Combined Therapy of Locally Advanced Oesophageal and Gastro-Oesophageal Junction Adenocarcinomas: State of the Art and Aspects of Predictive Factors
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, přehledy
PubMed
34572818
PubMed Central
PMC8469285
DOI
10.3390/cancers13184591
PII: cancers13184591
Knihovny.cz E-zdroje
- Klíčová slova
- adenocarcinoma, gastro-oesophageal junction, oesophagus, perioperative chemotherapy, preoperative chemoradiotherapy,
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
The following main treatment approaches are currently used in locally advanced adenocarcinomas of the oesophagus and gastrooesophageal junction (GOJ): preoperative chemoradiotherapy and surgery, and perioperative chemotherapy and surgery. While preoperative chemoradiotherapy is used primarily in oesophageal tumours, perioperative chemotherapy is the treatment of choice in Western countries for gastric cancer. The optimal treatment strategy for GOJ adenocarcinoma is still not clear. In comparison to other malignancies, biomarkers are used as predictive factors in distal oesophageal and GOJ adenocarcinomas in a very limited way, and moreover, only in metastatic stages (e.g., HER2 status, or microsatellite instability status). The aim of the article is to provide an overview of current treatment options in locally advanced adenocarcinomas of oesophagus and GOJ based on the latest evidence, including the possible potential of predictive biomarkers in optimizing treatment.
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Xie Y., Shi L., He X., Luo Y. Gastrointestinal cancers in China, the USA, and Europe. Gastroenterol. Rep. 2021;9:1–104. doi: 10.1093/gastro/goab010. PubMed DOI PMC
Pohl H., Welch H.G. The role of overdiagnosis and reclassification in the marked increase of esophageal adenocarcinoma incidence. J. Natl. Cancer Inst. 2005;97:142–146. doi: 10.1093/jnci/dji024. PubMed DOI
Kort E.J., Sevensma E., Fitzgerald T.L. Trends in esophageal cancer and body mass index by race and gender in the state of Michigan. BMC Gastroenterol. 2009;9:47. doi: 10.1186/1471-230X-9-47. PubMed DOI PMC
Marabotto E., Pellegatta G., Sheijani A.D., Ziola S., Zentilin P., De Marzo M.G., Giannini E.G., Ghisa M., Barberio B., Scarpa M., et al. Prevention Strategies for Esophageal Cancer-An Expert Review. Cancers. 2021;13:2183. doi: 10.3390/cancers13092183. PubMed DOI PMC
Uhlenhopp D.J., Then E.O., Sunkara T., Gaduputi V. Epidemiology of esophageal cancer: Update in global trends, etiology and risk factors. Clin. J. Gastroenterol. 2020;13:1010–1021. doi: 10.1007/s12328-020-01237-x. PubMed DOI
Siewert J.R., Hölscher A.H., Becker K., Gössner W. Cardia cancer: Attempt at a therapeutically relevant classification. Der Chir. Z. Geb. Oper. Medizen. 1987;58:25–32. PubMed
Siewert J.R., Stein H.J. Carcinoma of the cardia: Carcinoma of the gastroesophageal junction-classification, pathology and extent of resection. Dis. Esophagus. 1996;9:173–182.
International Union against Cancer (UICC) In: In TNM Classification of Malignant Tumours. 6th ed. Sobin L.H., Wittekind C., editors. Wiley-Blackwell; New York, NY, USA: 2009.
International Union against Cancer (UICC) In: In TNM Classification of Malignant Tumours. 7th ed. Sobin L.H., Gospodarowicz M.K., Wittekind C., editors. Wiley-Blackwell; New York, NY, USA: 2009. pp. 67–77.
International Union against Cancer (UICC) In: In TNM Classification of Malignant Tumours. 8th ed. Brierley J.D., Gospodarowicz M.K., Wittekind C., editors. Wiley-Blackwell; New York, NY, USA: 2017. pp. 57–67.
Kurokawa Y., Takeuchi H., Doki Y., Mine S., Terashima M., Yasuda T., Yoshida K., Daiko H., Sakuramoto S., Yoshikawa T., et al. Mapping of Lymph Node Metastasis From Esophagogastric Junction Tumors: A Prospective Nationwide Multicenter Study. Ann. Surg. 2021;274:120–127. doi: 10.1097/SLA.0000000000003499. PubMed DOI
Lordick F., Mariette C., Haustermans K., Obermannová R., Arnold D., ESMO Guidelines Committee Oesophageal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2016;27:v50–v57. doi: 10.1093/annonc/mdw329. PubMed DOI
Shah M.A., Kennedy E.B., Catenacci D.V., Deighton D.C., Goodman K.A., Malhotra N.K., Willett C., Stiles B., Sharma P., Tang L., et al. Treatment of Locally Advanced Esophageal Carcinoma: ASCO Guideline. J. Clin. Oncol. 2020;38:2677–2694. doi: 10.1200/JCO.20.00866. PubMed DOI
NCCN Clinical Practice Guidelines in Oncology, NCCN Guidelines Version 2. 2020. [(accessed on 9 June 2020)]. Esophageal and Esophagogastric Junction Cancer. Available online: https://www.nccn.org/professionals/physician_gls/pdf/esophageal.pdf.
