Ionizing radiation activates the translation of the gene coding for transforming growth factor-β (TGF-β) in the intestines. TGF-β is a potent fibrogenic and proinflammatory cytokine, leading to hyperplasia of connective tissue mast cells and leukocyte migration into the intestinal wall. TGF-β promotes intestinal fibrosis by stimulating the expression of collagen and fibronectin genes and the chemotaxis of fibroblasts. The extracellular matrix of the intestine is also increased as TGF-β inhibits its degradation. The increased expression of TGF-β is especially enhanced in areas with histopathologic changes consistent with radiation damage: areas with mucosal ulceration, mucosal and serosal thickening, inflammatory cell infiltrates, and vascular sclerosis.^3,⁴ TGF-β exists in three isoforms: TGF-β1, TGF- β2, and TGF- β3. All three isoforms are overexpressed in the early postradiation phase. However, only isoform β1 remains elevated six months after radiation exposure. In the first 2 weeks after radiation, TGF-β1 messenger RNA is increased in epithelial cells, fibroblasts of the submucosa and subserosa, vascular endothelial cells, and smooth muscle cells of the intestinal wall. However, at 26 weeks, the expression of TGF-β1 of epithelial cells returns to baseline level but TGF-β1 expression remains elevated in vascular endothelial cells, fibroblasts, and smooth muscle cells.⁵ Compared with control mouse intestine, the TGF-β1 immunoreactivity or overexpression is substantially increased in areas of radiation-induced acute and late bowel injury.^6,⁷ In addition, pathologic examination of bowel specimens from patients undergoing surgery for radiation enteropathy showed an increased TGF-β in areas with vascular sclerosis and fibrotic areas of the serosa and muscularis propria as compared with patients who have surgery for other causes.⁸ Neutralizing antibodies to TGF-β and gene therapy using decorin (a natural TGF-β inhibitor) have been shown to suppress or reverse fibrosis in preclinical models.⁹

Epidermal growth factors, interleukins, and tumor necrosis factors are also being investigated for their effects in chronic radiation injury.¹⁰ Another cytokine implicated in the development of radiation injury is connective tissue growth factor (CTGF). The CTGF expression is increased in intestinal radiation fibrosis associated with chronic radiation injury.¹¹ CTGF is found commonly in the extracellular region surrounding the area of active fibrosis or neovascularization. TGF-β1 may induce CTGF, which in turn functions as a mediator of intestinal radiation fibrosis by sustaining the activation of fibrogenesis in the irradiated gastrointestinal tract. Mechanisms underlying the pathogenesis of radiation-induced gastrointestinal damage remain an active area of investigation.

ESOPHAGUS

INCIDENCE AND CLINICAL FEATURES

Early and late injury of the esophagus often occurs following irradiation of malignances of the thorax and upper abdomen (e.g., esophageal/gastroesophageal junctional carcinomas and lung carcinomas). The normal esophageal mucosa undergoes continuous renewal or turnover. Acute esophageal side effects are believed to be primarily related to radiation damage to the basal epithelial layer, manifested histologically by vacuolization, resulting in epithelial thinning followed by denudation (Fig. 39-1). These changes manifest clinically as dysphagia, odynophagia, and substernal discomfort, usually occurring within two to three weeks following initiation of radiation therapy. Patients may describe a sudden, sharp, severe chest pain radiating to the back. As treatment progresses, pain may become constant and may not necessarily be related to swallowing. The symptoms may be confused with Candida esophagitis, which may occur in conjunction with radiation esophagitis. Concurrent chemotherapy exacerbates these toxic effects. Endoscopically, mucositis and ulceration may be observed. Perforation and bleeding are rare in the acute phase.¹² After treatment completion, basal proliferation returns and regeneration occurs, usually within three weeks.¹³

Figure 39-1. Acute radiation-induced esophageal injury. Acute esophageal ulceration with abundant fibroblasts is seen. (Hematoxylin and eosin, ×400.)

