
Gastrointestinal oncology
Welcome to our Center for Gastrointestinal Oncology in Karlshorst. We offer comprehensive care for gastrointestinal tumor diseases, including prevention, aftercare, diagnostics and drug-based tumor therapy – both for patients with statutory and private insurance.
Our team specializes in the treatment of a variety of cancers of the digestive system:
Esophageal carcinoma
Squamous cell carcinomas of the oesophagus are often caused by chronic damage to the mucous membrane. The main causes include smoking, alcohol consumption, very hot drinks, chemical burns, radiotherapy and achalasia. These factors cause chronic inflammation and mucosal changes that can eventually lead to carcinomas.
Esophageal carcinomas often require multimodal therapy that combines surgery, radiotherapy and chemotherapy. If diagnosed at an early stage, endoscopic resection of the tumor may be sufficient. In locally advanced stages, preoperative (neoadjuvant) chemotherapy and radiotherapy are used to shrink the tumor before surgery and increase the chances of complete removal. After surgery (adjuvant therapy), further treatments are often carried out to eliminate any remaining cancer cells and reduce the risk of recurrence.
Carcinomas of the esophageal junction
Carcinomas of the esophageal junction, also known as adenocarcinomas of the esophago-gastric junction (AEG), often develop due to chronic reflux disease. The reflux of gastric acid leads to mucosal changes known as Barrett’s esophagus1. These changes can develop further and ultimately lead to cancer.
Treatment is similar to that for gastric carcinomas. Superficial carcinomas in early stages can be cured by endoscopic resection. In locally advanced stages, surgical resection is necessary in many cases. In many cases, additional chemotherapy is carried out before and after chemotherapy. Preoperative therapy is used to shrink the tumor and make the operation easier. Postoperative treatment aims to minimize the risk of recurrence and maximize the chances of recovery.
Gastric carcinomas
Gastric carcinomas are often caused by chronic inflammation of the gastric mucosa, which can lead to malignant tumors. The main risk factors include an infection with Helicobacter pylori, an unhealthy diet (especially a diet high in salt and smoke), smoking, alcohol consumption, genetic predisposition and chronic inflammation of the stomach lining (gastritis). Typical symptoms are abdominal pain, nausea, weight loss, loss of appetite and blood in the stool or vomit.
Early diagnosis through procedures such as endoscopy and biopsy are crucial for treatment. In certain cases, early carcinomas can be removed endoscopically and cured without surgery. Otherwise, surgical removal of the tumor is often the primary treatment method. This may involve a total or partial gastrectomy (removal of the stomach), depending on the size and location of the tumor. Chemotherapy is often used in addition to this to reduce the risk of recurrence. Neoadjuvant therapies can shrink the tumor before surgery, while adjuvant therapies fight any remaining cancer cells after surgery. In advanced cases, various combined chemotherapy options are available to control the disease for as long as possible and minimize symptoms. Targeted molecular therapy and immunotherapies are increasingly being used here.
Small intestine carcinomas
Small bowel carcinomas are rare malignant tumors of the small intestine. The main causes include genetic predisposition, chronic inflammatory bowel diseases such as Crohn’s disease, and certain hereditary syndromes such as Lynch syndrome. Risk factors also include diet, smoking and alcohol consumption.
Symptoms can be non-specific and include abdominal pain, weight loss, nausea, vomiting and blood in the stool. Diagnosis is often made using imaging techniques such as CT or MRI scans as well as endoscopy and biopsy.
As long as the disease is localized, a cure can be achieved by surgical removal. Similar to colon cancer, adjuvant chemotherapy is offered in locally advanced cases.
In metastatic disease, chemotherapy can be used to slow the progression of the disease and alleviate symptoms. In some cases, targeted molecular therapies or immunotherapies can also be used.
Colon and rectal carcinomas
Colon and rectal cancers often arise from benign polyps that can develop into malignant tumors. The main risk factors include genetic predisposition, an unhealthy diet, alcohol consumption, tobacco use and obesity. Symptoms include blood in the stool, changes in bowel movements, unexplained weight loss and abdominal pain. Regular screening tests, such as colonoscopy and rectoscopy, are crucial for early diagnosis and treatment. Early detection and treatment significantly improve the chances of recovery.
Colon and rectal carcinomas can usually be removed endoscopically as long as they are limited to the surface of the bowel. Otherwise, surgical removal is the treatment of choice as long as the disease is localized. In certain stages of the disease, adjuvant chemotherapy is recommended after surgery to minimize the risk of recurrence. In advanced stages, neoadjuvant chemotherapy or radiotherapy may also be used to shrink the tumor before surgery.
In the metastatic situation, differentiated targeted molecular or immunotherapies are now available, which can be individually coordinated in combination with chemotherapy or in some cases even as the sole treatment.
Pancreatic carcinomas
Pancreatic carcinomas, also known as pancreatic cancer, often develop due to genetic predisposition, chronic inflammation of the pancreas (pancreatitis), smoking, obesity and diabetes. The disease can also develop due to a family history of pancreatic cancer. Typical symptoms include unintentional weight loss, abdominal and back pain, jaundice, loss of appetite and nausea.
Early diagnosis is often difficult, as pancreatic carcinomas are often asymptomatic in the early stages. Imaging procedures such as CT or MRI scans as well as endoscopic ultrasound examinations and biopsies are crucial for the diagnosis. Treatment options include surgery, chemotherapy and radiotherapy. Early detection and treatment significantly improve the chances of recovery, although the prognosis for pancreatic cancer is often serious.