Kelly R.J., Ajani J.A., Kuzdzal J., Zander T., Van Cutsem E., Piessen G., Mendez G., Feliciano J., Motoyama S., Lièvre A., et al. Adjuvant Nivolumab in Resected Esophageal or Gastroesophageal Junction Cancer. N. Engl. J. Med. 2021;384:1191–1203. doi: 10.1056/NEJMoa2032125. PubMed DOI
Cooper J.S., Guo M.D., Herskovic A., Macdonald J.S., Martenson J.A., Jr., Al-Sarraf M., Byhardt R., Russell A.H., Beitler J.J., Spencer S., et al. Chemoradiotherapy of locally advanced esophageal cancer: Long-term follow-up of a prospective randomized trial (RTOG 85–01) Radiat. Ther. Oncol. Group. JAMA. 1999;281:1623–1627. doi: 10.1001/jama.281.17.1623. PubMed DOI
Minsky B.D., Pajak T.F., Ginsberg R.J., Pisansky T.M., Martenson J., Komaki R., Okawara G., Rosenthal S.A., Kelsen D.P. INT 0123 (Radiation Therapy Oncology Group 94-05) phase III trial of combined-modality therapy for esophageal cancer: High-dose versus standard-dose radiation therapy. J. Clin. Oncol. 2002;20:1167–1174. doi: 10.1200/JCO.2002.20.5.1167. PubMed DOI
Urschel J.D., Vasan H. A meta-analysis of randomized controlled trials that compared neoadjuvant chemoradiation and surgery to surgery alone for resectable esophageal cancer. Am. J. Surg. 2003;185:538–543. doi: 10.1016/S0002-9610(03)00066-7. PubMed DOI
Fiorica F., Di Bona D., Schepis F., Licata A., Shahied L., Venturi A., Falchi A.M., Craxì A., Cammà C. Preoperative chemoradiotherapy for oesophageal cancer: A systematic review and meta-analysis. Gut. 2004;53:925–930. doi: 10.1136/gut.2003.025080. PubMed DOI PMC
Gebski V., Burmeister B., Smithers B.M., Foo K., Zalcberg J., Simes J. Survival benefits from neoadjuvant chemoradiotherapy or chemotherapy in oesophageal carcinoma: A metaanalysis. Lancet Oncol. 2007;8:226–234. doi: 10.1016/S1470-2045(07)70039-6. PubMed DOI
Walsh T.N., Noonan N., Hollywood D., Kelly A., Keeling N., Hennessy T.P. A comparison of multimodal therapy and surgery for esophageal adenocarcinoma. N. Engl. J. Med. 1996;335:462–467. doi: 10.1056/NEJM199608153350702. PubMed DOI
Walsh T.N., Grennell M., Mansoor S., Kelly A. Neoadjuvant treatment of advanced stage esophageal adenocarcinoma increases survival. Dis. Esophagus. 2002;15:121–124. doi: 10.1046/j.1442-2050.2002.00214.x. PubMed DOI
Urba S.G., Orringer M.B., Turrisi A., Iannettoni M., Forastiere A., Strawderman M. Randomized trial of preoperative chemoradiation versus surgery alone in patients with locoregional esophageal carcinoma. J. Clin. Oncol. 2001;19:305–313. doi: 10.1200/JCO.2001.19.2.305. PubMed DOI
Burmeister B.H., Smithers B.M., Gebski V., Fitzgerald L., Simes R.J., Devitt P., Ackland S., Gotley D.C., Joseph D., Millar J., et al. Trans-Tasman Radiation Oncology Group; Australasian Gastro-Intestinal Trials Group. Surgery alone versus chemoradiotherapy followed by surgery for resectable cancer of the oesophagus: A randomised controlled phase III trial. Lancet Oncol. 2005;6:659–668. doi: 10.1016/S1470-2045(05)70288-6. PubMed DOI
Tepper J., Krasna M.J., Niedzwiecki D., Hollis D., Reed C.E., Goldberg R., Kiel K., Willett C., Sugarbaker D., Mayer R. Phase III trial of trimodality therapy with cisplatin, fluorouracil, radiotherapy, and surgery compared with surgery alone for esophageal cancer: CALGB 9781. J. Clin. Oncol. 2008;26:1086–1092. doi: 10.1200/JCO.2007.12.9593. PubMed DOI PMC
van Hagen P., Hulshof M.C., van Lanschot J.J., Steyerberg E.W., van Berge Henegouwen M.I., Wijnhoven B.P., Richel D.J., Nieuwenhuijzen G.A.P., Hospers G.A.P., Bonenkamp J.J., et al. Preoperative chemoradiotherapy for esophageal or junctional cancer. N. Engl. J. Med. 2012;366:2074–2084. doi: 10.1056/NEJMoa1112088. PubMed DOI
