Renal Cell Cancer Clinical Trial
Official title:
Phase1/2 Study of Vaccination With DNP Modified Autologous Renal Cell Carcinoma in Combination With Sunitinib in Stage 4 RCC
While different lines of evidence support the notion that renal cell cancer is amenable for
immunologic vaccination, up to now the clinical benefit associated with vaccines has been
limited. One reason being probably the whole immunological state of the patients with RCC in
which the tumor releases various substances promoting tolerance of the immune system towards
the carcinoma. Recent data demonstrates that sunitinib has effects on the immune system
which might enhance effectivity of anti tumor vaccines.
Since in kidney cancer it is quite common to resect primary tumor when there are few
metastasis or or metastatic tumor resected (if there are few metastasis), the investigators
plan to use these tumor source to grow autologous carcinoma cell lines and use a method used
world wide for many years and in our institution for over a decade to modify these cells by
dinitro phenol and use irradiated cell for patients vaccination in combination with
sunitinib treatments.
The investigators will monitor clinical and immunological parameters in these patients.
Background: Renal cell carcinoma (RCC) constitutes around 3% of all solid tumors and cure
for metastatic sidease is reported for less than 5% of patients. Together with melanoma it
is considered the most immune responsive tumor, moreover it is a common practice to resect
primary tumor or large metastasis even in the metastatic settings. Antiangiogenesis
treatments are currently the favored antitumor drugs, however their use has rarely resulted
in complete response/ cure. Recently it has been demonstrated that these drugs can elicit a
shift in the immune environment in RCC patients (improved T1 responses reduced Treg
responses).Our department has experience in the treatment 200 melanoma patients with
cellular vaccination and in the preparation of primary tumor cell lines from various tumors
including RCC. Interestingly , immune modulators such as antiCTLA-4 Ab have demonstrated
impressive activity in patients previously vaccinated with cellular vaccinations.
Working hypothesis: Vaccination with autologous cellular vaccines of RCC patients will
induce clinical and immunological responses and help in formulation of better combined
vaccination strategies in this cancer. Our aims are: 1) Growth and characterization of
primary RCC cell lines,2)vaccination with autologous cellular vaccines in combination with
sunitinib. 3) Clinical and immunologic characterizations for derivation of prognostic and
predictive factors.
Methods: primary or metastatic tumor resected in one of several Israeli hospitals will be
used to derive autologous cell lines used for vaccinations following DNP modifications in
combination with the regular Sunitinib treatments. Immunological and clinical followup of
the patients will be performed and primary cell lines will be grown for further in-vitro
testing including possible future use for allogeneic vaccines. Expected result Good safety
profile combined with significant clinical and immunological responses are expected.
Importance: This research might result in clinical benefit to the treated patients and will
be important in the formulation of effective immune strategies in kidney cancer.
Probable implications to Medicine: RCC vaccine in combination with other therapies has the
potential to lead to longer survival and even cure the proposed study will help in the
formulation of such a vaccine.
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Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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