Dermatofibrosarcomas of DARIER FERRAND(DFSP) Clinical Trial
Official title:
A Phase IIa Open Multicenter, Trial, of Treatment With Pazopanib (Multi Tyrosine Kinase Inhibitor) in Dermatofibrosarcomas (DFSP), Unresectable Locally Advanced (Potentially Mutilating Surgery), Primary or Relapsing , Transformed or Not.
In relation to the activation of PDGF-mediated signalization due to the fusion gene COL1A1-PDGFb in DFSP, imatinib (800mg/day) has shown activity in advanced DFSP and has became the reference treatment option for these patients. Yet the activity observed does not allow for a downstaging compatible with successful resection in a number of patients and does not prevent subsequent tumour progression in case of residual tumour.Pazopanib in relation to 1) its multi tyrosine kinase inhibiting activity (VEGFR-1, VEGFR-2, VEGFR-3, PDGFR-α, PDGFR-β and c-kit with IC50 values of 10, 30, 47, 71, 84, and 74 nM, respectively) involving in particular PDGFR, and VEGFR which has been shown to be activated in DFSP, 2) its antitumour activity in sarcomas patients, and 3) its acceptable safety profile, is a logical candidate for therapeutic trials in DFSP both in patients not expected to derive a sufficient benefit from imatinib and in patients failing imatinib mesylate. Moreover, using quantitative RT-PCR and immunohistochemistry we have recently demonstrated high levels of VEGF and VEGFR2 expression in dermatofibrosarcoma.
Dermatofibrosarcoma protuberance (DFSP) is a rare soft tissue sarcoma of intermediate
malignant potential. Treatment relies on a wide local excision with negative margin and with
frequent need of reconstructive surgery. A translocation between chromosomes 17 and 22 that
places the platelet-derived growth factor-B (PDGFB) under the control of the collagen 1A1
promoter is present in > 90 % of the cases leading to an up regulation of PDGF-β expression
and activation of the tyrosinase kinase PDGFRβ. Imatinib mesylate has been approved in
unresectable and metastatic DFSP due to its activity on PDGFR. This study will evaluate the
benefit of pazopanib, a multikinase inhibitor in advanced DFSP. Administration of pazopanib
per os 800mg/ qd during 6 months until stable response according to primary endpoint , and
for a period of study not exceeding one year.In case of progression evaluated according to
the primary endpoint after a period of treatment superior to one month, or in the absence of
response at 3 months, the patient will be withdrawn from study, in order to get alternative
therapeutics. These patients will be considered as failures for analysis. After a 6-month
treatment period, and reaching a stable response, treatment continuation decision will be
based on the operability of patients.
Administration of pazopanib per os 800mg/ qd during 6 months until stable response according
to primary endpoint, with 3 monthly successive examinations, and for a period of study not
exceeding 18 months.In case of progression evaluated according to the primary endpoint after
a period of treatment superior to one month, or in the absence of response at 3 months, the
patient will be withdrawn from study, in order to get alternative therapeutics. These
patients will be considered as failures for analysis. After a 6-month treatment period, and
reaching a stable response, treatment continuation decision will be based on the operability
of patients Statistical analysis : The trial has been planned using a one-stage design
(Fleming TR. Et al) Analysis of the main endpoint will rely on a one-sided binomial test
comparing the observed response rate to the expected response rate under the null hypothesis
. The type I error rate is fixed at 0.025.For the main endpoint, a point estimate and a
two-sided 90% confidence interval will be presented, which will be consistent with the
one-sided test at a 0.025 level. For secondary endpoints, point estimates and 95% confidence
intervals will be presented.We intend to estimate the probability of tumour size reduction
of at least 30%. The sample size was calculated by FLEMMING method : Ho will be defined by a
RR ≤20% (decrease in tumour size of at least 30%) , H1 , response rate, 26 patients must be
included in order to demonstrate an efficacy as defined by a RR≥50%, with a 90% power and
alfa 2.5% one side.
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Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment