Abstract:Background The majority of oral cavity cancers arise in the oral tongue. The aim of this study was to evaluate the prognostic value of tumor budding in oral tongue squamous cell carcinoma, both as a separate variable and in combination with depth of invasion. We also assessed the prognostic impact of the 8th edition of the American Joint Committee on Cancer's TNM classification (TNM8), where depth of invasion (DOI) supplements diameter in the tumor size (T) categorization. Methods Patients diagnosed with prima… Show more
“…Regarding the emerging prognostic markers that are not included in the pathology report, the published studies revealed a promising prognostic value for cancer‐related histopathologic markers including cell‐in‐cell structures (one study), 19 tumor budding (seven studies), 13,15,25–29 and pattern of invasion (15 studies) which were evaluated either as mode of invasion, 22,30 pattern of invasion, 31–34 invasive pattern, 28 or WPOI 13,16,25,35–39 . At the same time, some of the relevant studies analyzed stromal‐related histopathologic markers including stromal infiltrating lymphocytes (one study) 18 and tumor–stroma ratio (TSR; three studies) 17,40,41 which were significantly associated with prognosis.…”
Section: Resultsmentioning
confidence: 99%
“…The meta‐analysis of OS revealed some heterogeneity ( I 2 = 44%). For DSS, two studies 15,25 were included in the meta‐analysis and are visualized using a forest plot (Figure 2B). Again, tumor budding was indicated to be a predictor of DSS (HR 1.89, 95% CI 1.13–3.15; p = 0.02).…”
Section: Resultsmentioning
confidence: 99%
“…Although these have shown good prognostic value for early‐stage OTSCC, they are not included in clinical implementation. Examples of such markers include tumor budding, 13–15 worst pattern of invasion (WPOI), 13,16 tumor stroma ratio (TSR), 17 tumor‐infiltrating lymphocytes (TILs), 18 and cell‐in‐cell phenomenon, 19 which has been recently studied in many cancers including early OTSCC 19 …”
Although there are many histopathologic prognosticators, grading of early oral tongue squamous cell carcinoma (OTSCC) is still based on morphological cell differentiation which has low prognostic value. Here we summarize the emerging histopathological markers showing powerful prognostic value, but are not included in pathology reports. Using PubMed, Scopus, Ovid Medline, and Web of Science databases, a systematic literature search was preformed to identify early OTSCC studies that investigated the prognostic significance of hematoxylin-eosin-based histopathologic markers. Our meta-analysis showed that tumor budding was associated with overall survival (hazard ratio[HR] 2.32; 95% CI 1.40-3.84; p < 0.01) and disease-specific survival (DSS) (1.89; 95% CI 1.13-3.15; p = 0.02). Worst pattern of invasion was associated with disease-free survival (DFS) (1.95; 95% CI 1.04-3.64; p = 0.04). Tumor-Alhadi Almangush and Tuula Salo jointly supervised this work.
“…Regarding the emerging prognostic markers that are not included in the pathology report, the published studies revealed a promising prognostic value for cancer‐related histopathologic markers including cell‐in‐cell structures (one study), 19 tumor budding (seven studies), 13,15,25–29 and pattern of invasion (15 studies) which were evaluated either as mode of invasion, 22,30 pattern of invasion, 31–34 invasive pattern, 28 or WPOI 13,16,25,35–39 . At the same time, some of the relevant studies analyzed stromal‐related histopathologic markers including stromal infiltrating lymphocytes (one study) 18 and tumor–stroma ratio (TSR; three studies) 17,40,41 which were significantly associated with prognosis.…”
Section: Resultsmentioning
confidence: 99%
“…The meta‐analysis of OS revealed some heterogeneity ( I 2 = 44%). For DSS, two studies 15,25 were included in the meta‐analysis and are visualized using a forest plot (Figure 2B). Again, tumor budding was indicated to be a predictor of DSS (HR 1.89, 95% CI 1.13–3.15; p = 0.02).…”
Section: Resultsmentioning
confidence: 99%
“…Although these have shown good prognostic value for early‐stage OTSCC, they are not included in clinical implementation. Examples of such markers include tumor budding, 13–15 worst pattern of invasion (WPOI), 13,16 tumor stroma ratio (TSR), 17 tumor‐infiltrating lymphocytes (TILs), 18 and cell‐in‐cell phenomenon, 19 which has been recently studied in many cancers including early OTSCC 19 …”
Although there are many histopathologic prognosticators, grading of early oral tongue squamous cell carcinoma (OTSCC) is still based on morphological cell differentiation which has low prognostic value. Here we summarize the emerging histopathological markers showing powerful prognostic value, but are not included in pathology reports. Using PubMed, Scopus, Ovid Medline, and Web of Science databases, a systematic literature search was preformed to identify early OTSCC studies that investigated the prognostic significance of hematoxylin-eosin-based histopathologic markers. Our meta-analysis showed that tumor budding was associated with overall survival (hazard ratio[HR] 2.32; 95% CI 1.40-3.84; p < 0.01) and disease-specific survival (DSS) (1.89; 95% CI 1.13-3.15; p = 0.02). Worst pattern of invasion was associated with disease-free survival (DFS) (1.95; 95% CI 1.04-3.64; p = 0.04). Tumor-Alhadi Almangush and Tuula Salo jointly supervised this work.
