<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.2 20190208//EN" "https://jats.nlm.nih.gov/publishing/1.2/JATS-journalpublishing1.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">Oncohematology</journal-id><journal-title-group><journal-title xml:lang="en">Oncohematology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкогематология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1818-8346</issn><issn publication-format="electronic">2413-4023</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">51</article-id><article-id pub-id-type="doi">10.17650/1818-8346-2012-7-3-30-37</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>HEMATOLOGIC MALIGNANCIES: DIAGNOSIS, TREATMENT, SUPPORTIVE CARE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ГЕМОБЛАСТОЗЫ: ДИАГНОСТИКА, ЛЕЧЕНИЕ, СОПРОВОДИТЕЛЬНАЯ ТЕРАПИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Predictive value of initial involvement and early response assessment using positron‑emission tomography with 18F‑FLT in patients with non‑Hodgkin lymphoma</article-title><trans-title-group xml:lang="ru"><trans-title>Прогностическое значение оценки инициального поражения и раннего ответа на терапию при помощи позитронно‑эмиссионной томографии с 18F‑ФЛТ у пациентов с неходжкинскими лимфомами</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Likar</surname><given-names>Yu. N.</given-names></name><name xml:lang="ru"><surname>Ликарь</surname><given-names>Ю. Н.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>likar2007@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Dubrovin</surname><given-names>M. M.</given-names></name><name xml:lang="ru"><surname>Дубровин</surname><given-names>М. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Dmitry Rogachev Federal Research Center of Pediatric Hematology, Oncology and Immunology, Ministry of Health of Russia Memorial Sloan‑Kettering Cancer Center</institution></aff><aff><institution xml:lang="ru">ФГБУ «Федеральный научно‑клинический центр детской гематологии, онкологии и иммунологии им. Дмитрия Рогачева» Минздрава России Memorial Sloan‑Kettering Cancer Center</institution></aff></aff-alternatives><content-language>ru</content-language><pub-date date-type="pub" publication-format="electronic" iso-8601-date="2012-08-22"><day>22</day><month>08</month><year>2012</year></pub-date><pub-date date-type="collection"><year>2012</year></pub-date><volume>7</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>30</fpage><lpage>37</lpage><history><date date-type="received" iso-8601-date="2014-07-22"><day>22</day><month>07</month><year>2014</year></date><date date-type="accepted" iso-8601-date="2014-07-22"><day>22</day><month>07</month><year>2014</year></date></history><pub-history><event event-type="received"><event-desc>Received:<date date-type="received" iso-8601-date="2014-07-22"><day>22</day><month>07</month><year>2014</year></date></event-desc></event><event event-type="accepted"><event-desc>Accepted:<date date-type="accepted" iso-8601-date="2014-07-22"><day>22</day><month>07</month><year>2014</year></date></event-desc></event><event event-type="pub"><event-desc>Published:<pub-date date-type="pub" publication-format="electronic" iso-8601-date="2012-08-22"><day>22</day><month>08</month><year>2012</year></pub-date></event-desc></event></pub-history><permissions><copyright-year>2012</copyright-year><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncohematology.abvpress.ru/ongm/article/view/51">https://oncohematology.abvpress.ru/ongm/article/view/51</self-uri><abstract xml:lang="en"><p>The monitoring of treatment efficacy in patients with diffuse large B‑cell lymphoma (DLBCL) is generally performed by common computed tomography (CT). However, CT cannot distinguish between a real and residual tissue mass and in addition cannot be very useful in assessment of early response. 