- Case report
- Open Access
RapidArc for centrally recurrent cervical cancer in the vaginal cuff following primary surgical therapy: a case report
© Lalya et al. 2016
Received: 30 September 2015
Accepted: 11 January 2016
Published: 22 January 2016
Pelvic recurrences of cervical cancer after primary surgical treatment can be potentially cured with radical hysterectomy or chemoradiation therapy. Combined radio-chemotherapy is believed to improve results compared to other option. Currently, RapidArc radiotherapy is considered an excellent technological advance that shows great potential for producing highly conformal doses to treatment volumes.
We present a case of a 67-year-old woman with history of early cervical cancer initially treated by radical laparoscopic hysterectomy. More than 5 years later, the patient presented with a central pelvic vaginal cuff recurrence that is histologically confirmed. Salvage radiotherapy using RapidArc with concurrent cisplatin-based chemotherapy was indicated. A high dose of 70 Gy was delivered to the gross recurrent disease with simultaneous integrated boost (SIB) to the subclinical disease and good sparing of organs at risk especially the rectum and sigmoid.
This case clearly demonstrates a large benefit for salvage RapidArc radiotherapy to central pelvic recurrences of gynecological cancers with an excellent rate of local control and less rate of toxicity.
Women with early-stage cervical cancer can be potentially cured with radical hysterectomy or chemoradiation therapy . In Morocco, most patients present first at gynecologic clinics and, as a result, the majority of patients of early stage become subjected to radical hysterectomy and lymphadenectomy. Unfortunately, up to 17 % of women develop either local and/or distant disease recurrence usually within the first 2 years of completing the treatment [2, 3].
Local recurrence of cervical cancer after primary surgical therapy is still problematic. It commonly occurs locally as central pelvic recurrences due to the extent of spread into contiguous tissues . Treatment directed to the site of recurrence can be performed with curative intent. Options include radiation therapy (RT) or pelvic exenteration, both resulting in suboptimal rates of local tumor control and rates of survival [5, 6]. Recently, RapidArc radiotherapy is considered an important technological advance that shows great potential for producing highly conformal doses to treatment volumes while sparing organs at risk (OARs).
We report an excellent complete response case of a centrally recurrent squamous cell cervical cancer of the vaginal cuff after radical laparoscopic hysterectomy, successfully managed by salvage RapidArc radiotherapy and concurrent cisplatin-based chemotherapy.
A 67-year-old female underwent a radical laparoscopic hysterectomy, with adnexectomy and bilateral pelvic lymphadenectomy for a FIGO stage IB1 squamous cell cervical cancer in January 2010. Final pathology report showed a 9-mm squamous cell carcinoma with deep stromal invasion, positive resection margins, and one metastatic lymph node, without vascular embolism or parametrium invasion. Based on pathologic risk factors, adjuvant radiation therapy with radiosensitizing cisplatin was suggested. Unfortunately, the patient was not compliant, she was lost to follow-up and the adjuvant treatment was never delivered.
After primary surgery for cervical cancer, subsequent pelvic recurrence is effectively managed with external beam radiotherapy and concurrent cisplatin-based chemotherapy due to the presentation of a centrally recurrent cervical cancer of the vaginal cuff, as seen in 35–40 % of cases . Surgical management is an option therapy but it imposes radical pelvic surgery in order to achieve surgical resection with curative intent. However, in locally recurrent disease, radiation offers long-term pelvic control and prolonged survival .
One recent retrospective study examining outcomes of patients undergoing salvage radiotherapy alone for recurrent cervical cancer following radical hysterectomy found that is an effective treatment for who recur at the vaginal cuff with relatively little morbidity but it is less effective in patients where recurrence lies outside the central pelvis . Generally, it is accepted that the increasing dose to the target volume in external beam radiotherapy will lead to increased local control. Intensity-modulated radiotherapy (IMRT) is seen as the way to achieve this. It facilitates the delivery of differential doses of radiation to a specified target volume and the escalating of dose prescription. Early experience found that IMRT were able to achieve excellent coverage of target volumes, and there was very little acute gastrointestinal toxicity as compared with conventional external beam radiotherapy techniques .
RapidArc radiotherapy is an excellent option used to salvage our patient with a central pelvic vaginal cuff recurrent lesion which seems to obtain better dosimetric results compared to IMRT, with fewer monitor units, and a significant decrease in treatment time . Pelvic radiation can lead to urinary symptoms and bowel changes. However, RapidArc might reduce acute rectal and bladder toxicity compared with conventional techniques . Concurrent cisplatin-based chemoradiotherapy has also been used in the management of recurrent cervical cancer. This approach has provided both better local control and survival with acceptable toxicities in women with locally recurrent cervical cancer in several studies [13, 14].
