Journal of Urology and Renal Diseases (ISSN: 2575-7903)

Article / case report

"Extended Progression-Free Survival of Renal Cell Carcinoma with Axitinib: Case Report"

Rene A. Muñoz¹, María C. Cabezas²,³*, José Antonio Castillo¹, Camila Miño²,³, Adelin Albert4  

¹Hospital Oncológico Solca, Quito General Eloy Alfaro Avenue 5394, Ecuador

²Pontificia Universidad Católica del Ecuador, Vicente Ramón Roca, Ecuador

³Health & Research Services, Amazonas River Avenue and Cristobal Colon, Ecuador

4University Hospital Liège, Avenue de l’Hôpital, Liège, Belgium

*Corresponding author: María C. Cabezas, Pontificia Universidad Católica del Ecuador. Amazonas River Avenue and Cristobal Colon, EC170524, Ecuador. Tel: +59324532645; Fax: +593024532645; Email: mariadelcarmencg@yahoo.com

Received Date: 04 July, 2018; Accepted Date: 13 July, 2018; Published Date: 19 July, 2018

1.       Abstract

Axitinib is a selective inhibitor of vascular endothelial growth factor receptors approved for second line treatment of advanced renal cell carcinoma. The case report concerns an 85-year-old man with renal cell carcinoma of clear cells initially treated by left nephrectomy who presented with pulmonary progression 7 years later. Systemic treatment with pazopanib was initiated but disease progression and gastrointestinal toxicity were observed after 4 months. A second line treatment implemented with axitinib (5 mg twice daily, later reduced to 5 mg once daily due to gastrointestinal toxicity) led to favorable outcome and control of pulmonary progression. This case report demonstrates that axitinib in reduced dose can improve progression free survival (34 months at present) and surpass data published in Phase III clinical trials on patients with localized renal cell carcinoma of clear cells. It further contributes to the limited information currently available on axitinib in Latin-American populations.

 

Keywords: Kidney Cancer; Metastatic Renal Carcinoma; Tyrosine Kinase Inhibitors

1.       Abbreviations

CT                          :                               Computer Tomography

ECOG                    :                               Eastern Cooperative Oncology Group

NCCN                    :                               National Comprehensive Cancer Network

OS                           :                               Overall Survival

PFS                         :                               Progression Free Survival

RCC                       :                               Renal Cell Carcinoma

RECIST 1.1          :                               Response Evaluation Criteria in Solid Tumors

VEGFR                 :                               Vascular Endothelial Growth Factor Receptors

2.       Introduction

Renal cancer varies greatly from region to region worldwide with an average incidence of 4.4 per 100,000 and a mortality of 1.8 per 100,000 for both genders [1]. In Central and Latin-American countries incidence rates of Renal Cell Carcinoma (RCC) range between 3.0 and 6.8 per 100,000 for men and between 2.5 and 6.4 per 100,000 for women [2]. In Ecuador, the estimated incidence of RCC is 4.2 per 100,000 for men and 3.0 per 100,000 for women [1,2]. Axitinib is a potent anti-angiogenic tyrosine kinase inhibitor approved for the second-line treatment setting in patients with metastatic RCC [3-5]. Two meta-analyses have evidenced a better objective response rate, disease control, progression-free survival (PFS: median 6.7 months) and overall survival (OS: median 20.1 months) after axitinib administration in comparison to sorafenib [6,7]. There is currently very limited information available on the use of axitinib in Latin-American populations compared to other regions. The present case report describes a patient with RCC and distant metastases to the lung, first treated with radical nephrectomy and pazopanib and thereafter, at time of progression, successfully controlled by axitinib in reduced dose with an extended PFS.

3.       Case Report

In November 2006, a 75-year-old man underwent a radical left nephrectomy consecutive to RCC incidentally detected by Computer Tomography (CT) scan. The patient had a medical history of splenectomy, due to a left renal retroperitoneal tumor, and pulmonary hypertension with bi-auricular severe dilatation for unknown reasons. No significant family history was reported. The patient had only routine clinical follow-up until December 2013 when he presented fever. Physical examination and laboratory data were normal, but an 11.5 cm left lung mass in the inferior left lobe was evidenced by CT scan. The RCC-related pulmonary metastasis was confirmed by biopsy some days later. Systemic treatment was initiated immediately with oral pazopanib at a daily dose of 400 mg until March 2014 when the drug was suspended due to diarrheic stools grade IV that compromised his life. Six months later, the patient started a second line therapy with axitinib at an oral dose of 5 mg twice a day, dose adjustments based on individual safety and tolerability. Axitinib was swallowed whole with a glass of water. The treatment was carried out according to the National Comprehensive Cancer Network (NCCN) recommendations and National Health Service policies. However, after one month the dose had to be reduced to a single daily dose of 5 mg due to gastrointestinal toxicity grade II (4-6 diarrheic stools per day). Moreover, in October 2014, the patient was transferred to our oncology clinic where medical imaging examinations, laboratory and histopathology tests were performed for a comprehensive management and control. Laboratory data were normal, but the physical examination showed hypophonetic heart sounds with systolic murmur grade 2 in aortic focus, significant edema in both lower extremities and signs compatible with pulmonary effusion. CT evidenced a large amount of left pleural effusion, right metastatic pulmonary nodules in segments II (2.2 cm of diameter) and IX (0.7 cm of diameter) plus left lower lobar atelectasis by occupational mass of 13 x 13.3 x 14 cm of diameter compatible with soft tissue (Figure 1).

