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Rapid Onsite Evaluation for Specimen Adequacy and Triage of Breast Masses in a Low-Resource Setting
Open accessAbstract
Context.—: Rapid onsite evaluation (ROSE) is critical in determining sample adequacy and triaging cytology samples. Although fine-needle aspiration biopsy (FNAB) is the primary method of initial tissue sampling in Tanzania, ROSE is not practiced. Objective.—: To investigate the performance of ROSE in determining cellular adequacy and providing preliminary diagnoses in breast FNAB in a low-resource setting. Design.—: Patients with breast masses were recruited prospectively from the FNAB clinic at Muhimbili National Hospital. Each FNAB was evaluated by ROSE for overall specimen adequacy, cellularity, and preliminary diagnosis. The preliminary interpretation was compared to the final cytologic diagnosis and histologic diagnosis, when available. Results.—: Fifty FNAB cases were evaluated, and all were adequate for diagnosis on ROSE and final interpretation. Overall percentage of agreement (OPA) between preliminary and final cytologic diagnosis was 84%, positive percentage of agreement (PPA) was 33%, and negative percentage of agreement (NPA) was 100% (κ = 0.4, P < .001). Twenty-one cases had correlating surgical resections. OPA between preliminary cytologic and histologic diagnoses was 67%, PPA was 22%, and NPA was 100% (κ = 0.2, P = .09). OPA between final cytologic and histologic diagnoses was 95%, PPA was 89%, and NPA was 100% (κ = 0.9, P = <.001). Conclusions.—: False-positive rates of ROSE diagnoses for breast FNAB are low. While preliminary cytologic diagnoses had a high false-negative rate, final cytologic diagnoses had overall high concordance with histologic diagnoses. Therefore, the role of ROSE for preliminary diagnosis should be considered carefully in low-resource settings, and it may need to be paired with additional interventions to improve pathologic diagnosis.
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“The use of the FNAB for accurate diagnoses of mass lesions has been reported as especially useful in low resource settings, including low-and middle-income countries (LMICs).4,5”
From Fine needle aspiration biopsy in low‐ and middle‐income countries (2024) · cites this paper as [4]
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The Influence of Rapid Onsite Evaluation on the Adequacy Rate of Fine-Needle Aspiration Cytology
Schmidt, R. L., Witt, B. L., Lopez-Calderon, L. E., & Layfield, L. J. (2013) · American Journal of Clinical Pathology · doi:10.1309/ajcpegzmjkc42vup · Cited by 149
Ng, D. L., Vuhahula, E., Zhang, L., Waterhouse, E. G., White, K. L., Mushi, B. P., Nyeriga, M. S., Philipo, G. S., Mmbaga, E. J., Sheth, S., et al. (2018) · Journal of Global Oncology · doi:10.1200/jgo.18.00134 · Cited by 15
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Research works printed but not linked: 48
- Burson AM, Soliman AS, Ngoma TA, et al. Clinical and epidemiologic profile of breast cancer in Tanzania. Breast Dis. 2010; 31(1): 33– 41. doi:10.3233/BD-2009-0296 · DOI
- Amadori D, Serra P, Bravaccini S, et al. Differences in biological features of breast cancer between Caucasian (Italian) and African (Tanzanian) populations. Breast Cancer Res Treat. 2014; 145(1): 177– 183. doi:10.1007/s10549-014-2903-0 · DOI
- Mwakigonja AR, Lushina NE, Mwanga A. Characterization of hormonal receptors and human epidermal growth factor receptor-2 in tissues of women with breast cancer at Muhimbili National Hospital, Dar es salaam, Tanzania. Infect Agents Cancer. 2017; 12: 60. doi:10.1186/s13027-017-0170-5 · DOI
- Rambau P, Chalya P, Manyama M, Jackson K. Pathological features of breast cancer seen in Northwestern Tanzania: a nine years retrospective study. BMC Res Notes. 2011; 4: 214. doi:10.1186/1756-0500-4-214 · DOI
- Rambau PF. Pathology practice in a resource-poor setting: Mwanza, Tanzania. Arch Pathol Lab Med. 2011; 135(2): 191– 193. doi:10.1043/1543-2165-135.2.191 · DOI
- Richards MA, Westcombe AM, Love SB, Littlejohns P, Ramirez AJ. Influence of delay on survival in patients with breast cancer: a systematic review. Lancet. 1999; 353(9159): 1119– 1126. doi:10.1016/s0140-6736(99)02143-1 · DOI
- Thomas J. Role of cytopathology in cancer control in low-resource settings: sub-Saharan Africa's perspective. Int Health. 2011; 3(1): 3– 6. doi:10.1016/j.inhe.2010.09.002 · DOI · Paper page
- Yu YH, Wei W, Liu JL. Diagnostic value of fine-needle aspiration biopsy for breast mass: a systematic review and meta-analysis. BMC Cancer. 2012; 12(1): 41. doi:10.1186/1471-2407-12-41 · DOI
