Follow-Up Strategy After Primary and Early Diagnosis


Guideline

MH & PE

CEA

Abdominal imaging

Chest imaging

Colonoscopy

ASCO [18]

Every 3–6 months for 5 years

Every 3–6 months for 5 years

CT of abdomen and pelvis annually for 3 years, for high risk patients every 6–12 months for 3 years and then annually for 2 years

CT of Chest annually for 3 years, for high risk patients every 6–12 months for 3 years

Colonoscopy at 1 year, subsequently according indings and every 5 years if normal.

Rectosigmoidoscopy every 6 months for 5 years in rectal cancer not irradiated

ASCRS [4]

Every 3–6 months for 2 years, then every 6 months for 3 years

Every 3–6 months for 2 years, then every 6 months for 3 years

CT of abdomen and pelvis annually for 5 years

CT of chest annually for 5 years

Rectosigmoidoscopy (+/- ERUS) every 6 to 12 months or every 6 months for 3 to 5 years in high risk patients (lymphatic and venous invasion, poorly differentiation, male sex, distal lesion, close distal margins, transanal local excision)

ESMO [19]

Every 6 months for 2 years

NR

NR

NR

Rectosigmoidoscopy every 6 months for 2 years; colonoscopy every 5 years

ACPGBI [20]

Audit is mandatory but not recommendation for frequency

NR

CT of abdomen within 2 years

CT of chest within 2 years

Colonoscopy every 5 years

NCCN [21]

Every 3–6 months for 2 years, then every 6 months for 3 years

Every 3–6 months for 2 years, then every 6 months for 3 years for T2 or greater lesions

CT of abdomen and pelvis annually for 5 years in high risk patients (lymphatic and venous invasion, poorly differentiation)

CT of chest annually for 5 years in high risk patients (lymphatic and venous invasion, poorly differentiation)

Colonoscopy at 1 year, repeat in 3 years then every 5 years


ASCO, American Society of Oncology; ASCRS, American Society of Colon Rectal Surgeons; ESMO, European Society for Medical Oncology; ACPGBI, Association of Coloproctology of Great Britain and Ireland; NCCN, National Comprehensive Cancer Network; MH & PE, medical history and physical examination; CEA, carcinoembryonic antigen; CT, computed tomography; ERUS, endorectal ultrasound; NR, not recommended





1.8 Follow-Up Following Complete Response After Chemoradiation


Neoadjuvant chemoradiation (CRT) for locally advanced rectal cancers induces tumor regression with size reduction (downsizing), in-depth penetration, and eventually lymph-node sterilization (downstaging): up to 25% of patients present complete pathological tumor regression with no residual disease at the time of surgery [6369]. These patients are referred to as having a pathologic complete response (pCR). In a recent systematic review of 16 studies involving 1,263 patients with pCR, the finding of pCR was associated with a local recurrence rate of 0.7% and a distant metastasis rate of 8.7%. The 5-year overall survival rate was 90.2% and the disease-free survival rate was 87% [70].

Considering morbidity and mortality associated with rectal surgery, a nonoperative approach was first proposed to patients with complete tumor regression by Habr-Gama et al. [71]. This alternative strategy is described also as “organsparing treatment”, “rectal preservation”, or a “watch-and-wait” approach. In this setting, patients with apparent clinical complete response (cCR) to CRT are ideal candidates for the conservative approach. cCR is obviously less clearly defined than pCR and usually describes the absence of tumor based on a combination of clinical, radiologic, and endoscopic investigations. The landmark paper based on this policy was published by the Habr-Gama group in 2004 [71]. In the updated series published in 2011, 67 (39%) patients were considered to have cCR. At a mean follow-up of >5 years overall and disease-free survival in nonoperative patients were, respectively, 96% and 72% [72]. Similar results are reported by other, smaller, studies [73, 74], but these amazing results have not been repeated by others, who report an 80% relapse rate of complete clinical responders within 10 months of observation [75, 76].

This novel approach brings into question whether surveillance protocols following curative resection are appropriate in this particular patient subset. Again, the Habr-Gama group [77] suggests a strict follow-up program combining digital rectal examination, rigid proctoscopy with biopsy of suspicious lesions, and CEA levels every 1–2 months for the first year, every 6 months in the second year, and yearly thereafter. Chest X-ray and abdominal CT scans are recommended at 6 and 12 months and yearly thereafter. However, the real challenge of this novel approach remains to identify a true pCR without a resection.


1.9 Conclusions


Surveillance following colorectal cancer resection is intuitively beneficial and appealing. There is limited evidence of benefits in terms of earlier detection of recurrence, which results in more surgical resections with curative intent and improved overall survival. Controversy remains on the ideal surveillance methods and the frequency with which they should be applied. Under debate are the cost-effectiveness of various surveillance strategies and quality-of-life implications. In this era of cost containment, it is necessary to improve stratification of risk recurrence, identifying the patient population that will benefit from a value-based strategy and avoiding unnecessary examination in low-risk patients. It must be emphasized that the main purpose of a surveillance program is early identification of recurrence while curative interventions are still possible.


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Jan 29, 2017 | Posted by in GASTROENTEROLOGY | Comments Off on Follow-Up Strategy After Primary and Early Diagnosis

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