CTOIJ.MS.ID.555555

Background and Purpose: Carcinoma of the anal canal is relatively uncommon, yet incidence is on the rise. The accepted current standard regimen for patients with stage I-III squamous cell carcinoma (SCC) of the anal canal is radiotherapy (50.4 Gy) with concurrent infusional 5-fluorouracil (5-FU) (825 mg/m2 per oral bi-daily) administered on radiation days during weeks one and five and mytomycin C (MMC) (12 mg/m2) administered on week one. This study describes the efficacy and safety of substituting oral capecitabine (Cap) for the infusional 5-FU and compares the planned versus delivered therapy, and describes treatment-related patient toxicities and early outcomes in a population-based setting.

Materials and Methods: A retrospective chart review was conducted on a sequential cohort of SCC patients treated at one of the five BC Cancer Agency treatment centers since February 2010.

Results: Of 66 patients were treated, 99% of patients received the planned radiation dose, 13 patients (20%) required Cap dose reductions and three patients (5%) required MMC dose reductions. Most patients experienced minor treatment-related toxicities.

Conclusion: As part of the therapeutic regimen for SCC of the anal canal, oral Cap can be substituted for infusional 5-FU; patients had favorable outcomes and the treatment was well tolerated.

Keywords: Overall survival; Toxicity; Squamous cell carcinoma; Patient outcomes; Chemoradiation

Abbrivations: APR: Abdomino-perineal Resection; BCCA: British Columbia Cancer Agency; Cap: Capecitabine; HPV: Human Papilloma Virus; IMRT: Intensity-Modulated RT; MMC: Mitomycin C; RT: Radiation Therapy; SCC: Squamous Cell Carcinoma; 3D-CRT: Three-dimensional Conformal RT; 5-FU: 5-fluorouracil

Introduction

Carcinoma of the anal canal is a relatively uncommon malignancy, accounting for approximately 2 percent of all gastrointestinal cancers [1]. The incidence of this disease has been on the rise for the past few decades [1], which is thought to be due, in part, to the increased sexual transmission of human papilloma virus (HPV) [2,3].

Squamous cell carcinoma (SCC) of the anal canal remains the only carcinoma of the gastrointestinal tract that is curable without the need for definitive surgery with 5 year survival rates nearing 90% for early stage disease [1,2,4,5]. Treatment regimens for SCC of the anal canal have evolved over the past decades, and studies have included comparisons of radiotherapy alone versus chemoradiation [6,7]; determining treatment benefits of mitomycin C (MMC) [8,9]; and comparisons of MMC with cisplatin [5,10,11]. The accepted current standard regimen for patients with stage I-III SCC of the anal canal is radiotherapy (50.4 Gy) with concurrent infusional 5-fluorouracil (5-FU) administered days one through four during weeks one and five and MMC administered on day one of week one [5

Capecitabine (Cap) is an oral fluorouracil shown to be equivalent to infusional 5-FU in the treatment of rectal adenocarcinoma [12,13]. Unlike 5-FU, which is intravenously infused, Cap is orally administered which provides resource benefits as it is more convenient for patients and staff, and does not require the use of a central venous infusional device. Limited evidence for the substitution of infusional 5-FU for capecitabine in the treatment of SCC of the anal canal has been described in the literature. In a previously published phase II study thirtyone patients with stage I-III SCC of the anal canal were treated with continuous radiation, Cap on radiation days and MMC on day 1. Therapy was well tolerated and 24 (77%) of patients had a complete clinical response after four weeks, while 3 (16%) had partial response. Three locoregional relapses occurred during the follow up period (median of 14 months) [14].

In this study, a retrospective chart review was conducted of a sequential cohort of patients with stage I-III SCC of the anal canal treated with standard radiation and concurrent Cap and MMC according to the previously described protocol [14]. The objectives of the study were to:

  1. Describe the dose intensity of radiation, Cap and MMC by comparing the planned versus the delivered dose of radiation, Cap and MMC;
  2. Describe treatment-related patient toxicities and
  3. Describe the early outcomes of therapy.

