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Comparison · NCT02400437-7e46a4fc

MYD88 Mutated, CXCR4 Wild-type vs MYD88 Mutated, CXCR4 Mutated: Overall Response Rate by MYD88 L265P and CXCR4-WHIM Status

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. MYD88 Mutated, CXCR4 Wild-type vs MYD88 Mutated, CXCR4 Mutated: Overall Response Rate by MYD88 L265P and CXCR4-WHIM Status. Trial comparisons, record NCT02400437-7e46a4fc. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02400437-7e46a4fc

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 110.7411wilson
Risk in group 20.9330.7020.988wilson
Risk difference, group 1 minus group 20.0667-0.1980.298newcombe hybrid score
Risk ratio, group 1 over group 21.070.9361.23log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one more participant with the outcome on MYD88 Mutated, CXCR4 Wild-type than on MYD88 Mutated, CXCR4 Mutated15from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1MYD88 Mutated, CXCR4 Wild-typeParticipants who were MYD88 mutated and did not have the CXCR4 mutation1111OG000
Group 2MYD88 Mutated, CXCR4 MutatedParticipants with both the MYD88 mutation and a CXCR4 mutation1415OG001

Outcome

Type
SECONDARY
Title
Overall Response Rate by MYD88 L265P and CXCR4-WHIM Status
Description
To evaluate the overall response rate of participants by MYD88 L265P and CXCR4-WHIM mutations in WM. Overall response is defined as achieving at least a minor response, or \>25% reduction in serum IgM from baseline.
Time frame
2 Years
Population
Number of participants who achieved a response by mutational status

Source ClinicalTrials.gov

Trial

Title
Trial of Ixazomib, Dexamethasone and Rituximab in Patients With Untreated Waldenstrom's Macroglobulinemia
NCT number
NCT02400437
Phases
PHASE2
Conditions
Waldenstrom's Macroglobulinemia
Interventions
Ixazomib, Dexamethasone, Rituximab
Lead sponsor
Dana-Farber Cancer Institute
Results first posted
2020-09-02

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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