Following recovery from acute injury, late effects such as benign stricture, persistent ulceration and fistula formation may occur months to years following treatment. These effects are believed primarily due to inflammation and scar formation within the esophageal muscle. The connective tissues surrounding the esophagus may also exhibit severe fibrosis over time.¹⁴ Small vessel telangiectasias may be seen endoscopically. Histologic studies of the esophagus in previously irradiated patients have demonstrated epithelial thickening, chronic inflammation, fibrosis of the submucosa and muscularis propria, and (rarely) chronic ulceration. Complete epithelial recovery from radiation effects may take 3 to 24 months.¹⁵ Late effects often manifest as dysphagia due to stricture as well as altered motility due to fibrosis or muscular damage, possibly with accompanying nerve injury. Fistula formation is unusual and radiation dose dependent. Barium swallow examination may show strictures as well as disruption of peristalsis at the level of the irradiated esophagus with repetitive and nonperistaltic waves above and below the irradiated region. Abnormal peristalsis has been reported at 1 to 3 months following treatment completion, whereas most strictures occur 4 to 8 months following treatment completion. Late effects are usually not seen until 3 months following completion of radiation therapy, with a median time to onset of 6 months in some series.^16,¹⁷

Development of radiation-related late complications is dose related. The TD_5/5 (i.e., dose at which 5% of patients will develop complications at five years) has been estimated to be 60 Gy when one third of the length of the esophagus is irradiated.¹⁸ Other series have reported complication rates of less than 1% to 30% with doses of approximately 60 Gy, with benign stricture as the primary complication. Seaman and Ackerman treated patients to doses of 60 to 75 Gy, resulting in severe esophagitis and stricture formation in some patients. They concluded that the upper limit of dose tolerance of the esophagus was 60 Gy given at 10 Gy per week.¹⁹ Other studies reported that patients receiving 60 Gy had late complication rates of 1.2% to 18%. With contemporary radiation doses of 50 Gy, late complication rates have been observed in 2% of patients or less.^20,²¹

Brachytherapy (the temporary insertion of a radioactive source into or adjacent to a tumor) has also been used as a technique for radiation dose escalation in esophageal cancer. Gaspar and colleagues reported the results of a phase I/II study examining the role of brachytherapy in addition to external beam radiation therapy in the treatment of esophageal cancer. The one-year actuarial fistula formation rate was 18%, and the authors recommended caution in the use of this approach, particularly in conjunction with concurrent chemotherapy.²² In contrast, other authors have reported much lower rates of fistula formation with brachytherapy.²³ The length of esophagus being irradiated may not closely correlate with the incidence of esophagitis after radiotherapy.^24,²⁵ However, the intensity of cancer treatment such as use of concurrent chemotherapy with radiation therapy increases the rate of acute esophagitis.²⁶ Maguire and colleagues evaluated 91 patients treated with radiation therapy for non–small cell lung cancer and found that the percent esophageal volume and surface area treated to greater than 50 Gy predicted late esophageal toxicity. Patients who had preexisting gastroesophageal reflux disease and esophageal erosions secondary to tumor were at increased risk for late toxicity. Hyperfractionation (multiple daily radiation treatments) was also associated with increased acute toxicity.²⁷ Singh and associates studied patients with non–small cell lung cancer who received conformal daily radiation therapy with or without concurrent chemotherapy; they found that a maximal esophageal “point” dose of 69 Gy (radiation therapy alone) and 58 Gy (with concurrent chemotherapy) predicted significant toxicity. Twenty-six percent of patients receiving concurrent chemoradiotherapy developed grade 3 or higher esophageal toxicity, whereas only 1.3% of patients who received radiation therapy alone experienced this degree of toxicity.²⁸ Ahn and colleagues found that the most powerful predictor of late esophageal toxicity in 254 patients treated for non–small cell lung cancer was the severity of acute esophageal toxicity. Severe acute toxicity was predicted by the use of twice daily radiation, older age, increasing nodal stage and a variety of dosimetric parameters. The overall incidence of late toxicity was 7%, with a median and maximal time to onset of 5 and 40 months, respectively.²⁹ The Radiation Therapy Oncology Group, using standard radiation therapy techniques, reported grade 3 or higher acute esophageal toxicity in 34% of patients treated with concurrent hyperfractionated radiation therapy and chemotherapy versus 1.3% of patients treated with standard thoracic radiotherapy alone.³⁰ Based on these and other data, it is clear that the addition of concurrent chemotherapy to radiation therapy increases the incidence of esophageal toxicity.