Methods and Materials

Treatment of SCC of the anal canal

Patients were treated at one of five cancer treatment centers throughout the province of British Columbia (BC), a Canadian province with a population of 4.4 million. The BC Cancer Agency (BCCA) is responsible for funding all systemic cancer therapy and is the sole provider of radiotherapy in BC. All patients in the province who require radiation therapy for a diagnosis of SCC anal cancer are referred to the BCCA for consultation and treatment delivery.

Chemoradiation was delivered according to GICART, a standardized protocol, introduced in February 2010 and posted on the BCCA website [15]. Eligibility criteria for this therapy include a diagnosis of stage I-III squamous cell or cloacogenic carcinoma of the anal canal and ECOG performance status of less than or equal to 2. Patients also need to have an adequate marrow reserve (ANC greater than or equal to 1.5 x 109/L, platelets greater than 100 x 109/L), with adequate renal (creatinine less than or equal to 1.5 x ULN) and liver function (bilirubin less than or equal to 26 mmol/L; AST/Alkaline Phosphatase less than or equal to 5 x ULN

Patients treated under the GICART protocol receive a combination of chemotherapy and radiotherapy. Continuous radiation at a dose of 50.4 Gy in 28 fractions over 5 1/2 weeks is recommended. Chemotherapy with Cap is delivered twice a day at a dose of 825 mg/m2, on days that radiotherapy is administered (days 1-5, 8-12, 15-19, 22-26, 29-33, 36-40), to a total daily dose of 1650 mg/m2. As specified in the GICART protocol, Cap is administered orally with food, with the second dose administered 10-12 hours after the first. MMC is administered on day one week one intravenously, at a dose of 12 mg/m2 to a maximum dose of 20 mg.

Study Cohort Selection and data extraction

All SCC anal cancer patients diagnosed at BCCA and treated with GICART protocol from the time of its introduction in February 2010 until April 4, 2013 were included in this study.

The charts from all SCC anal canal patients in this cohort were examined, and the variations in chemotherapy doses, the differences in radiation dosing and type of radiation technique delivered to each patient were determined, as well as patient outcomes including relapses and deaths updated until April 2013. To determine the levels of toxicity experienced by each patient in the cohort, a review was conducted of all the narratives dictated by the oncologist assigned to each patient. Nausea, vomiting, stomatitis and diarrhea toxicities were graded according to the GICART protocol while dermatitis data was extrapolated from the narratives provided by the physicians and a graded according to the Dermatitis Grading Scale from the BCCA Protocol Summary for Care of Radiation Skin Reactions. The most severe toxicity described for each patient was used in each case. For example, if a patient had grade 3 diarrhea but was experiencing grade 4 levels of nausea, they were classified as experiencing a grade 4 toxicity.

Sources of Research Support

The Provincial Pharmacy Database was used to identify eligible patients, and patient and tumor characteristics were identified through the BCCA Gastrointestinal Cancer Outcomes Unit (GICOU). The GICOU database prospectively documents standard pathologic and clinical criteria of patients referred to the BCCA. The study was conducted as a quality assurance initiative and was reviewed by the BCCA-University of British Columbia Research Ethics Board.

Results

Patient Characteristics

The characteristics and diagnostic status of the 66 patients included in this study are shown in Table 1. The majority of patients were female (62%), HIV negative (99%), non-smokers (74%) and non-drinkers (74%). Most patients (n= 61, 93%) presented with an ECOG status between 0-1, while three (5%) presented with an ECOG status of 2 and two patients (3%) had an ECOG status of 3. Staging was varied, as 26 patients (39%) presented with a stage I tumor, 15 (23%) presented with a stage II tumor and 25 (38%) presented with a stage III tumor.

