Emerging Trends for Radio-Immunotherapy in Rectal Cancer

被引:23
作者
Corro, Claudia [1 ,2 ]
Dutoit, Valerie [1 ,2 ]
Koessler, Thibaud [3 ]
机构
[1] Univ Geneva, Translat Res Ctr Oncohematol, Dept Med, Fac Med, CH-1205 Geneva, Switzerland
[2] Swiss Canc Ctr Leman, CH-1005 Lausanne, Switzerland
[3] Geneva Univ Hosp, Dept Oncol, CH-1205 Geneva, Switzerland
关键词
rectal cancer; radiotherapy; immune checkpoint inhibitors; tumor microenvironment; SHORT-COURSE RADIOTHERAPY; CONSENSUS MOLECULAR SUBTYPES; ADVANCED COLORECTAL-CANCER; MISMATCH REPAIR-DEFICIENT; TOTAL MESORECTAL EXCISION; PHASE-III TRIAL; PREOPERATIVE RADIOTHERAPY; LOCAL RECURRENCE; RANDOMIZED-TRIAL; POSTOPERATIVE CHEMORADIOTHERAPY;
D O I
10.3390/cancers13061374
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Despite recent advances in understanding the molecular biology of tumors, obstacles still exist in the treatment of patients affected by rectal cancer. Recent evidence shows that ionizing radiation may have profound immunostimulatory effects, hinting at the possibility of exploiting radiotherapy to boost anti-tumor immunity. A bulk of work in pre-clinical tumor models have highlighted the potential benefit of this approach. Following these results, a few clinical trials are now evaluating the combination of radiotherapy and immune checkpoint inhibition. Remarkably, encouraging safety and toxicity profiles from these studies indicate that radio-immunotherapy combinations could represent a valid opportunity for rectal cancer patients. Yet, the biological and clinical impact of a radio-immunotherapy combination in rectal cancer remains unclear and further studies need to be performed to optimize the effect of these combinations. Rectal cancer is a heterogeneous disease at the genetic and molecular levels, both aspects having major repercussions on the tumor immune contexture. Whilst microsatellite status and tumor mutational load have been associated with response to immunotherapy, presence of tumor-infiltrating lymphocytes is one of the most powerful prognostic and predictive biomarkers. Yet, the majority of rectal cancers are characterized by microsatellite stability, low tumor mutational burden and poor T cell infiltration. Consequently, these tumors do not respond to immunotherapy and treatment largely relies on radiotherapy alone or in combination with chemotherapy followed by radical surgery. Importantly, pre-clinical and clinical studies suggest that radiotherapy can induce a complete reprograming of the tumor microenvironment, potentially sensitizing it for immune checkpoint inhibition. Nonetheless, growing evidence suggest that this synergistic effect strongly depends on radiotherapy dosing, fractionation and timing. Despite ongoing work, information about the radiotherapy regimen required to yield optimal clinical outcome when combined to checkpoint blockade remains largely unavailable. In this review, we describe the molecular and immune heterogeneity of rectal cancer and outline its prognostic value. In addition, we discuss the effect of radiotherapy on the tumor microenvironment, focusing on the mechanisms and benefits of its combination with immune checkpoint inhibitors.
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页码:1 / 28
页数:28
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