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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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1138021 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
- ^8 |% V; Z9 y# D2 {NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 / j) S7 F6 ?6 W
+ Author Affiliations
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5 n( ^- n! _: k0 t; R+ ?1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 4 {, g6 T0 f7 L0 m5 x/ `
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan & a5 ^1 C: V% B8 W2 G) t
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan " T8 e' w& u0 X5 j* C( [
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 5 [- Q) S6 @7 J$ P1 p
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
/ B# G8 E2 x$ v1 y; j/ N# k( Z6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
6 P- e! x* ]  f$ S7Kinki University School of Medicine, Osaka 589-8511, Japan 1 C& |. g7 D. h( u5 A$ i
8Izumi Municipal Hospital, Osaka 594-0071, Japan 2 m/ n5 ~# q) c6 D
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
4 z( l! e/ [( n2 O3 D! ]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 ' u( n% u4 A) t/ u3 K  n
AbstractBackground: 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 5 M4 j2 R1 {0 ]1 E/ W$ z* G& g

  q) P! E% h  k4 Q0 G5 m) f' _( ?5 YAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
1 H3 q$ H  H: y: R$ M7 ^, V* f% l2 }8 o0 A" `; F5 y: J
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
0 F3 k& a9 A0 Z& Z) d, J! P; i4 v
- \8 B5 n$ ^2 M* O. ~Published online on: Thursday, December 1, 2011   l7 @2 v% O2 X0 s, m/ p  p3 i4 x
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Doi: 10.3892/ol.2011.507 + B1 C% ]/ }7 Q  n+ G8 V+ r  L
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Pages: 405-410 ( v; p: D, F# c/ O* W

( ^9 C+ `. M/ X; a& S  V4 tAbstract:, d7 M, N+ V4 M# G/ u+ z! O
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.
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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 population1 J9 K$ x2 j: n) T8 K+ ^8 {1 b
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
* I+ T. A* W; |1 I: T+ `3 ~+ Author Affiliations
1 }& Z, O0 a. r7 L. `/ _1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 1 x" j4 e9 L& \& `/ A* D& W
2Department of Thoracic Surgery, Kyoto University, Kyoto - y7 F/ q. ?$ x' s. s" c
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 5 n& B- P5 u% }
&#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 5 d3 y3 t' U- w
Received September 3, 2010.
) f  [$ q! ], s7 JRevision received November 11, 2010. 7 D& o. h' @% n4 \7 n
Accepted November 17, 2010.
! d+ U9 q/ w' Y' Z( D# vAbstract7 a0 a1 ]# ~5 k5 D& x+ y! E
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. * X4 b: z3 \& H
Patients 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. / r& i0 z4 a, L7 ]* q, b
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.
- J7 m, B# l+ [! G0 RConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ! }. g; A. L8 U: `7 G- M
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。
, v9 Y  j/ m! V1 }$ `9 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?9 J1 \2 D$ L6 }9 q' e2 Y( c
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
- e* j4 e: ]9 u( W, h2 d4 j; zhttp://clinicaltrials.gov/ct2/show/NCT01523587
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% E1 m) a. |- JBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC! R$ w$ W* i/ n5 @+ A% F. S4 O* ]
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
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5 _/ R( D6 `7 ]2 e2 t5 P- {2 d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。
' M% M) `1 ]0 p+ `% q/ R+ [% c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

$ ?2 n+ f6 [% O/ l2 e没有副作用是第一追求,效果显著是第二追求。
: M  C7 T' G  Q" R不错。

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