TREATMENT AND PREVENTION

The treatment and prevention of radiation-induced esophagitis have come under increased attention with the use of aggressive combination chemotherapy and radiation therapy regimens. The treatment of acute esophagitis is based on the grade of symptoms experienced by the patient. Treatment interruptions may ease the symptoms of acute esophagitis, but may also compromise the patient’s cancer treatment. Treatment interruption is reserved for severe cases. The management of acute esophagitis usually includes symptomatic management such as topical anesthetics (including viscous lidocaine-based regimens), oral analgesics (including anti-inflammatory agents and narcotics), gastric antisecretory drugs (histamine [H₂] blockers, proton pump inhibitors), promotility agents (such as metoclopramide), and treatment of superimposed infection (candidiasis). Dietary modification, including bland foods as well as pureed or soft foods and soups, can help patients maintain food and liquid intake. Other modifications include avoidance of smoking, alcohol, coffee, spicy or acidic foods or liquids, chips, crackers, fatty foods, and indigestible foods. A study of dietary modifications and pharmacologic prophylaxis for radiation-induced esophagitis reported decreased toxicity and fewer treatment interruptions. It was recommended to drink between meals and to eat six smaller meals per day, consisting of semisolid food, soup, high-calorie supplements, purees, puddings, milk, and soft breads.³¹ Additionally, ingestion of hot or cold foods should be avoided if possible; instead foods and liquids should be at room temperature. In severe cases, feeding tube placement may be required.

Radioprotective chemical agents have been investigated as a means of mitigating radiation-induced normal tissue toxicity. The best-studied of these is amifostine, an organic thiophosphate. This agent is a scavenger of free radicals and serves as an alternative target to nucleic acids for alkylating or platinum agents.³² In one trial, patients treated with chemotherapy and radiation therapy for non–small cell lung cancer were randomized to receive amifostine or no drug. Amifostine did not significantly reduce grade 3 or higher esophagitis in these patients. However, patient self-assessments suggested a significantly lower incidence of acute esophagitis in those who received amifostine.³³ Other trials have demonstrated a protective effect,^34,³⁵ whereas others have not confirmed this.³⁶ Larger, randomized and placebo-controlled trials are needed to determine the ultimate efficacy of amifostine in preventing radiation injury of the esophagus.

The management of late esophageal radiation stricture consists of endoscopic dilatation (often serially), usually resulting in symptomatic improvement. Additionally, long-term use of gastric antisecretory drugs as well as prokinetic agents such as metoclopramide have been recommended to decrease gastroesophageal (GE) reflux effects. Dilatations in advanced stricture can cause esophageal rupture and therefore their use should be approached cautiously. Uncommonly, tube feedings may be required for patients with significant weight loss or for those only able to take in liquids. Surgical intervention may be required for patients who develop perforation or fistula.

Finally, it is important to note that the clinical symptoms associated with late radiation injury are often difficult to distinguish from those caused by recurrent (or new) cancer. Therefore, patients with strictures or ulcerations should also be evaluated to differentiate chronic radiation changes from cancer recurrence.

STOMACH

INCIDENCE AND CLINICAL FEATURES

The stomach may be damaged following irradiation of the upper abdomen for cancer, including esophageal-GE junctional, gastric, and pancreatic carcinomas. Radiation to the stomach in animals using a very high single dose of irradiation results in erosive and ulcerative gastritis. A slightly lower single dose (23 Gy) results in gastric dilatation and gastroparesis, with replacement of the normal gastric mucosa by hyperkeratinized squamous epithelium. With even lower doses, gastric obstruction occurring months after irradiation was observed, with an atrophic gastric mucosa and intestinal metaplasia seen in surviving animals.³⁷

