Colon carcinoma

- internistic

  • Profilbild von Prof. Dr. med. Thomas Seufferlein

    Prof. Dr. med. Thomas Seufferlein

    Ärztlicher Direktor der Klinik für Innere Medizin I (Speiseröhre, Magen, Darm, Leber und Niere sowie Stoffwechselerkrankungen) und Sprecher des Darmzentrums

  • Profilbild von Dr. med. Thomas J. Ettrich

    Dr. med. Thomas J. Ettrich

    Oberarzt, Leiter Schwerpunkt GI-Onkologie, Leiter des klinischen Studienzentrums GI-Onkologie

    Schwerpunkte

    Gastrointestinale Onkologie, Klinische Studien

  • Profilbild von Dr. med. Angelika Kestler

    Dr. med. Angelika Kestler

    Funktionsoberärztin, Fachärztin für Innere Medizin und Gastroenterologie, Palliativmedizin, Ärztliche Referentin für GI-Onkologie am CCCU

    Schwerpunkte

    Gastrointestinale Onkologie, Privatambulanz Prof. Seufferlein

- Surgical

  • Profilbild von Prof. Dr. med. Nuh Rahbari, MHBA

    Prof. Dr. med. Nuh Rahbari, MHBA

    Ärztlicher Direktor

  • Profilbild von Prof. Dr. med. Marko Kornmann

    Prof. Dr. med. Marko Kornmann

    Stellv. Ärztlicher Direktor/ Koordinator Viszeral-Onkologisches Zentrum

    Schwerpunkte

    Bereichsleitung Bauchspeicheldrüsen-, Magen- und Speiseröhrenchirurgie

  • Profilbild von Priv.-Doz. Dr. med. Benjamin Müssle, M.Sc.

    Priv.-Doz. Dr. med. Benjamin Müssle, M.Sc.

    Schwerpunkte

    Bereichsleitung Darmchirurgie

- radiooncological

Description of the disease

Colon cancer is the most common cancer in the gastrointestinal tract. Colon carcinoma refers to malignant tumours of the large intestine.

Frequency and age of onset

Malignant bowel tumours account for around 14% of all malignant neoplasms in adults. In Germany, around 27,000 men and 30,000 women are diagnosed with carcinomas of the colon every year.

It is the third most common carcinoma in men and the most common in women. With a mean age of onset of almost 70 years, colon carcinoma is predominantly a disease of older people, with a particularly marked increase after the age of 50.

The vast majority of malignant tumours in the bowel develop in the large intestine, the so-called colon. Around 95% of all bowel tumours are carcinomas (also known as colon carcinoma or adenocarcinoma of the colon). The remaining 5% are neuroendocrine tumours, squamous cell carcinomas, lymphomas and small cell carcinomas.

Colon carcinomas usually develop from polyps of the colon mucosa. Around 64% of carcinomas are found in the sigmoid colon and rectum, 20% in the left colon, 6% in the transverse colon and around 10% in the right colon.

Causes and risk factors

Most colon carcinomas develop from polyps as part of a so-called adenoma-carcinoma sequence over the course of 5-10 years. In addition, there are familial syndromes with an increased risk of carcinoma, which account for around 5-6% of colorectal carcinomas.

Exogenous (external influences): Low physical activity, obesity, possibly dietary factors (red meat, alcohol consumption)

Endogenous (internal influences): Ulcerative colitis, Crohn's disease, colorectal intraepithelial neoplasia = adenomas

Genetic (hereditary): Positive family history (1st degree relatives with colorectal carcinoma (CRC) or adenomas), hereditary (inherited) cancer syndromes.

Signs of illness

As a rule, colon carcinomas rarely cause symptoms in the early stages and are therefore usually discovered by chance. Occasionally, abdominal pain, intestinal discomfort or constant fatigue occur. However, these symptoms are often due to harmless causes. If occult blood is found in the stool as part of a screening examination using a stool test, this leads to a colonoscopy being carried out, which can result in a diagnosis of colon cancer. Visible blood in the stool or a black discolouration of the stool can also be an indication of colon cancer.

Investigations

If colon carcinoma is suspected, various examinations are necessary, e.g. physical examination, laboratory tests (blood), ultrasound examination, colonoscopy and computer tomography (CT). If necessary, further examinations such as X-ray examination, magnetic resonance imaging (MRI) or skeletal scintigraphy may also be required.

