Delcath Systems, Inc. Announces Promising Results from Independent Study on Repeated Hepatic Chemosaturation for Liver Tumors
2024年8月27日 - 5:01AM
ビジネスワイヤ(英語)
Delcath Systems, Inc. (Nasdaq: DCTH) (“Company” or “Delcath”),
an interventional oncology company focused on the treatment of
primary and metastatic liver cancers, today announced the
publication of an independent study conducted by investigators at
the University Hospital of Leipzig, Germany, in the European
Society for Medical Oncology journal of Gastrointestinal Oncology.
The study, titled “Hepatic chemosaturation with melphalan in
patients with primary or secondary liver tumors with or without
extrahepatic tumor manifestation,” highlights the efficacy and
safety of repeated chemosaturation treatments using Delcath’s
CHEMOSAT® Hepatic Delivery System.
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Figure 1: Individual changes in tumor
sizes during CHEMOSAT treatment. (A) Individual changes in tumor
sizes during CHEMOSAT treatment. On the y-axis the change in tumor
size is indicated according to the baseline lesions. (B) Waterfall
plot of changes in the size of target lesions at the end of
observation. Dashed lines are thresholds for hepatic PD, hepatic
SD, hepatic PR and hepatic CR. CR, complete response; HCC,
hepatocellular carcinoma; ICC, intrahepatic cholangiocellular
carcinoma; other, ciliary body melanoma, angiosarcoma, tonsil and
pancreatic carcinoma; PD, progressive disease; PR, partial
response; SD, stable disease; UM, uveal melanoma. (Graphic:
Business Wire)
Key Findings from the Independent Study:
- Patient Population: This retrospective study evaluated
the efficacy of CHEMOSAT in 33 previously treated patients with
unresectable intrahepatic metastases from various cancers: uveal
melanoma (N=19), cholangiocarcinoma (N=8), hepatocellular carcinoma
(N=2), and one patient each with ciliary body melanoma, acinar cell
carcinoma, pancreatic cancer, or tonsil cancer (N=4). In addition
to hepatic metastases, 7 out of 33 patients also had limited
extrahepatic disease, which was found not to significantly impact
overall survival.
- Disease Control Rate: The study reported a disease
control rate (DCR) of 91%, with 30 out of 33 patients experiencing
either objective tumor response or stable disease. Notably, 6
patients (18.2%) achieved complete response (CR) in the liver,
including 5 patients with uveal melanoma and 1 patient with
cholangiocarcinoma, who received a median of 5 treatment
cycles.
- Hepatic Progression-Free Survival: Median hepatic
progression-free survival (hPFS) was 52 weeks across all patients,
with particularly strong outcomes for specific cancers:
- 69 weeks (16 months) median hPFS in patients with uveal
melanoma.
- 38 weeks (8.5 months) median hPFS in patients with
cholangiocarcinoma.
- Importance of Repeated Treatments: The investigators’
approach of using CHEMOSAT in the form of regularly repeated
treatment cycles as clinically indicated (Figure 1), similar to
systemic chemotherapy, resulted in long-term disease control in the
majority of patients and was well tolerated.
- Tolerability and Safety: The safety profile of CHEMOSAT
was consistent with published literature. Most patients experienced
transient hematological adverse events, which were routinely
managed with supportive care. Importantly, no significant liver
damage was reported, even in patients who underwent multiple
treatment cycles. Treatment was discontinued in 2 patients due to
adverse events, and 2 patients withdrew consent during the
treatment period.
Dr. Vojislav Vukovic, Chief Medical Officer of Delcath
Systems, commented, “The results of this independent study
reinforce the potential of our CHEMOSAT Hepatic Delivery System as
an essential tool in the management of primary and secondary liver
tumors, particularly for patients with limited treatment options.
The high rate of disease control observed, even in patients with
extrahepatic tumor spread, underscores the importance of continuing
to explore and refine this treatment approach in larger,
prospective trials.”
The publication is available here.
About Delcath Systems, Inc., HEPZATO KIT and CHEMOSAT
Delcath Systems, Inc. is an interventional oncology company
focused on the treatment of primary and metastatic liver cancers.
The company's proprietary products, HEPZATO KIT™ (HEPZATO
(melphalan) for Injection/Hepatic Delivery System) and CHEMOSAT®
Hepatic Delivery System for Melphalan percutaneous hepatic
perfusion (PHP), are designed to administer high-dose chemotherapy
to the liver while controlling systemic exposure and associated
side effects during a PHP procedure.
In the United States, HEPZATO KIT is considered a combination
drug and device product and is regulated and approved for sale as a
drug by the FDA. HEPZATO KIT is comprised of the chemotherapeutic
drug melphalan and Delcath's proprietary Hepatic Delivery System
(HDS). The HDS is used to isolate the hepatic venous blood from the
systemic circulation while simultaneously filtrating hepatic venous
blood during melphalan infusion and washout. The use of the HDS
results in loco-regional delivery of a relatively high melphalan
dose, which can potentially induce a clinically meaningful tumor
response with minimal hepatotoxicity and reduce systemic exposure.
HEPZATO KIT is approved in the United States as a liver-directed
treatment for adult patients with metastatic uveal melanoma (mUM)
with unresectable hepatic metastases affecting less than 50% of the
liver and no extrahepatic disease, or extrahepatic disease limited
to the bone, lymph nodes, subcutaneous tissues, or lung that is
amenable to resection or radiation. Please see the full Prescribing
Information, including BOXED WARNING for the HEPZATO KIT.
In Europe, the device-only configuration of the HDS is regulated
as a Class III medical device and is approved for sale under the
trade name CHEMOSAT Hepatic Delivery System for Melphalan, or
CHEMOSAT, where it has been used in the conduct of percutaneous
hepatic perfusion procedures at major medical centers to treat a
wide range of cancers of the liver.
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version on businesswire.com: https://www.businesswire.com/news/home/20240826877468/en/
Investor Relations: ICR Westwicke
investorrelations@delcath.com
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