Histologically, the tumours were classified as follows: of 66 patients, 62 (94%) had squamous cell carcinoma of which eight were described as keratinizing, and five as basaloid. Two patients (3%) had tubulovillous adenoma, and an additional two patients (3%) had adenocarcinoma. All 66 patients were included in the dose intensity and toxicity analysis, while only patients with SCC (62) were included in the outcome analysis.

Treatment Dose Intensity

All patients included in the study initiative therapy with both Cap and. The doses administered are shown in Table 2, along with the number of dose reductions, increases, omissions, and discontinuations for each therapy administered.

Patients received a median dose of 825 mg/m2 of Cap administered twice daily on radiation days. Dose reductions were recorded for 13 patients (20%) due to apparent toxicity during treatment. There were no recorded increases, omissions or discontinuations for this drug. The median duration of therapy of capecitabine was five and a half weeks on week-days, with a treatment range from three to six weeks. Seven patients initiated therapy at a lower dose of Cap (500-749 mg/m2) due to varying issues ranging from patient comorbidities, previous chemotherapy treatment, and the use of therapy purely for palliative purposes. None of the patients starting at this lower dose required a subsequent dose reduction.

The meandose of MCC delivered was 12 mg/m2 on day one, week one.Pre-planned dose reductions were recorded for three (5%) of patients, of which two cases were due to patient comorbidities and one was due to an infusion reaction.

Patients received a median dose of 825 mg/m2 of Cap administered twice daily on radiation days. Dose reductions were recorded for 13 patients (20%) due to apparent toxicity during treatment. There were no recorded increases, omissions or discontinuations for this drug. The median duration of therapy of capecitabine was five and a half weeks on week-days, with a treatment range from three to six weeks. Seven patients initiated therapy at a lower dose of Cap (500-749 mg/m2) due to varying issues ranging from patient comorbidities, previous chemotherapy treatment, and the use of therapy purely for palliative purposes. None of the patients starting at this lower dose required a subsequent dose reduction. The meandose of MCC delivered was 12 mg/m2 on day one, week one.Pre-planned dose reductions were recorded for three (5%) of patients, of which two cases were due to patient comorbidities and one was due to an infusion reaction.

Radiation techniques were also examined. Three-dimensional conformal RT (3D-CRT) was shown to be the primary technique used, with 50 patients (76%) receiving this treatment, while the remaining 16 patients (24%) received intensity-modulated RT (IMRT).

Patient toxicities

Toxicity grades of nausea, vomiting and stomatitis are described in Table 4. A total of 54 patients (82%) experienced grades 0-1 toxicity, including minor changes in bowel habits, one episode of nausea and vomiting per day as well as the presence of painless ulcers, erythema or mild soreness. A total of seven patients (11%) experienced grade 2 toxicity, including moderate changes in bowel habits, 2-5 episodes of nausea and vomiting a day and painful erythema, edema or ulcers. Two patient (3%) experience grade diarrhea and three patients (5%) were classified as having grade 4 diarrhea.

Peri-anal radiation dermatitis was experienced in varying degrees by numerous patients during the course of treatment (Table 5). Using the Dermatitis Grading Scale from the BCCA Protocol Summary for Care of Radiation Skin Reactions 16, there were a total of 19 patients (29%) that experienced grade 1 toxicities which encompassed minor skin changes such as numbness and tingling. Five patients (8%) experienced a grade two toxicity noted by erythema and swelling, and 42 patients (63%) who experienced a grade 3 toxicity highlighted by instances of moist desquamation and ulceration.

Patient Outcomes

Median follow from time of diagnosis was 20 months. Of patients with Squamous cell histology (N=62) 94% had no evidence of relapse as of April 2013. Four patients (6%), one stage I, one stage II and two stage III, had recorded relapses. One relapsed patient with initial stage II disease died, however, death was not attributed to treatment. Sorting the outcomes by cancer stage, one out of 26 patients (4%) with stage I tumours experienced a local relapse. For patients with stage II tumors, one out of 15 patients experienced a distant relapse, with two recorded deaths not attributed to treatment, and one out of the 25 patients with stage III tumours experiencing a distant relapse. Among 4 patients with tubulovillous adenoma and adenocarcinoma histology, 0% experienced a relapse.

