Chemotherapy Plus Vaccination to Treat Mantle Cell Lymphoma
Mantle Cell Lymphoma · Lymphoma, Mantle Cell
Bottom Line
View on ClinicalTrials.gov: NCT00005780 ↗Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- EPOCH-R (Drug); GM-CSF (Biological); Idiotype vaccine (Biological)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- National Cancer Institute (NCI)
- Primary completion
- Jun 2021
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Median Progression-free Survival (PFS) in Participants Treated With Etoposide, Prednisone, Vincristine, Cyclophosphamide, Doxorubicin, and Rituximab (EPOCH-R) |
23.5 | — |
| PRIMARY Percentage of Participants With an Antibody Response to Idiotype Vaccine |
30 | — |
| SECONDARY Percentage of Participants Whose Cancer Shrinks or Disappears After Treatment With Etoposide, Prednisone, Vincristine, Cyclophosphamide, Doxorubicin, and Rituximab (EPOCH-R) |
80.8; 7.7; 7.7; 0; 3.8 | — |
| SECONDARY Percentage of Participants With Grade 3 or Higher Serious and/or Non-serious Toxicity That Occurred That is at Least Possibly Related to Drug or Vaccine |
3.8; 0; 0; 69.2; 3.8; 0 | — |
| SECONDARY Overall Survival (OS) |
89.7 | — |
| SECONDARY Progression Free Survival (PFS) in Participants Who Received Idiotype Vaccine |
25.0 | — |
| SECONDARY Percentage of Participants With Antibodies to Keyhole Limpet Haemocyanin (KLH) |
74 | — |
| SECONDARY Percentage of Participants With Induction of Type 1 Cytokine T-cell Response |
87; 65; 52; 74 | — |
| SECONDARY Time to Recovery of CD4 T Lymphocytes (CD4+) |
3 | — |
Summary
Eligibility Criteria
- INCLUSION CRITERIA:
Tissue diagnosis of mantle cell lymphoma (confirmed in Laboratory of Pathology). Blastic cell variant will be eligible.
Age greater than or equal to 18.
Previously untreated with cytotoxic chemotherapy. Patients may have received local radiation or a short course of steroids for control of symptoms.
All stages of disease.
Lymph node of greater than or equal to 2 cm accessible for biopsy/harvest or greater than 1000/microliters of circulating tumor cells in the blood.
Eastern Cooperative Oncology Group (ECOG) performance status of less than or equal to 3.
Adequate major organ function (serum creatinine 1.5 mg/dl or creatinine clearance greater than 60 ml/min; bilirubin less than 2 mg/dl (total) except less than 5 mg/dl in patients with Gilbert's syndrome as defined by greater than 80% unconjugated; absolute neutrophil count (ANC) greater than 1000 and platelets greater than 100,000) unless impairment due to organ involvement by lymphoma.
No active symptomatic ischemic heart disease, myocardial infarction or congestive heart failure within the past year. If multigated acquisition (MUGA) scan is obtained, the left ventricular ejection fraction (LVEF) should exceed 40%.
Ability to give informed consent.
EXCLUSION CRITERIA
Antibodies to human immunodeficiency virus (HIV) or presence of hepatitis B surface antigen.
Pregnant or lactating.
Prior malignancy in past 5 years except squamous or basal cell carcinoma or curatively treated in situ of the cervix.
Involvement of central nervous system by lymphoma.
Data sourced from ClinicalTrials.gov (NCT00005780). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.