18F‑FDG Positron‑emission tomography (PET) has high prognostic implications at treatment completion but is limited as an early predictor. We present the results of a retrospective study where we have evaluated predictive value of initial and interim‑PET(I‑PET) with 18F‑FLT on clinical outcome.</p><p><bold>Methods</bold>. 39 patients were evaluated retrospectively with 18F‑FLT PET before treatment and interim 18F‑FLT PET after 1 cycles of chemotherapy. PET was performed 40−60 minutes after injection of 270−340 MBq of 18F‑FLT. Maximum standardized uptake values (SUVmax ) were calculated on a lesion. Response was assessed according to protocol during and in the end of therapy.</p><p><bold>Results.</bold> All lymphoma lesions identified by a reference method (18F‑FDG PET/CT or CT) showed increased focal tracer uptake of 18F‑FLT. Initial mean SUVmax was significantly higher in patients who showed progressive disease and partial response (SUVmax = 9.5 ± 3.2) than inpatients who achieved complete response (SUVmax = 6.3 ± 1.6) (p = 0.018). PFS for positive and negative patients after interim 18F‑FLT PET was 85.1 % and 35.7 %, respectively (р &lt; 0.05).</p><p><bold>Conclusion.</bold> High initial 18F‑FLT uptake is a negative treatment response predictor in patients with DLBCL. Positive I‑PET with 18F‑FLT is a negative PFS predictor compare to patients with negative I‑PET.</p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>PET</kwd><kwd>18F‑FDG</kwd><kwd>18F‑FLT</kwd><kwd>diffuse large B‑cell lymphoma</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>ПЭТ</kwd><kwd>18F‑ФДГ</kwd><kwd>18F‑ФЛТ</kwd><kwd>диффузная В‑клеточная крупноклеточная лимфома</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Coiffier B., Lepage E., Briere J. et al. CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large‑B‑cell lymphoma. N Engl J Med 2002;346:235−42.</mixed-citation><mixed-citation xml:lang="ru">Coiffier B., Lepage E., Briere J. et al. CHOP chemotherapy plus rituximab compared with CHOP alone in elderly patients with diffuse large‑B‑cell lymphoma. N Engl J Med 2002;346:235−42.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Pfreundschuh M., Trumper L., Osterborg A. et al. CHOP‑like chemotherapy plus rituximab versus CHOP‑like chemotherapy alone in young patients with good-prognosis diffuse large‑B-cell lymphoma: a randomised controlled trial by Group. Lancet Oncol 2006;7:379−91.</mixed-citation><mixed-citation xml:lang="ru">Pfreundschuh M., Trumper L., Osterborg A. et al. CHOP‑like chemotherapy plus rituximab versus CHOP‑like chemotherapy alone in young patients with good-prognosis diffuse large‑B-cell lymphoma: a randomised controlled trial by Group. Lancet Oncol 2006;7:379−91.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">3. Gisselbrecht C., Glass B., Mounier N. et al. Salvage regimens with autologous transplantation for relapsed large B‑cell lymphoma in the rituximab era. J Clin Oncol 2010;28(27):4184−90.</mixed-citation><mixed-citation xml:lang="ru">Gisselbrecht C., Glass B., Mounier N. et al. Salvage regimens with autologous transplantation for relapsed large B‑cell lymphoma in the rituximab era. J Clin Oncol 2010;28(27):4184−90.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">4. A predictive model for aggressive non‑Hodgkin's lymphoma. The International Non‑Hodgkin's Lymphoma Prognostic Factors Project. N Engl J Med 1993;329(14):987−94.</mixed-citation><mixed-citation xml:lang="ru">A predictive model for aggressive non‑Hodgkin's lymphoma. The International Non‑Hodgkin's Lymphoma Prognostic Factors Project. N Engl J Med 1993;329(14):987−94.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">5. Juweid M.E., Stroobants S., Hoekstra O.S. et al. Use of positron emission tomography for response assessment of lymphoma: consensus of the Imaging Subcommittee of International Harmonization Project in Lymphoma. J Clin Oncol 2007;25:571−8.