- Dong J, Ly A, Arpin R, Ahmed Q, Brachtel E. Breast fine needle aspiration continues to be relevant in a large academic medical center: experience from Massachusetts General Hospital. Breast Cancer Res Treat. 2016; 158(2): 297– 305. doi:10.1007/s10549-016-3886-9 · DOI
- Farras Roca JA, Tardivon A, Thibault F, et al. Diagnostic performance of ultrasound-guided fine-needle aspiration of nonpalpable breast lesions in a multidisciplinary setting: the Institut Curie's experience. Am J Clin Pathol. 2017; 147(6): 571– 579. doi:10.1093/ajcp/aqx009 · DOI
- Wong S, Rickard M, Earls P, Arnold L, Bako B, Field AS. The International Academy of Cytology Yokohama System for Reporting Breast Fine Needle Aspiration Biopsy Cytopathology: a single institutional retrospective study of the application of the system categories and the impact of rapid onsite evaluation. Acta Cytol. 2019; 63(4): 280– 291. doi:10.1159/000500191 · DOI
- Hoda RS, Brachtel EF. International Academy of Cytology Yokohama System for Reporting Breast Fine-Needle Aspiration Biopsy Cytopathology: a review of predictive values and risks of malignancy. Acta Cytol. 2019; 63(4): 292– 301. doi: 10.1159/000500704 · DOI
- Montezuma D, Malheiros D, Schmitt FC. Breast fine needle aspiration biopsy cytology using the newly proposed IAC Yokohama System for Reporting Breast Cytopathology: the experience of a single institution. Acta Cytol. 2019Feb15: 1– 6. doi: 10.1159/000492638 · DOI
- Nasuti JF, Gupta PK, Baloch ZW. Diagnostic value and cost-effectiveness of on-site evaluation of fine-needle aspiration specimens: review of 5,688 cases. Diagn Cytopathol. 2002; 27(1): 1– 4. doi:10.1002/dc.10065 · DOI
- Hamill J, Campbell ID, Mayall F, Bartlett ASJR, Darlington A. Improved breast cytology results with near patient FNA diagnosis. Acta Cytol. 2002; 46(1): 19– 24. doi:10.1159/000326710 · DOI
- Ljung BM, Drejet A, Chiampi N, et al. Diagnostic accuracy of fine-needle aspiration biopsy is determined by physician training in sampling technique. Cancer. 2001; 93(4): 263– 268. doi:10.1002/cncr.9040 · DOI · Paper page
- Philipo GS, Vuhahula E, Kimambo A, Mmbaga EJ, Van Loon K, Ng DL. Feasibility of fine-needle aspiration biopsy and rapid on-site evaluation for immediate triage in breast cancer screening in Tanzania. JCO Global Oncology. 2021; (7): 146– 152. doi:10.1200/GO.20.00279 · DOI · Paper page
- Agarwal P, Toi PC, Subramaniam H, Apoorva Lakshmi S. Prospective comparison of cytological specimen adequacy assessment by different rapid staining techniques for rapid on-site evaluation in fine needle aspiration cytology and their cost-effectiveness. Diagn Cytopathol. 2019; 47(5): 469– 474. doi:10.1002/dc.24139 · DOI
- Saba K, Niazi S, Bukhari MH, Imam SF. Use of supravital toluidine blue staining to improve the efficiency of fine-needle aspiration cytology reporting in comparison to Papanicolaou stain. Pak J Med Sci. 2015; 31(5): 1146– 1151. doi:10.12669/pjms.315.8411 · DOI
- Hewer E, Schmitt AM. Ultrafast toluidine blue staining for rapid on-site evaluation of cytological smears. Acta Cytol. 2020; 64(4): 375– 377. doi:10.1159/000505254 · DOI
- Rausch T, Rochat M-C, Moret M, Braunschweig R, Mihaescu A. Modified technique of toluidine blue staining in rapid on-site evaluation. Diagn Cytopathol. 2012; 40(9): 847– 848. doi:10.1002/dc.21753 · DOI
- Yadav K, Cree I, Field A, Vielh P, Mehrotra R. Importance of cytopathologic diagnosis in early cancer diagnosis in resource-constrained countries. JCO Glob Oncol. 2022; 8: e2100337. doi:10.1200/GO.21.00337 · DOI · Paper page
- Duggan C, Trapani D, Ilbawi AM, et al. National health system characteristics, breast cancer stage at diagnosis, and breast cancer mortality: a population-based analysis. Lancet Oncol. 2021; 22(11): 1632– 1642. doi:10.1016/S1470-2045(21)00462-9 · DOI
- Anderson BO, Ilbawi AM, Fidarova E, et al. The Global Breast Cancer Initiative: a strategic collaboration to strengthen health care for non-communicable diseases. Lancet Oncol. 2021; 22(5): 578– 581. doi:10.1016/S1470-2045(21)00071-1 · DOI
- Ljung BM, Drejet A, Chiampi N, et al. Diagnostic accuracy of fine-needle aspiration biopsy is determined by physician training in sampling technique. Cancer. 2001; 93(4): 263– 268. coi:10.1002/cncr.9040 · DOI · Paper page
- Field AS. Training for cytotechnologists and cytopathologists in the developing world. Cytopathology. 2016; 275):313–316.doi:10.1111/cyt.12372 · DOI
- Gui GP, Allum WH, Perry NM, et al. One-stop diagnosis for symptomatic breast disease. Ann R Coll Surg Engl. 1995; 77(1): 24– 27.