Medical history and physical examination

In a detailed discussion, all complaints and previous illnesses (including family hereditary diseases) are asked about and documented. This is followed by a thorough physical examination.

Laboratory tests

Your blood and urine will be analysed. The blood tests provide information about the patient's general condition and certain organ functions. Changes in the blood such as anaemia, changes in blood proteins, an increase in certain enzymes or an increase in blood cell count may indicate tumour disease. One tumour marker for colon carcinoma is the so-called CEA. This marker is particularly important for monitoring the progression of colon cancer. A normal CEA value after colon cancer surgery and an increased CEA value during the course of the disease indicates a recurrence of the colon cancer.

Ultrasound examination (sonography)

Sonography is a painless and radiation-free examination to detect colon cancer metastases in the liver or lymph nodes in the abdominal cavity.

Colonoscopy (colonoscopy)

A colonoscopy is performed to investigate the cause of abdominal complaints or to find a possible source of bleeding in the bowel in the event of anaemia or blood in the stool. During this examination, biopsies can also be taken from conspicuous areas of the intestinal mucosa to clearly identify the colon tumour.

CT colonography ("virtual colonoscopy")

Computed tomography (CT)

Computed tomography is a painless, special X-ray examination (with contrast medium) that illuminates the body layer by layer. This usually allows the size of the tumour and the exact spread of the tumour and any existing metastases, e.g. in the liver, lungs or lymph nodes, to be determined.

Magnetic resonance imaging (MRI)

MRI is not an X-ray examination, but is based on the effects of magnetic fields. However, this examination is only carried out in exceptional cases, e.g. in the case of contrast agent intolerance or impaired kidney function, sometimes in addition to computer tomography.

Skeletal scintigraphy (bone scintigraphy)

By administering a small amount of radioactive substance into the bloodstream, tumour metastases in the bones can be visualised. A special camera recognises the radioactively enriched areas in the diseased bone. This is a gentle examination in which the radiation decays quickly.

Classification and staging

In order to be able to determine the most suitable therapy, the exact extent to which the tumour has spread must be determined using the diagnostics described above before starting therapy, i.e. the tumour stage is determined. The TNM classification is used for this purpose (see table below).

T stands for the size and extent of the primary tumour, N stands for the number of affected regional lymph nodes and M stands for the occurrence and localisation of distant metastases (tumour metastases).

TNM colon carcinomas

Tx

Primary tumour cannot be assessed

T0

No evidence of primary tumour

Tis

Carcinoma in situ

T1

Tumour infiltrates the submucosa

T2

Tumour infiltrates the muscularis propria

T3

Tumour infiltrates the propria muscle into the subserosa or
into non-peritoneal pericolonic or perirectal tissue

T4

Tumour infiltrates directly into other organs or structures
and/or perforates the visceral peritoneum

NX

Neighbouring (regional) lymph nodes cannot be assessed

N0

No evidence of neighbouring lymph node metastases
(at least 12 lymph nodes were examined)

N1

Metastases in 1-3 regional lymph nodes

N2

Metastases in 4 or more regional lymph nodes

MX

Presence of distant metastases cannot be assessed

M0

No evidence of distant metastases

M1

Distant metastases occur most frequently in the liver, lungs
and lymph nodes, less frequently in the brain and skeleton.

 

An exact assessment of the TNM stage is often only possible after tumour surgery.
Two further criteria are decisive for further therapy. Microscopic examination of the tumour tissue provides an indication of the malignancy of the tumour. This involves comparing the similarity of the cancer cells with the organ cells (see table below).

Cell similarity = GRADING

GX

Preparation cannot be assessed histologically

G1

Highly differentiated tumour

G2

Moderately differentiated tumour

G3-4

Poorly differentiated/undifferentiated tumour


On the other hand, it is of decisive importance whether the tumour could be completely removed. The so-called R classification is used for this purpose (see table below).