Studies in which serial gastric biopsies were obtained following irradiation of patients for peptic ulcer disease noted coagulation necrosis of chief and parietal cells with mucosal thinning, edema, and chronic inflammatory infiltration.^17,³⁸ In addition, gastric acid production decreased after relatively low doses of gastric irradiation. In the past, radiotherapy had been used to decrease acid production in patients with peptic ulcer disease. Even with a relatively low dose of 18 Gy delivered in 10 fractions, approximately 40% of ulcer patients had a 50% reduction in gastric acid secretion that lasted for a year or more.³⁹

Clinically, radiation-induced gastritis may occur within a week of starting radiotherapy, with microscopic changes including edema, hemorrhage, and exudation. Histologic changes may also include disappearance of cytoplasmic details and granules in parietal and chief cells as early as one week into therapy. Cell damage and subsequent cell death are often seen first in the depths of glands, followed by thinning of the gastric mucosa.⁴⁰ Additional mucosal changes include deepening of the glandular pits and proliferation of cells in the glandular neck. Loss of glandular architecture and thickening of the mucosa can be seen by the third week of radiotherapy. Approximately three weeks after completing radiotherapy, histologic recovery may be seen. Signs of recovery of early radiation injury to the stomach include re-epithelialization and fibrosis.

Symptoms of acute radiation injury of the stomach consist primarily of nausea and vomiting, dyspepsia, anorexia, abdominal pain, and malaise. These are more common with the concurrent administration of chemotherapy. Radiation-induced nausea and vomiting may occur within the first 24 hours following treatment. It is estimated that approximately half of patients receiving upper abdominal radiation will experience emesis within two to three weeks following initiation of irradiation.⁴¹

Late effects of gastric irradiation have been classified into four categories: (1) acute ulceration (occurring shortly after completion of radiation therapy); (2) gastritis with smoothened mucosal folds and mucosal atrophy on endoscopy accompanied by radiographic evidence of antral stenosis (1 to 12 months following irradiation) (see Chapter 51); (3) dyspepsia, consisting of vague gastric symptoms without obvious clinical correlate (6 months to four years following irradiation); and (4) late ulceration (averaging 5 months after irradiation).^17,⁴² The TD_5/5 for treatment of the entire stomach has been estimated to be 50 Gy. Large studies of upper abdominal irradiation have suggested that prior abdominal surgery as well as using a higher radiation dose per fraction of radiation may increase the risk of late effects.⁴³ Studies from Walter Reed Army Medical Center delivering abdominal radiation using now antiquated techniques in testicular cancer patients have suggested that higher radiation doses lead to an increasing risk of late ulceration and perforation, with ulceration occurring in approximately 6% of patients treated to 45 to 50 Gy, 10% of patients treated to 50 to 60 Gy, and 38% of patients treated to greater than 60 Gy. No ulceration was seen in patients receiving less than 45 Gy. In this series, symptomatic gastritis occurred approximately 2 months following radiation completion, with ulcer formation occurring at a median of 5 months. Six of 233 patients (3%) required surgery for ulcer hemorrhage or pain related to ulcer disease, almost all of whom had received doses of greater than 50 Gy.^17,⁴⁵ Other studies of patients treated with radiation therapy for Hodgkin’s lymphoma or for testicular, gastric, or cervical cancer have established tolerance limits for gastric irradiation.⁴³^–⁴⁶ These studies delivered doses of 40 to 60 Gy. Patients who received doses greater than 50 Gy experienced gastric ulceration and gastric ulcer–associated perforation at rates of 15% and 10%, respectively. If indicated, the dose to the entire stomach with conventionally administered radiation therapy is limited to 45 to 50 Gy, with an estimated 5% to 10% risk of severe radiation toxicity. Where appropriate, reduced field boosts can be given to treat to doses up to 55 Gy with acceptable toxicity.

As in the esophagus, combining chemotherapy with radiation therapy decreases the tolerance of the gastric mucosa to radiation therapy. 5-Fluorouracil (5-FU) is the most common chemotherapy agent delivered concurrently with radiation therapy in the management of gastrointestinal tumors. This agent can be given in an adjuvant or neoadjuvant setting or as “definitive” therapy for gastroesophageal junction, gastric, pancreatic and biliary cancers. 5-FU is a radiation sensitizer, but has historically been given safely with radiation therapy at doses of 45 to 50 Gy without substantial increases in toxicity. Newer systemic agents have been shown to increase acute gastric toxicity when delivered with radiotherapy, including taxanes, gemcitabine, and epidermal growth factor inhibitors. These regimens remain the subject of investigation in the treatment of abdominal malignancies.

