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Phase 2 N=23 Treatment

Autologous Peripheral Blood Stem Cell Transplant for Germ Cell Tumors

Childhood Germ Cell Tumor · Ovarian Cancer · Teratoma

Enrolled (actual)
23
Serious AEs
34.8%
Results posted
May 2022
Primary outcome: Primary: Overall Survival (OS) — 86; 56 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
carboplatin (Drug); etoposide (Drug); ifosfamide (Drug); paclitaxel (Drug); thiotepa (Drug); autologous hematopoietic stem cell transplantation (Procedure); Mesna (Drug); filgrastim (Biological)
Age
Pediatric, Adult, Older Adult · 10+ yrs
Sex
All
Sponsor
Masonic Cancer Center, University of Minnesota
Primary completion
Mar 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Survival (OS)
86; 56
SECONDARY
Disease-free Survival (DFS)
64; 44
SECONDARY
Engraftment of Platelets
13; 8
SECONDARY
Numbers of Patients Unable to Mobilize Peripheral Blood Stem Cells
0; 0
SECONDARY
Engraftment of Neutrophils
13; 9

Summary

RATIONALE: Germ cell tumors (GCT) are highly sensitive to chemotherapy such that even with metastatic disease at diagnosis, many patients can be cured. Patients who fall into the poor risk category or others who relapse can be successfully salvaged with high dose chemotherapy and autologous stem cell transplant (AuSCT). As in other diseases such as myeloma, sequential high dose chemotherapy and AuSCT may improve overall and disease free survival. PURPOSE: Because prior investigations in GCT suggest that a subset of high risk or relapsed patients may be cured with sequential cycles of high dose chemotherapy and AuSCT, we propose investigating how well non-cross resistant conditioning regimens work in treating patients with relapsed or high risk GCT.

Eligibility Criteria

Inclusion Criteria

  • Diagnosis: Poor Prognosis Non-Seminomas Germ Cell Tumor in ≥ PR1/CR1 or Good or Intermediate Prognosis Seminomas and Non- Seminomas Germ Cell Tumor in ≥ PR1 or ≥ CR2 as defined by the International Germ Cell Cancer Consensus Classification. Patients with increasing tumor markers only (i.e. no imaging evidence of progressive disease) are eligible for transplant.
  • Age: ≥ 10 years and 8 gm/dL without transfusion and off erythropoietin for 14 days or Aranesp for 21 days
  • White blood cells (WBC) > 2.5 x 10^9/L with an absolute neutrophile count (ANC) > 1.5 x 10^9/L and off G-CSF or GM-CSF for 10 days or Neulasta for 21 days
  • Platelets > 100 x 10^9/L without transfusion and/or a bone marrow cellularity of ≥ 20%
  • Renal: Creatinine ≤ 2.0 mg/dl or creatinine clearance > 50 ml/min.
  • Hepatic: Total bilirubin ≤ 2.0 mg/dl, AST and alkaline phosphatase 50% of predicted).
  • Patients with a history of CNS tumor involvement are eligible if they have completed treatment for CNS disease (radiotherapy or surgery or chemotherapy), have recovered from or stabilization of the side effects associated with the therapy and have no evidence of progressive CNS disease at the time of enrollment.

Exclusion Criteria

  • Patients with serious uncontrolled infections will not be eligible.
  • Male and female patients of reproductive potential must use an approved contraceptive method if appropriate (for example, intrauterine device [IUD], birth control pills, or barrier device) during and for the duration of study participation. The drugs used in this study are pregnancy category D - clear evidence of risk in pregnancy.
  • Pregnant and breast feeding women will not be eligible.

Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care.

Additional Eligibility prior to Transplant Two:

  • Total Collection of ≥ 4 x 10^6 CD34 cells/kg prior to transplant one
  • Transplant able to occur between day +30 and day +90 from transplant one
  • Recovery of blood counts as demonstrated by:
  • WBC > 2.5 x 10^9/L with an ANC > 1.5 x 10^9/L and off G-CSF for 3 days
  • Platelets > 50 x 10^9/L without transfusion in the prior 7 days
  • Renal: Creatinine ≤ 2.0 mg/dl or creatinine clearance > 50 ml/min
  • Hepatic: Total bilirubin ≤ 2.0 mg/dl, AST and alkaline phosphatase < 5 x upper limit of normal
  • Infection: Patients with serious uncontrolled infections at the time of planned transplant will be excluded
  • Patients with progressive disease by Response Evaluation Criteria in Solid Tumors (RECIST) criteria by imaging techniques are not eligible to proceed to the second transplant. Tumor marker increase alone is not sufficient to diagnose disease progression.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00432094). 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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