Radiofrequency Ablation Treatment Shown to Improve Survival Rates and Patient
Outcomes Across Multiple Organs
FREMONT, Calif., Dec. 1 /PRNewswire-FirstCall/ -- RITA Medical Systems,
Inc. (Nasdaq: RITA), a publicly-traded medical device company focused solely
on cancer therapies, today announced the presentation of several clinical
studies featuring radiofrequency ablation (RFA) treatment of cancer at the
Radiology Society of North America (RSNA) 91st Scientific Assembly and Annual
Meeting in Chicago, Illinois. In addition to clinical information presented
during plenary sessions at the annual meeting, approximately 200 physicians
attended a symposium on interventional oncology presented by the RSNA and the
Society of Interventional Radiology (SIR) Foundation.
Dr. Jelle Kylstra, Vice President and Medical Director of RITA Medical
Systems commented, "Radiofrequency ablation was featured prominently at both
the symposium and regular RSNA meeting this year, demonstrating in my view a
determination among clinicians to expand the application of RFA in the
treatment of cancer." Dr. Kylstra continued, "It is exciting to see 2-year,
3-year, and 5-year survival data being published with large patient series
that I believe demonstrate comparable outcomes, and often with lower
associated procedure morbidities than reported series of surgical candidates."
The Company believes that the RAPTURE lung cancer clinical trial data
presented at RSNA is a starting point for comparative follow-on studies that
may eventually lead to broader adoption of the procedure in the community
based hospital setting. A description of the RAPTURE clinical trial data
presented at the RSNA meeting is provided below.
Stuart Singer, MD, an interventional radiologist at Crouse Hospital in
Syracuse, New York, said "I believe that the RAPTURE trial demonstrates that
RFA for small primary and metastatic lung carcinoma is a viable treatment
option for nonresectable patients with good intermediate survival results. I
have had a comparable experience in my community hospital practice over the
last 3 years in a similar cohort of patients."
RFA Treatment of Lung Cancer Clinical Data Presented
In a paper titled, "Radiofrequency Ablation of Pulmonary Tumors Response
Evaluation (RAPTURE) Trial: 2-Year Survival Outcomes," author Riccardo
Lencioni, MD, Professor of Radiology, University of Pisa, presented two-year
survival outcomes from a lung RFA clinical study in which 186 lung tumors were
treated in 106 patients. The study was a prospective, multicenter clinical
trial. All 106 patients were non-surgical candidates with 33 presenting with
primary non-small cell lung cancer (NSCLC), 53 presenting with colorectal
cancer (CRC) metastases, and 20 presenting with metastases from other primary
malignancies. Complete ablation of macroscopic tumor as evidenced at 3-month
computed tomography (CT) was achieved in 173 of 186 tumors. No
procedure-related deaths occurred. Overall survival was 69% at 1 year and 49%
at 2 years in patients with NSCLC; and 86% at 1 year and 62% at 2 years in
patients with CRC metastases. Cancer-specific survival was 91% at 1 year and
91% at 2 years in patients with NSCLC; and 88% at 1 year and 72% at 2 years in
patients with CRC metastases.
In a paper titled, "Percutaneous Radiofrequency Ablation of Stage 1A
Non-Small Cell Lung Cancer: A Prospective Multicenter Clinical Trial," author
Prof. Lencioni, MD, focused on the biopsy-proven Stage 1 non-small cell lung
cancer (NSCLC) patient data from the RAPTURE study reviewed above. 14 NSCLC
patients were all considered unfit for surgery and radical radiotherapy. RFA
was technically feasible in all 14 patients and a CT image obtained 1 month
post-RFA showed a round, ground-glass density area encompassing the treated
lesion in all cases. Complete ablation of the treated lesions was confirmed by
the absence of tumor re-growth over a period of 1 year or more in 8 patients.
Preliminary survival analysis by the Kaplan-Meier method showed 1 year and
2 year overall survival rates of 84% and 72%, respectively; and 1 year and
2 year cancer-specific survival rates of 92% and 92%, respectively.