- Delaloge S, Bonastre J, Borget I, et al. The challenge of rapid diagnosis in oncology: diagnostic accuracy and cost analysis of a large-scale one-stop breast clinic. Eur J Cancer. 2016; 66: 131– 137. doi:10.1016/j.ejca.2016.06.021 · DOI
- Ly A, Ono JC, Hughes KS, Pitman MB, Balassanian R. Fine-needle aspiration biopsy of palpable breast masses: patterns of clinical use and patient experience. J Natl Compr Canc Netw. 2016; 14(5): 527– 536. doi:10.6004/jnccn.2016.0061 · DOI
- Schmidt RL, Kordy MA, Howard K, Layfield LJ, Hall BJ, Adler DG. Risk-benefit analysis of sampling methods for fine-needle aspiration cytology: a mathematical modeling approach. Am J Clin Pathol. 2013; 139(3): 336– 344. doi:10.1309/AJCPEAKR4MO2GQBO · DOI
- Ammanagi AS, Dombale VD, Patil SS. On-site toluidine blue staining and screening improves efficiency of fine-needle aspiration cytology reporting. Acta Cytol. 2012; 56(4): 347– 351. doi:10.1159/000338725 · DOI
- Torous VF, Lopez SH, Xu C, Sweeney BJ, Pitman MB. Performance of rapid on-site evaluation in breast fine-needle aspiration biopsies: identifying areas of diagnostic challenge. Acta Cytol. 2022; 66(1): 1– 13. doi:10.1159/000518579 · DOI
- Brundyn K, Koegelenberg CFN, Diacon AH, et al. Transbronchial fine needle aspiration biopsy and rapid on-site evaluation in the setting of superior vena cava syndrome. Diagn Cytopathol. 2013; 41(4): 324– 329. doi:10.1002/dc.21857 · DOI
- Koegelenberg CFN, Diacon AH, Irusen EM, et al. The diagnostic yield and safety of ultrasound-assisted transthoracic biopsy of mediastinal masses. Respiration. 2011; 81(2): 134– 141. doi:10.1159/000322005 · DOI
- Diacon AH, Schuurmans MM, Theron J, et al. Utility of rapid on-site evaluation of transbronchial needle aspirates. Respiration. 2005; 72(2): 182– 188. doi:10.1159/000084050 · DOI
- Mfokazi A, Wright CA, Louw M, et al. Direct comparison of liquid-based and smear-based cytology with and without rapid on-site evaluation for fine needle aspirates of thoracic tumors. Diagn Cytopathol. 2016; 44(5): 363– 368. doi:10.1002/dc.23447 · DOI
- Geisler DL, Nestler RJ, Mosley BL, et al. Accuracy of definitive rapid on-site evaluation cytopathology diagnoses: assessment of potentially critical diagnoses as a quality assurance measure. J Am Soc Cytopathol. 2022; 11(3): 133– 141. doi:10.1016/j.jasc.2022.02.002 · DOI
- Sakuma T, Mimura A, Tanigawa N, Takamizu R, Morishima H, Matsunami N. Rapid on-site cytologic examination of 1500 breast lesions using the modified Shorr's stain. Breast Cancer. 2015; 22(3): 280– 286. doi:10.1007/s12282-013-0479-x · DOI
- Bofin AM, Lydersen S, Isaksen C, Hagmar BM. Interpretation of fine needle aspiration cytology of the breast: a comparison of cytological, frozen section, and final histological diagnoses. Cytopathology. 2004; 15(6): 297– 304. doi:10.1111/j.1365-2303.2004.00159.x · DOI
- Liew PL, Liu TJ, Hsieh MC, et al. Rapid staining and immediate interpretation of fine-needle aspiration cytology for palpable breast lesions: diagnostic accuracy, mammographic, ultrasonographic and histopathologic correlations. Acta Cytol. 2010; 55(1): 30– 37. doi:10.1159/000320869 · DOI
- Krishnamurthy S, Ashfaq R, Shin HJC, Sneige N. Distinction of phyllodes tumor from fibroadenoma. Cancer Cytopathol. 2000; 90(6): 342– 349. doi:10.1002/1097-0142(20001225)90:6<342::AID-CNCR4>3.0.CO;2-I · DOI
- El Hag IA, Aodah A, Kollur SM, Attallah A, Mohamed AAE, Al-Hussaini H. Cytological clues in the distinction between phyllodes tumor and fibroadenoma. Cancer Cytopathol. 2010; 118(1): 33– 40. doi:10.1002/cncy.20057 · DOI
- Dusenbery D, Frable WJ. Fine needle aspiration cytology of phyllodes tumor. Potential diagnostic pitfalls. Acta Cytol. 1992; 36(2): 215– 221.