Shapiro J., van Lanschot J.J., Hulshof M.C., van Hagen P., van Berge Henegouwen M.I., Wijnhoven B.P., van Laarhoven H.W., Nieuwenhuijzen G.A.P., Hospers G.A.P., Bonenkamp J.J., et al. Neoadjuvant chemoradiotherapy plus surgery versus surgery alone for oesophageal or junctional cancer (CROSS): Long-term results of a randomised controlled trial. Lancet Oncol. 2015;16:1090–1098. doi: 10.1016/S1470-2045(15)00040-6. PubMed DOI
Eyck B.M., van Lanschot J.J.B., Hulshof M.C.C.M., van der Wilk B.J., Shapiro J., van Hagen P., van Berge Henegouwen M.I., Wijnhoven B.P.L., van Laarhoven H.W.M., Nieuwenhuijzen G.A.P., et al. Ten-Year Outcome of Neoadjuvant Chemoradiotherapy Plus Surgery for Esophageal Cancer: The Randomized Controlled CROSS Trial. J. Clin. Oncol. 2021;39:1995–2004. doi: 10.1200/JCO.20.03614. PubMed DOI
Macdonald J.S., Smalley S.R., Benedetti J., Hundahl S.A., Estes N.C., Stemmermann G.N., Haller D.G., Ajani J.A., Gunderson L.L., Jessup J.M., et al. Chemoradiotherapy after surgery compared with surgery alone for adenocarcinoma of the stomach or gastroesophageal junction. N. Engl. J. Med. 2001;345:725–730. doi: 10.1056/NEJMoa010187. PubMed DOI
Smalley S.R., Benedetti J.K., Haller D.G., Hundahl S.A., Estes N.C., Ajani J.A., Gunderson L.L., Goldman B., Martenson J.A., Milburn Jessup J., et al. Updated analysis of SWOG-directed intergroup study 0116: A phase III trial of adjuvant radiochemotherapy versus observation after curative gastric cancer resection. J. Clin. Oncol. 2012;30:2327–2333. doi: 10.1200/JCO.2011.36.7136. PubMed DOI PMC
Fuchs C.S., Niedzwiecki D., Mamon H.J., Tepper J.E., Ye X., Swanson R.S., Enzinger P.C., Haller D.G., Dragovich T., Alberts S.R., et al. Adjuvant Chemoradiotherapy with Epirubicin, Cisplatin, and Fluorouracil Compared with Adjuvant Chemoradiotherapy with Fluorouracil and Leucovorin After Curative Resection of Gastric Cancer: Results From CALGB 80101 (Alliance) J. Clin. Oncol. 2017;35:3671–3677. doi: 10.1200/JCO.2017.74.2130. PubMed DOI PMC
Ychou M., Boige V., Pignon J.P., Conroy T., Bouché O., Lebreton G., Ducourtieux M., Bedenne L., Fabre J.-M., Saint-Aubert B., et al. Perioperative chemotherapy compared with surgery alone for resectable gastroesophageal adenocarcinoma: An FNCLCC and FFCD multicenter phase III trial. J. Clin. Oncol. 2011;29:1715–1721. doi: 10.1200/JCO.2010.33.0597. PubMed DOI
Cunningham D., Allum W.H., Stenning S.P., Thompson J.N., Van de Velde C.J., Nicolson M., Scarffe J.H., Lofts F.J., Falk S.J., Iveson T.J., et al. MAGIC Trial Participants. Perioperative chemotherapy versus surgery alone for resectable gastroesophageal cancer. N. Engl. J. Med. 2006;355:11–20. doi: 10.1056/NEJMoa055531. PubMed DOI
Al-Batran S.E., Homann N., Pauligk C., Goetze T.O., Meiler J., Kasper S., Kopp H.-G., Mayer F., Haag G.M., Luley K., et al. FLOT4-AIO Investigators. Perioperative chemotherapy with fluorouracil plus leucovorin, oxaliplatin, and docetaxel versus fluorouracil or capecitabine plus cisplatin and epirubicin for locally advanced, resectable gastric or gastro-oesophageal junction adenocarcinoma (FLOT4): A randomised, phase 2/3 trial. Lancet. 2019;393:1948–1957. doi: 10.1016/S0140-6736(18)32557-1. PubMed DOI
Allum W.H., Stenning S.P., Bancewicz J., Clark P.I., Langley R.E. Long-term results of a randomized trial of surgery with or without preoperative chemotherapy in esophageal cancer. J. Clin. Oncol. 2009;27:5062–5067. doi: 10.1200/JCO.2009.22.2083. PubMed DOI
Kelsen D.P., Ginsberg R., Pajak T.F., Sheahan D.G., Gunderson L., Mortimer J., Estes N., Haller D.G., Ajani J., Kocha W., et al. Chemotherapy followed by surgery compared with surgery alone for localized esophageal cancer. N. Engl. J. Med. 1998;339:1979–1984. doi: 10.1056/NEJM199812313392704. PubMed DOI