Two thoracenteses were performed with a drain of 1800 cc of pleural fluid. Pelvic echography reported a benign prostatism grade I treated with tamsolusin and prophylactic nitrofurantoin and a right renal nodule of 25 mm on the superior pole with a parapielic cyst without surgical criteria. Finally, the lamellae histopathological and immune-histochemical review revealed pulmonary metastases of RCC of clear cells with Fuhrman grade 2. With regards to baseline outcomes of axitinib therapy 34 months later the patient experienced a clinical benefit with stable disease according to RECIST 1.1 (Response evaluation criteria in solid tumors) based on CT scan [8] (Figure 2).

Nevertheless, the patient presented complications such as a deep venous thrombosis of the left safena vein treated with clinical treatment, fecal impaction and bladder balloon treated by enema and urinary catheter, respectively, and a multi-infarct disease in brain (bilateral white matter of the supratentorial area) without sequels controlled with levetiracetam. Additionally, he had subclinical asymptomatic hypothyroidism and reported asthenia, somnolence, dyspnea, periungual desquamation, need for supplemental oxygen for at least 16 hours a day, grade I retrolisthesis in C6, spondylosis and generalized osteopenia in the spine. At present, the 85-year-old patient continues with axitinib (dose of 5 mg orally daily) and has an OS of more than 10.5 years since RCC diagnosis and a PFS of 34 months with an ECOG (Eastern Cooperative Oncology Group) performance index equal to 1 and a Karnofsky score of 90%.

4.       Discussion

Cancer of the kidney and renal pelvis represents the sixth most common cancer in men worldwide [2]. Although metastatic cancers are traditionally associated with an overall poor prognosis, axitinib is a potential therapeutic option to consider in advanced RCC [3]. In the latest clinical guidelines, systemic treatment with tyrosine kinase inhibitors, such as sunitinib, pazopanib and axitinib, has been approved as first line therapy for RCC [3-5]. Pazopanib in a phase III trial reported a PFS of 10.5 months and a better toxicity profile in comparison to sunitinib although in this case study the patient experienced toxicity after only 4 months of pazopanib treatment [9]. In turn axitinib is a potent and selective second-generation inhibitor of Vascular Endothelial Growth Factor Receptors (VEGFR) that bears a relative potency 50-450 times greater than the first-generation VEGFR inhibitors [10]. International guidelines recommend axitinib at doses of 5 mg twice a day for an anti-neoplastic activity but in our case the dose had to be reduced to 5 mg once a day [3-5]. Despite the dose reduction our patient showed a notable therapeutic response with an extended PFS. Axitinib demonstrated to be a well-tolerated drug, with positive clinical outcomes and no negative impact on quality of life. Our patient experienced the classical adverse events reported in clinical trials such as fatigue, hypothyroidism, decrease appetite, nausea and asthenia [7]. Concomitantly, he presented with a major episode of fecal impaction and bladder balloon due to unidentified reasons. This case report which adds to the limited knowledge currently available about the use of axitinib for RCC in Latin-American populations shows that a reduced dose treatment regimen with axitinib can be as effective as the recommended doses and may prolong survival in advanced RCC. This hypothesis requires confirmation in randomized trials.


Figure 1: CT of October 2014 reported a large amount of left pleural effusion with an occupational mass of 13 x 13.3 x 14 cm of diameter compatible with soft tissue.




Figure 2: CT of May 2017 reported a tumor mass of heterogeneous density with multilobed contours, extends from the pulmonary hilum to the chest wall and measures 9.6 x 7.2 cm of diameter.




1.       WHO (2012) GLOBOCAN 2012: Estimated Cancer Incidence, Mortality and Prevalence Worldwide in 2012. International Agency for Research on Cancer 1: 6-11.

2.       Znaor A, Lortet-Tieulent J, Laversanne M, Jemal A, Bray F (2015) International variations and trends in renal cell carcinoma incidence and mortality. Eur Urol 67: 519-530.

3.       Escudier B, Porta C, Schmidinger M, Rioux-Leclercq N, Bex A, et al. (2016) Renal cell carcinoma: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol 27: v58-v68.

4.       Motzer R, Jonasch E, Agarwal N, Beard C, Bhayani S (2016) Kidney Cancer. NCCN Clinical Practice Guidelines in Oncology 2: 4-37.

5.       NICE (2015) Axitinib for treating advanced renal cell carcinoma after failure of prior systemic treatment. National Institute for Health and Care Excellence 1: 1-68.

6.       Escudier B, Michaelson MD, Motzer RJ, Hutson TE, Clark JI, et al. (2014) Axitinib versus sorafenib in advanced renal cell carcinoma: Subanalyses by prior therapy from a randomised phase III trial. Br J Cancer 110: 2821-2828.

7.       Wang H, Man L, Li G, Huang G, Wang J (2016) Comparative efficacy and safety of axitinib versus sorafenib in metastatic renal cell carcinoma: A systematic review and meta-analysis. Onco Targets Ther 9: 3423-3432.

8.       Seymour L, Bogaerts J, Perrone A, Ford R, Schwartz LH, et al. (2017) RECIST: guidelines for response criteria for use in trials testing immunotherapeutics. Lancet Oncol 18: 143-152.

9.       Motzer RJ, Hutson TE, Cella D, Reeves J, Hawkins R, et al. (2013) Pazopanib versus Sunitinib in Metastatic Renal-Cell Carcinoma. N Engl J Med 369: 22-31.

10.    Motzer RJ, Escudier B, Tomczak P, Hutson TE, Michaelson MD, et al. (2013) Axitinib versus sorafenib as second-line treatment for advanced renal cell carcinoma: Overall survival analysis and updated results from a randomised phase 3 trial. Lancet Oncol 14: 52-62.

Citation: Muñoz RA, Cabezas MC, Miño C, Albert A, Castillo JA (2018) Extended Progression-Free Survival of Renal Cell Carcinoma with Axitinib: Case Report. J Urol Ren Dis 20181102. DOI: 10.29011/2575-7903.001102

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