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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1178409 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type( k6 h" s5 z+ P+ u2 Z
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
/ x! d+ z9 ]  B9 K) b+ Author Affiliations
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; l# }2 R& p2 f- l9 M: G1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
1 y2 Z, t, ?  f; S& n( m5 c2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
- z) S) [3 e' ~  O3 Q; J$ R" [3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan # n) I' Y& x& @
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 9 S! B& O) `+ [5 d
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 7 \$ y0 u5 ]# u4 |0 T4 P: {3 M* @! G3 s
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
+ y1 E# H8 U) j& a7 c  [7Kinki University School of Medicine, Osaka 589-8511, Japan
$ K' b/ T8 Q0 I/ f8Izumi Municipal Hospital, Osaka 594-0071, Japan + w( M2 W; @9 k1 |2 X
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan - c; D1 |  l; [
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
6 j, y7 V4 i% j7 h& G/ sAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
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3 y7 R) l' i/ s# CAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
' p' [. Z( X+ \' M5 l  m4 X. j( F7 M6 q8 k: T/ @& _$ G
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ) R1 t! f5 Q2 `4 A7 ]& @

# T5 e1 a8 W0 t0 s( ?Published online on: Thursday, December 1, 2011
) ], ?0 |+ u. q& }& D- G! C' \; E
Doi: 10.3892/ol.2011.507
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Pages: 405-410 ) R$ ~4 v+ ?# w
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Abstract:* W( Y7 x  B/ m& _0 R
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.9 O  X; f8 N  U7 m; R" _5 J/ w

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population0 r' ~- h. J- \8 t: W, \, ?
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 / ~% I% F1 v% H! s
+ Author Affiliations5 ^; x4 O9 P: Y
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
" A3 V' H+ r/ O6 a3 \! S2Department of Thoracic Surgery, Kyoto University, Kyoto - M! C0 ?3 m: v& \1 }# `
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
9 b/ Q4 A* L; y* R&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp % k/ y; b5 G% {  m, ]8 F; z" k
Received September 3, 2010.
- S- z! c6 R4 {# G* B' Y% YRevision received November 11, 2010.
+ K* `& e4 o1 \- qAccepted November 17, 2010. 7 J. w" W' S/ R- p1 s  K) _- D1 u  C
Abstract- U. G* O1 W/ a: A0 a- J) g6 o2 t1 `* O
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
" r/ i3 r0 c7 I, W( bPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 7 B/ S+ `8 o+ `. b- W; ^
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. + h' p$ U. c: U0 f. n( @- v3 f( t
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 9 o+ |' I' J! A! Y7 q$ q
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。5 W/ R; F# J# C" I2 K, k
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?/ |" w4 Q/ T7 X3 i3 c+ i
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
4 ~0 E6 h  H$ {http://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC+ Z) t) A* U/ D' |( @: i
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 ! k3 {2 L/ O# t7 b2 O

- s. }# a1 [0 R8 E( i从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。) O! j. \/ U8 M, u
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 ) n3 e" H) U& S$ F3 B1 [/ `
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
4 b* h' ^/ O- p5 K  I! E至今为止,未出 ...

# l% G+ I7 @  C没有副作用是第一追求,效果显著是第二追求。$ v$ W2 _5 K7 q' o
不错。

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