Alderson D., Cunningham D., Nankivell M., Blazeby J.M., Griffin S.M., Crellin A., Grabsch H.I., Langer R., Pritchard S., Okines A., et al. Neoadjuvant cisplatin and fluorouracil versus epirubicin, cisplatin, and capecitabine followed by resection in patients with oesophageal adenocarcinoma (UK MRC OE05): An open-label, randomised phase 3 trial. Lancet Oncol. 2017;18:1249–1260. doi: 10.1016/S1470-2045(17)30447-3. PubMed DOI PMC
Sasako M., Sakuramoto S., Katai H., Kinoshita T., Furukawa H., Yamaguchi T., Nashimoto A., Fujii M., Nakajima T., Ohashi Y. Five-year outcomes of a randomized phase III trial comparing adjuvant chemotherapy with S-1 versus surgery alone in stage II or III gastric cancer. J. Clin. Oncol. 2011;29:4387–4393. doi: 10.1200/JCO.2011.36.5908. PubMed DOI
Noh S.H., Park S.R., Yang H.K., Chung H.C., Chung I.J., Kim S.W., Kim H.H., Choi J.H., Kim H.K., Yu W., et al. CLASSIC trial investigators. Adjuvant capecitabine plus oxaliplatin for gastric cancer after D2 gastrectomy (CLASSIC): 5-year follow-up of an open-label, randomised phase 3 trial. Lancet Oncol. 2014;15:1389–1396. doi: 10.1016/S1470-2045(14)70473-5. PubMed DOI
Cats A., Jansen E.P.M., van Grieken N.C.T., Sikorska K., Lind P., Nordsmark M., Kranenbarg E.M.K., Boot H., Trip A.K., Maurits Swellengrebel H.A., et al. CRITICS investigators; CRITICS investigators. Chemotherapy versus chemoradiotherapy after surgery and preoperative chemotherapy for resectable gastric cancer (CRITICS): An international, open-label, randomised phase 3 trial. Lancet Oncol. 2018;19:616–628. doi: 10.1016/S1470-2045(18)30132-3. PubMed DOI
Stahl M., Walz M.K., Stuschke M., Lehmann N., Meyer H.J., Riera-Knorrenschild J., Langer P., Engenhart-Cabillic R., Bitzer M., Königsrainer A., et al. Phase III comparison of preoperative chemotherapy compared with chemoradiotherapy in patients with locally advanced adenocarcinoma of the esophagogastric junction. J. Clin. Oncol. 2009;27:851–856. doi: 10.1200/JCO.2008.17.0506. PubMed DOI
Stahl M., Walz M.K., Riera-Knorrenschild J., Stuschke M., Sandermann A., Bitzer M., Wilke H., Wilfried Budach W. Preoperative chemotherapy versus chemoradiotherapy in locally advanced adenocarcinomas of the oesophagogastric junction (POET): Long-term results of a controlled randomised trial. Eur. J. Cancer. 2017;81:183–190. doi: 10.1016/j.ejca.2017.04.027. PubMed DOI
Reynolds J.V., Preston S.R., O’Neill B., Lowery M.A., Baeksgaard L., Crosby T., Cunningham M., Cuffe S., Griffiths G.O., Roy R., et al. Neo-AEGIS (Neoadjuvant trial in Adenocarcinoma of the Esophagus and Esophago-Gastric Junction International Study): Preliminary results of phase III RCT of CROSS versus perioperative chemotherapy (Modified MAGIC or FLOT protocol) J. Clin. Oncol. 2021;39((Suppl. 15)):4004. doi: 10.1200/JCO.2021.39.15_suppl.4004. DOI
Hoeppner J., Lordick F., Brunner T., Glatz T., Bronsert P., Röthling N., Schmoor C., Lorenz D., Ell C., Hopt U.T., et al. ESOPEC: Prospective randomized controlled multicenter phase III trial comparing perioperative chemotherapy (FLOT protocol) to neoadjuvant chemoradiation (CROSS protocol) in patients with adenocarcinoma of the esophagus (NCT02509286) BMC Cancer. 2016;16:503. doi: 10.1186/s12885-016-2564-y. PubMed DOI PMC
Leong T., Smithers B.M., Michael M., Gebski V., Boussioutas A., Miller D., Simes J., Zalcberg J., Haustermans K., Lordick F., et al. TOPGEAR: A randomised phase III trial of perioperative ECF chemotherapy versus preoperative chemoradiation plus perioperative ECF chemotherapy for resectable gastric cancer (an international, intergroup trial of the AGITG/TROG/EORTC/NCIC CTG) BMC Cancer. 2015;15:532. doi: 10.1186/s12885-015-1529-x. PubMed DOI PMC