Surveillance after primary curative therapy for cervical cancer is uniformly recommended, although its effectiveness is not well studied . The concept of long-term surveillance for patients treated with curative intent is based on the premise that early detection of recurrence may lead to treatments that have lower morbidity and increase survival. Early detection of recurrence is aimed at treating patients with potentially curative salvage therapy. This is most likely in patients who have an isolated central pelvic recurrence.
In summary, we have presented an excellent complete response case of centrally recurrent cervical cancer of the vaginal cuff following radical hysterectomy, which managed by salvage RapidArc radiotherapy with concurrent cisplatin-based chemotherapy. This case demonstrates a large benefit for local dose escalation to the residual tumor by the currently techniques with high rates of local control and less rate of toxicity.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of the journal.
All authors are thankful for providing the necessary facilities for the preparation of the manuscript. Special thanks are due to the Faculty of Medicine and Pharmacy of Rabat, the source(s) of funding for all authors.
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- Bansal N, Herzog TJ, Shaw RE, Burke WM, Deutsch I, Wright JD. Primary therapy for early-stage cervical cancer: radical hysterectomy vs radiation. Am J Obstet Gynecol. 2009;201:485.e1.Google Scholar
- Ries LAG, Harkins D, Krapcho M, et al. SEER Cancer Statistics Review, 1975 to 2003. Bethesda, MD: National Cancer Institute; 2006.Google Scholar
- SEER data for 2000–2004 http://seer.cancer.gov/ (Accessed on April 25, 2011).
- Di Saia PJ, Creasman WT, Mannel RS, McMeekin DS, Mutch DG. Invasive cervical cancer. In: Di Saia PJ, Creasman WT, editors. Clinical Gynecologic Oncology. 8th ed. Philadelphia: Elsevier; 2012. p. 51–119.Google Scholar
- Estape R, Angioli R. Surgical management of advanced and recurrent cervical cancer. Semin Surg Oncol. 1999;16:236–41.View ArticlePubMedGoogle Scholar
- Jobsen JJ, Leer JW, Cleton FJ, Hermans J. Treatment of locoregional recurrence of carcinoma of the cervix by radiotherapy after primary surgery. Gynecol Oncol. 1989;33:368–71.View ArticlePubMedGoogle Scholar
- Peiretti M, Zapardiel I, Zanagnolo V, Landoni F, Morrow CP, Maggioni A. Management of recurrent cervical cancer: a review of the literature. Surg Oncol. 2012;21:e59–66.View ArticlePubMedGoogle Scholar
- Cancer C. NIH Consens. Statement. 1996;14(1):1–38.Google Scholar
- Jain P, Hunter RD, Livsey JE, Coyley C, Swindellz R, Davidson SE. Salvaging locoregional recurrence with radiotherapy after surgery in early cervical cancer. Clin Oncol. 2007;19:763e768.Google Scholar
- Mundt AJ, Roeske JC, Lujan AE, et al. Initial clinical experience with intensity-modulated whole-pelvis radiation therapy in women with gynecologic malignancies. Gynecol Oncol. 2001;82:456.View ArticlePubMedGoogle Scholar
- De-Yin ZHAI, Yong YIN, Guan-Zhong GONG, Tong-Hai LIU, Jin-Hu CHEN, Chang-Sheng MA, et al. RapidArc radiotherapy for whole pelvic lymph node in cervical cancer with 6 and 15 MV: a treatment planning comparison with fixed field IMRT. J Radiat Res. 2013;54:166–73.View ArticleGoogle Scholar
- Renard-Oldrini S, Brunauda C, Huger S, Marchesi V, Tournier-Rangeard L, Bouzid D, et al. Dosimetric comparison between the intensity modulated radiotherapy with fixed field and RapidArc of cervix cancer. Cancer Radiother. 2012;16(3):209–14.View ArticlePubMedGoogle Scholar
- Singh AK, Grigsby PW, Rader JS, Mutch DG, Powell MA. Cervix carcinoma, concurrent chemoradiotherapy, and salvage of isolated paraaortic lymph node recurrence. Int J Radiat Oncol Biol Phys. 2005;61:450.View ArticlePubMedGoogle Scholar
- Miglietta L, Franzone P, Centurioni MG, et al. A phase II trial with cisplatinepaclitaxel cytotoxic treatment and concurrent external and endocavitary radiation therapy in locally advanced or recurrent cervical cancer. Oncology. 2006;70:19e24.View ArticleGoogle Scholar
- Elit L, Fyles AW, Devries MC, et al. Follow-up for women after treatment for cervical cancer: a systematic review. Gynecol Oncol. 2009;114:528.View ArticlePubMedGoogle Scholar