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Study of evaluating shortening of a hospitalization period after salvage therapy in patients with relapsed or refractory malignant lymphoma

Study of evaluating shortening of a hospitalization period after salvage therapy in patients with relapsed or refractory malignant lymphoma - Evaluation of post-salvage therapy hospitalization period in patients with malignant lymphoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000028082
Enrollment
25
Registered
2017-07-05
Start date
2017-07-12
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsed or refractory malignant lymphoma

Interventions

Patients receive a single subcutaneous injection of pegfilgrastim (3.6 mg) 2 days after chemotherapy.

Sponsors

National Hospital Organization Kyushu Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Relapsed or refractory non-hodgkins lymphoma and hodgkins lymphoma 2)Age >= 20 years old at informed consent 3)ECOG PS <= 2 4)Patients who are going to receive (R)EPOCH, CHASE(R), (R)DeVIC or (R)ESHAP regimen. 5)Patients who meet the following criteria within 14 days before salvage therapy. Neutrophil count >= 1,000/ul Platelet >= 50,000/ul Total bilirubin level <= 2 times the upper normal limit in institute Serum creatinine <= 1.5mg/dl

Exclusion criteria

Exclusion criteria: 1)Patients who have a possibility of severe infection after the entry or active infection at the entry. 2)Pregnant or breast-feeding females and females who have a possibility of pregnancy. 3)Patients who have any other inadequacy for this study by physicians.

Design outcomes

Primary

MeasureTime frame
Ratio of outpatient management period (days)

Secondary

MeasureTime frame
1) Readmission rate due to febrile neutropenia 2) All-cause readmission rate 3) Number of transfusions (RBC, Platelet) 4) Number of outpatient visits 5) Relative dose intensity 6) Cost analysis 7) Utilization rate of antibiotics 8) Patient satisfaction 9) Adverse events

Countries

Japan

Contacts

Public ContactTomoyuki Nukada

Kyowa Kirin Medical Affairs

ma.oncology@kyowa-kirin.co.jp03-5205-7200

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026