TREATMENT AND PREVENTION

Acute symptoms of gastric radiation in toxicity are treated with antiemetics (5-hydroxytryptamine-3 [5-HT₃] antagonists, phenothiazines, metoclopramide, glucocorticoids, benzodiazepines, antihistamines, or anticholinergics), as well as consumption of a light meal prior to delivery of radiation therapy. Randomized trials of prophylactic 5-HT₃ inhibitors have shown efficacy compared with placebo in preventing radiation-induced nausea and vomiting.⁴⁷ A randomized trial of 211 patients receiving upper abdominal radiation compared the 5-HT₃ inhibitor ondansetron given twice daily, with or without dexamethasone delivered daily for the first five fractions of treatment. Patients receiving dexamethasone showed a trend toward improved complete control of nausea (50% versus 38%) and significant improvement in complete control over emesis. The authors concluded that the addition of dexamethasone resulted in modest improvement in protection against radiation-induced emesis.⁴⁸ Narcotic and non-narcotic agents are often used for pain. Additionally, it is generally recommended that patients be placed on antacid medications, including proton pump inhibitors. Careful nutritional support along with antiemetic therapy is essential for patients undergoing radiotherapy to the abdomen. Acute symptoms generally resolve within one to two weeks following completion of radiation therapy.

Late gastritis-related symptoms are often treated with antacids (H₂ antagonists, proton pump inhibitors, sucralfate, and so on). These may be used on a long-term basis to avoid late ulceration. With more severe complications of bleeding, ulceration, gastric outlet obstruction, fistula formation, or perforation, patients may require endoscopic therapeutic approaches or rarely surgical intervention with partial gastrectomy.

SMALL INTESTINE

Small bowel injury, or radiation enteritis, is the primary treatment-limiting toxicity in the radiotherapeutic management of abdominal and pelvic malignancies. The small bowel can be damaged during radiation treatment of malignances of the stomach, pancreas, rectum, and anus, as well as during treatment of gynecologic malignancies. The first case of radiation enteropathy was described in 1897.⁴⁹

INCIDENCE AND CLINICAL FEATURES

The epithelium of the gastrointestinal tract has a high proliferative rate, making it susceptible to radiation- and chemotherapy-induced mucositis. The intestinal lining is normally replaced every three to five days, reflecting this high cellular turnover rate. Irradiation of intestinal mucosa primarily affects the clonogenic intestinal stem cells within the crypts of Lieberkühn (cells that provide, via self-replication and eventual maturation, replacement cells in the intestinal villi). Stem cell damage, either as a primary result of radiation damage or as a result of radiation-induced microvascular damage, leads to a decrease in cellular reserves for the intestinal villi, resulting in mucosal denudement, shortened villi, and decreased absorptive area, with associated intestinal inflammation and edema. Histologic changes are seen within hours of irradiation. Within two to four weeks, an infiltration of leukocytes with crypt abscess (microabscess) formation can be seen (Fig. 39-2). Ulceration may also occur. This acute injury can result in impaired absorption of fats, carbohydrates, proteins, bile salts, and vitamin B₁₂, with associated loss of water, electrolytes, and protein. Additionally, impaired ileal bile salt absorption increases loads of conjugated bile salts entering the colon, which are in turn deconjugated by colonic bacteria, resulting in intraluminal water retention with resultant diarrhea. Furthermore, impaired digestion of lactose may occur following radiation, leading to increased bacterial fermentation with associated flatulence, distention, and diarrhea, possibly accompanied by bacterial overgrowth. There is also evidence of acutely altered gut motility following radiation therapy.⁵⁰

Figure 39-2. Microabscesses and radiation-related fibroblasts. Submucosal reaction shows large, bizarre radiation fibroblasts that have both cytomegaly and nucleomegaly. Smooth muscle cells also have reactive changes. Microabscesses composed of excess neutrophils infiltrate the stroma. (Hematoxylin and eosin, ×400.)