Leong T., Smithers B.M., Haustermans K., Michael M., Gebski V., Miller D., Zalcberg J., Boussioutas A., Findlay M., O’Connell R.L., et al. TOPGEAR: A Randomized, Phase III Trial of Perioperative ECF Chemotherapy with or Without Preoperative Chemoradiation for Resectable Gastric Cancer: Interim Results from an International, Intergroup Trial of the AGITG, TROG, EORTC and CCTG. Ann. Surg. Oncol. 2017;24:2252–2258. doi: 10.1245/s10434-017-5830-6. PubMed DOI
Cunningham D., Stenning S.P., Smyth E.C., Okines A.F., Allum W.H., Rowley S., Stevenson L., Grabsch H.I., Alderson D., Crosby T., et al. Peri-operative chemotherapy with or without bevacizumab in operable oesophagogastric adenocarcinoma (UK Medical Research Council ST03): Primary analysis results of a multicentre, open-label, randomised phase 2–3 trial. Lancet Oncol. 2017;18:357–370. doi: 10.1016/S1470-2045(17)30043-8. PubMed DOI PMC
Bang Y.J., Van Cutsem E., Feyereislova A., Chung H.C., Shen L., Sawaki A., Lordick F., Ohtsu A., Omuro Y., Satoh T., et al. ToGA Trial Investigators. Trastuzumab in combination with chemotherapy versus chemotherapy alone for treatment of HER2-positive advanced gastric or gastro-oesophageal junction cancer (ToGA): A phase 3, open-label, randomised controlled trial. Lancet. 2010;376:687–697. doi: 10.1016/S0140-6736(10)61121-X. PubMed DOI
Safran H., Winter K.A., Wigle D.A., DiPetrillo T.A., Haddock M.G., Hong T.S., Leichman L.P., Rajdev L., Resnick M.B., Kachnic L.A., et al. Trastuzumab with trimodality treatment for esophageal adenocarcinoma with HER2 overexpression: NRG Oncology/RTOG 1010. J. Clin. Oncol. 2020;38:4500. doi: 10.1200/JCO.2020.38.15_suppl.4500. PubMed DOI PMC
Hofheinz R.D., Haag G.M., Ettrich T.J., Borchert K., Kretzschmar A., Teschendorf C., Siegler G.M., Ebert M.P., Goekkurt E., Welslau M., et al. Perioperative trastuzumab and pertuzumab in combination with FLOT versus FLOT alone for HER2-positive resectable esophagogastric adenocarcinoma: Final results of the PETRARCA multicenter randomized phase II trial of the AIO. J. Clin. Oncol. 2020;38((Suppl. 15)):4502. doi: 10.1200/JCO.2020.38.15_suppl.4502. DOI
Tabernero J., Hoff P.M., Shen L., Ohtsu A., Shah M.A., Cheng K., Song C., Wu H., Eng-Wong J., Kim K., et al. Pertuzumab plus trastuzumab and chemotherapy for HER2-positive metastatic gastric or gastro-oesophageal junction cancer (JACOB): Final analysis of a double-blind, randomised, placebo-controlled phase 3 study. Lancet Oncol. 2018;19:1372–1384. doi: 10.1016/S1470-2045(18)30481-9. PubMed DOI
Wagner A.D., Grabsch H.I., Mauer M., Marreaud S., Caballero C., Thuss-Patience P., Mueller L., Elme A., Moehler M.H., Martens U., et al. EORTC-1203-GITCG-the “INNOVATION”-trial: Effect of chemotherapy alone versus chemotherapy plus trastuzumab, versus chemotherapy plus trastuzumab plus pertuzumab, in the perioperative treatment of HER2 positive, gastric and gastroesophageal junction adenocarcinoma on pathologic response rate: A randomized phase II-intergroup trial of the EORTC-Gastrointestinal Tract Cancer Group, Korean Cancer Study Group and Dutch Upper GI-Cancer group. BMC Cancer. 2019;19:494. doi: 10.1186/s12885-019-5675-4. PubMed DOI PMC
Homann N., Lorenzen S., Schenk M., Thuss-Patience P.C., Goekkurt E., Hofheinz R.D., Kretzschmar A., Bolling C., Angermeier S., Wicki A., et al. Interim safety analysis of the DANTE trial: Perioperative atezolizumab in combination with FLOT versus FLOT alone in patients with resectable esophagogastric adenocarcinoma—A randomized, open-label phase II trial of the German Gastric Group at the AIO and SAKK. J. Clin. Oncol. 2020;38((Suppl. 15)):4549.
