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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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1206590 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
# t1 R( n0 i6 W# n0 PNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
; ?3 N/ u* A$ ~9 G' K) G+ Author Affiliations
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; x) H+ W9 E( u( l6 P0 ]) W% o1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 5 O8 S5 C# W% J/ E+ l& M5 L
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan : N- ^* O( l) i1 M6 K' I
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; e0 ?* I& s% y2 ^) s! S  J; g
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan % |1 C) z5 Z; R4 H* q1 _5 ?1 \
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan % h9 J1 \( g; h3 R) M. O
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan % T2 |& O' D( H  U+ j& c
7Kinki University School of Medicine, Osaka 589-8511, Japan
  g" U! c. L% c! u" u: V8Izumi Municipal Hospital, Osaka 594-0071, Japan + f( o8 F2 j8 v* ~: A  S; N+ {9 y
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
6 Q3 U! h/ `2 d! a# f! JCorrespondence 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 * f* u9 Y9 H; g6 V/ i
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
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/ F  f0 X. o0 T9 ?/ w7 uAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 5 U* h1 @2 H  b9 B2 ^2 ]0 X' v6 y
$ J9 S" W' U4 J4 ~' m/ O  p
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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# p. B1 r- w. X2 ]) T7 pPublished online on: Thursday, December 1, 2011
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% m: l2 \: F+ K* K* e& h2 DDoi: 10.3892/ol.2011.507 % }* q7 O8 q( Q6 F
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Pages: 405-410 2 e  \; I% i! Y$ k7 Q, U9 m. E
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Abstract:
. u( f3 R. l6 M5 R3 ?: d5 \. eS-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.4 _# v- \: ~1 M$ h

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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 population
7 A7 `3 m, z2 S% L0 I& ]4 YF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
1 o/ _- O$ Y/ q" S1 G8 v+ Author Affiliations, t0 L) u4 M5 Z& k9 A  B* Q0 i: w
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
( P( ~# p& G+ q2Department of Thoracic Surgery, Kyoto University, Kyoto
) i% }# b9 f/ l5 k3 o4 t3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan & v: N, d6 N# z% i) h1 }5 ]
&#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
% z+ s# S6 Y3 ]6 U/ y0 p; M5 |0 NReceived September 3, 2010. 7 X* v6 X7 s! m2 e$ R4 Z& f; ]
Revision received November 11, 2010.
. [1 N/ d' F0 P8 u- bAccepted November 17, 2010.
% S% [1 ?# ~# C5 `7 L" g% S( jAbstract
7 N0 U; h2 S9 C9 h5 ?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. " j& g1 B5 l: |% W* p1 ^
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.
4 R7 |7 K+ j5 ^' Y( d! o0 u9 rResults: 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.
- @* B; J1 ]6 L4 y) GConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. " E- \' U! ^$ _7 h
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。
- Y) P5 @# B, F; f  ^0 q7 ?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?
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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
. d$ G% t5 v* C2 F0 {http://clinicaltrials.gov/ct2/show/NCT01523587& {$ U- f3 O: k9 ~( X9 R8 l- W

# K/ ^; R* ^  Q, ~BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC* V0 E, r" e7 x! _  c; Q  c6 {. A
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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3 V! Y8 W2 f( d% |! U7 E1 o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。9 S' ]- J' X# P6 E+ g0 B/ s
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

3 \- B* r1 s" d+ r没有副作用是第一追求,效果显著是第二追求。
* k7 z5 i4 f5 v不错。

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