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Phase 3 N=166 Treatment

Combination Chemotherapy and Radiation Therapy in Treating Young Patients With Newly Diagnosed Hodgkin Lymphoma

Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma · Stage III Childhood Hodgkin Lymphoma · Stage IV Childhood Hodgkin Lymphoma

Enrolled (actual)
166
Serious AEs
0.0%
Results posted
May 2017
Primary outcome: Primary: Second-event-free Survival — 0.91 Probability of survival

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
bleomycin sulfate (Biological); doxorubicin hydrochloride (Drug); liposomal vincristine sulfate (Drug); vinorelbine tartrate (Drug); cyclophosphamide (Drug); etoposide phosphate (Drug); prednisone (Drug); filgrastim (Biological); ifosfamide (Drug)
Age
Pediatric, Adult
Sex
All
Sponsor
Children's Oncology Group
Primary completion
Mar 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
Second-event-free Survival
0.94; 0.88
PRIMARY
Safety Analysis and Monitoring of Toxic Death
SECONDARY
Event Free Survival
0.83; 0.78
SECONDARY
Second-event-free Survival
0.94; 0.88
SECONDARY
Event-free Survival for Rapid Early Response (RER) Positron Emission Tomography(PET)-1 Positive, RER PET-1 Negative
0.84; 0.82; 0.90
SECONDARY
Relapse-free Survival
0.82; 0.83; 0.79
SECONDARY
Grade 3 and 4 Non-hematologic Toxicities During Protocol Therapy
72
SECONDARY
Overall Survival
0.97; 0.97; 0.97

Summary

This phase III trial is studying how well giving combination chemotherapy together with radiation therapy works in treating young patients with newly diagnosed Hodgkin lymphoma. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high energy x-rays to kill cancer cells. Giving combination chemotherapy together with radiation therapy may kill more cancer cells.

Eligibility Criteria

Inclusion Criteria

  • Pathologically confirmed newly diagnosed Hodgkin lymphoma (HL) meeting one of the following criteria:
  • Classical disease
  • Nodular lymphocyte-predominant disease
  • Stage III or IV disease with B symptoms, as defined by ≥ 1 of the following:
  • Unexplained weight loss > 10% within the past 6 months
  • Unexplained recurrent fever > 38°C within the past month
  • Recurrent drenching night sweats within the past month
  • Creatinine clearance or radioisotope GFR ≥ 70 mL/min OR maximum serum creatinine based on age/gender as follows:
  • 0.4 mg/dL (1 to 5 months)
  • 0.5 mg/dL (6 to 11 months)
  • 0.6 mg/dL (12 to 23 months)
  • 0.8 mg/dL (2 to 5 years)
  • 1 mg/dL (6 to 9 years)
  • 1.2 mg/dL (10 to 12 years)
  • 1.5 mg/dL (males) or 1.4 mg/dL (females) (13 to 15 years)
  • 1.7 mg/dL (males) or 1.4 mg/dL (females) (≥ 16 years)
  • Total bilirubin ≤ 1.5 times upper limit of normal (ULN) for age
  • AST or ALT 60% by pulmonary function tests (PFT) (unless due to large mediastinal mass fromHL)
  • For children who are unable to cooperate for PFTs, the criteria are:
  • No evidence of dyspnea at rest
  • No exercise intolerance
  • Pulse oximetry > 92% on room air
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • No pathologic prolongation of QTc interval (> 450 milliseconds) on 12-lead ECG
  • No prior chemotherapy, biological response modifiers (e.g., monoclonal antibody therapy), or radiotherapy
  • At least 28 days since prior corticosteroids except for emergent treatment for respiratory distress or spinal cord compression, or for treatment of allergy to contrast agent required for CT scan
  • No other concurrent cancer chemotherapy or immunomodulating agents (including steroids)
  • Concurrent corticosteroid therapy as treatment or prophylaxis for anaphylactic reactions allowed
  • No concurrent pegfilgrastim
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01026220). 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.

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