(Courtesy Dr. Robin Amirkahn, Dallas, Tex.)

Patients with acute radiation enteritis experience diarrhea, abdominal cramping or pain, nausea and vomiting, anorexia, and malaise. Radiation-induced diarrhea often appears during the third week of a fractionated radiation course, with reported rates of 20% to 70%.⁵¹ Acute radiation enteropathy with diarrhea may be seen in some patients after delivery of doses of 18 to 22 Gy using conventional fractionation, and in most patients receiving doses of 40 Gy. The symptoms and pathologic findings typically subside and spontaneously disappear two to six weeks following completion of radiation therapy.⁵² However, growing evidence suggests that patients who develop acute small intestine toxicity may be at higher risk for chronic effects.⁵³

Histologic changes of chronic toxicity to the small intestine include progressive occlusive vasculopathy with foam cell invasion of the intima and hyaline thickening of the arteriolar walls, as well as collagen deposition and fibrosis, often in the submucosal layer of the bowel wall. The small bowel becomes thickened with development of telangiectasias, whereas the vessel walls of small arterioles are obliterated, causing ischemia (Fig. 39-3).⁵⁴ As the vasculopathy progresses, mucosal ulceration, necrosis, and occasionally perforation of the intestinal wall can be seen, resulting in fistula and abscess formation. Lymphatic damage results in constriction of the lymphatic channels, which contributes to mucosal edema and inflammation.⁵⁵ Histologically, the mucosa atrophies, with atypical hyperplastic glands and intestinal wall fibrosis (Fig. 39-4).¹⁵ As the ulcers heal, there can be fibrosis with narrowing of the intestinal lumen with subsequent stricture formation and even obstruction with dilatation of the proximal bowel. Bacterial overgrowth may be an indirect complication arising from stasis in a dilated loop of bowel proximal to the stricture. Although the affected segments of intestine and serosa appear thickened with areas of telangiectasias,⁵⁶ it should be noted that even if the gut appears normal, patients can still be at risk of spontaneous perforation.⁵⁷

Figure 39-3. Submucosal arteriole in chronic radiation enteropathy. Radiation-induced changes include thickening of vessel walls and subintimal hydropic change and fibrosis. Vessel wall thickening results in luminal narrowing/occlusion and subsequent tissue ischemia. (Hematoxylin and eosin, ×200.)

(Courtesy Dr. Robin Amirkahn, Dallas, Tex.)

Figure 39-4. Small intestinal submucosal fibrosis following radiation therapy. The patient presented with small intestinal obstruction due to this stricture. (Hematoxylin and eosin, ×40.)

(Courtesy Dr. Robin Amirkahn, Dallas, Tex.)

Chronic radiation enteritis can cause significant morbidity. This complication tends to be progressive, with an onset at least 6 months after radiotherapy. Late radiation injury to the small intestine occurs at a median of 8 to 12 months following radiation therapy, though it can appear years later.¹⁷ There are numerous clinical manifestations of the chronic phase of radiation enteritis (Table 39-1). These include malabsorption and diarrhea, with more rapid transit times occurring in the affected bowel. Rarely, chronic malnutrition may develop, resulting in anemia and hypoalbuminemia. There can be bleeding from ulceration and pain and bloating from strictures, as well as fevers from abscess. Fibrosis and vasculitis of the bowel may lead to dysmotility, stricture, and malabsorption.^58,⁵⁹ Malabsorption and other complications may require surgical intervention and parenteral alimentation (discussed in Chapters 4 and 5 and following). Patients with severe chronic radiation enteritis have a poor long-term prognosis with a mortality rate of approximately 10%.⁶⁰^–⁶⁶ The overall incidence of chronic radiation enteritis has not been precisely defined. Retrospective series suggest an incidence of 5% to 15%; however, these studies often include a large number of patients who were lost to follow-up or died between the end of radiation therapy and the completion of the study. A review of randomized trials of adjuvant radiation therapy for rectal cancer shows severe long-term complications as low as 1.2% and as high as 15%.⁶⁷ In older series of radiotherapy for abdominal cancers, symptoms of chronic bowel dysfunction were present in many patients, although such symptoms are often multifactorial and influenced by other treatment modalities including surgery and chemotherapy.^68,⁶⁹ However, it appears that advances in radiation therapy treatment techniques have reduced chronic small intestinal toxicity rates.

