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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorTissera, Natalia Soledad
dc.contributor.authorEsteso, Federico
dc.contributor.authorLuca, Romina
dc.contributor.authorEnrico, Diego
dc.contributor.authorWaisberg, Federico
dc.contributor.authorRodríguez, Andrés
dc.date.accessioned2023-09-14T11:07:19Z
dc.date.available2023-09-14T11:07:19Z
dc.date.issued2023-06-30
dc.identifier.citationTissera NS, Esteso F, Luca R, Enrico D, Waisberg F, Rodriguez A, et al. Atypical pattern of response in rectal cancer after neoadjuvant pembrolizumab treatment: a case report, literature review, and proposed management model. J Gastrointest Oncol. 2023 Jun 30;14(3):1635-42.
dc.identifier.issn2219-679X
dc.identifier.urihttps://hdl.handle.net/11351/10278
dc.descriptionRectal cancer; Neoadjuvant; Pembrolizumab
dc.description.abstractBackground: Immunotherapy is the first-line treatment in patients with advanced microsatellite instability-high (MSI-H) or deficient mismatch repair (dMMR) colorectal cancer (CRC). Although immune checkpoint inhibitors (ICIs) for locally advanced rectal cancer (LARC) are not yet a standard, the results are very encouraging and raise the question of whether patients with clinical complete response (cCR) could receive nonoperative management (NOM). However, different patterns of response have challenged management strategies. Case Description: A 34-year-old woman diagnosed with dMMR LARC started treatment with capecitabine 2,000 mg/m2 on day 1 to 14 and oxaliplatin 130 mg/m2 on day 1 and every 21 days. Magnetic resonance imaging (MRI), performed three cycles later, showed local progression of the primary rectal lesion, which at that time had new peritoneal reflex involvement. A new hepatic lesion in segment V was observed. Due to disease progression, she was administered pembrolizumab 200 mg every 21 days. After three cycles, a discordant radiological response was observed on a new MRI scan that showed a complete response of the liver lesion and magnetic resonance tumor regression grade (mrTRG) 1 in the rectum. However, new involvement of the mesentery and enlargement of the regional lymph nodes (LNs) were also evident. A new colonoscopic biopsy was performed, showing no cancerous cells. She underwent surgery on the rectum and liver lesion. Pathology showed a complete response of the rectal wall and liver lesion, but 1 of 22 LNs was positive for adenocarcinoma (ypT0 N1 M0). The patient continued on pembrolizumab, and 14 months after surgery, she had not relapsed. Conclusions: Neoadjuvant immunotherapy for rectal cancer requires new recommendations for the assessment of clinical response. Pseudoprogression should be ruled out as an atypical response before deciding on surgical treatment. We propose an algorithm to address pseudoprogression in this setting.
dc.language.isoeng
dc.publisherAME Publishing Company
dc.relation.ispartofseriesJournal of Gastrointestinal Oncology;14(3)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectRecte - Càncer - Immunoteràpia
dc.subjectCòlon - Càncer - Immunoteràpia
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subject.meshColorectal Neoplasms
dc.subject.mesh/drug therapy
dc.subject.meshNeoadjuvant Therapy
dc.subject.meshTreatment Outcome
dc.titleAtypical pattern of response in rectal cancer after neoadjuvant pembrolizumab treatment: a case report, literature review, and proposed management model
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.21037/jgo-22-1140
dc.subject.decsneoplasias colorrectales
dc.subject.decs/farmacoterapia
dc.subject.decstratamiento neoadyuvante
dc.subject.decsresultado del tratamiento
dc.relation.publishversionhttp://dx.doi.org/10.21037/jgo-22-1140
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Tissera NS] Upper Gastrointestinal Cancer Translational Research Group, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Esteso F, Luca R] Department of Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina. [Enrico D, Waisberg F, Rodriguez A] Department of Oncology, Alexander Fleming Cancer Institute, Buenos Aires, Argentina. Research Unit, Alexander Fleming Cancer Institute, Buenos Aires, Argentina
dc.identifier.pmid37435212
dc.identifier.wos001017659000001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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