe et al. [35]

1st

CR

NA

Sakurai et al. [25]

1st

CR

NA

Takizawa et al. [32]

1st

CR

NA

Nakano et al. [22]

1st

NC

NA

Kotake et al. [21]

2nd

CR

NA

Shinoda et al. [28]

2nd

CR

NA

Shimada et al. [1]

2nd

CR

None

Ishizuka et al. [17]

2nd

CR

NA

Iwagami et al. [18]

2nd

CR

NA

Kashizaki et al. [19]

2nd

CR

Unspecified*

Kobayashi et al. [20]

2nd

PR

NA

Sakurai et al. [25]

2nd

CR

None

Suzuki et al. [29]

2nd

CR

NA

Tadokoro et al. [30]

2nd

CR

NA

Our other case

1st

CR

Grade 1 fever, chills, hypoxia

Present case

1st

NA

Death

  1. NA, not applicable; CR, complete response; NC, no change; PR, partial response. *In this case, rituximab administration was attempted during the first course, but an infusion reaction was observed and the rituximab injection was discontinued. However, rituximab was administered according to protocol during the second course.