Discussion

In this study, the charts of 66 patients with stage I-III SCC of the anal canal treated at BCCA with multimodality therapy – Cap, MMC and radiation – were retrospectively reviewed. Although the global standard of care for SCC of the anal canal is concurrent radiotherapy with 5-FU and MMC, a standard protocol substituting infusional 5-FU with oral capecitabine was introduced in 2010 as a an alternative non-infusional regimen.5 Results of the study showed that while the majority of patients experienced some form of chemotherapy or radiation induced toxicity, protocol therapy was well tolerated; despite some dose reductions due to apparent toxicities there were no treatment discontinuations. The majority of patients who underwent this therapy since its initiation in 2010 currently have their tumors in remission with only a few reported cases of relapses and no treatment-related deaths.

Limitations encountered in this study centered on the retrospective nature of the collection of toxicity data. While the number of patients included was modest, the current study adds to the description of efficacy and outcomes of this regimen. Results compare favorably to the previous publication of the phase II study on which the current GICART protocol was based [14]. To our knowledge, there are no other prospective or retrospective studies describing this treatment regimen.

Patient characteristics

The patient cohort was similar to those described in published clinical trials [5,17]. Median age was 60 and the majority of tumors were stage I-II at presentation. It was noteworthy that there were almost twice as many female subjects in the study cohort as males. A significant increase in SCC has been documented in both men and women [18]. Most study subjects did not smoke, and there was only one HIV-positive subject included in the cohort. The preferred institutional chemotherapy regimen for HIV-positive patients is cisplatin-capecitabine due to the more favorable hematological toxicity described with cisplatin over MMC.5

Chemotherapy Tolerance

Toxicity grades for nausea, vomiting and diarrhea were low despite the high dose intensity of chemotherapy drugs administered (Table 4). Most patients experienced only grade 0-1 toxicities indicating favorable outcomes with low side effects, while 12 patients (19%) experienced grade 2-4 toxicities for nausea, vomiting and diarrhea.

Overall, the starting doses of Cap (generally of 825 mg/ m2 BID on each radiotherapy day) were well tolerated by the patients; however, 20% of patients required dose reductions, likely for reasons of apparent toxicity. The protocol specifies a dose reduction with grade 2 or more hand foot toxicity. Because it is difficult to abstract hand-foot syndrome grade by chart review, it was not included in the study, however, we speculate that Cap dose reductions may have been made for this reason. The chart review revealed that while all of the patients involved in this study experienced some degree of dermatitis during radiotherapy treatment, only one patient required radiation dose reduction. Generally, radiation treatment of any degree causes some sort of reaction in the treated and neighboring skin layers so the results themselves are not unexpected given the duration and intensity of the radiation doses.

Radiation Therapy

The GICART protocol specified 50.4 Gy in 28 fractions over 5.5 weeks, however, there were significant variances in the planned radiation dose, technique and treatment duration received by patients in the cohort. The reason for this variability is likely because radiation oncologists selected the best treatment for each individual patient based on patient factors and tumour characteristics. Generally, patients with a higher tumour stage or patients physically able to withstand higher doses of radiation were given larger radiation doses, while patients with lower stage tumors were treated with lower radiation doses. In a previous phase II study, escalating doses of radiation were prospectively defined in the following manner: patients with stage T1 tumours were given a dose of 45 Gy in 25 fractions, patients with stage T2 tumours were given a dose of 55 Gy in 30 fractions, and patients with stage T3–4 tumours were given 59 Gy in 32 fractions [19]. Radiation oncologists involved in the current study used similar criteria to justify dose variation according to tumor stage. There was no discernible difference in outcomes between the patients treated with the two radiation techniques, 3D-CRT and IMRT.