R = Residual tumour (residual tumour after surgery)

RX

Residual tumour cannot be determined

R0

No residual tumour

R1

Microscopically detected residual tumour

R2

Visible residual tumour

 

The UICC classification is used for the stage-appropriate treatment stratification of patients with colorectal cancer. There is also the Dukes classification:

UICC 2010

TNM system

Stage 0

Tis

N0

M0

Stage I

T1/T2

N0

M0

Stage IIA

T3

N0

M0

Stage IIB/C

T4a/T4b

N0

M0

Stage III

Any T

N1,N2

M0

Stage IV

Any T

Any N

M1

Treatment options

The treatment methods depend on the stage of the tumour. The earlier colon cancer is detected, the more favourable the prognosis for the patient. Whether the tumour has spread to other organs, i.e. whether and in how many organs there are metastases, plays a key role. It is also important how many metastases are found in the affected organ.

Curative (healing) surgery

As a rule, only the earlier stages of the tumour can be cured by surgical therapy. As a rule, an en bloc resection (removal as a whole) of the tumour-bearing section of bowel and the regional lymph drainage area is performed. The mortality rate for this operation is less than 3%, even in older patients. In the event of complications such as intestinal obstruction (ileus) and tumour perforation, etc., the surgical procedure must be adapted, e.g. as an extended en-bloc resection. Local surgical tumour removal (excision) or endoscopic resection is only indicated in the early stages (pT1, G1-G2 without lymph vessel infiltration and with complete removal in healthy tissue). Curative resection of individual distant metastases or liver metastases confined to one lobe of the liver can be discussed and should be performed if possible, as this can significantly improve the prognosis.

Palliative (symptom-relieving) surgery

Approximately 25% of all colorectal cancer patients already have lymph node or distant metastases at the time of diagnosis. In the case of obstructing carcinomas without the possibility of complete resection, a bypass anastomosis or an artificial bowel outlet (anus-praeter anastomosis) is performed if a complete resection of the tumour is not possible.

Metastatic surgery and special local ablative procedures

Curative resection of solitary distant metastases or liver metastases confined to one lobe of the liver is now standard practice. This can reduce symptoms and prolong survival.

Secondary resection after chemotherapy

Even if the size or location of the metastases does not permit primary surgery, in certain cases chemotherapy can be used to reduce the size of the metastases. Due to the high response rates of combination chemotherapy (> 50%; see below), approx. 20%-30% of metastases can be removed secondarily (resectable). In the case of partial remissions, resectability must always be checked in good time as long as metastases are still recognisable.

Local ablative (ablative) procedures

Local ablative procedures such as radiofrequency ablation or laser-induced thermotherapy (LITT) are similarly effective as surgical therapy for solitary distant metastases.

Palliative endoscopic procedures

In the case of narrowing (stenosing) colon carcinomas, if surgery is not possible, the passage can be restored using endoscopic procedures. This may include procedures such as dilatation, argon plasma coagulation, cryotherapy and laser therapy as well as implantation of a metal mesh stent.

Chemotherapy

Cytostatic drugs are intended to kill fast-growing tumour cells in the body. Stage-dependent adjuvant (post-operative) and palliative chemotherapy is a recognised component of the treatment of colon carcinomas. Significant progress has been made in recent years with the introduction of new chemotherapeutic agents. The introduction of antibodies and so-called small molecules, which block the effect of tumour-specific growth factors (e.g. epidermal growth factor (EGF)) or angiogenic cytokines (vascular growth factor (VEGF)), in combination with chemotherapy, can achieve further improvements in therapy.

Systemic chemotherapy should be initiated at an early stage. If successful, the therapy can also be interrupted and resumed if the tumour progresses. Whether a real break or a lighter chemotherapy is given during the "break" is discussed individually with the patient. At the University Hospital, innovative treatment options are available for many types of tumour as part of studies. We are constantly endeavouring to improve the treatment of patients through current studies.
Current studies can be found here LINK.


Palliative radiotherapy

Colon carcinomas are relatively insensitive to radiation. For this reason, radiotherapy is almost only used at an advanced stage to relieve pain, particularly in the case of bone metastases.

Course of the disease

If a recurrence (reappearance of the tumour in the former tumour area) occurs, it should be surgically removed if possible. If metastases have also formed or the recurrent tumour is too large (has grown together with other organs), a decision must be made on a case-by-case basis as to whether surgery or another therapy is appropriate. If the tumour is at an advanced stage, palliative (symptom-relieving) and supportive (supportive) treatment can be carried out.