Literature DB >> 29146617

Cure in Advanced Renal Cell Cancer: Is It an Achievable Goal?

Dhanusha Sabanathan1,2, John J Park3,2, Manuel Marquez2, Louise Francisco2, Natalie Byrne3, Howard Gurney3,2.   

Abstract

BACKGROUND: Immunotherapy has historically been of interest in the management of metastatic renal cell cancer (mRCC) because of its relative chemoresistance and the reproducible but low incidence of spontaneous remission in metastatic disease. Recently, targeted immunotherapies in the form of checkpoint inhibitors have shown durable responses in approximately 20%-30% of patients with solid tumors, with a much more acceptable side-effect profile. Anti-programmed death receptor 1 (PD-1)/programmed death receptor ligand 1 antibodies rely on the presence of host T cells in the tumor microenvironment to be stimulated in order to activate an antitumor response. The presence of tumor antigens augments this stimulation. This has led to further research into combination therapy with anti-PD-1 inhibitors and radiotherapy, chemotherapy, or targeted therapy with the aim of increasing the response rate to these agents.
MATERIALS AND METHODS: We describe three cases of patients with mRCC treated with anti-PD-1 antibody therapy in combination with targeted therapy (bevacizumab), anti-cytotoxic T lymphocyte antigen 4 therapy (ipilimumab), or radiotherapy. We perform a comprehensive literature review on combination immunotherapy and the scope for the future.
RESULTS: Two patients had a complete clinical response within 3 months of commencing treatment. The third patient had a further significant response to radiotherapy outside the field of treatment after initial response to anti-PD-1 therapy, which lasted for over 12 months.
CONCLUSION: We are now in the era of immunotherapy with promising results in select patients. However, the number of complete remissions with single agents are low. This report demonstrates the potential for combination therapy in mRCC to produce complete responses and improved survival rates. Whether these results equate to cure in a subset of patients requires longer follow-up. Further evaluation of dosing regimens, sequencing methods, and biomarkers to select patient population is required to advance this treatment strategy. IMPLICATIONS FOR PRACTICE: Multiple phase I-III studies exploring the benefit of combination immunotherapy are currently under way. Further research into predictive biomarkers to identify the cohort of patients who gain this benefit is pertinent. This case series demonstrates that the combination of immunotherapy with other treatments can lead to complete responses, even in patients with initially bulky disease. Combination therapy with immunotherapy seems to cause more durable responses in patients with metastatic renal cell cancer compared with monotherapy. Significantly longer follow-up is necessary to determine whether durable complete response confers a cure in a select group of patients. © AlphaMed Press 2017.

Entities:  

Keywords:  Combination therapy; Complete response rate; Immunotherapy; Renal cell carcinoma; Targeted therapy

Mesh:

Substances:

Year:  2017        PMID: 29146617      PMCID: PMC5728040          DOI: 10.1634/theoncologist.2017-0159

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  32 in total

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3.  Vascular endothelial growth factor affects dendritic cell maturation through the inhibition of nuclear factor-kappa B activation in hemopoietic progenitor cells.

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4.  Nivolumab and ipilimumab versus ipilimumab in untreated melanoma.

Authors:  Michael A Postow; Jason Chesney; Anna C Pavlick; Caroline Robert; Kenneth Grossmann; David McDermott; Gerald P Linette; Nicolas Meyer; Jeffrey K Giguere; Sanjiv S Agarwala; Montaser Shaheen; Marc S Ernstoff; David Minor; April K Salama; Matthew Taylor; Patrick A Ott; Linda M Rollin; Christine Horak; Paul Gagnier; Jedd D Wolchok; F Stephen Hodi
Journal:  N Engl J Med       Date:  2015-04-20       Impact factor: 91.245

Review 5.  The interplay of immunotherapy and chemotherapy: harnessing potential synergies.