The Company noted that in a series of 347 patients reported in the medical
journal CHEST titled, "The Curative Treatment by Radiotherapy Alone of Stage 1
Non-Small Cell Carcinoma of the Lung" (S Gauden, J Ramsay, and L Tripcony Nov
1995; 108: 1278 - 1282), the largest such reported retrospective radiation
therapy series in early lung cancer patients, patients with inoperable disease
treated with definitive radiation therapy achieved an overall survival at
2 years of 54%. A copy of the abstract of the Gauden study may be found on the
CHEST Journal website, http://www.chestjournal.org .
RFA Treatment of Liver Cancer Clinical Data Presented
In a paper titled, "Comparing the Outcomes of Surgical Resection and
Radiofrequency Ablation in Cirrhotic Patients with a Single Small
Hepatocellular Carcinoma and Well-Preserved Hepatic Function," author
Prof. Riccardo Lencioni, MD, presented clinical data comparing surgical
resection to percutaneous RF ablation in a matched case-control study. In the
study 162 patients were matched and the rate of local tumor progression and
the incidence of tumor recurrence were compared. Dr. Lencioni concluded that
overall survival and rate of tumor recurrence was similar in the two groups.
Although there was a higher rate of local tumor progression in the RF group in
the study, RF ablation was "found to be as effective as surgical resection for
the treatment of a single small hepatocellular carcinoma (HCC) in patients
with well-preserved liver function."
In a paper titled, "Radiofrequency Ablation in Patients with Small (less
than 4cm) Solitary Colorectal Liver Metastases," Allison Gillams, MD,
Middlesex Hospital, London, UK, presented clinical data from a retrospective
review of a sub-group of 35 patients from the institution's database of
221 patients with colorectal liver metastases treated with RFA. The
35 patients in the sub-group had a solitary liver metastasis, less than 4 cm
in diameter. Survival data showed that median 3-year and 5-year survival from
first ablation was 40 months, 65% and 43% respectively. The author concluded
that "survival following RFA for small solitary colorectal liver metastases is
extremely good."
The Company noted that in a series of 456 patients reported in the Journal
of Clinical Oncology (Fong et al., JCO1997;15:938-946), 3-year and 5-year
survival rates for patients with colorectal liver metastases treated with open
liver resection were 59% and 38% respectively. The same study noted an
overall complication rate of 24% following surgical resection, including a
peri-operative mortality rate of 2.8%.
In a paper titled, "Complications after Percutaneous Radiofrequency
Ablation (RFA) of Focal Hepatic Tumors," Ralf-Thorsten Hoffmann, MD, Professor
of Radiology, University of Munich, Germany, reported study data assessing the
number and degree of complications after RFA in patients suffering from liver
tumors or metastases of the liver. Over a 5 year period 840 procedures were
performed in 393 patients. 95 patients suffered from primary HCC, 126 had
metastases of colorectal cancer, 124 of breast cancer, and 48 had metastases
of other tumors. The size of tumors treated ranged from 5mm to 60mm (mean
27mm). Study data showed that the overall complication rate in the series was
less than 5% with a major complication rate of about 1%. The author concluded
that RFA is a "very safe therapeutical option for patients suffering from
focal liver tumors."
RFA Treatment of Kidney Cancer Clinical Data Presented
In a paper titled, "Radiofrequency Ablation (RFA) of 25 Renal Masses in
Patients with Solitary of Functionally Solitary Kidneys: Trends in Creatinine
Levels with and without Obstructive Complications," Debra Gervais, MD,
Director of Abdominal and Interventional Radiology at Mass General Hospital
and an Assistant Professor of Radiology at Harvard Medical School, reported
the results of a retrospective review of 141 tumors ablated in 125 patients.
The study review revealed 25 tumors (median 3.1 cm) in 21 patients with
solitary or functionally solitary kidneys. Complete ablation was achieved in
23 of 25 (92%) of tumors, with a mean follow up of 2.8 years during which no
local recurrences were reported following complete necrosis of the tumor. The
author concluded that "RF ablation of renal masses is a safe option for
patients with solitary kidneys compared to surgical removal and in most cases
preserves renal function sufficient to avoid dialysis."