“…The major pitfalls of our study are its retrospective nature, lack of centralized pathology revision, and the lack of a pathological nodal staging for half of the patients. Moreover, other prognosticators such as the pattern of invasion, PNI density foci, and tumor budding, which were recently demonstrated to be expression of tumor biological behavior, were not available [ 18 , 19 , 20 ].…”
Background: This study investigated the role of depth of infiltration (DOI) as an independent prognosticator in early stage (T1-T2N0M0) oral cavity tumors and to evaluate the need of postoperative radiotherapy in the case of patients upstaged to pT3 for DOI > 10 mm in the absence of other risk factors. Methods: We performed a retrospective analysis on patients treated with surgery and re-staged according to the 8th edition of malignant tumors classification (TNM). The role of DOI as well as other clinical/pathological features was investigated at both univariable and multivariable analyses on overall survival (OS), disease free survival (DFS), relapse free survival (RFS), and local RFS. Results: Among the 94 included patients, 23 would have been upstaged to pT3 based on DOI. Multivariable analysis showed that DOI was not an independent prognostic factor for any of the considered outcomes. The presence of perineural invasion was associated with a significant worse RFS (p = 0.02) and LRFS (p = 0.04). PORT was found to be significantly associated with DFS (p = 0.04) and RFS (p = 0.06). Conclusions: The increasing DOI alone was not sufficient to impact the prognosis, and therefore, should not be sufficient to dictate PORT indications in early-stage patients upstaged on the sole basis of DOI.
“…Piazza et al (2019) and Bjerkli et al (2020) suggested that the 8th edition of the AJCC staging system improved the prognostic value of the T category than the previous one in early-stage oral tongue SCC [ 19 , 20 ]. Contrary to Piazza et al (2019) and Bjerkli et al (2020), our results are more relevant to Kano et al (2018) As this study included a relatively small number of patients and all oral cavity subsites, additional studies using a larger patient population are needed.…”
The aim of this study was to compare the effect of using depth of invasion (DOI) versus tumor thickness (TT) as a prognostic factor for early-stage oral squamous cell carcinoma (OSCC). A total of 57 patients with early-stage OSCC treated surgically from 2009 to 2014 at our institution were reviewed retrospectively. Histopathological measurement of DOI and TT was performed. The validation of DOI and TT as prognostic factors was conducted using a Kaplan–Meier survival analysis. TT had no association with disease-specific survival (DSS) or progression-free survival (PFS) in this cohort; however, increased DOI was significantly associated with decreased DSS but not correlated to decreased PFS. The T category of the 7th edition of AJCC was statistically associated with both DSS and PFS; however, the T category of the 8th edition of the AJCC was only associated with DSS. In this study group, TT could not be used as a prognostic factor, and DOI was not by itself sufficient to predict prognosis for early-stage OSCC. The T category in AJCC 8th Edition cannot be considered the sole prognostic factor for early OSCC, so additional prognostic factors may need to be considered.
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