Table 39-1 Clinical Complications of Chronic Radiation Enteritis or Proctitis *

COMPLICATION	LESION(S)	SYMPTOMS
Obstruction	Stricture	Constipation, nausea, vomiting, postprandial abdominal pain
Infection	Abscess	Abdominal pain, fever, chills, sepsis, peritonitis
Fistulization	Fistula	Fecal, vaginal, or bladder discharge; pneumaturia
Bleeding	Ulceration	Rectal pain, tenesmus, rectal bleeding, anemia
Malabsorption	Small bowel damage	Diarrhea, steatorrhea, weight loss, malnutrition, cachexia

* From Girvent M, Carlson GL, Anderson I, et al: Intestinal failure after surgery for complicated radiation enteritis. Ann R Coll Surg Engl 2000; 82:198.

Certain factors have been found to predispose patients to radiation toxicity to the small intestine. Women, older patients, and thin patients may have a larger amount of small bowel in the pelvic cul-de-sac, which can increase the probability of radiation injury in the treatment of pelvic malignancies.⁷⁰ Patients with a history of pelvic inflammatory disease or endometriosis also appear to be at higher risk of radiation complications.^71,⁷² Patients who have had previous abdominal surgery can develop adhesions that decrease the mobility of the small bowel, thereby allowing it to be consistently exposed to fractionated radiation therapy.^73,⁷⁴ In addition, patients with prior pelvic surgery may have an increase in the amount of small bowel within the pelvis, allowing increased exposure during pelvic irradiation. In a series published by Eifel and associates, the risk of small bowel complications was significantly higher in women who had undergone a previous laparotomy.⁷⁵ With modern treatment approaches (allowing direct visualization of the volume of bowel in treatment field) and use of improved treatment techniques (discussed later), as well as a shift toward neoadjuvant approaches, this risk factor may not be as relevant as in prior years. Patients with diabetes, hypertension, and cardiovascular disease also have an increased risk of pre-existing vascular damage or occlusion.⁷⁶ These comorbid conditions are compounded by the pathologic changes of chronic radiation injury, which include vasculopathy and ischemia, predisposing these patients to radiation-related small bowel toxicity. Patients with collagen vascular disease and inflammatory bowel disease also have a higher risk of acute as well as chronic radiation-induced injury. Patients with these diseases may have pathologic changes which include transmural fibrosis, collagen deposition, and inflammatory infiltration of the mucosa. The late effects induced by radiation therapy to the small bowel are likely additive to these preexisting changes, and studies have shown that these patients have a lower gastrointestinal tolerance to radiation therapy.⁷⁷^–⁷⁹ Patients whose inflammatory bowel disease or nonmalignant systemic disease is quiescent or well controlled appear to fare better than patients with active disease.

Studies have also addressed the effect of radiation dose on occurrence of small bowel toxicity. Volume of the treatment field, volume of irradiated small bowel, total radiation dose, fraction size, treatment time, and treatment technique all influence small bowel tolerance. The TD_5/5 for small volumes of small bowel has been estimated to be 50 Gy. Patients can generally receive 45 to 50 Gy in 1.8 to 2 Gy daily fractions to a pelvic field without a significant rate of toxicity.⁸⁰ For postoperative patients, radiation to 45 to 50 Gy in five weeks is associated with an approximate 5% incidence of small bowel obstruction requiring surgery, whereas at doses greater than 50 Gy, the incidence rises to as high as 25% to 50%.⁷⁰ Doses greater than 2 Gy per fraction in the postoperative setting also increase the risk of toxicity.⁸¹ At radiation doses of 70 Gy or greater, the incidence of toxicity rises precipitously.⁸² A study of different treatment techniques to minimize the effect of pelvic radiation on the small bowel showed that irradiating smaller volumes of bowel yielded less toxicity.⁸³ In addition, treating patients in the prone position with external compression and bladder distention decreased side effects, likely from exclusion of portions of the small bowel from the radiation field. Another study treating postoperative patients with pelvic radiation therapy noted less small bowel toxicity by placing patients in the decubitus position.⁸⁴ Studies have also analyzed dose-volume parameters associated with acute small bowel toxicity in patients undergoing treatment with 5-FU–based chemoradiation therapy for rectal cancer.^85,⁸⁶ These found strong correlations between acute toxicity and the amount of small bowel irradiated at each dose level analyzed. Another analysis evaluating rectal cancer patients treated preoperatively with chemoradiotherapy also showed a strong correlation between the occurrence of severe diarrhea and irradiated small bowel volume, surmising that limiting the volume of small bowel receiving greater than 15 Gy may significantly improve treatment tolerance.⁸⁷ These and other studies imply that attention to detail in radiation planning with the use of modern treatment techniques are important considerations in patient treatment.