Pancreatic carcinomas are often removed surgically. Surgery may include a Whipple procedure (pancreaticoduodenectomy) or a distal pancreatectomy, depending on the location of the tumor. In addition to surgery, chemotherapy is often used to minimize the risk of recurrence and improve quality of life.
In cases where surgery is not possible, palliative chemotherapy can help to alleviate symptoms and prolong life. In addition, targeted therapies or immunotherapies are sometimes used for advanced tumors.
Bile duct carcinomas
Bile duct carcinomas, also known as cholangiocarcinomas, are rare malignant tumors of the bile ducts. The main causes include chronic inflammation of the bile ducts, in particular primary sclerosing cholangitis, infections with hepatitis B and C viruses and certain parasites in Asia. Other risk factors include genetic predisposition, liver cirrhosis and certain toxic substances such as nicotine and alcohol.
Typical symptoms are jaundice, unintentional weight loss, loss of appetite and abdominal pain. Diagnosis is based on a combination of blood tests, imaging procedures and endoscopy.
The main treatment method for bile duct carcinomas is surgical removal of the tumor. In cases where surgery is not possible, local ablative measures and chemotherapy can be used. In advanced stages, targeted therapies aimed at molecular changes in the tumor are also available
Gallbladder carcinomas
Gallbladder carcinomas, also known as gallbladder cancer, are malignant tumors of the gallbladder. The main causes include chronic inflammation of the gallbladder, often caused by gallstones, as well as certain chronic infections. Other risk factors include genetic predisposition, obesity, an unhealthy diet and certain chemical exposures.
Typical symptoms include jaundice, upper abdominal pain, nausea, vomiting and unexplained weight loss. Diagnosis is often made using imaging techniques such as ultrasound, CT or MRI scans as well as endoscopy and biopsy.
Treatment options usually include surgical removal of the gallbladder and surrounding tissue, often supplemented by chemotherapy or radiotherapy, depending on the stage of the disease. Early detection and treatment are crucial to improve the chances of recovery.
Small intestine carcinomas
Small bowel carcinomas are rare malignant tumors of the small intestine. The main causes include genetic predisposition, chronic inflammatory bowel diseases such as Crohn’s disease, and certain hereditary syndromes such as Lynch syndrome. Risk factors also include diet, smoking and alcohol consumption.
Symptoms can be non-specific and include abdominal pain, weight loss, nausea, vomiting and blood in the stool. Diagnosis is often made using imaging techniques such as CT or MRI scans as well as endoscopy and biopsy.
As long as the disease is localized, a cure can be achieved by surgical removal. Similar to colon cancer, adjuvant chemotherapy is offered in locally advanced cases.
In metastatic disease, chemotherapy can be used to slow the progression of the disease and alleviate symptoms. In some cases, targeted molecular therapies or immunotherapies can also be used.
Gallbladder carcinomas
Gallbladder carcinomas, also known as gallbladder cancer, are malignant tumors of the gallbladder. The main causes include chronic inflammation of the gallbladder, often caused by gallstones, as well as certain chronic infections. Other risk factors include genetic predisposition, obesity, an unhealthy diet and certain chemical exposures.
Typical symptoms include jaundice, upper abdominal pain, nausea, vomiting and unexplained weight loss. Diagnosis is often made using imaging techniques such as ultrasound, CT or MRI scans as well as endoscopy and biopsy.
Treatment options usually include surgical removal of the gallbladder and surrounding tissue, often supplemented by chemotherapy or radiotherapy, depending on the stage of the disease. Early detection and treatment are crucial to improve the chances of recovery.
Outpatient specialty care (ASV)
Our practice participates in outpatient specialty care (ASV) in cooperation with renowned clinics:
- the Elisabeth Herzberge Clinic,
- the Vivantes Klinikum im Friedrichshain
- DTZ Berlin-Friedrichshain
- and the DRK Klinikum Köpenick.
These collaborations enable comprehensive and specialized care for patients with gastrointestinal tumours who have statutory health insurance. Interdisciplinary cooperation and access to state-of-the-art technology and specialists guarantee optimal care. Privately insured patients benefit from this care structure in the same way.
Our team is at your side with extensive experience and state-of-the-art technology to provide you with the best possible care and coordinate the treatment path tailored to your individual needs. For further information and a personal consultation, please arrange a “Gastrointestinal Oncology Consultation”.

You are currently viewing a placeholder content from Google Maps. To access the actual content, click the button below. Please note that doing so will share data with third-party providers. More Information
Specialist practice for gastroenterology Karlshorst
Ehrenfelsstraße 47,
10318 Berlin
Phone: 030 5293310
karlshorst@gastroenterologie-
brunk.de
Opening hours
Mon., Tue. & Wed.: 07:30 – 15:30
Thurs.: 07:30 – 17:30
Fri.: 07:30 – 15:30
or by appointment!
Closing times: 23.12.2024 and 02.01.2025
Specialist practice for gastroenterology at Wittenbergplatz
Ansbacher Straße 13,
10787 Berlin
Phone: 030 21 00 57 20
wittenbergplatz@gastroenterologie-
brunk.de
Opening hours
Mon.: 07:30 – 15:00
Tue & Wed: 07:30 – 15:00
Thurs.: 08:00 – 15:30
Fri.: closed
Closing times: 23.12.2024 and 02.01.2025