Bang Y.J., Van Cutsem E., Fuchs C.S., Ohtsu A., Tabernero J., Ilson D.H., Hyung W.J., Strong V.E., Goetze T.O., Yoshikawa T., et al. KEYNOTE-585: Phase III study of perioperative chemotherapy with or without pembrolizumab for gastric cancer. Future Oncol. 2019;15:943–952. doi: 10.2217/fon-2018-0581. PubMed DOI
Smyth E., Knödler M., Giraut A., Mauer M., Nilsson M., Van Grieken N., Wagner A.D., Moehler M., Lordick F. VESTIGE: Adjuvant Immunotherapy in Patients With Resected Esophageal, Gastroesophageal Junction and Gastric Cancer Following Preoperative Chemotherapy With High Risk for Recurrence (N+ and/or R1): An Open Label Randomized Controlled Phase-2-Study. Front. Oncol. 2020;9:1320. doi: 10.3389/fonc.2019.01320. PubMed DOI PMC
Paver E.C., Cooper W.A., Colebatch A.J., Ferguson P.M., Hill S.K., Lum T., Shin J.S., O’Toole S., Anderson L., Scolyer R.A., et al. Programmed death ligand-1 (PD-L1) as a predictive marker for immunotherapy in solid tumours: A guide to immunohistochemistry implementation and interpretation. Pathology. 2021;53:141–156. doi: 10.1016/j.pathol.2020.10.007. PubMed DOI
Park R., Da Silva L.L., Saeed A. Immunotherapy Predictive Molecular Markers in Advanced Gastroesophageal Cancer: MSI and Beyond. Cancers. 2021;13:1715. doi: 10.3390/cancers13071715. PubMed DOI PMC
Högner A., Thuss-Patience P. Immune Checkpoint Inhibition in Oesophago-Gastric Carcinoma. Pharmaceuticals. 2021;14:151. doi: 10.3390/ph14020151. PubMed DOI PMC
Marabelle A., Le D.T., Ascierto P.A., Di Giacomo A.M., De Jesus-Acosta A., Delord J.P., Geva R., Gottfried M., Penel N., Hansen A.R., et al. Efficacy of Pembrolizumab in Patients With Noncolorectal High Microsatellite Instability/Mismatch Repair-Deficient Cancer: Results From the Phase II KEYNOTE-158 Study. J. Clin. Oncol. 2020;38:1–10. doi: 10.1200/JCO.19.02105. PubMed DOI PMC
Marabelle A., Fakih M., Lopez J., Shah M., Shapira-Frommer R., Nakagawa K., Chung H.C., Kindler H.L., Lopez-Martin J.A., Miller W.H., Jr., et al. Association of tumour mutational burden with outcomes in patients with advanced solid tumours treated with pembrolizumab: Prospective biomarker analysis of the multicohort, open-label, phase 2 KEYNOTE-158 study. Lancet Oncol. 2020;21:1353–1365. doi: 10.1016/S1470-2045(20)30445-9. PubMed DOI
Fuchs C.S., Doi T., Jang R.W., Muro K., Satoh T., Machado M., Sun W., Jalal S.I., Shah M.A., Metges J.P., et al. Safety and efficacy of pembrolizumab monotherapy in patients with previously treated advanced gastric and gastroesophageal junction cancer: Phase 2 clinical KEYNOTE-059 Trial. JAMA Oncol. 2018;4:e180013. doi: 10.1001/jamaoncol.2018.0013. PubMed DOI PMC
Marrelli D., Polom K., Pascale V., Vindigni C., Piagnerelli R., De Franco L., Ferrara F., Roviello G., Garosi L., Petrioli R., et al. Strong prognostic value of microsatellite instability in intestinal type non-cardia gastric cancer. Ann. Surg. Oncol. 2016;23:943–950. doi: 10.1245/s10434-015-4931-3. PubMed DOI
Haag G.M., Czink E., Ahadova A., Schmidt T., Sisic L., Blank S., Heger U., Apostolidis L., Berger A.K., Springfeld C., et al. Prognostic significance of microsatellite-instability in gastric and gastroesophageal junction cancer patients undergoing neoadjuvant chemotherapy. Int. J. Cancer. 2019;144:1697–1703. doi: 10.1002/ijc.32030. PubMed DOI
Hashimoto T., Kurokawa Y., Takahashi T., Miyazaki Y., Tanaka K., Makino T., Yamasaki M., Nakajima K., Ikeda J.I., Mori M., et al. Predictive value of MLH1 and PD-L1 expression for prognosis and response to preoperative chemotherapy in gastric cancer. Gastric Cancer. 2019;22:785–792. doi: 10.1007/s10120-018-00918-4. PubMed DOI
Kim S.Y., Choi Y.Y., An J.Y., Shin H.B., Jo A., Choi H., Seo S.H., Bang H.J., Cheong J.H., Hyung W.J., et al. The benefit of microsatellite instability is attenuated by chemotherapy in stage II and stage III gastric cancer: Results from a large cohort with subgroup analyses. Int. J. Cancer. 2015;137:819–825. doi: 10.1002/ijc.29449. PubMed DOI