Authors:  Leisha A Emens; Gary Middleton
Journal:  Cancer Immunol Res       Date:  2015-05       Impact factor: 11.151

6.  Survival, Durable Response, and Long-Term Safety in Patients With Previously Treated Advanced Renal Cell Carcinoma Receiving Nivolumab.

Authors:  David F McDermott; Charles G Drake; Mario Sznol; Toni K Choueiri; John D Powderly; David C Smith; Julie R Brahmer; Richard D Carvajal; Hans J Hammers; Igor Puzanov; F Stephen Hodi; Harriet M Kluger; Suzanne L Topalian; Drew M Pardoll; Jon M Wigginton; Georgia D Kollia; Ashok Gupta; Dan McDonald; Vindira Sankar; Jeffrey A Sosman; Michael B Atkins
Journal:  J Clin Oncol       Date:  2015-03-30       Impact factor: 44.544

7.  PD-1 and CTLA-4 combination blockade expands infiltrating T cells and reduces regulatory T and myeloid cells within B16 melanoma tumors.

Authors:  Michael A Curran; Welby Montalvo; Hideo Yagita; James P Allison
Journal:  Proc Natl Acad Sci U S A       Date:  2010-02-16       Impact factor: 11.205

8.  Three-year follow-up of advanced melanoma patients who received ipilimumab plus fotemustine in the Italian Network for Tumor Biotherapy (NIBIT)-M1 phase II study.

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Journal:  Ann Oncol       Date:  2014-12-23       Impact factor: 32.976

9.  Pretreatment serum VEGF is associated with clinical response and overall survival in advanced melanoma patients treated with ipilimumab.

Authors:  Jianda Yuan; Jun Zhou; Zhiwan Dong; Sapna Tandon; Deborah Kuk; Katherine S Panageas; Philip Wong; Xinqi Wu; Jarushka Naidoo; David B Page; Jedd D Wolchok; F Stephen Hodi
Journal:  Cancer Immunol Res       Date:  2014-02       Impact factor: 11.151

10.  Abscopal effects of radiotherapy on advanced melanoma patients who progressed after ipilimumab immunotherapy.

Authors:  Antonio M Grimaldi; Ester Simeone; Diana Giannarelli; Paolo Muto; Sara Falivene; Valentina Borzillo; Francesca Maria Giugliano; Fabio Sandomenico; Antonella Petrillo; Marcello Curvietto; Assunta Esposito; Miriam Paone; Marco Palla; Giuseppe Palmieri; Corrado Caracò; Gennaro Ciliberto; Nicola Mozzillo; Paolo A Ascierto
Journal:  Oncoimmunology       Date:  2014-05-14       Impact factor: 8.110

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  4 in total

1.  Interleukin-2 Can Cure Kidney Cancer.

Authors:  Janice P Dutcher; Peter H Wiernik
Journal:  Oncologist       Date:  2018-08-13

2.  Inhibition of Sirt6 suppresses tumor growth by inducing G1/S phase arrest in renal cancer cells.

Authors:  Yu Ding; Sisi Wu; Yuwei Huo; Xuemei Chen; Li Chai; Yan Wang; Xiangxiu Wang; Guonian Zhu; Wei Jiang
Journal:  Int J Clin Exp Pathol       Date:  2019-07-01

3.  Development and Validation of an Inflammatory Response-Related Gene Signature for Predicting the Prognosis of Pancreatic Adenocarcinoma.

Authors:  Zu-Liang Deng; Ding-Zhong Zhou; Su-Juan Cao; Qing Li; Jian-Fang Zhang; Hui Xie
Journal:  Inflammation       Date:  2022-03-23       Impact factor: 4.092

4.  Cytokine Measurements for Diagnosing and Characterizing Leukemoid Reactions and Immunohistochemical Validation of a Granulocyte Colony-Stimulating Factor and CXCL8-Producing Renal Cell Carcinoma.

Authors:  Maria Åström; Walid Tajeddinn; Mats G Karlsson; Olle Linder; Jan Palmblad; Per Lindblad
Journal:  Biomark Insights       Date:  2018-08-17
  4 in total

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