RFA Treatment of Bone Tumors Clinical Data Presented
In a paper titled, "Radiofrequency Ablation: An Algorithm for the
treatment of Spinal Mets and Myeloma," Gregory Gordon, MD, Department of
Vascular and Interventional Radiology, Decatur Memorial Hospital, Decatur,
Illinois, reported on the effectiveness RFA to reduce pain in 31 patients with
45 lesions. In the study 8 patients (25.8%) had a complete response (reduction
in pain), 13 patients (42%) had a greater than 50% reduction in pain, and
7 patients (22.6%) had between 20% and 50% reduction in pain. The author
concluded that "RFA is a promising new technique which helps in the treatment
of pain from osteolytic metastases and myeloma," with an overall response rate
in the series of greater than 90%.
In a paper titled, "Combination of Radiofrequency Ablation and
Percutaneous Cementoplasty in Painful Bone Metastasis: Experience in
75 Cases," Afshin Gangi, MD, PhD, Professor of Radiology, University Hospital
of Strasbourg, France, presented study results assessing the ability of the
combination of RFA and cementoplasty to manage pain and consolidate
load-bearing bone to prevent fractures. A total of 75 patients were treated
for painful bone metastases by means of percutaneous RF ablation, with a mean
tumor diameter of 4.5 cm. The author reported that "92% of the patients
experienced a notable reduction in pain and an improvement in mobility within
24 to 72 hours."
RSNA and the SIR Foundation Present Week-Long Interventional Oncology
Symposium Featuring Multiple Presentations on Radiofrequency Ablation
The use of RFA to treat several types of cancer was among procedures
highlighted in a press release issued by the SIR Foundation on Monday,
November 28, 2005. Applications of RFA mentioned in the release included: RFA
treatment of liver cancer; RFA treatment of bone tumors; RFA treatment of
renal (kidney) tumors; and RFA treatment of lung cancer. The full text of the
SIR Foundation press release may be found on the Society of Interventional
Radiology website, http://sirweb.org/news/news.shtml .
About RITA Medical Systems, Inc.
RITA Medical Systems develops, manufactures and markets innovative
products for cancer patients including radiofrequency ablation (RFA) systems
for treating cancerous tumors as well as percutaneous vascular and spinal
access systems. The Company's oncology product lines include implantable
ports, some of which feature its proprietary Vortex(R) technology; tunneled
central venous catheters; and safety infusion sets and peripherally inserted
central catheters used primarily in cancer treatment protocols. The product
line also includes the HABIB 4X resection device which coagulates a "surgical
resection plane" and is designed to facilitate a fast dissection in order to
minimize blood loss and blood transfusion during surgery. The proprietary RITA
RFA system uses radiofrequency energy to heat tissue to a high enough
temperature to ablate it or cause cell death. In March 2000, RITA became the
first RFA Company to receive specific FDA clearance for unresectable liver
lesions in addition to its previous general FDA clearance for the ablation of
soft tissue. In October 2002, RITA again became the first company to receive
specific FDA clearance, this time for the palliation of pain associated with
metastatic lesions involving bone. The RITA Medical Systems website is at
www.ritamedical.com.
The statements in this news release related to the efficacy, benefits and
safety of RFA technology, including without limitation physician adoption of
RFA treatment for lung, liver, kidney and bone cancer and other cancers, are
forward-looking statements involving risks and uncertainties that could cause
actual results to differ materially from those in such forward-looking
statements. Such risks and uncertainties include but are not limited to: the
Company's ability to compete with companies with greater resources; the
existence of alternative therapies that could prove to be superior to RFA; the
lack of long-term data regarding the safety and efficacy of its RFA products;
delay of product introductions or modifications as a result of the FDA
regulatory process; and the Company's success in its physician training
efforts. Information regarding these risks and other risks and uncertainties
is included in the Company's filings with the Securities and Exchange
Commission.
SOURCE RITA Medical Systems, Inc.
12/01/2005
CONTACT: investors, Doug Sherk, dsherk@evcgroup.com, or
Jennifer Beugelmans, +1-415-896-6820, or media, Steve DiMattia,
+1-646-277-8706, or sdimattia@evcgroup.com, all of EVC Group, for RITA Medical
Systems, Inc.; or Stephen Pedroff, VP Marketing Communications of RITA Medical
Systems, Inc., +1-510-771-0400, or spedroff@ritamed.com
Web site: http://www.chestjournal.org
Web site: http://sirweb.org/news/news.shtml
Web site: http://www.ritamedical.com
(RITA)