</mixed-citation><mixed-citation xml:lang="ru">Juweid M.E., Stroobants S., Hoekstra O.S. et al. Use of positron emission tomography for response assessment of lymphoma: consensus of the Imaging Subcommittee of International Harmonization Project in Lymphoma. J Clin Oncol 2007;25:571−8.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">6. Cheson B.D., Pfistner B., Juweid M.E. et al. Revised response criteria for malignant lymphoma. J Clin Oncol 2007;25:579−86.</mixed-citation><mixed-citation xml:lang="ru">Cheson B.D., Pfistner B., Juweid M.E. et al. Revised response criteria for malignant lymphoma. J Clin Oncol 2007;25:579−86.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">7. Cheson B.D. Role of functional imaging in the management of lymphoma. J Clin Oncol 2011;29:1844−54.</mixed-citation><mixed-citation xml:lang="ru">Cheson B.D. Role of functional imaging in the management of lymphoma. J Clin Oncol 2011;29:1844−54.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">8. Hutchings M., Barrington S.F. PET/CT for therapy response assessment in lymphoma. J Nucl Med 2009;50 Suppl 1: 21S–30S.</mixed-citation><mixed-citation xml:lang="ru">Hutchings M., Barrington S.F. PET/CT for therapy response assessment in lymphoma. J Nucl Med 2009;50 Suppl 1: 21S–30S.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">9. Jerusalem G., Beguin Y., Fassotte M.F. et al. Persistent tumor 18F‑FDG uptake after a few cycles of polychemotherapy is predictive of treatment failure in non‑Hodgkin's lymphoma. Haematologica 2000;85:613−8.</mixed-citation><mixed-citation xml:lang="ru">Jerusalem G., Beguin Y., Fassotte M.F. et al. Persistent tumor 18F‑FDG uptake after a few cycles of polychemotherapy is predictive of treatment failure in non‑Hodgkin's lymphoma. Haematologica 2000;85:613−8.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">10. Spaepen K., Stroobants S., Dupont P. et al. Early restaging positron emission tomography with (18)F‑fluorodeoxyglucose predicts outcome in patients with aggressive non‑Hodgkin's lymphoma. Ann Oncol 2002;13: 1356−63.</mixed-citation><mixed-citation xml:lang="ru">Spaepen K., Stroobants S., Dupont P. et al. Early restaging positron emission tomography with (18)F‑fluorodeoxyglucose predicts outcome in patients with aggressive non‑Hodgkin's lymphoma. Ann Oncol 2002;13: 1356−63.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">11. Itti E., Lin C., Dupuis J. et al. Prognostic value of interim 18F‑FDG PET in patients with diffuse large B‑cell lymphoma: SUV‑based assessment at 4 cycles of chemotherapy. J Nucl Med 2009;50:527−33.</mixed-citation><mixed-citation xml:lang="ru">Itti E., Lin C., Dupuis J. et al. Prognostic value of interim 18F‑FDG PET in patients with diffuse large B‑cell lymphoma: SUV‑based assessment at 4 cycles of chemotherapy. J Nucl Med 2009;50:527−33.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">12. Haioun C., Itti E., Rahmouni A. et al. [18F]fluoro-2‑deoxy-D‑glucose positron emission tomography (FDG‑PET) in aggressive lymphoma: an early prognostic tool for predicting patient outcome. Blood 2005;106:1376−81.</mixed-citation><mixed-citation xml:lang="ru">Haioun C., Itti E., Rahmouni A. et al. [18F]fluoro-2‑deoxy-D‑glucose positron emission tomography (FDG‑PET) in aggressive lymphoma: an early prognostic tool for predicting patient outcome. Blood 2005;106:1376−81.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">13. Moskowitz C.H., Schoder H., Teruya‑Feldstein J. et al. Risk‑adapted dose‑dense mmunochemotherapy determined by interim FDG‑PET in Advanced-stage diffuse large B‑cell lymphoma. J Clin Oncol 2010; 28:1896−903.