All patients included in the study achieved initial remission of disease. Subsequent relapses were infrequent and occurred in only 4% of stage I, 7% of stage II patients and in 6% of patients with stage III disease. Due to limited follow-up time, no conclusion regarding the efficacy of the regimen can be made at this time. However, phase III evidence from other disease settings show equivalence of capecitabine to infusional 5-FU in multiple settings. One randomized head-to-head study of infusional 5-FU versus capecitabine in combination with radiation for stage II/III rectal cancer demonstrated equivalent efficacy and toxicity [13]. In phase III studies, capecitabine was documented to be equivalent in efficacy to bolus 5-FU in colon cancer and equivalent to infusional 5-FU in combination with pelvic radiation among patients with rectal cancer (R04) [13,20]. Given the high observed dose intensity for both capecitabine and radiation, it is unlikely that the use of capecitabine in the GICART regimen will result in inferior future outcomes.

In this study there was a wide variation in radiation doses. At this point in time, the variations in administered radiation doses do not correlate with different outcomes, suggesting that lower radiation doses may be considered in some patients. Longer term follow up of patients in this cohort is necessary to ensure that patients who received lower doses of radiation and chemotherapy have similar outcomes to those who received larger doses. Our intention is to follow this cohort to see if additional correlations between radiation and chemotherapy and long term survival outcomes can be made.

Conclusion

Combined modality therapy of capecitabine plus mitomycin and radiotherapy is well tolerated and allows high dose intensity of radiation and chemotherapy in a population based setting. Substitution of capecitabine for infusional 5-FU is feasible and may be a reasonable consideration for patients and physicians who prefer to avoid the inconvenience and potential complications of a central infusional device. A significant amount of variability in planned radiation dose was observed related to both oncologist preference and tumor stage. Prospective studies to determine optimal radiation dose would be justified.

