TY - JOUR
T1 - Adherence to the guidelines and the pathological diagnosis of high-risk gastrointestinal stromal tumors in the real world
AU - The members of the STAR ReGISTry Study Group
AU - Nishida, Toshirou
AU - Sakai, Yoshiharu
AU - Takagi, Masakazu
AU - Ozaka, Masato
AU - Kitagawa, Yuko
AU - Kurokawa, Yukinori
AU - Masuzawa, Toru
AU - Naito, Yoichi
AU - Kagimura, Tatsuo
AU - Hirota, Seiichi
AU - Saito, Takuro
AU - Komatsu, Yoshito
AU - Kondo, Masato
AU - Hayashi, Tsutomu
AU - Gotoda, Naoto
AU - Takiguchi, Nobuhiro
AU - Maki, Atsuhiko
AU - Baba, Hideo
AU - Orita, Hajime
AU - Yabusaki, Hiroshi
AU - Chiguchi, Gaku
AU - Manaka, Dai
AU - Nabeshima, Kazuhito
AU - Akabane, Hiromitsu
AU - Ono, Koichi
AU - Wada, Norihito
AU - Kaji, Masahide
AU - Yoshida, Kazuhiro
AU - Takahashi, Ikuo
AU - Fujitani, Kazumasa
AU - Matsumoto, Sohei
AU - Tamamori, Yutaka
AU - Saito, Hiroaki
AU - Ueda, Shugo
AU - Yamamura, Masahiro
AU - Fujii, Hirofumi
AU - Yoshino, Shigefumi
AU - Suzuki, Akihiro
AU - Otsuji, Eigo
AU - Kawachi, Shigeyuki
AU - Takahashi, Tsuyoshi
AU - Muguruma, Kazuya
AU - Ishikawa, Suguru
AU - Mitsutsuji, Masaaki
AU - Takamori, Hiroshi
AU - Kaiho, Takashi
AU - Sako, Akihiro
AU - Ito, Seiji
AU - Mori, Masahiro
AU - Tokuhara, Makoto
N1 - Publisher Copyright:
© 2019, The Author(s).
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Background: A multidisciplinary approach based on guidelines and pathological diagnosis by specialized pathologists are important for improving the prognosis and QoL of GIST patients. This study examined the adherence to the guidelines and the concordance of the pathological diagnosis of high-risk GISTs. Patients and methods: Among 541 patients with high-risk GISTs recruited to the prospective registry between Dec. 2012 and Dec. 2015, 534 patients were analyzed after central pathology with KIT and DOG1 IHC and genotyping of KIT and PDGFRA. Results: Of the 534 patients, 432 (81%) received imatinib adjuvant therapy at a starting dose of 400 or 300 mg/day. Multivariate analysis indicated that age (HR 0.71; 95% CI 0.58–0.88), tumor size (HR for > 10 cm vs < 5 cm, 3.87; 95% CI 1.72–8.74), mitosis (HR for > 10 vs < 5, 3.54; 95% CI 1.84–6.79), tumor rupture (HR 3.69; 95% CI 1.43–9.52) and performance status (HR 0.55; 95% CI 0.31–0.99) were independently related to adjuvant therapy. Among the 534 high-risk GISTs diagnosed locally, 19 tumors (3.6%) were diagnosed as non-GISTs, and the other 93 (18.1%) GISTs were reclassified into lower risk categories by central pathology. Among 10 patients with non-GISTs and 8 patients with PDGFRA D842V mutations, 4 (40%) and 3 (38%) patients, respectively, continued the therapy after receiving the central pathology results. Conclusions: The adherence to guidelines and the concordance of pathological diagnoses were comparatively good for high-risk GISTs. Central pathology may contribute to improved diagnosis, but further refinements may be required.
AB - Background: A multidisciplinary approach based on guidelines and pathological diagnosis by specialized pathologists are important for improving the prognosis and QoL of GIST patients. This study examined the adherence to the guidelines and the concordance of the pathological diagnosis of high-risk GISTs. Patients and methods: Among 541 patients with high-risk GISTs recruited to the prospective registry between Dec. 2012 and Dec. 2015, 534 patients were analyzed after central pathology with KIT and DOG1 IHC and genotyping of KIT and PDGFRA. Results: Of the 534 patients, 432 (81%) received imatinib adjuvant therapy at a starting dose of 400 or 300 mg/day. Multivariate analysis indicated that age (HR 0.71; 95% CI 0.58–0.88), tumor size (HR for > 10 cm vs < 5 cm, 3.87; 95% CI 1.72–8.74), mitosis (HR for > 10 vs < 5, 3.54; 95% CI 1.84–6.79), tumor rupture (HR 3.69; 95% CI 1.43–9.52) and performance status (HR 0.55; 95% CI 0.31–0.99) were independently related to adjuvant therapy. Among the 534 high-risk GISTs diagnosed locally, 19 tumors (3.6%) were diagnosed as non-GISTs, and the other 93 (18.1%) GISTs were reclassified into lower risk categories by central pathology. Among 10 patients with non-GISTs and 8 patients with PDGFRA D842V mutations, 4 (40%) and 3 (38%) patients, respectively, continued the therapy after receiving the central pathology results. Conclusions: The adherence to guidelines and the concordance of pathological diagnoses were comparatively good for high-risk GISTs. Central pathology may contribute to improved diagnosis, but further refinements may be required.
KW - Adjuvant therapy
KW - Gastrointestinal stromal tumor
KW - Guidelines
KW - Multidisciplinary board
KW - Pathological diagnosis
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U2 - 10.1007/s10120-019-00966-4
DO - 10.1007/s10120-019-00966-4
M3 - Article
C2 - 31041650
AN - SCOPUS:85065223920
SN - 1436-3291
VL - 23
SP - 118
EP - 125
JO - Gastric Cancer
JF - Gastric Cancer
IS - 1
ER -