</mixed-citation><mixed-citation xml:lang="ru">Moskowitz C.H., Schoder H., Teruya‑Feldstein J. et al. Risk‑adapted dose‑dense mmunochemotherapy determined by interim FDG‑PET in Advanced-stage diffuse large B‑cell lymphoma. J Clin Oncol 2010; 28:1896−903.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">14. Shields A.F., Grierson J.R., Dohmen B.M. et al. Imaging proliferation in vivo with [F18]FLT and positron emission tomography. Nat Med 1998;4:1334−6.</mixed-citation><mixed-citation xml:lang="ru">Shields A.F., Grierson J.R., Dohmen B.M. et al. Imaging proliferation in vivo with [F18]FLT and positron emission tomography. Nat Med 1998;4:1334−6.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">15. Turcotte E., Wiens L.W., Grierson J.R. et al. Toxicology evaluation of radiotracer doses of 3'‑deoxy‑3'-[18F]fluorothymidine (18F‑FLT) for human PET imaging: Laboratory analysis of serial blood samples and comparison to previously investigated therapeutic FLT doses. BMC Nucl Med2007;7:3.</mixed-citation><mixed-citation xml:lang="ru">Turcotte E., Wiens L.W., Grierson J.R. et al. Toxicology evaluation of radiotracer doses of 3'‑deoxy‑3'-[18F]fluorothymidine (18F‑FLT) for human PET imaging: Laboratory analysis of serial blood samples and comparison to previously investigated therapeutic FLT doses. BMC Nucl Med2007;7:3.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">16. Spence A.M., Muzi M., Link J.M. et al. NCI‑sponsored trial for the evaluation of safety and preliminary efficacy of FLT as a marker of proliferation in patients with recurrent gliomas: safety studies. Mol Imaging Biol 2008;10:271−80.</mixed-citation><mixed-citation xml:lang="ru">Spence A.M., Muzi M., Link J.M. et al. NCI‑sponsored trial for the evaluation of safety and preliminary efficacy of FLT as a marker of proliferation in patients with recurrent gliomas: safety studies. Mol Imaging Biol 2008;10:271−80.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">17. Buck A.K., Bommer M., Stilgenbauer S. et al. Molecular imaging of proliferation in malignant lymphoma. Cancer Res 2006; 66:11055−61.</mixed-citation><mixed-citation xml:lang="ru">Buck A.K., Bommer M., Stilgenbauer S. et al. Molecular imaging of proliferation in malignant lymphoma. Cancer Res 2006; 66:11055−61.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">18. Buck A.K., Halter G., Schirrmeister H. et al. Imaging proliferation in lung tumors with PET: 18F‑FLT versus 18F‑FDG. J Nucl Med 2003;44:1426−31.</mixed-citation><mixed-citation xml:lang="ru">Buck A.K., Halter G., Schirrmeister H. et al. Imaging proliferation in lung tumors with PET: 18F‑FLT versus 18F‑FDG. J Nucl Med 2003;44:1426−31.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">19. Eckel F., Herrmann K., Schmidt S. et al. Imaging of proliferation in hepatocellular carcinoma with the in vivo marker 18F‑fluorothymidine. J Nucl Med 2009;50:1441−7.</mixed-citation><mixed-citation xml:lang="ru">Eckel F., Herrmann K., Schmidt S. et al. Imaging of proliferation in hepatocellular carcinoma with the in vivo marker 18F‑fluorothymidine. J Nucl Med 2009;50:1441−7.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">20. Herrmann K., Wieder H.A., Buck A.K. et al. Early response assessment using 3'‑deoxy-3'‑[18F]fluorothymidine-positron emission tomography in high‑grade non‑Hodgkin's lymphoma. Clin Cancer Res 2007;13:3552−8.</mixed-citation><mixed-citation xml:lang="ru">Herrmann K., Wieder H.A., Buck A.K. et al. Early response assessment using 3'‑deoxy-3'‑[18F]fluorothymidine-positron emission tomography in high‑grade non‑Hodgkin's lymphoma. Clin Cancer Res 2007;13:3552−8.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">21. Kenny L.M., Vigushin D.M., Al‑Nahhas A. et al. Quantification of cellular proliferation in tumor and normal tissues of patients with breast cancer by [18F] fluorothymidine-positron emission tomography imaging: evaluation of analytical methods. Cancer Res 2005;65:10104−12. 