Beghelli S., de Manzoni G., Barbi S., Tomezzoli A., Roviello F., Di Gregorio C., Vindigni C., Bortesi L., Parisi A., Saragoni L., et al. Microsatellite instability in gastric cancer is associated with better prognosis in only stage II cancers. Surgery. 2006;139:347–356. doi: 10.1016/j.surg.2005.08.021. PubMed DOI
Shitara K., Özgüroğlu M., Bang Y.J., Di Bartolomeo M., Mandalà M., Ryu M.H., Fornaro L., Olesiński T., Caglevic C., Chung H.C., et al. Pembrolizumab versus paclitaxel for previously treated, advanced gastric or gastro-oesophageal junction cancer (KEYNOTE061): A randomised, open-label, controlled, phase 3 trial. Lancet. 2018;392:123–133. doi: 10.1016/S0140-6736(18)31257-1. PubMed DOI
Oki E., Kakeji Y., Zhao Y., Yoshida R., Ando K., Masuda T., Ohgaki K., Morita M., Yoshihiko Maehara Y. Chemosensitivity and survival in gastric cancer patients with microsatellite instability. Ann. Surg. Oncol. 2009;16:2510–2515. doi: 10.1245/s10434-009-0580-8. PubMed DOI
Miceli R., An J., Di Bartolomeo M., Morano F., Kim S.T., Park S.H., Choi M.G., Lee J.H., Raimondi A., Fucà G., et al. Prognostic impact of microsatellite instability in Asian gastric cancer patients enrolled in the ARTIST trial. Oncology. 2019;97:38–43. doi: 10.1159/000499628. PubMed DOI
Dos Santos N.R., Seruca R., Constância M., Seixas M., Sobrinho-Simões M. Microsatellite instability at multiple loci in gastric carcinoma: Clinicopathologic implications and prognosis. Gastroenterology. 1996;110:38–44. doi: 10.1053/gast.1996.v110.pm8536886. PubMed DOI
Fang W.L., Chang S.C., Lan Y.T., Huang K.H., Chen J.H., Lo S.S., Hsieh M.C., Li A.F.Y., Wu C.W., Chiou S.H. Microsatellite instability is associated with a better prognosis for gastric cancer patients after curative surgery. World J. Surg. 2012;36:2131–2138. doi: 10.1007/s00268-012-1652-7. PubMed DOI
Zhu L., Li Z., Wang Y., Zhang C., Liu Y., Qu X. Microsatellite instability and survival in gastric cancer: A systematic review and meta-analysis. Mol. Clin. Oncol. 2015;3:699–705. doi: 10.3892/mco.2015.506. PubMed DOI PMC
Choi Y.Y., Bae J.M., An J.Y., Kwon I.G., Cho I., Shin H.B., Eiji T., Aburahmah M., Kim H.I., Cheong J.H., et al. Is microsatellite instability a prognostic marker in gastric cancer? A systematic review with meta-analysis. J. Surg. Oncol. 2014;110:129–135. doi: 10.1002/jso.23618. PubMed DOI
Smyth E.C., Wotherspoon A., Peckitt C., Gonzalez D., Hulkki-Wilson S., Eltahir Z., Fassan M., Rugge M., Valeri N., Okines A., et al. Mismatch repair deficiency, microsatellite instability, and survival: An exploratory analysis of the Medical Research Council Adjuvant Gastric Infusional Chemotherapy (MAGIC) Trial. JAMA Oncol. 2017;3:1197–1203. doi: 10.1001/jamaoncol.2016.6762. PubMed DOI PMC
Choi Y.Y., Kim H., Shin S.-J., Kim H.Y., Lee J., Yang H.K., Kim W.H., Kim Y.W., Kook M.C., Park Y.K., et al. Microsatellite instability and programmed cell death-ligand 1 expression in stage II/III gastric cancer: Post hoc analysis of the CLASSIC randomized controlled study. Ann. Surg. 2019;270:309–316. doi: 10.1097/SLA.0000000000002803. PubMed DOI
Pietrantonio F., Miceli R., Raimondi A., Kim Y.W., Kang W.K., Langley R.E., Choi Y.Y., Kim K.M., Nankivell M.G., Morano F., et al. Individual patient data meta-analysis of the value of microsatellite instability as a biomarker in gastric cancer. J. Clin. Oncol. 2019;37:3392–3400. doi: 10.1200/JCO.19.01124. PubMed DOI
Smyth E.C. Chemotherapy for resectable microsatellite instability-high gastric cancer? Lancet Oncol. 2020;21:204. doi: 10.1016/S1470-2045(20)30025-5. PubMed DOI
Shibata D., Weiss L.M. Epstein-Barr virus-associated gastric adenocarcinoma. Am. J. Pathol. 1992;140:769–774. PubMed PMC
Dai C., Geng R., Wang C., Wong A., Qing M., Hu J., Sun Y., Lo A.W.I., Li J. Concordance of immune checkpoints within tumor immune contexture and their prognostic significance in gastric cancer. Mol. Oncol. 2016;10:1551–1558. doi: 10.1016/j.molonc.2016.09.004. PubMed DOI PMC