  1. Bilimoria KY, Bentrem DJ, Rock CE, Stewart AK, Ko CY, et al. (2009) Outcomes and prognostic factors for squamous-cell carcinoma of the anal canal: analysis of patients from the National Cancer Data Base. Dis Colon Rectum 52(4): 624-631.
  2. Ryan DP, Mayer RJ (2000) Anal carcinoma: histology, staging, epidemiology, treatment. Curr Opin Oncol 12(4): 345-52.
  3. Moscicki AB, Schiffman M, Burchell A, Albero G, Giuliano AR, et al. (2012) Updating the natural history of human papillomavirus and anogenital cancers. Vaccine Suppl 5: F24-F33.
  4. Poggio J (2011) Premalignant Lesions of the Anal Canal and Squamous Cell Carcinoma of the Anal Canal. Clin Colon Rectal Surg 24(3): 177-192.
  5. James R (2009) ACT II: The second UK phase III analcancer trial. a randomised trial of chemoradiation using mitomycin or cisplatin,with or without maintenance cisplatin/5FU in squamous cell carcinoma of the anus. Presented at the ASCO Annual Meeting, Florida, May 2009.
  6. Epidermoid anal cancer: results from the UKCCCR randomised trial of radiotherapy alone versus radiotherapy, 5-fluorouracil, and mitomycin. UKCCCR Anal Cancer Trial Working Party. UK Co-ordinating Committee on Cancer Research. (1996) Lancet 348(9034): 1049-1054.
  7. Bartelink H, Roelofsen F, Eschwege F, Rougier P, Bosset JF, et al. (1997) Concomitant radiotherapy and chemotherapy is superior to radiotherapy alone in the treatment of locally advanced anal cancer: results of a phase III randomized trial of the European Organization for Research and Treatment of Cancer Radiotherapy and Gastrointestinal Cooperative Groups. J Clin Oncol 15(5): 2040-2049.
  8. Flam M, John M, Pajak TF, Petrelli N, Myerson R, et al. (1996) Role of mitomycin in combination with fluorouracil and radiotherapy, and of salvage chemoradiation in the definitive nonsurgical treatment of epidermoid carcinoma of the anal canal: results of a phase III randomized intergroup study. J Clin Oncol 14(9): 2527-2539.
  9. Cummings BJ, Keane TJ, O'Sullivan B, Wong CS, Catton CN, et al. (1991) Epidermoid anal cancer: treatment by radiation alone or by radiation and 5-fluorouracil with and without mitomycin C. Int J Radiat Oncol Biol Phys 21(5): 1115-1125.
  10. Peiffert D, Seitz JF, Rougier P, Francois E, Cvitkovic F, et al. (1997) Preliminary results of a phase II study of high-dose radiation therapy and neoadjuvant plus concomitant 5-fluorouracil with CDDP chemotherapy for patients with anal canal cancer: a French cooperative study. Ann Oncol 8(6): 575-581.
  11. Martenson JA, Lipsitz SR, Wagner H, Kaplan EH, Otteman LA, et al. (1996) Initial results of a phase II trial of high dose radiation therapy, 5-fluorouracil, and cisplatin for patients with anal cancer (E4292): an Eastern Cooperative Oncology Group study. Int J Radiat Oncol Biol Phys 35(4): 745-749.
  12. De Paoli A, Chiara S, Luppi G, Friso ML, Beretta GD, et al. (2006) Capecitabine in combination with preoperative radiation therapy in locally advanced, resectable, rectal cancer: a multicentric phase II study. Annals of Oncology 17: 246-251.
  13. Roh MS, Yothers GA, O'Connell MJ, Beart RW, Pitot HC, et al. (2011) The impact of capecitabine and oxaliplatin in the preoperative multimodality treatment in patients with carcinoma of the rectum: NSABP R-04., ASCO Annual Meeting, J Clin Oncol 29(15): 15_suppl.
  14. Glynne-Jones R, Meadows H, Wan S, Gollins S, Leslie M, et al. (2008) EXTRA--a multicenter phase II study of chemoradiation using a 5 day per week oral regimen of capecitabine and intravenous mitomycin C in anal cancer. Int J Radiat Oncol Biol Phys 72(1): 119-126.
  15. British Columbia Cancer Agency Protocol Summary for Curative Combined Modality Therapy for Carcinoma of the Anal Canal using Mitomycin, Capecitabine and Radiation Therapy (GICART)
  16. Columbia Cancer Agency Protocol Summary for Care of Radiation Skin Reactions
  17. Gerard JP, Ayzac L, Hun D, Romestaing P, Coquard R, et al. (1998) Treatment of anal canal carcinoma with high dose radiation therapy and concomitant fluorouracil-cisplatinum. Long-term results in 95 patients. Radiother Oncol 46(3): 249-256.
  18. Grulich AE, Poynten IM, Machalek DA, et al. (2012) The epidemiology of anal cancer. Sex Health 9(6): 504-508.
  19. Eng C, Chang GJ, Das P, Rodriguez-Bigas M, Skibber JM, et al. (2009) Phase II study of capecitabine and oxaliplatin with concurrent radiation therapy (XELOX-XRT) for squamous cell carcinoma of the anal canal. ASCO Annual Meeting.
  20. Twelves C, Wong A, Nowacki MP, Abt M, Burris H, et al. (2005) Capecitabine as adjuvant treatment for stage III colon cancer. N Engl J Med 352(26): 2696-2704.
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    Table 1: Characteristics of patients included in study (n=66).

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    Table 2: Chemotherapy dosings (n=66).

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    Table 3: DRadiation dose, techniques and treatment received by patients in study (n=66).

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    Table 4: Nausea, Vomiting, Stomatitis or Diarrhea experienced by patients in study [16].rors.

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    Table 5: Radiation dermatitis experienced by patients in this study (n=66).

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