22. Pio B.S., Park C.K., Pietras R. et al. Usefulness of 3'‑[F18]fluoro-3'‑deoxythymidine with positron emission tomography in predicting breast cancer response to therapy. Mol Imaging Biol 2006;8:36−42.</mixed-citation><mixed-citation xml:lang="ru">Kenny L.M., Vigushin D.M., Al‑Nahhas A. et al. Quantification of cellular proliferation in tumor and normal tissues of patients with breast cancer by [18F] fluorothymidine-positron emission tomography imaging: evaluation of analytical methods. Cancer Res 2005;65:10104−12. 22. Pio B.S., Park C.K., Pietras R. et al. Usefulness of 3'‑[F18]fluoro-3'‑deoxythymidine with positron emission tomography in predicting breast cancer response to therapy. Mol Imaging Biol 2006;8:36−42.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">23. Herrmann K., Buck A.K., Schuster T. et al. A pilot study to evaluate 3'‑deoxy- 3'‑18F‑fluorothymidine pet for initial and early response imaging in mantle cell lymphoma. J Nucl Med 2011;52:1898−902.</mixed-citation><mixed-citation xml:lang="ru">Herrmann K., Buck A.K., Schuster T. et al. A pilot study to evaluate 3'‑deoxy- 3'‑18F‑fluorothymidine pet for initial and early response imaging in mantle cell lymphoma. J Nucl Med 2011;52:1898−902.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">24. Machulla H.J., Blocher A., Kuntzsch M. et al. Simplified labeling approach for synthesizing 3'‑deoxy-3'‑[18F]fluorothymidine ([18F]FLT). J Radioanal Nucl Chem 2000;243:843−6.</mixed-citation><mixed-citation xml:lang="ru">Machulla H.J., Blocher A., Kuntzsch M. et al. Simplified labeling approach for synthesizing 3'‑deoxy-3'‑[18F]fluorothymidine ([18F]FLT). J Radioanal Nucl Chem 2000;243:843−6.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">25. Meignan M., Gallamini A., Meignan M. et al. Report on the First International Workshop on Interim-PET-Scan in Lymphoma. Leuk Lymphoma 2009; 50:1257−60.</mixed-citation><mixed-citation xml:lang="ru">Meignan M., Gallamini A., Meignan M. et al. Report on the First International Workshop on Interim-PET-Scan in Lymphoma. Leuk Lymphoma 2009; 50:1257−60.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">26. Cheson B.D., Horning S.J., Coiffier B. et al. Report of an international workshop to standardize response criteria for non‑Hodgkin's lymphomas. NCI Sponsored International Working Group. J Clin Oncol 1999;17:1244.</mixed-citation><mixed-citation xml:lang="ru">Cheson B.D., Horning S.J., Coiffier B. et al. Report of an international workshop to standardize response criteria for non‑Hodgkin's lymphomas. NCI Sponsored International Working Group. J Clin Oncol 1999;17:1244.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">27. Terasawa T., Lau J., Bardet S. et al. Fluorine-18-fluorodeoxyglucose positron emission tomography for interim response assessment of advanced-stage Hodgkin's lymphoma and diffuse large B‑cell lymphoma: a systematic review. J Clin Oncol 2009;27:1906−14.</mixed-citation><mixed-citation xml:lang="ru">Terasawa T., Lau J., Bardet S. et al. Fluorine-18-fluorodeoxyglucose positron emission tomography for interim response assessment of advanced-stage Hodgkin's lymphoma and diffuse large B‑cell lymphoma: a systematic review. J Clin Oncol 2009;27:1906−14.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">28. Kostakoglu L., Goldsmith S.J., Leonard J.P. et al. FDG‑PET after 1 cycle of therapy predicts outcome in diffuse large cell lymphoma and classic Hodgkin disease. Cancer 2006;107:2678−87.</mixed-citation><mixed-citation xml:lang="ru">Kostakoglu L., Goldsmith S.J., Leonard J.P. et al. FDG‑PET after 1 cycle of therapy predicts outcome in diffuse large cell lymphoma and classic Hodgkin disease. Cancer 2006;107:2678−87.</mixed-citation></citation-alternatives></ref></ref-list></back></article>