Kim S.T., Cristescu R., Bass A.J., Kim K.M., Odegaard J.I., Kim K., Liu X.Q., Sher X., Jung H., Lee M., et al. Comprehensive molecular characterization of clinical responses to PD-1 inhibition in metastatic gastric cancer. Nat. Med. 2018;24:1449–1458. doi: 10.1038/s41591-018-0101-z. PubMed DOI
Stanland L.J., Luftig M.A. The Role of EBV-Induced Hypermethylation in Gastric Cancer Tumorigenesis. Viruses. 2020;12:1222. doi: 10.3390/v12111222. PubMed DOI PMC
Choi S.J., Shin Y.S., Kang B.W., Kim J.G., Won K.J., Lieberman P.M., Cho H., Kang H. DNA hypermethylation induced by Epstein-Barr virus in the development of Epstein-Barr virus-associated gastric carcinoma. Arch. Pharm. Res. 2017;40:894–905. doi: 10.1007/s12272-017-0939-5. PubMed DOI
Setia N., Wang C.X., Lager A., Maron S., Shroff S., Arndt N., Peterson B., Kupfer S.S., Ma C., Misdraji J., et al. Morphologic and molecular analysis of early-onset gastric cancer. Cancer. 2020;127:103–114. doi: 10.1002/cncr.33213. PubMed DOI
Koh J., Nam S.K., Roh H., Kim J., Lee B.C., Kim J.W., Ahn S.H., Park D.J., Kim H.H., Park K.U., et al. Somatic mutational profiles of stage II and III gastric cancer according to tumor microenvironment immune type. Genes Chromosomes Cancer. 2019;58:12–22. doi: 10.1002/gcc.22683. PubMed DOI
Grosser B., Kohlruss M., Slotta-Huspenina J., Jesinghaus M., Pfarr N., Steiger K., Novotny A., Gaida M.M., Schmidt T., Hapfelmeier A., et al. Impact of Tumor Localization and Molecular Subtypes on the Prognostic and Predictive Significance of p53 Expression in Gastric Cancer. Cancers. 2020;12:1689. doi: 10.3390/cancers12061689. PubMed DOI PMC
Vošmik M., Vošmiková H., Sieglová K., Sirák I., Laco J., Ryška A., Petera J., Melichar B., Soumarová R. HPV Status and Mutation Analysis Using Multiparallel Sequencing in Distal Oesophageal and Gastro-oesophageal Junction Adenocarcinomas. Folia Biol. 2018;64:41–45. PubMed
Schulz-Heddergott R., Moll U.M. Gain-of-Function (GOF) Mutant p53 as Actionable Therapeutic Target. Cancers. 2018;10:188. doi: 10.3390/cancers10060188. PubMed DOI PMC
Zhu G., Pan C., Bei J.X., Li B., Liang C., Xu Y., Fu X. Mutant p53 in Cancer Progression and Targeted Therapies. Front. Oncol. 2020;10:595187. doi: 10.3389/fonc.2020.595187. PubMed DOI PMC
Graziano F., Humar B., Guilford P. The role of the E-cadherin gene (CDH1) in diffuse gastric cancer susceptibility: From the laboratory to clinical practice. Ann Oncol. 2003;14:1705–1713. doi: 10.1093/annonc/mdg486. PubMed DOI
Zhao H., Hu H., Chen B., Xu W., Zhao J., Huang C., Xing Y., Lv H., Nie C., Wang J., et al. Overview on the Role of E-Cadherin in Gastric Cancer: Dysregulation and Clinical Implications. Front. Mol. Biosci. 2021;8:689139. doi: 10.3389/fmolb.2021.689139. PubMed DOI PMC
Doebele R.C., Drilon A., Paz-Ares L., Siena S., Shaw A.T., Farago A.F., Blakely C.M., Seto T., Cho B.C., Tosi D., et al. trial investigators. Entrectinib in patients with advanced or metastatic NTRK fusion-positive solid tumours: Integrated analysis of three phase 1–2 trials. Lancet Oncol. 2020;21:271–282. doi: 10.1016/S1470-2045(19)30691-6. PubMed DOI PMC
Hong D.S., DuBois S.G., Kummar S., Farago A.F., Albert C.M., Rohrberg K.S., van Tilburg C.M., Nagasubramanian R., Berlin J.D., Federman N., et al. Larotrectinib in patients with TRK fusion-positive solid tumours: A pooled analysis of three phase 1/2 clinical trials. Lancet Oncol. 2020;21:531–540. doi: 10.1016/S1470-2045(19)30856-3. PubMed DOI PMC
Cancer Genome Atlas Research Network Comprehensive molecular characterization of gastric adenocarcinoma. Nature. 2014;513:202–209. doi: 10.1038/nature13480. PubMed DOI PMC
Cancer Genome Atlas Research Network Integrated genomic characterization of oesophageal carcinoma. Nature. 2017;541:169–175. doi: 10.1038/nature20805. PubMed DOI PMC