- Scolyer RA, McKenzie PR, Achmed D, Lee CS. Can phyllodes tumours of the breast be distinguished from fibroadenomas using fine needle aspiration cytology? Pathology . 2001; 33(4): 437– 443. doi:10.1080/00313020120083151 · DOI
- Veneti S, Manek S. Benign phyllodes tumour vs fibroadenoma: FNA cytological differentiation. Cytopathology. 2001; 12(5): 321– 328. doi:10.1046/j.1365-2303.2001.00334.x · DOI
- Maritz RM, Michelow PM. Cytological criteria to distinguish phyllodes tumour of the breast from fibroadenoma. Acta Cytol. 2017; 61(6): 418– 424. doi:10.1159/000477573 · DOI
- Tummidi S, Kothari K, Agnihotri M, Naik L, Sood P. Fibroadenoma versus phyllodes tumor: a vexing problem revisited! BMC Cancer . 2020; 20(1): 648. doi:10.1186/s12885-020-07129-0 · DOI
- Koshikawa T, Kyotake A, Tsukamoto R, Itoh T. Standard and rapid stains in fine-needle aspiration cytology and rapid on-site evaluation with a short column (standard and rapid stains in fine-needle aspiration cytology and rapid on-site evaluation). In: KakudoK,ed. Thyroid FNA Cytology: Differential Diagnoses and Pitfalls. Singapore: Springer; 2019: 505– 509. doi:10.1007/978-981-13-1897-9_66 · DOI
Cited by
Sorted by citations
Fine needle aspiration biopsy in low‐ and middle‐income countries
Khorsandi, N., Balassanian, R., & Vohra, P. (2024) · Diagnostic Cytopathology · doi:10.1002/dc.25317 · Cited by 4
Metadata
- Authors
- Kimambo, A. H., Vuhahula, E. A., Philipo, G. S., Mushi, B. P., Mmbaga, E. J., Van Loon, K., & Ng, D. L.
- Affiliations
- Muhimbili University of Health and Allied Sciences (TZ)
- the Division of Hematology and Oncology in the Department of Medicine (Van Loon), the Helen Diller Family Comprehensive Cancer Center (Van Loon, Ng)
- Memorial Sloan Kettering Cancer Center (US)
- Corresponding author
- Ng, Dianna L.
- ORCID
- Venue
- Archives of Pathology & Laboratory Medicine
- Published
- 2023-06-19
- Volume
- 148
- Issue
- 1
- Pages
- e9-e17
- ISSN
- 0003-9985 (ISSN-L)
- 1543-2165
- PMC
- PMC10728347
- OpenAlex
- W4380925291
- Cited by
- 6
- References
- 2
- Citations by year
- 2026: 4 · 2024: 2
- FWCI
- 1.19
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Locations
- Archives of Pathology & Laboratory Medicine (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (UL1TR001873, UL1TR002384)
- National Cancer Institute (P30CA008748, K08CA263299)
- Fogarty International Center (D43TW009343, D43TW011598)
- National Center for Advancing Translational Sciences
- Topics
- Health Sciences › Medicine › Pathology and Forensic Medicine › Breast Lesions and Carcinomas
- Physical Sciences › Computer Science › Artificial Intelligence › AI in cancer detection
- Health Sciences › Medicine › Pathology and Forensic Medicine › Lymphadenopathy Diagnosis and Analysis
- Keywords
- rapid on-site evaluation, breast mass, fine-needle aspiration, specimen adequacy, resource-limited settings, Tanzania
- MeSH terms
- Breast, Humans, Tanzania, Triage, Biopsy, Fine-Needle
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