The combination of radiation and chemotherapy (e.g., 5-FU) increases the risk of small bowel toxicity. In a randomized trial delivering 40 to 48 Gy using parallel, opposed fields to patients with rectal cancer, the incidence of severe small bowel complications was significantly higher in patients who received chemotherapy and radiation therapy than in patients who received radiation therapy alone. There were two treatment-related deaths (4%) in the combination therapy arm.^88,⁸⁹ In other trials in which multiple field radiation techniques were used, bolus 5-FU and radiation therapy showed no increase in chronic toxicity when chemotherapy and radiation therapy were combined. There was, however, a mild increase in acute diarrhea symptoms.^83,⁹⁰ The use of continuous infusional 5-FU as opposed to bolus 5-FU combined with radiation therapy also has been studied. Continuous 5-FU with radiation to 50.4 Gy in 1.8-Gy fractions was associated with more acute diarrhea, but no significant increase in chronic or severe small bowel toxicity as compared with bolus 5-FU therapy.⁹¹ Capecitabine, a prodrug that is converted to 5-FU in the tumor, also appears to enhance acute diarrhea rates when combined with radiation therapy.⁹² Although the addition of concurrent chemotherapy increases the acute toxicity of external radiotherapy (e.g., diarrhea, bowel frequency, cramping), its contribution to late bowel toxicity is poorly defined.¹⁷

There is investigation in integration of novel chemotherapeutic and “targeted” agents with radiation therapy in the neoadjuvant therapy of gastrointestinal cancers. Data from phase I and phase II trials using novel agents such as oxaliplatin, irinotecan, and epidermal growth factor receptor inhibitors suggest that the addition of these agents may significantly increase grades 3 and 4 gastrointestinal toxicity rates relative to conventional neoadjuvant chemoradiotherapy regimens, further emphasizing the importance of careful radiation planning to maximize normal tissue sparing in these patients.⁹³^–⁹⁵

Diagnosis of chronic enteropathy is often a clinical one. The cause of symptoms can be variable from patient to patient. Therefore, individualization of diagnostic and therapeutic approaches is indicated. General diagnostic evaluation procedures and therapeutic options are displayed in Tables 39-2 and 39-3. Consultation with the treating radiation oncologist should be requested if the clinical presentation is consistent with radiation enteritis. Review of the patient’s previous radiation treatment record will reveal the total dose, fractionation, volume of treatment, and other radiation parameters. Analysis of the treatment plan may show areas of high dose, especially if the patient had an intracavitary implant or brachytherapy. Lesions encountered at endoscopy or x-ray studies are usually localized in the area of high dose. Ulceration of the mucosa, thickening of jejunal folds, and thickening of the intestinal loops are radiologic signs that suggest radiation damage to the small bowel (Fig. 39-5). Faster intestinal transit and reduced bile acid and lactose absorption are observed in patients with chronic radiation enteritis.⁹⁶ These effects may be improved after the administration of loperamide. Antibiotics are indicated if there is small bowel bacterial overgrowth syndrome (see Chapter 102).^97,⁹⁸

Table 39-2 Pathophysiologic Features of Patients with Late Radiation Enteropathy

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